Modified transferrin fusion proteins comprising duplicate transferrin amino or carboxy terminal domains

FIELD OF THE INVENTION

The present invention relates to therapeutic proteins or peptides with extended serum stability and/or in vivo circulatory half-life, particularly to therapeutic proteins or peptides fused to or inserted in a transferrin molecule modified to reduce or inhibit glycosylation, iron binding and/or transferrin receptor binding.

BACKGROUND OF THE INVENTION

Therapeutic proteins or peptides in their native state or when recombinantly produced are typically labile molecules exhibiting short periods of serum stability or short in vivo circulatory half-lives. In addition, these molecules are often extremely labile when formulated, particularly when formulated in aqueous solutions for diagnostic and therapeutic purposes.

Few practical solutions exist to extend or promote the stability in vivo or in vitro of proteinaceous therapeutic molecules. Polyethylene glycol (PEG) is a substance that can be attached to a protein, resulting in longer-acting, sustained activity of the protein. If the activity of a protein is prolonged by the attachment to PEG, the frequency that the protein needs to be administered may be decreased. PEG attachment, however, often decreases or destroys the protein's therapeutic activity. While in some instance PEG attachment can reduce immunogenicity of the protein, in other instances it may increase immunogenicity.

Therapeutic proteins or peptides have also been stabilized by fusion to a protein capable of extending the in vivo circulatory half-life of the therapeutic protein. For instance, therapeutic proteins fused to albumin or to antibody fragments may exhibit extended in vivo circulatory half-life when compared to the therapeutic protein in the unfused state. See U.S. Pat. Nos. 5,876,969 and 5,766,883.

Another serum protein, glycosylated human transferrin (Tf) has also been used to make fusions with therapeutic proteins to target delivery to the interior of cells or to carry agents across the blood-brain barrier. These fusion proteins comprising glycosylated human Tf have been used to target nerve growth factor (NGF) or ciliary neurotrophic factor (CNTF) across the blood-brain barrier by fusing full-length Tf to the agent. See U.S. Pat. Nos. 5,672,683 and 5977,307. In these fusion proteins, the Tf portion of the molecule is glycosylated and binds to two atoms of iron, which is required for Tf binding to its receptor on a cell and, according to the inventors of these patents, to target delivery of the NGF or CNTF moiety across the blood-brain barrier. Transferrin fusion proteins have also been produced by inserting an HIV-1 protease target sequence into surface exposed loops of glycosylated transferrin to investigate the ability to produce another form of Tf fusion for targeted delivery to the inside of a cell via the Tf receptor (Ali et al. (1999) J. Biol. Chem. 274(34):24066-24073).

Serum transferrin (Tf) is a monomeric glycoprotein with a molecular weight of 80,000 daltons that binds iron in the circulation and transports it to various tissues via the transferrin receptor (TfR) (Aisen et al. (1980) Ann. Rev. Biochem. 49: 357-393; MacGillivray et al. (1981) J. Biol. Chem. 258: 3543-3553, U.S. Pat. No. 5,026,651). Tf is one of the most common serum molecules, comprising up to about 5-10% of total serum proteins. Carbohydrate deficient transferrin occurs in elevated levels in the blood of alcoholic individuals and exhibits a longer half life (approximately 14-17 days) than that of glycosylated transferrin (approximately 7-10 days). See van Eijk et al. (1983) Clin. Chim. Acta 132:167-171, Stibler (1991) Clin. Chem. 37:2029-2037 (1991), Arndt (2001) Clin. Chem. 47(1):13-27 and Stibler et al. in “Carbohydrate-deficient consumption”, Advances in the Biosciences, (Ed Nordmann et al.), Pergamon, 1988, Vol. 71, pages 353-357).

The structure of Tf has been well characterized and the mechanism of receptor binding, iron binding and release and carbonate ion binding have been elucidated (U.S. Pat. Nos. 5,026,651, 5,986,067 and MacGillivray et al. (1983) J. Biol. Chem. 258(6):3543-3546).

Transferrin and antibodies that bind the transferrin receptor have also been used to deliver or carry toxic agents to tumor cells as cancer therapy (Baselga and Mendelsohn, 1994), and transferrin has been used as a non-viral gene therapy vector to deliver DNA to cells (Frank et al., 1994; Wagner et al., 1992). The ability to deliver proteins to the central nervous system (CNS) using the transferrin receptor as the entry point has been demonstrated with several proteins and peptides including CD4 (Walus et al., 1996), brain derived neurotrophic factor (Pardridge et al., 1994), glial derived neurotrophic factor (Albeck et al.), a vasointestinal peptide analogue (Bickel et al., 1993), a beta-amyloid peptide (Saito et al., 1995), and an antisense oligonucleotide (Pardridge et al., 1995).

Transferrin fusion proteins have not, however, been modified or engineered to extend the in vivo circulatory half-life of a therapeutic protein nor peptide or to increase bioavailability by reducing or inhibiting glycosylation of the Tf moiety nor to reduce or prevent iron and/or Tf receptor binding.

SUMMARY OF THE INVENTION

As described in more detail below, the present invention includes modified Tf fusion proteins comprising at least one therapeutic protein, polypeptide or peptide entity, wherein the Tf portion or moiety is engineered to comprise at least two N domains from native or wild-type transferrin, at least two modified C domains or one N and one C domain, wherein the C domain has been modified to function substantially like an N domain. The invention also includes pharmaceutical formulations and compositions comprising the fusion proteins, methods of extending the serum stability, in vivo circulatory half-life and bioavailability of a therapeutic protein by fusion to modified transferrin, nucleic acid molecules encoding the modified Tf fusion proteins, and the like. Another aspect of the present invention relates to methods of treating a patient with a modified Tf fusion protein.

DETAILED DESCRIPTION

General Description

It has been discovered that a therapeutic protein (e.g., a polypeptide, antibody, or peptide, or fragments and variants thereof) can be stabilized to extend the in vivo circulatory half-life and/or retain the therapeutic protein's activity for extended periods of time in vivo by genetically fusing or chemically conjugating the therapeutic protein, polypeptide or peptide to a modified transferrin comprising at least two N domains from native or wild-type transferrin, at least two modified C domains or one N and one C domain, wherein the C domain has been modified to function substantially like and N domain. The modified transferrin fusion proteins include a transferrin protein or domain covalently linked to, a therapeutic protein or peptide, wherein the transferrin portion is modified to contain one or more amino acid substitutions, insertions or deletions compared to a wild-type transferrin sequence. In one embodiment, Tf fusion proteins are engineered to reduce or prevent glycosylation within the Tf or a Tf domain. In other embodiments, the Tf protein or Tf domain(s) is modified to exhibit reduced or no binding to iron or carbonate ion, or to have a reduced affinity or not bind to a Tf receptor (TfR).

The present invention therefore includes transferrin fusion proteins, therapeutic compositions comprising the fusion proteins, and methods of treating, preventing, or ameliorating diseases or disorders by administering the fusion proteins. A transferrin fusion protein of the invention includes at least a fragment or variant of a therapeutic protein and at least a fragment or variant of modified transferrin, which are associated with one another, preferably by genetic fusion (i.e., the transferrin fusion protein is generated by translation of a nucleic acid in which a polynucleotide encoding all or a portion of a therapeutic protein is joined in-frame with a polynucleotide encoding all or a portion of modified transferrin) or chemical conjugation to one another. The therapeutic protein and transferrin protein, once part of the transferrin fusion protein, may be referred to as a “portion”, “region” or “moiety” of the transferrin fusion protein (e.g., a “therapeutic protein portion’ or a “transferrin protein portion”).

In one embodiment, the invention provides a transferrin fusion protein comprising, or alternatively consisting of, a therapeutic protein and a modified serum transferrin protein. In other embodiments, the invention provides a transferrin fusion protein comprising, or alternatively consisting of, a biologically active and/or therapeutically active fragment of a therapeutic protein and a modified transferrin protein. In other embodiments, the invention provides a transferrin fusion protein comprising, or alternatively consisting of, a biologically active and/or therapeutically active variant of a therapeutic protein and modified transferrin protein. In further embodiments, the invention provides a transferrin fusion protein comprising a therapeutic protein, and a biologically active and/or therapeutically active fragment of modified transferrin. In another embodiment, the therapeutic protein portion of the transferrin fusion protein is the active form of the therapeutic protein.

Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although any methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, the preferred methods and materials are described.

DEFINITIONS

As used herein, the term “biological activity” refers to a function or set of activities performed by a therapeutic molecule, protein or peptide in a biological context (i.e., in an organism or an in vitro facsimile thereof). Biological activities may include but are not limited to the functions of the therapeutic molecule portion of the claimed fusion proteins, such as, but not limited to, the induction of extracellular matrix secretion from responsive cell lines, the induction of hormone secretion, the induction of chemotaxis, the induction of mitogenesis, the induction of differentiation, or the inhibition of cell division of responsive cells. A fusion protein or peptide of the invention is considered to be biologically active if it exhibits one or more biological activities of its therapeutic protein's native counterpart.

As used herein, an “amino acid corresponding to” or an “equivalent amino acid” in a transferrin sequence is identified by alignment to maximize the identity or similarity between a first transferrin sequence and at least a second transferrin sequence. The number used to identify an equivalent amino acid in a second transferrin sequence is based on the number used to identify the corresponding amino acid in the first transferrin sequence. In certain cases, these phrases may be used to describe the amino acid residues in human transferrin compared to certain residues in rabbit serum transferrin.

As used herein, the terms “fragment of a Tf protein” or “Tf protein,” or “portion of a Tf protein” refer to an amino acid sequence comprising at least about 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 96%, 97%, 98%, 99% or 100% of a naturally occurring Tf protein or mutant thereof.

As used herein, the term “gene” refers to any segment of DNA associated with a biological function. Thus, genes include, but are not limited to, coding sequences and/or the regulatory sequences required for their expression. Genes can also include nonexpressed DNA segments that, for example, form recognition sequences for other proteins. Genes can be obtained from a variety of sources, including cloning from a source of interest or synthesizing from known or predicted sequence information, and may include sequences designed to have desired parameters.

As used herein, a “heterologous polynucleotide” or a “heterologous nucleic acid” or a “heterologous gene” or a “heterologous sequence” or an “exogenous DNA segment” refers to a polynucleotide, nucleic acid or DNA segment that originates from a source foreign to the particular host cell, or, if from the same source, is modified from its original form. A heterologous gene in a host cell includes a gene that is endogenous to the particular host cell, but has been modified. Thus, the terms refer to a DNA segment which is foreign or heterologous to the cell, or homologous to the cell but in a position within the host cell nucleic acid in which the element is not ordinarily found. As an example, a signal sequence native to a yeast cell but attached to a human Tf sequence is heterologous.

As used herein, an “isolated” nucleic acid sequence refers to a nucleic acid sequence which is essentially free of other nucleic acid sequences, e.g., at least about 20% pure, preferably at least about 40% pure, more preferably about 60% pure, even more preferably about 80% pure, most preferably about 90% pure, and even most preferably about 95% pure, as detelrnied by agarose gel electrophoresis. For example, an isolated nucleic acid sequence can be obtained by standard cloning procedures used in genetic engineering to relocate the nucleic acid sequence from its natural location to a different site where it will be reproduced. The cloning procedures may involve excision and isolation of a desired nucleic acid fragment comprising the nucleic acid sequence encoding the polypeptide, insertion of the fragment into a vector molecule, and incorporation of the recombinant vector into a host cell where multiple copies or clones of the nucleic acid sequence will be replicated. The nucleic acid sequence may be of genomic, cDNA, RNA, semisynthetic, synthetic origin, or any combinations thereof.

As used herein, two or more DNA coding sequences are said to be “joined” or “fused” when, as a result of in-frame fusions between the DNA coding sequences, the DNA coding sequences are translated into a fusion polypeptide.

As used herein, the term “fusion” in reference to Tf fusions includes, but is not limited to, attachment of at least one therapeutic protein, polypeptide or peptide, preferably an antibody variable region, to the N-terminal end of Tf, attachment to the C-terminal end of Tf, insertion between any two amino acids within Tf, and/or replacement of a portion of Tf sequence such as the Tf loop.

“Modified transferrin” as used herein refers to a transferrin molecule that exhibits at least one modification of its amino acid sequence, compared to wildtype transferrin to produce a transferrin molecule comprising at least two N domains, at least two C domains or and N and a C domain, wherein the C domain has been modified so that it functions substantially like an N domain.

“Modified transferrin fusion protein” as used herein refers to a protein formed by the fusion of at least one molecule of modified transferrin (or a fragment or variant thereof) to at least one molecule of a therapeutic protein (or fragment or variant thereof).

As used herein, the terms “nucleic acid” or “polynucleotide” refer to deoxyribonucleotides or ribonucleotides and polymers thereof in either single- or double-stranded form. Unless specifically limited, the terms encompass nucleic acids containing analogues of natural nucleotides that have similar binding properties as the reference nucleic acid and are metabolized in a manner similar to naturally occurring nucleotides. Unless otherwise indicated, a particular nucleic acid sequence also implicitly encompasses conservatively modified variants thereof (e.g. degenerate codon substitutions) and complementary sequences as well as the sequence explicitly indicated. Specifically, degenerate codon substitutions may be achieved by generating sequences in which the third position of one or more selected (or all) codons is substituted with mixed-base and/or deoxyinosine residues (Batzer et al. (1991) Nucleic Acid Res. 19:5081; Ohtsuka et al. (1985) J. Biol. Chem. 260:2605-2608; Cassol et al. (1992); Rossolini et al. (1994) Mol. Cell. Probes 8:91-98). The term nucleic acid is used interchangeably with gene, cDNA, and mRNA encoded by a gene.

As used herein, a DNA segment is referred to as “operably linked” when it is placed into a functional relationship with another DNA segment. For example, DNA for a signal sequence is operably linked to DNA encoding a fusion protein of the invention if it is expressed as a preprotein that participates in the secretion of the fusion protein; a promoter or enhancer is operably linked to a coding sequence if it stimulates the transcription of the sequence. Generally, DNA sequences that are operably linked are contiguous, and in the case of a signal sequence or fusion protein both contiguous and in reading phase. However, enhancers need not be contiguous with the coding sequences whose transcription they control. Linking, in this context, is accomplished by ligation at convenient restriction sites or at adapters or linkers inserted in lieu thereof.

As used herein, the term “promoter” refers to a region of DNA involved in binding RNA polymerase to initiate transcription.

As used herein, the term “recombinant” refers to a cell, tissue or organism that has undergone transformation with a new combination of genes or DNA.

As used herein, a targeting entity, protein, polypeptide or peptide refers to a molecule that binds specifically to a particular cell type [normal (e.g., lymphocytes) or abnormal e.g., (cancer cell)] and therefore may be used to target a Tf fusion protein or compound (drug, or cytotoxic agent) to that cell type specifically.

As used herein, “therapeutic protein” refers to proteins, polypeptides, peptides or fragments or variants thereof, having one or more therapeutic and/or biological activities. Therapeutic proteins encompassed by the invention include but are not limited to proteins, polypeptides, peptides, antibodies, and biologics. The terms peptides, proteins, and polypeptides are used interchangeably herein. Additionally, the term “therapeutic protein” may refer to the endogenous or naturally occurring correlate of a therapeutic protein. By a polypeptide displaying a “therapeutic activity” or a protein that is “therapeutically active” is meant a polypeptide that possesses one or more known biological and/or therapeutic activities associated with a therapeutic protein such as one or more of the therapeutic proteins described herein or otherwise known in the art. As a non-limiting example, a “therapeutic protein” is a protein that is useful to treat, prevent or ameliorate a disease, condition or disorder. Such a disease, condition or disorder may be in humans or in a non-human animal, e.g., veterinary use.

As used herein, the term “transformation” refers to the transfer of nucleic acid (i.e., a nucleotide polymer) into a cell. As used herein, the term “genetic transformation” refers to the transfer and incorporation of DNA, especially recombinant DNA, into a cell.

As used herein, the term “transformant” refers to a cell, tissue or organism that has undergone transformation.

As used herein, the term “transgene” refers to a nucleic acid that is inserted into an organism, host cell or vector in a manner that ensures its function.

As used herein, the term “transgenic” refers to cells, cell cultures, organisms, bacteria, fungi, animals, plants, and progeny of any of the preceding, which have received a foreign or modified gene and in particular a gene encoding a modified Tf fusion protein by one of the various methods of transformation, wherein the foreign or modified gene is from the same or different species than the species of the organism receiving the foreign or modified gene.

“Variants or variant” refers to a polynucleotide or nucleic acid differing from a reference nucleic acid or polypeptide, but retaining essential properties thereof. Generally, variants are overall closely similar, and, in many regions, identical to the reference nucleic acid or polypeptide. As used herein, “variant” refers to a therapeutic protein portion of a transferrin fusion protein of the invention, differing in sequence from a native therapeutic protein but retaining at least one functional and/or therapeutic property thereof as described elsewhere herein or otherwise known in the art.

As used herein, the term “vector” refers broadly to any plasmid, phagemid or virus encoding an exogenous nucleic acid. The term is also be construed to include non-plasmid, non-phagemid and non-viral compounds which facilitate the transfer of nucleic acid into virions or cells, such as, for example, polylysine compounds and the like. The vector may be a viral vector that is suitable as a delivery vehicle for delivery of the nucleic acid, or mutant thereof, to a cell, or the vector may be a non-viral vector which is suitable for the same purpose. Examples of viral and non-viral vectors for delivery of DNA to cells and tissues are well known in the art and are described, for example, in Ma et al. (1997, Proc. Natl. Acad. Sci. U.S.A. 94:12744-12746). Examples of viral vectors include, but are not limited to, a recombinant vaccinia virus, a recombinant adenovirus, a recombinant retrovirus, a recombinant adeno-associated virus, a recombinant avian pox virus, and the like (Cranage et al., 1986, EMBO J. 5:3057-3063; International Patent Application No. WO94/17810, published Aug. 18, 1994; International Patent Application No. WO94/23744, published Oct. 27, 1994). Examples of non-viral vectors include, but are not limited to, liposomes, polyamine derivatives of DNA, and the like.

As used herein, the term “wild type” refers to a polynucleotide or polypeptide sequence that is naturally occurring.

Transferrin and Transferrin Modifications

Any transferrin may be used to make modified Tf fusion proteins of the invention. As an example, the wild-type human Tf (Tf) is a 679 amino acid protein of approximately 75 kDa (not accounting for glycosylation), with two main domains, N (about 330 amino acids) and C (about 340 amino acids), which appear to originate from a gene duplication. See GenBank accession numbers NM001063, XM002793, M12530, XM039845, XM 039847 and S95936 (www.ncbi.nlm.nih.gov/), all of which are herein incorporated by reference in their entirety, as well as SEQ ID NOS 1, 2 and 3. The two domains have diverged over time but retain a large degree of identity/similarity.

Each of the N and C domains is further divided into two subdomains, N1 and N2, C1 and C2. The function of Tf is to transport iron to the cells of the body. This process is mediated by the Tf receptor (TfR), which is expressed on all cells, particularly actively growing cells. TfR recognizes the iron bound form of Tf (two molecules of which are bound per receptor), endocytosis then occurs whereby the TfR/Tf complex is transported to the endosome, at which point the localized drop in pH results in release of bound iron and the recycling of the TfR/Tf complex to the cell surface and release of Tf (known as apoTf in its un-iron bound form). Receptor binding is through the C domain of Tf. The two glycosylation sites in the C domain do not appear to be involved in receptor binding as unglycosylated iron bound Tf does bind the receptor.

Each Tf molecule can carry two iron ions (Fe³⁺). These are complexed in the space between the N1 and N2, C1 and C2 sub domains resulting in a conformational change in the molecule. Tf crosses the blood brain barrier (BBB) via the Tf receptor.

In human transferrin, the iron binding sites comprise at least amino acids Asp 63 (Asp 82 of SEQ ID NO: 2 which includes the native Tf signal sequence), Asp 392 (Asp 411 of SEQ ID NO: 2), Tyr 95 (Tyr 114 of SEQ ID NO: 2), Tyr 426 (Tyr 445 of SEQ ID NO: 2), Tyr 188 (Tyr 207 of SEQ ID NO: 2), Tyr 514 or 517 (Tyr 533 or Tyr 536 SEQ ID NO: 2), His 249 (His 268 of SEQ ID NO: 2), and His 585 (His 604 of SEQ ID NO: 2) of SEQ ID NO: 3. The hinge regions comprise at least N domain amino acid residues 94-96, 245- 247 and/or 316-318 as well as C domain amino acid residues 425-427, 581-582 and/or 652-658 of SEQ ID NO: 3. The carbonate binding sites comprise at least amino acids Thr 120 (Thr 139 of SEQ ID NO: 2), Thr 452 (Thr 471 of SEQ ID NO: 2), Arg 124 (Arg 143 of SEQ ID NO: 2), Arg 456 (Arg 475 of SEQ ID NO: 2), Ala 126 (Ala 145 of SEQ ID NO: 2), Ala 458 (Ala 477 of SEQ ID NO: 2), Gly 127 (Gly 146 of SEQ ID NO: 2), and Gly 459 (Gly 478 of SEQ ID NO: 2) of SEQ ID NO: 3.

In one embodiment of the invention, the modified transferrin fusion protein includes a modified human transferrin, although any animal Tf molecule may be used to produce the fusion proteins of the invention, including human Tf variants, cow, pig, sheep, dog, rabbit, rat, mouse, hamster, echnida, platypus, chicken, frog, hornworm, monkey, as well as other bovine, canine and avian species. All of these Tf sequences are readily available in GenBank and other public databases. The human Tf nucleotide sequence is available (see SEQ ID NOS 1, 2 and 3 and the accession numbers described above and available at www.ncbi.nlm.nih.gov) and can be used to make genetic fusions between Tf or a domain of Tf and the therapeutic molecule of choice. Fusions may also be made from related molecules such as lacto transferrin (lactoferrin) GenBank Acc: NM_—002343) or melanotransferrin (GenBank Acc. NM_—013900, murine melanotransferrin).

Melanotransferrin is a glycosylated protein found at high levels in malignant melanoma cells and was originally named human melanoma antigen p97 (Brown et al., 1982, Nature, 296: 171-173). It possesses high sequence homology with human serum transferrin, human lactoferrin, and chicken transferrin (Brown et al., 1982, Nature, 296: 171-173; Rose et al., Proc. Natl. Acad. Sci. USA, 1986, 83: 1261-1265). However, unlike these receptors, no cellular receptor has been identified for melanotransferrin. Melanotransferrin reversibly binds iron and it exists in two forms, one of which is bound to cell membranes by a glycosyl phosphatidylinositol anchor while the other form is both soluble and actively secreted (Baker et al., 1992, FEBS Lett, 298: 215-218; Alemany et al., 1993, J. Cell Sci., 104: 1155-1162; Food et al., 1994, J. Biol. Chem. 274: 7011-7017).

Lactoferrin (Lf), a natural defense iron-binding protein, has been found to possess antibacterial, antimycotic, antiviral, antineoplastic and anti-inflammatory activity. The protein is present in exocrine secretions that are commonly exposed to normal flora: milk, tears, nasal exudate, saliva, bronchial mucus, gastrointestinal fluids, cervico-vaginal mucus and seminal fluid. Additionally, Lf is a major constituent of the secondary specific granules of circulating polymorphonuclear neutrophils (PMNs). The apoprotein is released on degranulation of the PMNs in septic areas. A principal function of Lf is that of scavenging free iron in fluids and inflamed areas so as to suppress free radical-mediated damage and decrease the availability of the metal to invading microbial and neoplastic cells. In a study that examined the turnover rate of ¹²⁵I Lf in adults, it was shown that Lf is rapidly taken up by the liver and spleen, and the radioactivity persisted for several weeks in the liver and spleen (Bennett et al. (1979), Clin. Sci. (Lond.) 57: 453-460).

In one embodiment, the transferrin portion of the transferrin fusion protein of the invention includes a transferrin splice variant. In one example, a transferrin splice variant can be a splice variant of human transferrin. In one specific embodiment, the human transferrin splice variant can be that of Genbank Accession AAA61140.

In another embodiment, the transferrin portion of the transferrin fusion protein of the invention includes a lactoferrin splice variant. In one example, a human serum lactoferrin splice variant can be a novel splice variant of a neutrophil lactoferrin. In one specific embodiment, the neutrophil lactoferrin splice variant can be that of Genbank Accession AAA59479. In another specific embodiment, the neutrophil lactoferrin splice variant can comprise the following amino acid sequence EDCIALKGEADA (SEQ ID NO: 8), which includes the novel region of splice-variance.

In another embodiment, the transferrin portion of the transferrin fusion protein of the invention includes a melanotransferrin variant.

Modified Tf fusions may be made with N or C domains from any Tf protein, fragment, domain, or engineered domain. For instance, fusion proteins may be produced using the full-length Tf sequence, with or without the native Tf signal sequence. Tf fusion proteins may also be made using a single Tf domain in duplicate, such as an individual N or C domain. In some embodiments, the use of a double N domain is advantageous as the Tf glycosylation sites reside in the C domain and the N domain, on its own, does not bind iron or the Tf receptor. In other embodiments, fusions of a therapeutic protein to a double C domain may be produced, wherein the C domain is altered to function like an N domain, for instance to reduce, inhibit or prevent glycosylation, iron binding and/or Tf receptor binding.

As used herein, a C terminal domain or lobe modified to function as an N-like domain is modified to exhibit glycosylation patterns or iron binding properties substantially like that of a native or wild-type N domain or lobe. In a preferred embodiment, the C domain or lobe is modified so that it is not glycosylated and does not bind iron by substitution of the relevant C domain regions or amino acids to those present in the corresponding regions or sites of a native or wild-type N domain.

As used herein, a Tf moiety comprising “two N domains or lobes” includes a Tf molecule that is modified to replace the native C domain or lobe with a second native or wild-type N domain or lobe or a modified N domain or lobe or contains a C domain that has been modified to function substantially like a wild-type or modified N domain.

Analysis of the two domains by overlay of the 3-dimensional structure of the two domains (Swiss PDB Viewer 3.7b2, Iterative Magic Fit) and by direct amino acid alignment (ClustalW multiple alignment) reveals that the two domains have diverged over time. Amino acid alignment shows 42% identity and 59% similarity between the two domains. However, approximately 80% of the N domain matches the C domain for structural equivalence. The C domain also has several extra disulfide bonds compared to the N domain.

Alignment of molecular models for the N and C domain reveals the following structural equivalents:

N 4-2436-72 94-136138-139149-164168-173178-198domain75-88200-214(1-330)C340-361365-415425-437470-471475-490492-497507-542domain439-468(340-679)N219-255259-260263-268271-275279-280283-288309-327domain290-304(1-330)C555-591593-594597-602605-609614-615620-640645-663domain(340-679)

The disulfide bonds for the two domains align as follows:

NCC339-C596C9-C48C345-C377C19-C39C355-C368C402-C674C418-C637C118-C194C450-C523C137-C331C474-C665C158-C174C484-C498C161-C179C171-C177C495-C506C227-C241C563-C577C615-C620
Bold aligned disulfide bonds

Italics bridging peptide

In one embodiment, the transferrin portion of the transferrin fusion protein includes at least two N terminal lobes of transferrin. In further embodiments, the transferrin portion of the transferrin fusion protein includes at least two N terminal lobes of transferrin derived from human serum transferrin.

In another embodiment, the transferrin portion of the transferrin fusion protein includes, comprises of consists of at least two N terminal lobes of transferrin having a mutation in at least one amino acid residue selected from the group consisting of Asp63, Gly65, Tyr95, Tyr188, and His249 of SEQ ID NO:3.

In another embodiment, the transferrin portion of the modified transferrin fusion protein includes a recombinant human serum transferrin N-terminal lobe mutant having a mutation at Lys206 or His207 of SEQ ID NO:3.

In another embodiment, the transferrin portion of the transferrin fusion protein includes, comprises or consists of at least two C terminal lobes of transferrin. In further embodiments, the transferrin portion of the transferrin fusion protein includes at least two C terminal lobes of transferrin derived from human serum transferrin.

In a further embodiment the C terminal lobe mutant further includes a mutation of at least one of Asn413 and Asn611 of SEQ ID NO:3 to an amino acid which does not allow glycosylation.

In another embodiment, the transferrin portion of the transferrin fusion protein includes at least two C terminal lobes of transferrin having a mutation in at least one amino acid residue selected from the group consisting of Asp392, Tyr426, Tyr514, Tyr517 and His585 of SEQ ID NO:3, wherein the mutant retains the ability to bind metal ions. In an alternate embodiment, the transferrin portion of the transferrin fusion protein includes at least two C terminal lobes of transferrin having a mutation in at least one amino acid residue selected from the group consisting of Tyr426, Tyr514, Tyr517 and His585 of SEQ ID NO: 3, wherein the mutant has a reduced ability to bind metal ions. In another embodiment, the transferrin portion of the transferrin fusion protein includes at least two C terminal lobes of transferrin having a mutation in at least one amino acid residue selected from the group consisting of Asp392, Tyr426, Tyr517 and His585 of SEQ ID NO:3, wherein the mutant does not retain the ability to bind metal ions and functions substantially like and N domain.

In some embodiments, the Tf or Tf portion will be of sufficient length to increase the in vivo circulatory half-life in vitro solution stability, stability in serum, or bioavailability of the therapeutic protein compared to the in vivo circulatory half-life in vitro solution stability, stability in serum, or bioavailability of the therapeutic protein in an unfused state. Such an increase in in vivo circulatory half-life in vitro solution stability, stability in serum, or bioavailability may be about a 30%, 50%, 70%, 80%, 90% or more increase over the unfused therapeutic protein. In some cases, the modified transfenin fusion proteins exhibit a serum half-life of about 10-20 or more days, about 12-18 days or about 14-17 days.

When the C domain of Tf is part of the fusion protein, the two N-linked glycosylation sites, amino acid residues corresponding to N413 and N611 of SEQ ID NO:3 may be mutated for expression in a yeast system to prevent glycosylation or hypermannosylationn and extend the in vivo circulatory half-life of the fusion protein and/or therapeutic protein (to produce asialo-, or in some instances, monosialo-Tf or disialo-Tf). In addition to Tf amino acids corresponding to N413 and N611, mutations may be to the adjacent residues within the N—X—S/T glycosylation site to prevent or substantially reduce glycosylation. See U.S. Pat. No. 5,986,067 of Funk et al. It has also been reported that the N domain of Tf expressed in Pichia pastoris is becomes O-linked glycosylated with a single hexose at S32 which also may be mutated or modified to prevent such glycosylation. Moreover, O-linked glycosylation may be reduced or eliminated in a yeast host cell with mutations in the PMT genes.

Accordingly, in one embodiment of the invention, the transferrin fusion protein includes a modified transferrin molecule wherein the transferrin exhibits reduced glycosylation, including but not limited to asialo- monosialo- and disialo- forms of Tf. In another embodiment, the transferrin portion of the transferrin fusion protein includes a recombinant transferrin mutant that is mutated to prevent glycosylation. In another embodiment, the transferrin portion of the transferrin fusion protein includes a recombinant transferrin mutant that is fully glycosylated. In a further embodiment, the transferrin portion of the transferrin fusion protein includes a recombinant human serum transferrin mutant that is mutated to prevent glycosylation, wherein at least one of Asn413 and Asn6 11 of SEQ ID NO:3 are mutated to an amino acid which does not allow glycosylation. In another embodiment, the transferrin portion of the transferrin fusion protein includes a recombinant human serum transferrin mutant that is mutated to prevent or substantially reduce glycosylation, wherein mutations may be to the adjacent residues within the N—X—S/T glycosylation site. Moreover, glycosylation may be reduced or prevented by mutating the serine or threonine residue. Further, changing the X to proline is known to inhibit glycosylation.

As discussed below in more detail, modified Tf fusion proteins comprising a C domain of the invention may also be engineered to not bind iron and/or not bind the Tf receptor. In other embodiments of the invention, the iron binding is retained and the iron binding ability of Tf may be used in two ways, one to deliver a therapeutic protein or peptide(s) to the inside of a cell and/or across the BBB. These embodiments that bind iron and/or the Tf receptor will often be engineered to reduce or prevent glycosylation to extend the serum half-life of the therapeutic protein. The N domain alone will not bind to TfR when loaded with iron, and the iron bound C domain will bind TfR but not with the same affinity as the whole molecule.

In another embodiment, the transferrin portion of the transferrin fusion protein includes a recombinant transferrin mutant having a mutation wherein the mutant does not retain the ability to bind metal ions. In an alternate embodiment, the transferrin portion of the transferrin fusion protein includes a recombinant transferrin mutant having a mutation wherein the mutant has a weaker binding avidity for metal ions than wild-type serum transferrin. In an alternate embodiment, the transferrin portion of the transferrin fusion protein includes a recombinant transferrin mutant having a mutation wherein the mutant has a stronger binding avidity for metal ions than wild-type serum transferrin.

In another embodiment, the transferrin portion of the transferrin fusion protein includes a recombinant transferrin mutant having a mutation wherein the mutant does not retain the ability to bind to the transferrin receptor. In an alternate embodiment, the transferrin portion of the transferrin fusion protein includes a recombinant transferrin mutant having a mutation wherein the mutant has a weaker binding avidity for the transferrin receptor than wild-type serum transferrin. In an alternate embodiment, the transferrin portion of the transferrin fusion protein includes a recombinant transferrin mutant having a mutation wherein the mutant has a stronger binding avidity for the transferrin receptor than wild-type serum transferrin.

In another embodiment, the transferrin portion of the transferring fusion protein includes a recombinant transferrin mutant having a mutation wherein the mutant does not retain the ability to bind to carbonate ions. In an alternate embodiment, the transferrin portion of the transferrin fusion protein includes a recombinant transferrin mutant having a mutation wherein the mutant has a weaker binding avidity for carbonate ions than wild-type serum transferrin. In an alternate embodiment, the transferrin portion of the transferrin fusion protein includes a recombinant transferrin mutant having a mutation wherein the mutant has a stronger binding avidity for carbonate ions than wild-type serum transferrin.

In another embodiment, the transferrin portion of the transferrin fusion protein includes a recombinant human serum transferrin mutant having a mutation in at least one amino acid residue selected from the group consisting of Asp63, Gly65, Tyr95, Tyr188, His249, Asp392, Tyr426, Tyr514, Tyr517 and His585 of SEQ ID NO:3, wherein the mutant retains the ability to bind metal ions. In an alternate embodiment, a recombinant human serum transferrin mutant having a mutation in at least one amino acid residue selected from the group consisting of Asp63, Gly65, Tyr95, Tyr188, His249, Asp392, Tyr426, Tyr514, Tyr517 and His585 of SEQ ID NO:3, wherein the mutant has a reduced ability to bind metal ions. In another embodiment, a recombinant human serum transferrin mutant having a mutation in at least one amino acid residue selected from the group consisting of Asp63, Gly65, Tyr95, Tyr188, His249, Asp392, Tyr426, Tyr517 and His585 of SEQ ID NO:3, wherein the mutant does not retain the ability to bind metal ions.

In another embodiment, the transferrin portion of the transferrin fusion protein includes a recombinant human serum transferrin mutant having a mutation at Lys206 or His207 of SEQ ID NO:3, wherein the mutant has a stronger binding avidity for metal ions than wild-type human serum transferrin (see U.S. Pat. No. 5,986,067, which is herein incorporated by reference in its entirety). In an alternate embodiment, the transferrin portion of the transferrin fusion protein includes a recombinant human serum transferrin mutant having a mutation at Lys206 or His207 of SEQ ID NO:3, wherein the mutant has a weaker binding avidity for metal ions than wild-type human serum transferrin. In a further embodiment, the transferrin portion of the transferrin fusion protein includes a recombinant human serum transferrin mutant having a mutation at Lys206 or His207 of SEQ ID NO:3, wherein the mutant does not bind metal ions.

Any available technique may be used to make the fusion proteins of the invention, including but not limited to molecular techniques commonly available, for instance, those disclosed in Sambrook et al. Molecular Cloning: A Laboratory Manual, 2nd Ed., Cold Spring Harbor Laboratory Press, 1989. When carrying out nucleotide substitutions using techniques for accomplishing site-specific mutagenesis that are well known in the art, the encoded amino acid changes are preferably of a minor nature, that is, conservative amino acid substitutions, although other, non-conservative, substitutions are contemplated as well, particularly when producing a modified transferrin portion of a Tf fusion protein, e.g., a modified Tf fusion protein exhibiting reduced glycosylation, reduced iron binding and the like. Specifically contemplated are amino acid substitutions, small deletions or insertions, typically of one to about 30 amino acids; insertions between transferrin domains; small amino- or carboxyl-terminal extensions, such as an amino-terminal methionine residue, or small linker peptides of less than 50, 40, 30, 20 or 10 residues between transferrin domains or linking a transferrin protein and a therapeutic protein or peptide; or a small extension that facilitates purification, such as a poly-histidine tract, an antigenic epitope or a binding domain.

Examples of conservative amino acid substitutions are substitutions made within the same group such as within the group of basic amino acids (such as arginine, lysine, histidine), acidic amino acids (such as glutamic acid and aspartic acid), polar amino acids (such as glutamine and asparagine), hydrophobic amino acids (such as leucine, isoleucine, valine), aromatic amino acids (such as phenylalanine, tryptophan, tyrosine) and small amino acids (such as glycine, alanine, serine, threonine, methionine).

Non-conservative substitutions encompass substitutions of amino acids in one group by amino acids in another group. For example, a non-conservative substitution would include the substitution of a polar amino acid for a hydrophobic amino acid. For a general description of nucleotide substitution, see e.g. Ford et al. (1991), Prot. Exp. Pur. 2: 95-107. Non-conservative substitutions, deletions and insertions are particularly useful to produce Tf fusion proteins of the invention that exhibit no or reduced binding of iron and/or no or reduced binding of the fusion protein to the Tf receptor.

In the polypeptide and proteins of the invention, the following system is followed for designating amino acids in accordance with the following conventional list:

TABLE OF AMINO ACIDSONE-LETTERTHREE-LETTERAMINO ACIDSYMBOLSYMBOLAlanineAAlaArginineRArgAsparagineNAsnAspartic AcidDAspCysteineCCysGlutamineQGlnGlutamic AcidEGluGlycineGGlyHistidineHHisIsoleucineIIleLeucineLLeuLysineKLysMethionineMMetPhenylalanineFPheProlinePProSerineSSerThreonineTThrTryptophanWTrpTyrosineYTyrValineVVal

Iron binding and/or receptor binding may be reduced or disrupted by mutation, including deletion, substitution or insertion into, amino acid residues corresponding to one or more of Tf N domain residues Asp63, Tyr95, Tyr188, His249 and/or C domain residues Asp 392, Tyr 426, Tyr 514 and/or His 585 of SEQ ID NO: 3. Iron binding may also be affected by mutation to amino acids Lys206, His207 or Arg632 of SEQ ID NO: 3. Carbonate binding may be reduced or disrupted by mutation, including deletion, substitution or insertion into, amino acid residues corresponding to one or more of Tf N domain residues Thr120, Arg124, Ala126, Gly 127 and/or C domain residues Thr 452, Arg 456, Ala 458 and/or Gly 459 of SEQ ID NO: 3. A reduction or disruption of carbonate binding may adversely affect iron and/or receptor binding.

Binding to the Tf receptor may be reduced or disrupted by mutation, including deletion, substitution or insertion into, amino acid residues corresponding to one or more of Tf N domain residues described above for iron binding.

As discussed above, glycosylation may be reduced or prevented by mutation, including deletion, substitution or insertion into, amino acid residues corresponding to one or more of Tf C domain residues around the N—X—S/T sites corresponding to C domain residues N413 and/or N611 (See U.S. Pat. No. 5,986,067). For instance, the N413 and/or N611 may be mutated to Glu residues.

The carbohydrates on the fusion protein may also be reduced or completely removed enzymatically by treating the fusion protein with deglycosylases. Deglycosylases are well known in the art. Examples of deglycosylases include but are not limited to galactosidase, PNGase A, PNGase F, glucosidase, mannosidase, fucosidase, and Endo H deglycosylase.

In instances where the Tf fusion proteins of the invention are not modified to prevent glycosylation, iron binding, carbonate binding and/or receptor binding, glycosylation, iron and/or carbonate ions may be stripped from or cleaved off of the fusion protein. For instance, available deglycosylases may be used to cleave glycosylation residues from the fusion protein, in particular the sugar residues attached to the Tf portion, yeast deficient in glycosylation enzymes may be used to prevent glycosylation and/or recombinant cells may be grown in the presence of an agent that prevents glycosylation, e.g., tunicamycin.

Additional mutations may be made with Tf to alter the three dimensional structure of Tf, such as modifications to the hinge region to prevent the conformational change needed for iron binding and Tf receptor recognition. For instance, mutations may be made in or around N domain amino acid residues 94-96, 245-247 and/or 316-318 as well as C domain amino acid residues 425-427, 581-582 and/or 652-658. In addition, mutations may be made in or around the flanking regions of these sites to alter Tf structure and function.

In one aspect of the invention, the transferrin fusion protein can function as a carrier protein to extend the half life or bioavailability of the therapeutic protein as well as, in some instances, delivering the therapeutic protein inside a cell and/or across the blood brain barrier. In an alternate embodiment, the transferrin fusion protein includes a modified transferrin molecule wherein the transferrin does not retain the ability to cross the blood brain barrier.

In another embodiment, the transferrin fusion protein includes a modified transferrin molecule wherein the transferrin molecule retains the ability to bind to the transferrin receptor and transport the therapeutic peptide inside cells. In an alternate embodiment, the transferrin fusion protein includes a modified transferrin molecule wherein the transferrin molecule does not retain the ability to bind to the transferrin receptor and transport the therapeutic peptide inside cells.

In further embodiments, the transferrin fusion protein includes a modified transferrin molecule wherein the transferrin molecule retains the ability to bind to the transferrin receptor and transport the therapeutic peptide inside cells and retains the ability to cross the blood brain barrier. In an alternate embodiment, the transferrin fusion protein includes a modified transferrin molecule wherein the transferrin molecule retains the ability to cross the blood brain barrier, but does not retain the ability to bind to the transferrin receptor and transport the therapeutic peptide inside cells.

Modified Transferrin Fusion Proteins

The fusion proteins of the invention may contain one or more copies of the therapeutic protein or polypeptide attached to the N-terminus and/or the C-terminus of the Tf moiety. In some embodiments, the therapeutic protein or polypeptide is attached to both the N- and C-terminus of the Tf moiety and the fusion protein may contain one or more equivalents of the therapeutic protein or polypeptide on either or both ends of Tf. In other embodiments, the therapeutic protein or polypeptide is inserted into known domains of the Tf protein, for instance, into one or more of the loops of Tf (see Ali et al. (1999) J. Biol. Chem. 274(34):24066-24073). In other embodiments, the therapeutic protein or therapeutic peptide is inserted between the N and C domains of Tf.

Generally, the transferrin fusion protein of the invention may have one modified transferrin-derived region and one therapeutic protein-derived region. Multiple regions of each protein, however, may be used to make a transferrin fusion protein of the invention. Similarly, more than one therapeutic protein may be used to make a transferrin fusion protein of the invention, thereby producing a multi-functional modified Tf fusion protein.

The present invention provides transferrin fusion protein containing a therapeutic protein or polypeptide or portion thereof fused to a transferrin molecule or portion thereof. In one embodiment, the transferrin fusion protein of the invention contains a therapeutic protein or polypeptide fused to the N terminus of a transferrin molecule. In an alternate embodiment, the transferrin fusion protein of the invention contains a therapeutic protein fused to the C terminus of a transferrin molecule. The present invention also provides transferrin fusion protein containing a therapeutic protein or polypeptide or protion thereof fused to a modified transferrin morlecule or portion thererof.

In other embodiments, the transferrin fusion protein of the inventions contains a therapeutic protein fused to both the N-terminus and the C-terminus of modified transferrin. In another embodiment, the therapeutic proteins fused at the N- and C- termini are the same therapeutic proteins. In an alternate embodiment, the therapeutic proteins fused at the N- and C-termini are different therapeutic proteins. In another alternate embodiment, the therapeutic proteins fused to the N- and C-termini are different therapeutic proteins which may be used to treat or prevent the same disease, disorder, or condition. In another embodiment, the therapeutic proteins fused to the N- and C-termini are different therapeutic proteins which may be used to treat or prevent diseases or disorders which are known in the art to commonly occur in patients simultaneously.

Additionally, transferrin fusion protein of the invention may also be produced by inserting the therapeutic protein or peptide of interest (e.g., a therapeutic protein or peptide as disclosed herein, or, for instance, a single chain antibody that binds a therapeutic protein or a fragment or variant thereof) into an internal region of the modified transferrin. Internal regions of modified transferrin include, but are not limited to, the iron binding sites, the hinge regions, the bicarbonate binding sites, or the receptor binding domain. There is also a proline near the N-terminus. In one aspect of the invention, the prolines at the N- and C-termini may be changed out. In another aspect of the invention, the C-terminal disulfide bond may e eliminated to untether the C-terminus.

Within the protein sequence of the modified transferrin molecule a number of loops or turns exist, which are stabilized by disulfide bonds. These loops are useful for the insertion, or internal fusion, of therapeutically active peptides, particularly those requiring a secondary structure to be functional, or therapeutic proteins, to generate a modified transferrin molecule with specific biological activity.

When therapeutic proteins or peptides are inserted into or replace at least one loop of a Tf molecule, insertions may be made within any of the surface exposed loop regions, in addition to other areas of Tf. For instance, insertions may be made within the loops comprising Tf amino acids 32-33, 74-75, 256-257, 279-280 and 288-289 (Ali et al., Supra). As previously described, insertions may also be made within other regions of Tf such as the sites for iron and bicarbonate binding, hinge regions, and the receptor binding domain as described in more detail below. The loops in the Tf protein sequence that are amenable to modification/replacement for the insertion of proteins or peptides may also be used for the development of a screenable library of random peptide inserts. Any procedures may be used to produce nucleic acid inserts for the generation of peptide libraries, including available phage and bacterial display systems, prior to cloning into a Tf domain and/or fusion to the ends of Tf.

The N-terminus of Tf is free and points away from the body of the molecule. Fusions of proteins or peptides on the N-terminus may therefore be a preferred embodiment. Such fusions may include a linker region, such as but not limited to a poly-glycine stretch, to separate the therapeutic protein or peptide from Tf. Attention to the junction between the leader sequence, the choice of leader sequence, and the structure of the mRNA by codon manipulation/optimization (no major stem loops to inhibit ribosome progress) will increase secretion and can be readily accomplished using standard recombinant protein techniques.

The C-terminus of Tf appears to be more buried and secured by a disulfide bond 6 amino acids from the C-terminus. In human Tf, the C-terminal amino acid is a proline which, depending on the way that it is orientated, will either point a fusion away or into the body of the molecule. A linker or spacer moiety at the C-terminus may be used in some embodiments of the invention. There is also a proline near the N-terminus. In one aspect of the invention, the proline at the N- and/or the C-termini may be changed out. In another aspect of the invention, the C-terminal disulfide bond may be eliminated to untether the C-terminus.

In yet other embodiments, small molecule therapeutics may be complexed with iron and loaded on a modified Tf protein fusion for delivery to the inside of cells and across the BBB. The addition of a targeting peptide or, for example, a single chain antibody (SCA) can be used to target the payload to a particular cell type, e.g., a cancer cell.

Nucleic Acids

Nucleic acid molecules are also provided by the present invention. These encode a modified Tf fusion protein comprising a transferrin protein or a portion of a transferrin protein covalently linked or joined to a therapeutic protein. As discussed in more detail below, any therapeutic protein may be used. The fusion protein may further comprise a linker region, for instance a linker less than about 50, 40, 30, 20, or 10 amino acid residues. The linker can be covalently linked to and between the transferrin protein or portion thereof and the therapeutic protein. Nucleic acid molecules of the invention may be purified or not.

Host cells and vectors for replicating the nucleic acid molecules and for expressing the encoded fusion proteins are also provided. Any vectors or host cells may be used, whether prokaryotic or eukaryotic, but eukaryotic expression systems, in particular yeast expression systems, may be preferred. Many vectors and host cells are known in the art for such purposes. It is well within the skill of the art to select an appropriate set for the desired application.

DNA sequences encoding transferrin, portions of transferrin and therapeutic proteins of interest may be cloned from a variety of genomic or cDNA libraries known in the art. The techniques for isolating such DNA sequences using probe-based methods are conventional techniques and are well known to those skilled in the art. Probes for isolating such DNA sequences may be based on published DNA or protein sequences (see, for example, Baldwin, G. S. (1993) Comparison of Transferrin Sequences from Different Species. Comp. Biochem. Physiol. 106B/1:203-218 and all references cited therein, which are hereby incorporated by reference in their entirety). Alternatively, the polymerase chain reaction (PCR) method disclosed by Mullis et al. (U.S. Pat. No. 4,683,195) and Mullis (U.S. Pat. No. 4,683,202), incorporated herein by reference may be used. The choice of library and selection of probes for the isolation of such DNA sequences is within the level of ordinary skill in the art.

As known in the art, “similarity” between two polynucleotides or polypeptides is determined by comparing the nucleotide or amino acid sequence and its conserved nucleotide or amino acid substitutes of one polynucleotide or polypeptide to the sequence of a second polynucleotide or polypeptide. Also known in the art is “identity” which means the degree of sequence relatedness between two polypeptide or two polynucleotide sequences as determined by the identity of the match between two strings of such sequences. Both identity and similarity can be readily calculated (Computational Molecular Biology, Lesk, A. M., ed., Oxford University Press, New York, 1988; Biocomputing: Informatics and Genome Projects, Smith, D. W., ed., Academic Press, New York, 1993; Computer Analysis of Sequence Data, Part I, Griffin, A. M., and Griffin, H. G., eds., Humana Press, New Jersey, 1994; Sequence Analysis in Molecular Biology, von Heinje, G., Academic Press, 1987; and Sequence Analysis Primer, Gribskov, M. and Devereux, J., eds., M Stockton Press, New York, 1991).

While there exist a number of methods to measure identity and similarity between two polynucleotide or polypeptide sequences, the terms “identity” and “similarity” are well known to skilled artisans (Sequence Analysis in Molecular Biology, von Heinje, G., Academic Press, 1987; Sequence Analysis Primer, Gribskov, M. and Devereux, J., eds., M Stockton Press, New York, 1991; and Carillo, H., and Lipman, D., SIAM J. Applied Math., 48: 1073 (1988). Methods commonly employed to determine identity or similarity between two sequences include, but are not limited to those disclosed in Guide to Huge Computers, Martin J. Bishop, ed., Academic Press, San Diego, 1994, and Carillo, H., and Lipman, D., SIAM J. Applied Math. 48:1073 (1988).

Preferred methods to determine identity are designed to give the largest match between the two sequences tested. Methods to determine identity and similarity are codified in computer programs. Preferred computer program methods to determine identity and similarity between two sequences include, but are not limited to, GCG program package (Devereux, et al., Nucl. Acid Res. 12(1):387 (1984)), BLASTP, BLASTN, FASTA (Atschul, et al., J. Mol. Biol. 215:403 (1990)). The degree of similarity or identity referred to above is determined as the degree of identity between the two sequences, often indicating a derivation of the first sequence from the second. The degree of identity between two nucleic acid sequences may be determined by means of computer programs known in the art such as GAP provided in the GCG program package (Needleman and Wunsch (1970) J. of Mol. Biol. 48:443-453). For purposes of determining the degree of identity between two nucleic acid sequences for the present invention, GAP is used with the following settings: GAP creation penalty of 5.0 and GAP extension penalty of 0.3.

Codon Optimization

The degeneracy of the genetic code permits variations of the nucleotide sequence of a transferrin protein and/or therapeutic protein of interest, while still producing a polypeptide having the identical amino acid sequence as the polypeptide encoded by the native DNA sequence. The procedure, known as “codon optimization” (described in U.S. Pat. No. 5,547,871 which is incorporated herein by reference in its entirety) provides one with a means of designing such an altered DNA sequence. The design of codon optimized genes should take into account a variety of factors, including the frequency of codon usage in an organism, nearest neighbor frequencies, RNA stability, the potential for secondary structure formation, the route of synthesis and the intended future DNA manipulations of that gene. In particular, available methods may be used to alter the codons encoding a given fusion protein with those most readily recognized by yeast when yeast expression systems are used.

The degeneracy of the genetic code permits the same amino acid sequence to be encoded and translated in many different ways. For example, leucine, serine and arginine are each encoded by six different codons, while valine, proline, threonine, alanine and glycine are each encoded by four different codons. However, the frequency of use of such synonymous codons varies from genome to genome among eukaryotes and prokaryotes. For example, synonymous codon-choice patterns among mammals are very similar, while evolutionarily distant organisms such as yeast (such as S. cerevisiae), bacteria (such as E. coli) and insects (such as D. melanogaster) reveal a clearly different pattern of genomic codon use frequencies (Grantham, R., et al., Nucl. Acids Res., 8, 49-62 (1980); Grantham, R., et al., Nucl. Acid Res., 9, 43-74 (1981); Maroyama, T., et al., Nucl. Acid Res., 14, 151-197 (1986); Aota, S., et al., Nucl. Acid Res., 16, 315-402 (1988); Wada, K., et al., Nucl. Acid Res., 19 Supp., 1981-1985 (1991); Kurland, C. G., FEBS Lett., 285, 165-169 (1991)). These differences in codon-choice patterns appear to contribute to the overall expression levels of individual genes by modulating peptide elongation rates. (Kurland, C. G., FEBS Lett., 285, 165-169 (1991); Pedersen, S., EMBO J., 3, 2895-2898 (1984); Sorensen, M. A., J. Mol. Biol., 207, 365-377 (1989); Randall, L. L., et al., Eur. J. Biochem., 107, 375-379 (1980); Curran, J. F., and Yarus, M., J. Mol. Biol., 209, 65-77 (1989); Varenne, S., et al., J. Mol. Biol., 180, 549-576 (1984), Varenne, S., et al., J. Mol. Biol., 180, 549-576 (1984); Garel, J.-P., J. Theor. Biol., 43, 211-225 (1974); Ikemura, T., J. Mol. Biol., 146,1-21 (1981); Ikemura, T., J. Mol. Biol., 151, 389-409 (1981)).

The preferred codon usage frequencies for a synthetic gene should reflect the codon usages of nuclear genes derived from the exact (or as closely related as possible) genome of the cell/organism that is intended to be used for recombinant protein expression, particularly that of yeast species. As discussed above, in one preferred embodiment the human Tf sequence is codon optimized, before or after modification as herein described for yeast expression as may be the therapeutic protein nucleotide sequence(s).

Vectors

Expression units for use in the present invention will generally comprise the following elements, operably linked in a 5′ to 3′ orientation: a transcriptional promoter, a secretory signal sequence, a DNA sequence encoding a modified Tf fusion protein comprising transferrin protein or a portion of a transferrin protein joined to a DNA sequence encoding a therapeutic protein or peptide of interest and a transcriptional terminator. As discussed above, any arrangement of the therapeutic protein or peptide fused to or within the Tf portion may be used in the vectors of the invention. The selection of suitable promoters, signal sequences and terminators will be determined by the selected host cell and will be evident to one skilled in the art and are discussed more specifically below.

Suitable yeast vectors for use in the present invention are described in U.S. Pat. No. 6,291,212 and include YRp7 (Stuhl et al., Proc. Natl. Acad. Sci. USA 76: 1035-1039, 1978), YEp13 (Broach et al., Gene 8: 121-133, 1979), pJDB249 and pJDB219 (Beggs, Nature 275:104-108, 1978), pPPC0005, pSeCHSA, pScNHSA, pC4 and derivatives thereof. Useful yeast plasmid vectors also include pRS403-406, pRS413-416 and the Pichia vectors available from Stratagene Cloning Systems, La Jolla, Calif. 92037, USA. Plasmids pRS403, pRS404, pRS405 and pRS406 are Yeast Integrating plasmids (YIPs) and incorporate the yeast selectable markers HIS3, TRP1, LEU2 and URA3. Plasmids pRS413˜41.6 are Yeast Centromere plasmids (YCps).

Such vectors will generally include a selectable marker, which may be one of any number of genes that exhibit a dominant phenotype for which a phenotypic assay exists to enable transformants to be selected. Preferred selectable markers are those that complement host cell auxotrophy, provide antibiotic resistance or enable a cell to utilize specific carbon sources, and include LEU2 (Broach et al. ibid.), URA3 (Botstein et al., Gene 8: 17, 1979), HIS3 (Struhl et al., ibid.) or POT1 (Kawasaki and Bell, EP 171,142). Other suitable selectable markers include the CAT gene, which confers chloramphenicol resistance on yeast cells. Preferred promoters for use in yeast include promoters from yeast glycolytic genes (Hitzeman et al., J Biol. Chem. 225: 12073-12080, 1980; Alber and Kawasaki, J. Mol. Appl. Genet. 1: 419-434, 1982; Kawasaki, U.S. Pat. No. 4,599,311) or alcohol dehydrogenase genes (Young et al., in Genetic Engineering of Microorganisms for Chemicals, Hollaender et al., (eds.), p. 355, Plenum, N.Y., 1982; Ammerer, Meth. Enzymol. 101: 192-201, 1983). In this regard, particularly preferred promoters are the TPI1 promoter (Kawasaki, U.S. Pat. No. 4,599,311) and the ADH2-4.sup.C [see U.S. Pat. No. 6,291,212] promoter (Russell et al., Nature 304: 652-654, 1983). The expression units may also include a transcriptional terminator. A preferred transcriptional terminator is the TPI1 terminator (Alber and Kawasaki, ibid.). Other preferred vectors and preferred components such as promoters and terminators of a yeast expression system are disclosed in European Patents EP 0258067, EP 0286424, EP0317254, EP 0387319, EP 0386222, EP 0424117, EP 0431880, and EP 1002095; European Patent Publications EP 0828759, EP 0764209, EP 0749478, and EP 0889949; PCT Publication WO 00/44772 and WO 94/04687; and U.S. Pat. Nos. 5,739,007; 5,637,504; 5,302,697; 5,260,202; 5,667,986; 5,728,553; 5,783,423; 5,965,386; 6150,133; 6,379,924; and 5,714,377; which are herein incorporated by reference in their entirety.

In addition to yeast, modified fusion proteins of the present invention can be expressed in filamentous fungi, for example, strains of the fungi Aspergillus. Examples of useful promoters include those derived from Aspergillus nidulans glycolytic genes, such as the adh3 promoter (McKnight et al., EMBO J. 4: 2093-2099, 1985) and the tpiA promoter. An example of a suitable terminator is the adh3 terminator (McKnight et al., ibid.). The expression units utilizing such components may be cloned into vectors that are capable of insertion into the chromosomal DNA of Aspergillus, for example.

Mammalian expression vectors for use in carrying out the present invention will include a promoter capable of directing the transcription of the modified Tf fusion protein. Preferred promoters include viral promoters and cellular promoters. Preferred viral promoters include the major late promoter from adenovirus 2 (Kaufman and Sharp, Mol. Cell. Biol. 2: 1304-13199, 1982) and the SV40 promoter (Subramani et al., Mol. Cell. Biol. 1: 854-864, 1981). Preferred cellular promoters include the mouse metallothionein 1 promoter (Palmiter et al., Science 222: 809-814, 1983) and a mouse V.sub.kappa. [see U.S. Pat. No. 6,291,212] promoter (Grant et al., Nuc. Acids Res. 15: 5496, 1987). A particularly preferred promoter is a mouse V.sub.H [see U.S. Pat. No. 6,291,212] promoter (Loh et al., ibid.). Such expression vectors may also contain a set of RNA splice sites located downstream from the promoter and upstream from the DNA sequence encoding the transferrin fusion protein. Preferred RNA splice sites may be obtained from adenovirus and/or immunoglobulin genes.

Also contained in the expression vectors is a polyadenylation signal located downstream of the coding sequence of interest. Polyadenylation signals include the early or late polyadenylation signals from SV40 (Kaufman and Sharp, ibid.), the polyadenylation signal from the adenovirus 5 E1B region and the human growth hormone gene terminator (DeNoto et al., Nucl. Acid Res. 9: 3719-3730, 1981). A particularly preferred polyadenylation signal is the V_H[see U.S. Pat. No. 6,291,212] gene terminator (Loh et al., ibid.). The expression vectors may include a noncoding viral leader sequence, such as the adenovirus 2 tripartite leader, located between the promoter and the RNA splice sites. Preferred vectors may also include enhancer sequences, such as the SV40 enhancer and the mouse .mu. [see U.S. Pat. No. 6,291,212] enhancer (Gillies, Cell 33: 717-728, 1983). Expression vectors may also include sequences encoding the adenovirus VA RNAs.

Transformation

Techniques for transforming fungi are well known in the literature, and have been described, for instance, by Beggs (ibid.), Hinnen et al. (Proc. Natl. Acad. Sci. USA 75: 1929-1933, 1978), Yelton et al., (Proc. Natl. Acad. Sci. USA 81: 1740-1747, 1984), and Russell (Nature 301: 167-169, 1983). Other techniques for introducing cloned DNA sequences into fungal cells, such as electroporation (Becker and Guarente, Methods in Enzymol. 194: 182-187, 1991) may be used. The genotype of the host cell will generally contain a genetic defect that is complemented by the selectable marker present on the expression vector. Choice of a particular host and selectable marker is well within the level of ordinary skill in the art.

Cloned DNA sequences comprising modified Tf fusion proteins of the invention may be introduced into cultured mammalian cells by, for example, calcium phosphate-mediated transfection (Wigler et al., Cell 14: 725, 1978; Corsaro and Pearson, Somatic Cell Genetics 7: 603, 1981; Graham and Van der Eb, Virology 52: 456, 1973.) Other techniques for introducing cloned DNA sequences into mammalian cells, such as electroporation (Neumann et al., EMBO J. 1: 841-845, 1982), or lipofection may also be used. In order to identify cells that have integrated the cloned DNA, a selectable marker is generally introduced into the cells along with the gene or cDNA of interest. Preferred selectable markers for use in cultured mammalian cells include genes that confer resistance to drugs, such as neomycin, hygronmycin, and methotrexate. The selectable marker may be an amplifiable selectable marker. A preferred amplifiable selectable marker is the DHFR gene. A particularly preferred amplifiable marker is the DHFR.sup.r [see U.S. Pat. No. 6,291,212] cDNA (Simonsen and Levinson, Proc. Natl. Adac. Sci. USA 80: 2495-2499, 1983). Selectable markers are reviewed by Thilly (Mammalian Cell Technology, Butterworth Publishers, Stoneham, Mass.) and the choice of selectable markers is well within the level of ordinary skill in the art.

Host Cells

The present invention also includes a cell, preferably a yeast cell transformed to express a modified transferrin fusion protein of the invention. In addition to the transformed host cells themselves, the present invention also includes a culture of those cells, preferably a monoclonal (clonally homogeneous) culture, or a culture derived from a monoclonal culture, in a nutrient medium. If the polypeptide is secreted, the medium will contain the polypeptide, with the cells, or without the cells if they have been filtered or centrifuged away.

Host cells for use in practicing the present invention include eukaryotic cells, and in some cases prokaryotic cells, capable of being transformed or transfected with exogenous DNA and grown in culture, such as cultured mammalian, insect, fungal, plant and bacterial cells.

Fungal cells, including species of yeast (e.g., Saccharomyces spp., Schizosaccharomyces spp., Pichia spp.) may be used as host cells within the present invention. Examples of fungi including yeasts contemplated to be useful in the practice, of the present invention as hosts for expressing the, transferrin fusion protein of the inventions are Pichia (some species of which were formerly classified as Hansenula), Saccharomyces, Kluyveromyces, Aspergillus, Candida, Torulopsis, Torulaspora, Schizosaccharomyces, Citeromyces, Pachysolen, Zygosaccharomyces, Debaromyces, Trichoderma, Cephalosporium, Humicola, Mucor, Neurospora, Yarrowia, Metschunikowia, Rhodosporidium, Leucosporidium, Botryoascus, Sporidiobolus, Endomycopsis, and the like. Examples of Saccharomyces spp. are S. cerevisiae, S. italicus and S. rouxii. Examples of Kluyveromyces spp. are K. fragilis, K. lactis and K. marxianus. A suitable Torulaspora species is T. delbrueckii. Examples of Pichia spp. are P. angusta (formerly H. polymorpha), P. anomala (formerly H. anomala) and P. pastoris.

Particularly useful host cells to produce the Tf fusion proteins of the invention are the methylotrophic Pichia pastoris (Steinlein et al. (1995) Protein Express. Purif. 6:619-624). Pichia pastoris has been developed to be an outstanding host for the production of foreign proteins since its alcohol oxidase promoter was isolated and cloned; its transformation was first reported in 1985. P. pastoris can utilize methanol as a carbon source in the absence of glucose. The P. pastoris expression system can use the methanol-induced alcohol oxidase (AOX1) promoter, which controls the gene that codes for the expression of alcohol oxidase, the enzyme which catalyzes the first step in the metabolism of methanol. This promoter has been characterized and incorporated into a series of P. pastoris expression vectors. Since the proteins produced in P. pastoris are typically folded correctly and secreted into the medium, the fermentation of genetically engineered P. pastoris provides an excellent alternative to E. coli expression systems. A number of proteins have been produced using this system, including tetanus toxin fragment, Bordatella pertussis pertactin, human serum albumin and lysozyme.

Strains of the yeast Saccharomyces cerevisiae are another preferred host. In a preferred embodiment, a yeast cell, or more specifically, a Saccharomyces cerevisiae host cell that contains a genetic deficiency in a gene required for asparagine-linked glycosylation of glycoproteins is used. S. cerevisiae host cells having such defects may be prepared using standard techniques of mutation and selection, although many available yeast strains have been modified to prevent or reduce glycosylation or hypermannosylation. Ballou et al. (J. Biol. Chem. 255: 5986-5991, 1980) have described the isolation of mannoprotein biosynthesis mutants that are defective in genes which affect asparagine-linked glycosylation. Gentzsch and Tanner (Glycobiology 7:481-486, 1997) have described a family of at least six genes (PMT1-6) encoding enzymes responsible for the first step in O-glycosylation of proteins in yeast. Mutants defective in one or more of these genes show reduced O-linked glycosylation and/or altered specificity of O-glycosylation.

To optimize production of the heterologous proteins, it is also preferred that the host strain carries a mutation, such as the S. cerevisiae pep4 mutation (Jones, Genetics 85: 23-33, 1977), which results in reduced proteolytic activity. Host strains containing mutations in other protease encoding regions are particularly useful to produce large quantities of the Tf fusion proteins of the invention.

Host cells containing DNA constructs of the present invention are grown in an appropriate growth medium. As used herein, the term “appropriate growth medium” means a medium containing nutrients required for the growth of cells. Nutrients required for cell growth may include a carbon source, a nitrogen source, essential amino acids, vitamins, minerals and growth factors. The growth medium will generally select for cells containing the DNA construct by, for example, drug selection or deficiency in an essential nutrient which is complemented by the selectable marker on the DNA construct or co-transfected with the DNA construct. Yeast cells, for example, are preferably grown in a chemically defined medium, comprising a carbon source, e.g. sucrose, a non-amino acid nitrogen source, inorganic salts, vitamins and essential amino acid supplements. The pH of the medium is preferably maintained at a pH greater than 2 and less than 8, preferably at pH 5.5-6.5. Methods for maintaining a stable pH include buffering and constant pH control. Preferred buffering agents may include citrate-phosphate or succinic acid and Bis-Tris (Sigma Chemical Co., St. Louis, Mo.). Yeast cells having a defect in a gene required for asparagine-linked glycosylation are preferably grown in a medium containing an osmotic stabilizer. A preferred osmotic stabilizer is sorbitol supplemented into the medium at a concentration between 0.1 M and 1.5 M., preferably at 0.5 M or 1.0 M.

Cultured mammalian cells are generally grown in commercially available serum-containing or serum-free media. Selection of a medium appropriate for the particular cell line used is within the level of ordinary, skill in the art. Transfected mammalian cells are allowed to grow for a period of time, typically 1-2 days, to begin expressing the DNA sequence(s) of interest. Drug selection is then applied to select for growth of cells that are expressing the selectable marker in a stable fashion. For cells that have been transfected with an amplifiable selectable marker the drug concentration may be increased in a stepwise manner to select for increased copy number of the cloned sequences, thereby increasing expression levels.

Baculovirus/insect cell expression systems may also be used to produce the modified Tf fusion proteins of the invention. The BacPAK™ Baculovirus Expression System (BD Biosciences (Clontech)) expresses recombinant proteins at high levels in insect host cells. The target gene is inserted into a transfer vector, which is cotransfected into insect host cells with the linearized BacPAK6 viral DNA. The BacPAK6 DNA is missing an essential portion of the baculovirus genome. When the DNA recombines with the vector, the essential element is restored and the target gene is transferred to the baculovirus genome. Following recombination, a few viral plaques are picked and purified, and the recombinant phenotype is verified. The newly isolated recombinant virus can then be amplified and used to infect insect cell cultures to produce large amounts of the desired protein.

Tf fusion proteins of the present invention may also be produced using transgenic plants and animals. For example, sheep and goats can make the therapeutic protein in their milk. Or tobacco plants can include the protein in their leaves. Both transgenic plant and animal production of proteins comprises adding a new gene coding the fusion protein into the genome of the organism. Not only can the transgenic organism produce a new protein, but it can also pass this ability onto its offspring.

Secretory Signal Sequences

The terms “secretory signal sequence” or “signal sequence” or “secretion leader sequence” are used interchangeably and are described, for example in U.S. Pat. No. 6,291,212 and U.S. Pat. No. 5,547,871, both of which are herein incorporated by reference in their entirety. Secretory signal sequences or signal sequences or secretion leader sequences encode secretory peptides. A secretory peptide is an amino acid sequence that acts to direct the secretion of a mature polypeptide or protein from a cell. Secretory peptides are generally characterized by a core of hydrophobic amino acids and are typically (but not exclusively) found at the amino termini of newly synthesized proteins. Very often the secretory peptide is cleaved from the mature protein during secretion. Secretory peptides may contain processing sites that allow cleavage of the signal peptide from the mature protein as it passes through the secretory pathway. Processing sites may be encoded within the signal peptide or may be added to the signal peptide by, for example, in vitro mutagenesis.

Secretory peptides may be used to direct the secretion of modified Tf fusion proteins of the invention. One such secretory peptide that may be used in combination with other secretory peptides is the alpha mating factor leader sequence. Secretory signal sequences or signal sequences or secretion leader sequences are required for a complex series of post-translational processing steps which result in secretion of a protein. If an intact signal sequence is present, the protein being expressed enters the lumen of the rough endoplasmic reticulum and is then transported through the Golgi apparatus to secretory vesicles and is finally transported out of the cell. Generally, the signal sequence immediately follows the initiation codon and encodes a signal peptide at the amino-terminal end of the protein to be secreted. In most cases, the signal sequence is cleaved off by a specific protease, called a signal peptidase. Preferred signal sequences improve the processing and export efficiency of recombinant protein expression using viral, mammalian or yeast expression vectors. In some cases, the native Tf signal sequence may be used to express and secrete fusion proteins of the invention.

Linkers

The Tf moiety and therapeutic protein moiety(s) of the modified transferrin fusion proteins of the invention can be fused directly or using a linker peptide of various lengths to provide greater physical separation and allow more spatial mobility between the fused proteins and thus maximize the accessibility of the therapeutic protein portion, for instance, for binding to its cognate receptor. The linker peptide may consist of amino acids that are flexible or more rigid. For example, a linker such as but not limited to a poly-glycine stretch. The linker can be less than about 50, 40, 30, 20, or 10 amino acid residues. The linker can be covalently linked to and between the transferrin protein or portion thereof and the therapeutic protein.

Detection of Tf Fusion Proteins

Assays for detection of biologically active modified transferrin-therapeutic protein fusions may include Western transfer, protein blot or colony filter as well as activity based assays that detect the fused therapeutic protein. A Western transfer filter may be prepared using the method described by Towbin et al. (Proc. Natl. Acad. Sci. USA 76: 4350-4354, 1979). Briefly, samples are electrophoresed in a sodium dodecylsulfate polyacrylamide gel. The proteins in the gel are electrophoretically transferred to nitrocellulose paper. Protein blot filters may be prepared by filtering supernatant samples or concentrates through nitrocellulose filters using, for example, a Minifold (Schleicher & Schuell, Keene, N. H.). Colony filters may be prepared by growing colonies on a nitrocellulose filter that has been laid across an appropriate growth medium. In this method, a solid medium is preferred. The cells are allowed to grow on the filters for at least 12 hours. The cells are removed from the filters by washing with an appropriate buffer that does not remove the proteins bound to the filters. A preferred buffer comprises 25 mM Tris-base, 19 mM glycine, pH 8.3, 20% methanol.

Fusion proteins of the invention may also be detected by assaying for the activity of the therapeutic protein moiety. Such assays are readily available, including but not limited to, those assays described in Table 1. Specifically, transferrin fusion proteins of the invention may be assayed for functional activity (e.g., biological activity or therapeutic activity) using the assay referenced in the “Exemplary Activity Assay” column of Table 1. Additionally, one of skill in the art may routinely assay fragments of a therapeutic protein corresponding to a therapeutic protein portion of a fusion protein of the invention, for activity using assays referenced in its corresponding row of Table 1. Further, one of skill in the art may routinely assay fragments of a modified transferrin protein for activity using assays known in the art.

For example, in one embodiment where one is assaying for the ability of a transferrin fusion protein of the invention to bind or compete with a therapeutic protein for binding to an anti-therapeutic polypeptide antibody and/or anti-transferrin antibody, various immunoassays known in the art can be used, including but not limited to, competitive and non-competitive assay systems using techniques such as radioimmunoassays, ELISA (enzyme linked immunosorbent assay), sandwich immunoassays, immunoradiometric assays, gel diffusion precipitation reactions, immunodiffusion assays, in situ immunoassays (using colloidal gold, enzyme or radioisotope labels, for example), western blots, precipitation reactions, agglutination assays (e.g., gel agglutination assays), complement fixation assays, immunofluorescence assays, protein A assays, and immunoelectrophoresis assays, etc. In one embodiment, antibody binding is detected by detecting a label on the primary antibody. In another embodiment, the primary antibody is detected by detecting binding of a secondary antibody or reagent to the primary antibody. In a further embodiment, the secondary antibody is labeled. Many means are known in the art for detecting binding in an immunoassay and are within the scope of the present invention.

In a further embodiment, where a binding partner (e.g., a receptor or a ligand) of a therapeutic protein is identified, binding to that binding partner by a transferrin fusion protein containing that therapeutic protein as the therapeutic protein portion of the fusion can be assayed, e.g., by means well-known in the art, such as, for example, reducing and non-reducing gel chromatography, protein affinity chromatography, and affinity blotting. Other methods will be known to the skilled artisan and are within the scope of the invention.

Isolation/Purification of Modified Transferrin Fusion Proteins

Secreted, biologically active, modified transferrin fusion proteins may be isolated from the medium of host cells grown under conditions that allow the secretion of the biologically active fusion proteins. The cell material is removed from the culture medium, and the biologically active fusion proteins are isolated using isolation techniques known in the art. Suitable isolation techniques include precipitation and fractionation by a variety of chromatographic methods, including gel filtration, ion exchange chromatography and affinity chromatography.

A particularly preferred purification method is affinity chromatography on an iron binding or metal chelating column or an immunoaffinity chromatography using an antibody directed against the transferrin or therapeutic protein or peptide portion of the polypeptide fusion. The antibody is preferably immobilized or attached to a solid support or substrate. A particularly preferred substrate is CNBr-activated Sepharose (Pharmacia LKB Technologies, Inc., Piscataway, N.J.). By this method, the medium is combined with the antibody/substrate under conditions that will allow binding to occur. The complex may be washed to remove unbound material, and the transferrin fusion protein is released or eluted through the use of conditions unfavorable to complex formation. Particularly useful methods of elution include changes in pH, wherein the immobilized antibody has a high affinity for the ligand at a first pH and a reduced affinity at a second (higher or lower) pH; changes in concentration of certain chaotropic agents; or through the use of detergents.

Labeled Modified Transferrin Fusion Proteins

Transferrin fusion proteins of the present invention may also be labeled with a radioisotope or other imaging agent and used for in vivo diagnostic purposes. Preferred radioisotope imaging agents include iodine-125 and technetium-99, with technetium-99 being particularly preferred. Methods for producing protein-isotope conjugates are well known in the art, and are described by, for example, Eckelman et al. (U.S. Pat. No. 4,652,440), Parker et al. (WO 87/05030) and Wilber et al. (EP 203,764). Alternatively, the transferrin fusion proteins may be bound to spin label enhancers and used for magnetic resonance (MR) imaging. Suitable spin label enhancers include stable, sterically hindered, free radical compounds such as nitroxides. Methods for labeling ligands for MR imaging are disclosed by, for example, Coffman et al. (U.S. Pat. No. 4,656,026). For administration, the labeled transferrin fusion proteins are combined with a pharmaceutically acceptable carrier or diluent, such as sterile saline or sterile water. Administration is preferably by bolus injection, preferably intravenously.

Production of Fusion Proteins

The present invention further provides methods for producing a modified fusion protein of the invention using nucleic acid molecules herein described. In general terms, the production of a recombinant form of a protein typically involves the following steps.

A nucleic acid molecule is first obtained that encodes a transferrin fusion protein of the invention. The nucleic acid molecule is then preferably placed in operable linkage with suitable control sequences, as described above, to form an expression unit containing the protein open reading frame. The expression unit is used to transform a suitable host and the transformed host is cultured under conditions that allow the production of the recombinant protein. Optionally the recombinant protein is isolated from the medium or from the cells; recovery and purification of the protein may not be necessary in some instances where some impurities may be tolerated.

Each of the foregoing steps can be accomplished in a variety of ways. For example, the construction of expression vectors that are operable in a variety of hosts is accomplished using appropriate replicons and control sequences, as set forth above. The control sequences, expression vectors, and transformation methods are dependent on the type of host cell used to express the gene and were discussed in detail earlier and are otherwise known to persons skilled in the art. Suitable restriction sites can, if not normally available, be added to the ends of the coding sequence so as to provide an excisable gene to insert into these vectors. A skilled artisan can readily adapt any host/expression system known in the art for use with the nucleic acid molecules of the invention to produce a desired recombinant protein.

As discussed above, any expression system may be used, including yeast, bacterial, animal, plant, eukaryotic and prokaryotic systems. In some embodiments, yeast, mammalian cell culture and transgenic animal or plant production systems are preferred. In other embodiments, yeast systems that have been modified to reduce native yeast glycosylation, hyper-glycosylation or proteolytic activity may be used.

Therapeutic Molecules

Any therapeutic molecule may be used as the fusion partner to Tf according to the methods and compositions of the present invention. As used herein, a therapeutic molecule is typically a protein or peptide capable of exerting a beneficial biological effect in vitro or in vivo and includes proteins or peptides that exert a beneficial effect in relation to normal homeostasis, physiology or a disease state. Therapeutic molecules do not include fusion partners commonly used as markers or protein purification aids, such as bacterial galactosidases (see for example, U.S. Pat. No. 5,986,067 and Aldred et al. (1984) Biochem. Biophys. Res. Commun. 122: 960-965). For instance, a beneficial effect as related to a disease state includes any effect that is advantageous to the treated subject, including disease prevention, disease stabilization, the lessening or alleviation of disease symptoms or a modulation, alleviation or cure of the underlying defect to produce an effect beneficial to the treated subject.

A modified transferrin fusion protein of the invention includes at least a fragment or variant of a therapeutic protein and at least a fragment or variant of modified serum transferrin, which are associated with one another, preferably by genetic fusion.

In one embodiment, the transferrin fusion protein includes a modified transferrin molecule linked to a neuropharmaceutical agent. In another embodiment, the modified transferrin fusion protein includes transferrin at the carboxyl terminus linked to a neuropharmaceutical agent at the amino terminus. In an alternate embodiment, the modified transferrin fusion protein includes transferrin at the amino terminus linked to a neuropharmaceutical agent at the carboxy terminus. In specific embodiments, the neuropharmaceutical agent is either nerve growth factor or ciliary neurotrophic factor.

In further embodiments, a modified transferrin fusion protein of the invention may contain at least a fragment or variant of a therapeutic protein, and/or at least a fragment or variant of an antibody. In a further embodiment, the transferrin fusion proteins can contain peptide fragments or peptide variants of proteins or antibodies wherein the variant or fragment retains at least one biological or therapeutic activity. The transferrin fusion proteins can contain therapeutic proteins that can be peptide fragments or peptide variants at least about 4, at least 5, at least 6, at least 7, at least 8, at least 9, at least 10, at least 11, at least 12, at least 13, at least 14, at least 15, at least 20, at least 25, at least 30, at least 35, or at least about 40, at least about 50, at least about 55, at least about 60 or at least about 70 or more amino acids in length fused to the N and/or C termini, inserted within, or inserted into a loop of a modified transferrin.

In another embodiment, the modified transferrin fusion molecules contain a therapeutic protein portion that can be fragments of a therapeutic protein that include the full length protein as well as polypeptides having one or more residues deleted from the amino terminus of the amino acid sequence.

In another embodiment, the modified transferrin fusion molecules contain a therapeutic protein portion that can have one or more amino acids deleted from both the amino and the carboxy termini.

In another embodiment, the modified transferrin fusion molecules contain a therapeutic protein portion that is at least about 80%, 85%, 90%, 95%, 96%, 97%, 98% or 99% identical to a reference therapeutic protein set forth herein, or fragments thereof. In further embodiments, the transferrin fusion molecules contain a therapeutic protein portion that is at least about 80%, 85%, 90%, 95%, 96%, 97%, 98% or 99% identical to reference polypeptides having the amino acid sequence of N- and C-terminal deletions as described above.

In another embodiment, the modified transferrin fusion molecules contain the therapeutic protein portion that is at least about 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99% or 100%, identical to, for example, the native or wild-type amino acid sequence of a therapeutic protein. Fragments, of these polypeptides are also provided.

The therapeutic proteins corresponding to a therapeutic protein portion of a modified transferrin fusion protein of the invention, such as cell surface and secretoiy proteins, can be modified by the attachment of one or more oligosaccharide groups. The modification referred to as glycosylation, can significantly affect the physical properties of proteins and can be important in protein stability, secretion, and localization. Glycosylation occurs at specific locations along the polypeptide backbone. There are usually two major types of glycosylation: glycosylation characterized by O-linked oligosaccharides, which are attached to serine or threonine residues; and glycosylation characterized by N-linked oligosaceharides, which are attached to asparagine residues in an Asn-X-Ser/Thr sequence, where X can be an amino acid except proline. Variables such as protein structure and cell type influence the number and nature of the carbohydrate units within the chains at different glycosylation sites. Glycosylation isomers are also commnon at the same site within a given cell type. For example, several types of human interferon are glycosylated.

Therapeutic proteins corresponding to a therapeutic protein portion of a transferrin fusion protein of the invention, as well as analogs and variants thereof, may be modified so that glycosylation at one or more sites is altered as a result of manipulation(s) of their nucleic acid sequence by the host cell in which they are expressed, or due to other conditions of their expression. For example, glycosylation isomers may be produced by abolishing or introducing glycosylation sites, e.g., by substitution or deletion of amino acid residues, such as substitution of glutamine for asparagine, or unglycosylated recombinant proteins may be produced by expressing the proteins in host cells that will not glycosylate them, e.g. in glycosylation-deficient yeast. These approaches are known in the art.

Therapeutic proteins and their nucleic acid sequences are well known in the art and available in public databases such as Chemical Abstracts Services Databases (e.g., the CAS Registry), GenBank, and GenSeq. The Accession Numbers and sequences referred to below are herein incorporated by reference in their entirety.

In other embodiments, the transferrin fusion proteins of the invention are capable of a therapeutic activity and/or biologic activity, corresponding to the therapeutic activity and/or biologic activity of the therapeutic protein listed in the corresponding row of Table 1 and elsewhere in this application. (See, e.g., the “Biological Activity” and “Therapeutic Protein X” columns of Table 1.) In further embodiments, the therapeutically active protein portions of the transferrin fusion proteins of the invention are fragments or variants of the reference sequences cited herein.

The present invention is further directed to modified Tf fusion proteins comprising fragments of the therapeutic proteins herein described. Even if deletion of one or more amino acids from the N-terminus of a protein results in modification or loss of one or more biological functions of the therapeutic protein portion, other therapeutic activities and/or functional activities (e.g., biological activities, ability to multimerize, ability to bind a ligand) may still be retained. For example, the ability of polypeptides with N-terminal deletions to induce and/or bind to antibodies which recognize the complete or mature forms of the polypeptides generally will be retained with less than the majority of the residues of the complete polypeptide removed from the N-terminus. Whether a particular polypeptide lacking N-terminal residues of a complete polypeptide retains such immunologic activities can be assayed by routine methods described herein and otherwise known in the art. It is not unlikely that a mutant with a large number of deleted N-terminal amino acid residues may retain some biological or immunogenic activities. In fact, peptides composed of as few as six amino acid residues may often evoke an immune response.

Also as mentioned above, even if deletion of one or more amino acids from the N-terminus or C-terminus of a therapeutic protein results in modification or loss of one or more biological functions of the protein, other functional activities (e.g., biological activities, ability to multimerize, ability to bind a ligand) and/or therapeutic activities may still be retained. For example the ability of polypeptides with C-terminal deletions to induce and/or bind to antibodies which recognize the complete or mature forms of the polypeptide generally will be retained when less than the majority of the residues of the complete or mature polypeptide are removed from the C-terminus. Whether a particular polypeptide lacking the N-terminal and/or, C-terminal residues of a reference polypeptide retains therapeutic activity can readily be determined by routine methods described herein and/or otherwise known in the art.

Peptide fragments of the therapeutic proteins can be fragments comprising, or alternatively, consisting of, an amino acid sequence that displays a therapeutic activity and/or functional activity (e.g. biological activity) of the polypeptide sequence of the therapeutic protein of which the amino acid sequence is a fragment.

The peptide fragments of the therapeutic protein may comprise only the N- and C-termini of the protein, i.e., the central portion of the therapeutic protein has been deleted. Alternatively, the peptide fragments may comprise non-adjacent and/or adjacent portions of the central part of the therapeutic protein.

Other polypeptide fragments are biologically active fragments. Biologically active fragments are those exhibiting activity similar, but not necessarily identical, to an activity of a therapeutic protein used in the present invention. The biological activity of the fragments may include an improved desired activity, or a decreased undesirable activity.

Generally, variants of proteins are overall very similar, and, in many regions, identical to the amino acid sequence of the therapeutic protein corresponding to a therapeutic protein portion of a transferrin fusion protein of the invention. Nucleic acids encoding these variants are also encompassed by the invention.

Further therapeutic polypeptides that may be used in the invention are polypeptides encoded by polynucleotides which hybridize to the complement of a nucleic acid molecule encoding an amino acid sequence of a therapeutic protein under stringent hybridization conditions which are known to those of skill in the art. (see, for example, Ausubel, F.M. et al., eds., 1989 Current Protocols in Molecular Biology, Green Publishing Associates, Inc., and John Wiley & Sons Inc., New. York). Polynucleotides encoding these polypeptides are also encompassed by the invention.

By a polypeptide having an amino acid sequence at least, for example, 95% “identical” to a query amino acid sequence of the present invention, it is intended that the amino acid sequence of the subject polypeptide is identical to the query sequence except that the subject polypeptide sequence may include up to five amino acid alterations per each 100 amino acids of the query amino acid sequence. In other words, to obtain a polypeptide having an amino acid sequence at least 95% identical to a query amino acid sequence, up to 5% of the amino acid residues in the subject sequence may be inserted, deleted, or substituted with another amino acid. These alterations of the reference sequence may occur at the amino- or carboxy-terminal positions of the reference amino acid sequence or anywhere between those terminal positions, interspersed either individually among residues in the reference sequence, or in one or more contiguous groups within the reference sequence.

As a practical matter, whether any particular polypeptide is at least about 80%, 85%, 90%, 95%, 96%, 97%, 98% or 99% identical to, for instance, the amino acid sequence of a transferrin fusion protein of the invention or a fragment thereof (such, as the therapeutic protein portion of the transferrin fusion protein or the transferrin portion of the transferrin fusion protein), can be determined conventionally using known computer programs. A preferred method for determining the best overall match between a query sequence (a sequence of the present invention) and a subject sequence, also referred to as a global sequence alignment, can be determined using the FASTDB computer program based on the algorithm of Brufiag—et al. (Comp. App. Biosci 245—(1990)).

The polynucleotide variants of the invention may contain alterations in the coding regions, non-coding regions, or both. Polynucleotide variants containing alterations which produce silent substitutions, additions, or deletions, but do not alter the properties or activities of the encoded polypeptide may be used to produce modified Tf fusion proteins. Nucleotide variants produced by silent substitutions due to the degeneracy of the genetic code can be utilized. Moreover, polypeptide variants in which less than about 50, less than 40, less than 30, less than 20, less than 10, or 5-50, 5-25, 5-10, 1-5, or 1-2 amino acids are substituted, deleted, or added in any combination can also be utilized. Polynucleotide variants can be produced for a variety of reasons, e.g., to optimize codon expression for a particular host (change codons in the human mRNA to those preferred by a host, such as, yeast or E. coli as described above).

In other embodiments, the therapeutic protein moiety has conservative substitutions compared to the wild-type sequence. By “conservative substitutions” is intended swaps within groups such as replacement of the aliphatic or hydrophobic amino acids Ala, Val, Leu and Ile; replacement of the hydroxyl residues Ser and Thr; replacement of the acidic residues Asp and Glu; replacement of the amide residues Asn and Gln, replacement of the basic residues Lys, Arg, and His; replacement of the aromatic residues Phe, Tyr, and Trp, and replacement of the small-sized amino acids Ala, Ser, Thr, Met, and Gly. Guidance concerning how to make phenotypically silent amino acid substitutions is provided, for example, in Bowie et al., “Deciphering the Message in Protein Sequences: Tolerance to Amino Acid Substitutions,” Science 247:1306-1310 (1990). In specific embodiments, the polypeptides of the invention comprise, or alternatively, consist of, fragments or variants of the amino acid sequence of a therapeutic protein described herein and/or serum transferrin, and/modified transferrin protein of the invention, wherein the fragments or variants have 1-5, 5-10, 5-25, 5-50, 10-50 or 50-150 amino acid residue additions, substitutions, and/or deletions when compared to the reference amino acid sequence. In further embodiments, the amino acid substitutions are conservative. Nucleic acids encoding these polypeptides are also encompassed by the invention.

The modified fusion proteins of the present invention can be composed of amino-acids joined to each other by peptide bonds or modified peptide bonds and may contain amino acids other than the 20 gene-encoded amino acids. The polypeptides may be modified by either natural processes, such as post-translational processing, or by chemical modification techniques which are well known in the art. Such modifications are well described in basic texts and in more detailed monographs, as well as in a voluminous research literature.

Modifications can occur anywhere in a polypeptide, including the peptide backbone, the amino acid side-chains and the amino or carboxy termini. It will be appreciated that the same type of modification may be present in the same or varying degrees at several sites in a given polypeptide. Also, a given polypeptide may contain many types of modifications. Polypeptides may be branched, for example, as a result of ubiquitination, and they may be cyclic, with or without branching. Cyclic, branched, and branched cyclic polypeptides may result from posttranslation natural processes or may be made by synthetic methods. Modifications include acetylation, acylation, ADP-ribosylation, amidation, covalent attachment of flavin, covalent attachment of a heme moiety, covalent attachment of a nucleotide or nucleotide derivative, covalent attachment of a lipid or lipid derivative, covalent attachment of phosphotidylinositol, cross-linking, cyclization, disulfide bond formation, demethylation, formation of covalent cross-links, formation of cysteine, glycosylation, GPI anchor formation, hydroxylation, iodination, methylation, myristylation, oxidation, pegylation, proteolytic processing, phosphorylation, prenylation, racemization, sulfation, transfer-RNA mediated addition of amino acids to proteins such as arginylation, and ubiquitination. (See, for instance, PROTEINS—STRUCTURE AND MOLECULAR PROPERTIES, 2nd Ed., T. E. Creighton, W. H. Freeman and Company, New York(1993); POST-TRANSLATIONAL COVALENT MODIFICATION OF PROTEINS, B. C. Johnson, Ed., Academic Press, New York, pgs. 1-12 (1983); Seifter et al. (1990) Meth. Enzymol. 182:626-646; Rattan et al., Ann. N.Y. Acad. Sci. 663:48-62.

Therapeutic molecules that may be fused to or inserted into Tf include, but are not limited to, hormones, matrix proteins, immunosuppressants, bronchodilators, cardiovascular agents, enzymes, CNS agents, neurotransmitters, receptor proteins or peptides, growth hormones, growth factors, antiviral peptides, fusogenic inhibitor peptides, cytokines, lymphokines, monokines, interleukins, colony stimulating factors, differentiation factors, angiogenic factors, receptor ligands, cancer-associated proteins, antineoplastics, viral peptides, antibiotic peptides, blood proteins, antagonist proteins, transcription factors, anti-angiogenic factors, antagonist proteins or peptides, receptor antagonists, antibodies, single chain antibodies and cell adhesion molecules. Different therapeutic molecules may be combined into a single fusion protein to produce a bi or multi-functional therapeutic molecule. Different molecules may also be used in combination to produce a fusion protein with a therapeutic entity and a targeting entity.

Cytokines are soluble proteins released by cells of the immune system, which act nonenzymatically through specific receptors to regulate immune responses. Cytokines resemble hormones in that they act at low concentrations bound with high affinity to a specific receptor. The term “cytokine” is used herein to describe naturally occurring or recombinant proteins, analogs thereof, and fragments thereof which elicit a specific biological response in a cell which has a receptor for that cytokine. Cytokines preferably include interleukins such as interleukin-2 (IL-2) (GenBank Acc. No. S77834), IL-3 (GenBank Acc. No. M14743), IL-4 (GenBank Acc. No. M23442), IL-5 (GenBank Acc. No. J03478), IL-6 (GenBank Acc. No. M14584), IL-7 (GenBank Acc. No. NM_—000880), IL-10 (GenBank Acc. No. NM_—000572), IL-12 (GenBank Acc. No.AF180562 and GenBank Acc. No. AF180563), IL-13 (GenBank Acc. No. U10307), IL-14 (GenBank Acc. No. XM_—170924), IL-15 (GenBank Acc. No. X91233), IL-16 (GenBank Acc. No. NM_—004513), IL-17 (GenBank Acc. No. NM_—002190) and IL-18 (GenBank Acc. No. NM_—001562), hematopoietic factors such as granulocyte-macrophage colony stimulating factor (GM-CSF) (GenBank Acc. No. X03021), granulocyte colony stimulating factor (G-CSF) (GenBank Acc. No. X03656), platelet activating factor (GenBank Acc. No. NM_—000437) and erythropoeitin (GenBank Acc. No. X02158), tumor necrosis factors (TNF) such as TNFα (GenBank Acc. No. X02910), lymphokines such as lymphotoxin-α (GenBank Acc. No. X02911), lymphotoxin-β (GenBank Acc. No. L11016), leukoregulin, macrophage migration inhibitory factor (GenBank Ace. No. M25639), and neuroleukin (GenBank Acc. No. K03515), regulators of metabolic processes such as leptin (GenBank Ace. No. U43415), interferons such as interferon α (IFNα) (GenBank Acc. No. M54886), IFNβ (GenBank Acc. No. V00534), IFNγ (GenBank Ace. No. J00219), IFNo (GenBank Ace. No. NM_—002177), thrombospondin 1 (THBS1) (GenBank Acc. No. NM_—003246), THBS2 (GenBank Acc. No. L12350), THBS3 (GenBank Acc. No. L38969), THBS4 (GenBank Acc. No. NM_—003248), and chemokines. Preferably, the modified transferrin-cytokine fusion protein of the present invention displays cytokine biological activity.

The term “hormone” is used herein to describe any one of a number of biologically active substances that are produced by certain cells or tissues and that cause specific biological changes or activities to occur in another cell or tissue located elsewhere in the body. Hormones preferably include GLP-1 of glucagon preproprotein (GenBank Acc. No. NM_—002045), proinsulin (GenBank Acc. No. V00565), insulin (GenBank Acc. No. NM_—000207), growth hormone 1 (GenBank Acc. No. V00520), growth hormone 2 (GenBank Acc. No. F006060), growth hormone release factor (GenBank Acc. No. NM_—021081), insulin-like growth factor I (GenBank Acc. No. M27544), insulin-like growth factor II (GenBank Acc. No. NM_—000612), insulin-like growth factor binding protein 1 (IGFBP-1) (GenBank Acc. No. M59316), IGFBP-2 (GenBank Acc. No. X16302), IGFBP-3 (GenBank Acc. No. NM_—000598), IGFBP-4 (GenBank Acc. No. Y12508), IGFBP-5 (GenBank Acc. No. M65062), IGFBP-6 (GenBank Acc. No. NM_—002178), IGFBP-7 (GenBank Acc. No. NM_—001553), chorionic gonadotropin β chain (GenBank Acc. No. NM_—033142), chorionic gonadotropin α chain (GenBank Acc. No. NM_—000735), luteinizing hormone β (GenBank Acc. No. X00264), follicle-stimulating hormone β (GenBank Acc. No. NM_—000510), thyroid-stimulating hormone β (GenBank Acc. No. NM_—000549), prolactin (GenBank Acc. No. NM_—000948), pro-opiomelanocortin (GenBank Acc. No. V01510), corticotropin (ACTH), β-lipotropin, α-melanocyte stimulating hormone (α-MSH), γ-lipotropin, β-MSH, β-endorphin, and corticotropin-like intermediate lobe peptide (CLIP).

The term “growth factor” is used herein to describe any protein or peptide that binds to a receptor to stimulate cell proliferation. Growth factors preferably include platelet-derived growth factor-α (PDGF-α) (GenBank Acc. No. X03795), PDGF-β (GenBank Acc. No. X02811), hormones, epidermal growth factor (EGF) (GenBank Acc. No. NM_—001963), fibroblast growth factors such as fibroblast growth factor 1 (FGF1) (GenBank Acc. No. NM_—000800), FGF2 (GenBank Acc. No. NM_—002006), FGF3 (GenBank Acc. No. NM_—005247), FGF4 (GenBank Acc. No. NM_—002007), FGF5 (GenBank Acc. No. M37825), FGF6 (GenBank Acc. No. X57075), FGF7 (GenBank Acc. No. NM_—002009), FGF8 (GenBank Acc. No. AH006649), FGF9 (GenBank Acc. No. NM_—002010), FGF10 (GenBank Acc. No. AB002097), FGF11 (GenBank Acc. No. NM_—004112), FGF12 (GenBank Acc. No. NM_—021032), FGF13 (GenBank Acc. No. NM_—004114), FGF14 (GenBank Acc. No. NM_—004115), FGF16 (GenBank Acc. No. AB009391), FGF17 (GenBank Acc. No. NM_—003867), FGF18 (GenBank Acc. No. AF075292), FGF19 (GenBank Acc. No. NM_—005117), FGF20 (GenBank Acc. No. NM_—019851), FGF21 (GenBank Acc. No. NM_—019113), FGF22 (GenBank Acc. No. NM_—020637), and FGF23 (GenBank Acc. No. NM_—020638), angiogenin (GenBank Acc. No. M11567), brain-derived neurotrophic factor (GenBank Ace. No. M61176), ciliary neurotrophic growth factor (GenBank Acc. No. X60542), transforming growth factor-α (TGF-α) (GenBank Acc. No. X70340), TGF-β (GenBank Acc. No. X02812), nerve growth factor-α (NGF-α) (GenBank Acc. No. NM_—010915), NGF-β (GenBank Acc. No. X52599), tissue inhibitor of metalloproteinase 1 (TIMP1) (GenBank Acc. No. NM_—003254), TIMP2 (GenBank Ace. No. NM_—003255), TIMP3 (GenBank Ace. No. U02571), TIMP4 (GenBank Ace. No. U76456) and macrophage stimulating 1 (GenBank Ace. No. L11924).

The term “matrix protein” is used herein to describe proteins or peptides that are normally found in the extracellular matrix. These proteins may be functionally important for strength, filtration, or adhesion. Matrix proteins preferably include collagens such as collagen I (GenBank Ace. No. Z74615), collagen II (GenBank Ace. No. X16711), collagen III (GenBank Ace. No. X14420), collagen IV (GenBank Acc. No. NM_—001845), collagen V (GenBank Acc. No. NM_—000393), collagen VI (GenBank Ace. No. NM_—058175), collagen VII (GenBank Acc. No. L02870), collagen VIII (GenBank Acc. No. NM_—001850), collagen IX (GenBank Ace. No. X54412), collagen X (GenBank Ace. No. X60382), collagen XI (GenBank Ace. No. J04177), and collagen XII (GenBank Ace. No. U73778), laminin proteins such as LAMA2 (GenBank Acc. No. NM_—000426), LAMA3 (GenBank Acc. No. L34155), LAMA4 (GenBank Ace. No. NM_—002290), LAMB1 (GenBank Acc. No. NM_—002291), LAMB3 (GenBank Acc. No. L25541), LAMC1 (GenBank Acc. No. NM_—002293), nidogen (GenBank Ace. No. NM_—002508), α-tectorin (GenBank Acc. No. NM_—005422), β-tectorin (GenBank Ace. No. NM_—058222), and fibronectin (GenBank Acc. No. X02761).

The term “blood proteins” are traditionally defined as those sourced from plasma, many now commonly produced by recombinant means, and include, but are not limited to native serum proteins, derivatives, fragments and mutants or variants thereof, blood clotting factors, derivatives, mutants, variants and fragments (including factors VII, VIII, IX, X), protease inhibitors (antithrombin III, alpha-1 antitrypsin), urokinase-type plasminogen activator, immunoglobulins, von Willebrand factor and von Willebrand mutants, fibronectin, fibrinogen, thrombin and hemoglobin.

The term “enzyme” is used herein to describe any protein or proteinaceous substance which catalyzes a specific reaction without itself being permanently altered or destroyed. Enzymes preferably include coagulation factors such as F2 (GenBank Acc. No. XM_—170688), F7 (GenBank Acc. No. XM_—027508), F8 (GenBank Acc. No. XM_—013124), F9 (GenBankAcc. No. NM_—000133), F10 (GenBankAcc. No. AF503510) and others, matrix metalloproteinases such as matrix metalloproteinase I (GenBank Acc. No. MMP1) (GenBank Acc. No. NM_—002421), MMP2 (GenBank Acc. No. NM_—004530), MMP3 (GenBank Acc. No. NM_—002422), MMP7 (GenBank Acc. No. NM_—002423), MMP8 (GenBank Acc. No. NM_—002424), MMP9 (GenBank Acc. No. NM_—004994), MMP10 (GenBank Acc. No. NM_—002425), MMP12 (GenBank Acc. No. NM_—002426), MMP13 (GenBank Acc. No. X75308), MMP20 (GenBank Acc. No. NM_—004771), adenosine deaminase (GenBank Acc. No. NM_—000022), mitogen activated protein kinases such as MAPK3 (GenBank Acc. No. XM_—055766), MAP2K2 (GenBank Acc. No. NM_—030662), MAP2K1 (GenBank Acc. No. NM_—002755), MAP2K4 (GenBank Acc. No. NM_—003010), MAP2K7 (AF013588), and MAPK12 (NM_—002969), kinases such as JNKK1 (GenBank Acc. No. U17743), JNKK2 (GenBank Acc. No. AF014401), JAK1 (M64174), JAK2 (NM_—004972), and JAK3 (NM_—000215), and phosphatases such as PPM1A (GenBank Acc. No. NM_—021003) and PPMID (GenBank Acc. No. NM_—003620).

The term “transcription factors” is used herein to describe any protein or peptide involved in the transcription of protein-coding genes. Transcription factors may include Sp1, Sp2 (GenBank Acc. No. NM_—003110), Sp3 (GenBank Acc. No. AY070137), Sp4 (GenBank Acc. No. NM_—003112) NFYB (GenBank Acc. No. NM_—006166), Hap2 (GenBank Acc. No. M59079), GATA-1 (GenBank Acc. No. NM_—002049), GATA-2 (GenBank Acc. No. NM_—002050), GATA-3 (GenBank Acc. No. X55122), GATA-4 (GenBank Ace. No. L34357), GATA-5, GATA-6 (GenBank Acc. No. NM_—005257), FOG2 (NM_—012082), Eryf1 (GenBank Acc. No. X17254), TRPS1 (GenBank Acc. No. NM_—014112), NF-E2 (GenBank Acc. No. NM_—006163), NF-E3, NF-E4, TFCP2 (GenBank Acc. No. NM_—005653), Oct-1 (GenBank Acc. No. X13403), homeobox proteins such as HOXB2 (GenBank Acc. No. NM_—002145), HOX2H (GenBank Acc. No. X16665), hairless homolog (GenBank Acc. No. NM_—005144), mothers against decapentaplegic proteins such as MADH1 (GenBank Acc. No. NM_—005900), MADH2 (GenBank Acc. No. NM_—005901), MADH3 (GenBank Acc. No. NM_—005902), MADH4 (GenBank Acc. No. NM_—005359), MADH5 (GenBank Acc. No. AF009678), MADH6 (GenBank Acc. No. NM_—005585), MADH7 (GenBank Acc. No. NM_—005904), MADH9 (GenBank Acc. No. NM_—005905), and signal transducer and activator of transcription proteins such as STAT1 (GenBank Acc. No. )(XM_—010893), STAT2 (GenBank Acc. No. NM_—005419), STAT3 (GenBank Acc. No. AJ012463), STAT4 (GenBank Acc. No. NM_—003151), STAT5 (GenBank Acc. No. L41142), and STAT6 (GenBank Acc. No. NM_—003153).

In yet another embodiment of the invention, the therapeutic molecule is a non-human or non-mammalian protein. For example, HIV gp120, HIV Tat, surface proteins of other viruses such as hepatitis, herpes, influenza, adenovirus and RSV, other HIV components, parasitic surface proteins such as malarial antigens, and bacterial surface proteins are preferred. These non-human proteins may be used, for example, as antigens, or because they have useful activities. For example, the therapeutic molecule may be streptokinase, staphylokinase, asparaginase, or other proteins with useful enzymatic activities.

In an alternative embodiment, the therapeutic molecule is a ligand-binding protein with biological activity. Such ligand-binding proteins may, for example, (1) block receptor-ligand interactions at the cell surface; or (2) neutralize the biological activity of a molecule in the fluid phase of the blood, thereby preventing it from reaching its cellular target. In some embodiments, the modified transferrin fusion proteins include a modified transferrin molecule fused to a ligand-binding domain of a receptor selected from the group consisting of, but not limited to, a low density lipoprotein (LDL) receptor, an acetylated LDL receptor, a tumor necrosis factor α receptor, a transforming growth factor β receptor, a cytokine receptor, an immunoglobulin Fc receptor, a hormone receptor, a glucose receptor, a glycolipid receptor, and a glycosaminoglycan receptor. In other embodiments, ligand-binding proteins include CD2 (M14362), CD3G (NM_—000073), CD3D (NM_—000732), CD3E (NM_—000733), CD3Z (J04132), CD28 (NM_—006139), CD4 (GenBank Acc. No. NM_—000616), CD1A (GenBank Acc. No. M28825), CD1B (GenBank Acc. No. NM_—001764), CD1C (GenBank Acc. No. NM_—001765), CD1D (GenBank Acc. No. NM_—001766), CD80 (GenBank Acc. No. NM_—005191), GNB3 (GenBank Acc. No. AF501884), CTLA-4 (GenBank Acc. No. NM_—005214), intercellular adhesion molecules such as ICAM-1 (NM_—000201), ICAM-2 (NM_—000873), and ICAM-3 (NM_—002162), tumor necrosis factor receptors such as TNFRSF1A (GenBank Acc. No. X55313), TNFR1SFB (GenBank Acc. No. NM_—001066), TNFRSF9 (GenBank Acc. No. NM_—001561), TNFRSF10B (GenBank Acc. No. NM_—003842), TNFRSF11B (GenBank Acc. No. NM_—002546), and TNFRSF13B (GenBank Acc. No. NM_—006573), and interleukin receptors such as IL2RA (GenBank Acc. No. NM_—000417), IL2RG (GenBank Acc. No. NM_—000206), IL4R (GenBank Acc. No. AF421855), IL7R (GenBank Acc. No. NM_—002185), IL9R (GenBank Acc. No. XM_—015989), and IL13R (GenBank Acc. No. X95302). Preferably, the Tf-ligand-binding protein fusion of the present invention displays the biological activity of the ligand-binding protein.

The term “cancer-associated proteins” is used herein to describe proteins or polypeptides whose expression is associated with cancer or the maintenance of controlled cell growth, such as proteins encoded by tumor suppressor genes or oncogenes. Cancer-associated proteins may include p16 (GenBank Acc. No. AH005371), p53 (GenBank Acc. No. NM_—000546), p63 (GenBank Acc. No. NM_—003722), p73 (GenBank Acc. No. NM_—005427), BRCA1 (GenBank Acc. No. U14680), BRCA2 (GenBank Acc. No. NM_—000059), CTBP interacting protein (GenBank Acc. No. U72066), DMBT1 (GenBank Acc. No. NM_—004406), HRAS (GenBank Acc. No. NM_—005343), NCYM (GenBank Acc. No. NM_—006316), FGR (GenBank Acc. No. NM_—005248), myb (GenBank Acc. No. AF104863), raf1 (GenBank Acc. No. NM_—002880), erbB2 (GenBank Acc. No. NM_—004448), VAV (GenBank Acc. No. X16316), c-fos (V GenBank Acc. No. 01512), c-fes (GenBank Acc. No. X52192), c-jun (GenBank Acc. No. NM_—002228), MAS1 (GenBank Acc. No. M13150), pim-1 (GenBank Acc. No. M16750), TIF1 (GenBank Acc. No. NM_—003852), c-fms (GenBank Acc. No. X03663), EGFR (GenBank Acc. No. NM_—005228), erbA (GenBank Acc. No. X04707), c-src tyrosine kinase (GenBank Acc. No. XM_—044659), c-abl (GenBank Acc. No. M14752), N-ras (GenBank Acc. No. X02751), K-ras (GenBank Acc. No. M54968), jun-B (GenBank Acc. No. M29039), c-myc (GenBank Acc. No. AH001511), RB1 (GenBank Acc. No. M28419), DCC (GenBank Acc. No. X76132), APC (GenBank Ace. No. NM_—000038), NF1 (GenBank Acc. No. M89914), NF2 (GenBank Acc. No. Y18000), and bcl-2 (GenBank Acc. No. M13994).

“Fusogenic inhibitor peptides” is used herein to describe peptides that show antiviral activity, anti-membrane fusion capability, and/or an ability to modulate intracellular processes, for instance, those involving coiled-coil peptide structures. Antiviral activity includes, but is not limited to, the inhibition of HIV-1, HIV-2, RSV, SIV, EBV, measles virus, influenza virus, or CMV transmission to uninfected cells. Additionally, the antifusogenic capability, antiviral activity or intracellular modulatory activity of the peptides merely requires the presence of the peptides and specifically does not require the stimulation of a host immune response directed against such peptides. Antifusogenic refers to a peptide's ability to inhibit or reduce the level of membrane fusion events between two or more moieties relative to the level of membrane fusion which occurs between said moieties in the absence of the peptide. The moieties may be, for example, cell membranes or viral structures, such as viral envelopes or pili. The term “antiviral peptide”, as used herein, refers to the peptide's ability to inhibit viral infection of cells or some viral activity required for productive viral infection and/or viral pathogenesis, via, for example, cell-cell fusion or free virus infection. Such infection may involve membrane fusion, as occurs in the case of enveloped viruses, or some other fusion event involving a viral structure and a cellular structure. Fusogenic inhibitor peptides and antiviral peptides often have amino acid sequences that are derived from greater than one viral protein (e.g., an HIV-1, HIV-2, RSV, and SIV-derived polypeptide).

Examples of fusogenic inhibitor peptides and antiviral peptides can be found in WO 94/2820, WO 96/19495, WO 96/40191, WO 01/64013 and U.S. Pat. Nos. 6,333,395, 6,258,782, 6,228,983, 6,133,418, 6,093,794, 6,068,973, 6,060,065, 6,054,265, 6,020,459, 6,017,536, 6,013,263, 5,464,933, 5,346,989, 5,603,933, 5,656,480, 5,759,517, 6,245,737; 6,326,004, and 6,348,568; all of which are herein incorporated by reference. In a preferred embodiment, antifusogenic peptides are selected from the group consisting of HIV T-20 (FWNWLSAWKDLELLEQENKEQQNQSEEILSHILSTY, SEQ ID NO: 4), HIV T-1249, RSV T786 (VYPSDEYDASISQVNEEINQALAYIRKADELLENV, SEQ ID NO: 5), RSV T1584 (AVSKVLHLEGEVNKIKSALLSTNKAVVSLSNGVSVLTSKVLDLKNYIDKQL, SEQ ID NO: 6) and RSV T112 (VFPSDEFDASISQVNEKINQSLAFIRESDELLHNV, SEQ ID NO: 7).

Examples of other types of peptides, include fragments of therapeutic proteins as described herein, in particular, fragments of human proteins that retain at least one activity of the parent molecule. Peptides that may be used to produce modified Tf fusion proteins of the invention also include mimetic peptides and peptides that exhibit a biological activity of a therapeutic protein but differ in sequence or three-dimensional structure from a full-length therapeutic protein. As a non-limited example, peptides include erythropoeitin mimetic peptides disclosed by Johnson et al. (2000) Nephrol. Dial. Transplant 15(9): 1274-7, Kuai et al. (2000) J. Pept. Res. 56(2):59-62, Barbone et al. (1999) Nephrol. Dial. Transplant. 14 Supp 2:80-4, Middleton et al. (1999) J. Biol. Chem. 274(20):14163-9, Johnson et al. (1998) Biochemistry 37(11):3699-710, Johnson et al. (1997) Chem. Biol. 12:939-50, Wrighton et al. (1997) Nat. Biotechnol. 15(12):1261-5, Livnah et al. (1996) Science 273:464-71, and Wrighton et al., (1996) Science 273:458-64.

Therapeutic molecules also include allergenic proteins and digested fragments thereof. These include pollen allergens from ragweed, rye, June grass, orchard grass, sweet vernal grass, red top grass, timothy grass, yellow dock, wheat, corn, sagebrush, blue grass, California annual grass, pigweed, Bermuda grass, Russian thistle, mountain cedar, oak, box elder, sycamore, maple, elm, etc., dust mites, bee venom, food allergens, animal dander, and other insect venoms.

Other therapeutic molecules include microbial vaccines which include viral, bacterial and protozoal vaccines and their various components such as surface antigens. These include vaccines which contain glycoproteins, proteins or peptides derived from these proteins. Such vaccines are prepared from Staphylococcus aureus, Streptococcus pyogenes, Streptococcus pneumonia, Neisseria meningitidis, Neisseria gonorrhoeae, Salmonella spp., Shigella spp., Escherichia coli, Klebsiella spp., Proteus spp., Vibrio cholerae, Campylobacter pylori, Pseudomonas aeruginosa, Haemophilus influenzae, Bordetella pertussis, Mycobacterium tuberculosis, Legionella pneumophila, Treponema pallidum, chlamydia, tetanus toxoid, diphtheria toxoid, influenza viruses, adenoviruses, paramyxoviruses (mumps, measles), rubella viruses, polio viruses, hepatitis viruses, herpes viruses, rabies virus, HIV-1, HIV-2, RSV and papilloma viruses.

Preferred fusion molecules may contain anti-HIV viral peptides, anti-RSV peptides, human growth hormone, α and/or β interferons, erythropoietin (EPO), EPO like peptides, granulocyte-colony stimulating factor (GCSF), granulocyte-macrophage colony-stimulating factor (GMCSF), insulin, insulin-like growth factor (IGF), thrombopoeitin, peptides corresponding to the CDR of an antibody, Islet Neogenesis Associated Protein (INGAP), calcitonin, angiostatin, endostatin, interleukin-2, growth hormone releasing factor, human parathyroid hormone, anti-tumor necrosis factor (TNF) peptides, interleukin-1 (IL-1) receptor and/or single chain antibodies.

Fusion proteins of the invention may also be prepared to include peptides or polypeptides derived from peptide libraries to screen for molecules with new or novel functions. Such peptide libraries may include those commercially or publicly available, e.g., American Peptide Co. Inc., Cell Sciences Inc., Invitrogen Corporation, Phoenix Pharmaceuticals Inc., United States Biological, as well as those produced by available technologies, e.g., bacteriophage and bacterial display libraries made using standard procedures.

In yet other embodiments of the invention, Tf fusion proteins may be prepared by using therapeutic protein moieties as known in the art and exemplified by the peptides and proteins currently approved by the Food and Drug Administration at (www.fda.gov/cber/efoi/approve.htm) as well as PCT Patent Publication Nos. WO 01/79258, WO 01/77137, WO 01/79442, WO 01/79443, WO 01/79444 and WO 01/79480, all of which are herein incorporated by reference in their entirety.

Table 1 (adapted from PCT International Publication No. WO 01/79444) provides a non-exhaustive list of therapeutic proteins that correspond to a therapeutic protein portion of a modified transferrin fusion protein of the invention. The “Therapeutic Protein X” column discloses therapeutic protein molecules followed by parentheses containing scientific and brand names that comprise or alternatively consist of that therapeutic protein molecule or a fragment or variant thereof. “Therapeutic protein X” as used herein may refer either to an individual therapeutic protein molecule (as defined by the amino acid sequence obtainable from the CAS and GenBank accession numbers), or to the entire group of therapeutic proteins associated with a given therapeutic protein molecule disclosed in this column. The ‘Exemplary Identifier’ column provides Chemical Abstracts Services (CAS) Registry Numbers (published by the American Chemical Society) and/or GenBank Accession Numbers (e.g., Locus ID, NP-XXXXX (Reference Sequence Protein), and XP-XXXXX (Model Protein) identifiers available through the National Center for Biotechnology Information (NCBI) webpage (www.ncbi.nlm.nih.gov) that correspond to entries in the CAS Registry or GenBank database which contain an amino acid sequence of the protein molecule or of a fragment or variant of the therapeutic protein molecule. In addition GenSeq Accession numbers and/or journal publication citations are given to identify the exemplary amino acid sequence for some polypeptides.

The summary pages associated with each of these CAS and GenBank and GenSeq Accession Numbers as well as the cited journal publications are available (e.g., PubMed ID number (PMID)) and are herein incorporated by reference in their entirety. The PCT/Patent Reference column provides U.S. Patent numbers, or PCT International Publication Numbers corresponding to patents and/or published patent-applications that describe the therapeutic protein molecule all of which are herein incorporated by reference in their entirety. The Biological Activity column describes biological activities associated with the therapeutic protein molecule. The Exemplary Activity Assay column provides references that describe assays which may be used to test the therapeutic and/or biological activity of a therapeutic protein or a transferrin fusion protein of the invention comprising a therapeutic protein X portion. These references are also herein incorporated by reference in their entirety. “The Preferred Indication Y” column describes disease, disorders, and/or conditions that may be treated, prevented, diagnosed, or ameliorated by therapeutic protein X or a transferrin fusion protein of the invention comprising a therapeutic protein X portion.

TABLE 1TherapeuticExemplaryPCT/PatentProtein XIdentifierReferenceBiological ActivityExemplary Activity AssayPreferred Indication YBMP-1GeneSeq AcessionWO8800205BMP1 belongs to the transforming growthBMP-1 activity can be determined using the followingInduction of Cartilage,P80618factor-beta (TGFB) superfamily. Boneassays known in the art: Nat Genet. 2001Tissue and Bonemorphogenic proteins induce cartilage andJan; 27(1): 84-8; Eur J Biochem 1996 AprGrowth, and Diabetesbone formation, play important role in1; 237(1): 295-302; J Biol Chem, Vol. 274, Issue 16,nephrogesis, and play an important role in the10897-10902, Apr. 16, 1999; and Hogan, B. L. M.development of many organs, including lung,(1996) Genes Dev. 10, 1580-1594.heart, teeth, gut, skin, and particularly thekidney.BMP-2GeneSeqWO8800205BMP-2 belongs to the transforming growthBMP-2 activity can be determined using the followingInduction of Cartilage,Accession P80619factor-beta (TGFB) superfamily. Boneassays known in the art: Nat Genet. 2001 Jan;Tissue and Bonemorphogenic protein induces bone formation.27(1): 84-8; Eur J Biochem 1996 Apr 1; 237(1): 295-302;Growth, and DiabetesJ Biol Chem, Vol. 274, Issue 16, 10897-10902,Apr. 16, 1999; and Hogan, B. L. M. (1996) GenesDev. 10, 1580-1594.BMP-2BGeneSeqUS5631142BMP-2b belongs to the transforming growthBMP-2b activity can be determined using theInduction of Cartilage,Accession W24850factor-beta (TGFB) superfamily. Bonefollowing assays known in the art: Nat Genet. 2001Tissue and Bonemorphogenic protein induces bone formation.Jan; 27(1): 84-8; Eur J Biochem 1996 AprGrowth, and Diabetes1; 237(1): 295-302; I Biol Cbcre, Vol. 274, Issue 16,10897-10902, Apr. 16, 1999; and Hogan, B. L. M.(1996) Genes Dev. 10, 1580-1594.BMP-4GeneSeqWO0020591BMP-4 belongs to the transforming growthBMP-4 activity can be determined using the followingInduction of Cartilage,Accessionfactor-beta (TGFB) superfamily. Boneassays known in the art: Nat Genet. 2001 Jan;Tissue and BoneB02796morphogenic protein induces bone formation.27(1): 84-8; Eur J Biochem 1996 Apr 1; 237(1): 295-302;Growth, and DiabetesJ Biol Chem, Vol. 274, Issue 16, 10897-10902,Apr. 16, 1999; and Hogan, B. L. M. (1996) GenesDev. 10, 1580-1594.BMP-5GeneSeqWO0020591BMP-5 belongs to the transforming growthBMP-5 activity can be determined using the followingInduction of Cartilage,Accessionfactor-beta (TGFB) superfamily. Boneassays known in the art: Nat Genet. 2001 Jan;Tissue and BoneB02797morphogenic protein induces bone formation.27(1): 84-8; Eur J Biochem 1996 Apr 1; 237(1): 295-302;Growth, and DiabetesJ Biol Chem, Vol. 274, Issue 16, 10897-10902,Apr. 16, 1999; and Hogan, B. L. M. (1996) GenesDev. 10, 1580-1594.BMP-6GeneSeqUS5187076BMP-6 belongs to the transforming growthBMP-6 activity can be determined using the followingInduction of Cartilage,Accessionfactor-beta (TGFB) superfamily. Boneassays known in the art: Nat Genet. 2001 Jan;Tissue and BoneR32904morphogenic protein induces bone formation.27(1): 84-8; Eur J Biochem 1996 Apr 1; 237(1): 295-302;Growth, and DiabetesJ Biol Chem, Vol. 274, Issue 16, 10897-10902,Apr. 16, 1999; and Hogan, B. L. M. (1996) GenesDev. 10, 1580-1594.OsteogenicGeneSeqWO973462OP-1 belongs to the transforming growthOP-1 activity can be determined using the followingInduction of Cartilage,Protein-1; OP-1;Accessionfactor-beta (TGFB) superfamily. Boneassays known in the art: Nat Genet. 2001 Jan;Tissue and BoneBMP-7W34783morphogenic protein induces bone formation.27(1): 84-8; Eur J Biochem 1996 Apr 1; 237(1): 295-302;Growth, and DiabetesJ Biol Chem, Vol. 274, Issue 16, 10897-10902,Apr. 16, 1999; and Hogan, B. L. M. (1996) GenesDev. 10, 1580-1594.OsteogenicGeneSeq AccessionWO9406399OP-2 belongs to the transforming growthOP-2 activity can be determined using the followingInduction of Cartilage,Protein-2R57973factor-beta (TGFB) superfamily. Boneassays known in the art: Nat Genet. 2001 Jan;Tissue and Bonemorphogenic protein induces bone formation.27(1): 84-8; Eur J Biochem 1996 Apr 1; 237(1): 295-302;Growth, and DiabetesJ Biol Chem, Vol. 274, Issue 16, 10897-10902,Apr. 16, 1999; and Hogan, B. L. M. (1996) GenesDev. 10, 1580-1594.GDP-1GeneSeq AccessionWO9406449Members of the TGF-beta family of proteinsThe effect of GDF-1 on signaling can be assayed byDevelopmentalR60961initiate cell signaling by binding to heteromerictreating Primary BAECs transferred with a constructdisorders, Induction ofreceptor complexes of type I (TbetaRI) andcalled p3TP-Lux, containing a TGF-beta responsiveCartilage, Tissue andtype II (TbetaRII) serine/threonine kinasepromoter fused to a reporter gene, and measuringBone Growth, andreceptors (reviewed by Massague, J. et al.luciferase gene expression (Wrana et al., 1994, NatureDiabetes(1994) Trends Cell Biol. 4: 172 178; Miyazono, K.370: 341-347).et al. (1994) Adv. Immunol. 55: 181-220).Activation of this heteromeric receptorcomplex occurs when TGF-beta binds toTbetaRII, which then recruits andphosphorylates TbetaRI. Activated TbetaRIthen propagates the signal to downstreamtargets (Chen, F. and Weinberg, R. A. (1995)PNA892: 1565-1569; Wrana, J. L. et al. (1994)Nature 370: 341 347).BMP-9GeneSeq AccessionWO9533830BMP-9 belongs to the transforming growthBMP-9 activity can be determined using the followingInduction of Cartilage,R86903factor-beta (TGFB) superfamily. Boneassays known in the art: Nat Genet. 2001 Jan;Tissue and Bonemorphogenic protein induces bone formation.27(1): 84-8; Eur J Biochem 1996 Apr 1; 237(1): 295-302;Growth, and DiabetesJ Biol Chem, Vol. 274, Issue 16, 10897-10902,Apr. 16, 1999; and Hogan, B. L. M. (1996) GenesDev. 10, 1580-1594.BMP-10GeneSeq AccessionWO9426893BMP-10 belongs to the transforming growthBMP-10 activity can be determined using theInduction of Cartilage,R66202factor-beta (TGFB) superfamily. Bonefollowing assays known in the art: Nat Genet. 2001Tissue and Bonemorphogenic protein induces bone formation.Jan; 27(1): 84-8; Eur J Biochem 1996 Apr 1;Growth, and Diabetes237(1): 295-302; J Biol Chem, Vol. 274, Issue 16,10897-10902, Apr. 16, 1999; and Hogan, B. L. M.(1996) Genes Dev. 10, 1580-1594.BMP-12GeneSeq AccessionWO9516035BMP-12 belongs to the transforming growthBMP-12 activity can be determined using theInduction of Cartilage,R78734factor-beta (TGFB) superfamily. Bonefollowing assays known in the art: Nat Genet. 2001Tissue and Bonemorphogenic protein induces bone formation.Jan; 27(1): 84-8; Eur J Biochem 1996 Apr 1;Growth, and Diabetes237(1): 295-302; J Biol Chem, Vol. 274, Issue 16,10897-10902, Apr. 16, 1999; and Hogan, B. L. M.(1996) Genes Dev. 10, 1580-1594.BMP-15GeneSeq AccessionWO9636710BMP-15 belongs to the transforming growthBMP-15 activity can be determined using theInduction of Cartilage,W11261factor-beta (TGFB) superfamily. Bonefollowing assays known in the art: Nat Genet. 2001Tissue and Bonemorphogenic protein induces bone formation.Jan; 27(1): 84-8; Eur J Biochem 1996 Apr 1;Growth, and Diabetes237(1): 295-302; J Biol Chem, Vol. 274, Issue 16,10897-10902, Apr. 16, 1999; and Hogan, B. L. M.(1996) Genes Dev. 10, 1580-1594.BMP-17GeneSeq AccessionWO9929718BMP-17 belongs to the transforming growthBMP-17 activity can be determined using theInduction of Cartilage,Y17870factor-beta (TGFB) superfamily. Bonefollowing assays known in the art: Nat Genet. 2001Tissue and Bonemorphogenic protein induces bone formation.Jan; 27(1): 84-8; Eur J Biochem 1996 Apr 1;Growth, and Diabetes237(1): 295-302; J Biol Chem, Vol. 274, Issue 16,10897-10902, Apr. 16, 1999; and Hogan, B. L. M.(1996) Genes Dev. 10, 1580-1594.BMP-18GeneSeqWO9929718BMP-18 belongs to the transforming growthBMP-18 activity can be determined using theInduction of Cartilage,Accession Y17871factor-beta (TGFB) superfamily. Bonefollowing assays known in the art: Nat Genet. 2001Tissue and Bonemorphogenic protein induces bone formation.Jan; 27(1): 84-8; Eur J Biochem 1996 Apr 1;Growth, and Diabetes237(1): 295-302; J Biol Chem, Vol. 274, Issue 16,10897-10902, Apr. 16, 1999; and Hogan, B. L. M.(1996) Genes Dcv. 10, 1580-1594.Inhibin alphaGeneSeqWO0020591The inhibin beta A subunit joins the alphaTumor suppressor activity of inhibin can be determinedTumor suppression.Accession B02806subunit to form a pituitary FSH secretionusing assays known in the art: Matzuk et al., Natureinhibitor. Inhibin has been shown to regulate1992 Nov. 26: 360 (6402); 313-9.gonadal stromal cell proliferation negativelyand to have tumour-suppressor activity. Inaddition, serum levels of inbibin bave beenshown to reflect the size of granulosa-celltumors and can therefore be used as a markerfor primary as well as recurrent disease.Inhibin betaGeneSeqWO0020591The inhibin beta A subunit joins the alphaTumor suppressor activity of inhibin can be determinedTumor suppression.Accessionsubunit to form a pituitary FSH secretionusing assays known in the art: Matzuk et al., NatureH02808inhibitor. Inhibin has been shown to regulate1992 Nov. 26: 360 (6402); 313-9.gonadal stromal cell proliferation negativelyand to have tumour-suppressor activity. Inaddition, serum levels of inhibin have beenshown to reflect the size of granulosa-celltumors and can therefore be used as a markerfor primary as well as recurrent disease.Cerebus ProteinGeneSeqWO9849296Cerebus is believed to be involved in theBMP activity, in the presence of the antagonistBMP Antagonist usefulAccessioninhibition of BMP activityCerebus, can be determined using the following assaysfor Osteosarcoma,W86032known in the art: Nat Genet. 2001 Jan; 27(1): 84-8; Eurabnormal bone growth.J Biochem 1996 Apr 1; 237(1): 295-302; J Biol Chem,Vol. 274, Issue 16, 10897-10902, Apr. 16, 1999; andHogan, B. L. M. (1996) Genes Dev. 10, 1580-1594.Soluble BMPGeneSeqWO9614579Soluble BMP receptor kinase protein-3 isBMP activity, in the presence of the soluble antagonistBMP Antagonist usefulReceptor KinaseAccessioninvolved in the binding of BMPs. SolubleBMP receptor kinase protein-3, can be determinedfor Osteosarcoma,Protein-3R95227BMP receptor kinase protein-3 is useful as anusing the following assays known in the art: Nat Genet.abnormal bone growth.antagonist for the inhibition of BMP activity.2001 Jan; 27(1): 84-8; Eur J Biochem 1996 Apr 1;237(1): 295-302; J Biol Chem, Vol. 274, Issue 16,10897-10902, Apr. 16, 1999; and Hogan, B. L. M.(1996) Genes Dev. 10, 1580-1594.BMP ProcessingGeneSeqWO9741250BMPs belong to the transforming growthBMP activity, in the presence of the Furin, can beBone formation orEnzyme FurinAccessionfactor-beta (TGFB) superfamily. Bonedetermined using the following assays known in theRegenerationW36099morphogenic protein induces bone formation.art: Nat Genet. 2001 Jan; 27(1): 84-8; Eur J BiochemAbnormalities1996 Apr 1; 237(1): 295-302; J Biol Chem, Vol. 274,Issue 16, 10897-10902, Apr. 16, 1999; and Hogan, B. L. M.(1996) Genes Dev. 10, 1580-1594.TGF-beta 1GeneSeqWO9216228Members of the TGF-beta family of proteinsThe effect of TGF betas on signaling can be assayed byUseful for treatingAccessioninitiate cell signaling by binding to heteromerictreating Primary BAECs transfected with a constructcancer and to promoteR29657receptor complexes of type I (TbetaRI) andcalled p3TP-Lux, containing a TGF-beta responsivewound healing.type II (TbetaRII) serine/threonine kinasepromoter fused to a reporter gene, and measuringreceptors (reviewed by Massague, J. et al.luciferase gene expression (Wrana et al., 1994, Nature(1994) Trends Cell Biol. 4: 172 178; Miyazono, K.370: 341-347).et al. (1994) Adv. Immunol. 55: 181-220).Activation of this heteromeric receptorcomplex occurs when TGF-beta. binds toTbetaRII, which then recruits andphosphorylates TbetaRI. Activated TbetaRIthen propagates the signal to downstreamtargets (Chen, F. and Weinberg. R. A. (1995)PNA892: 1565-1569; Wrana, J. L. et al. (1994)Nature 370: 341.TGF-beta 2GeneSeqEP542679Members of the TGF-beta family of proteinsThe effect of TGF betas on signaling can be assayed byUseful for treatingAccessioninitiate cell signaling by binding to heteromerictreating Primary BAECs transfected with a constructcancer and to promoteR39659receptor complexes of type I (TbetaRI) andcalled p3TP-Lux, containing a TGF-beta responsivewound healing.type II (TbetaRII) serine/threonine kinasepromoter fused to a reporter gene, and measuringreceptors (reviewed by Massague, J. et al.luciferase gene expression (Wrana et al., 1994, Nature(1994) Trends Cell Biol. 4: 172 178; Miyazono, K.370: 341-347).et al. (1994) Adv. Immunol. 55: 181-220).Activation of this heteromeric receptorcomplex occurs when TGF-beta. binds toTbetaRII, which then recruits andphosphorylates TbetaRI. Activated TbetaRIthen propagates the signal to downstreamtargets (Chen, F. and Weinberg. R. A. (1995)PNA892: 1565-1569; Wrana, J. L. et al. (1994)Nature 370: 341.ZTGF-beta 9GeneSeqWO0015798Members of the TGF-beta family of proteinsThe effect of TGF betas on signaling can be assayed byUseful for treatingAccessioninitiate cell signaling by binding to heteromerictreating Primary BAECs transfected with a constructcancer and to promoteY70654receptor complexes of type I (TbetaRI) andcalled p3TP-Lux, containing a TGF-beta responsivewound healing.type II (TbetaRII) serine/threonine kinasepromoter fused to a reporter gene, and measuringreceptors (reviewed by Massague, J. et al.luciferase gene expression (Wrana et al., 1994, Nature(1994) Trends Cell Biol. 4: 172 178; Miyazono, K.370: 341-347).et al. (1994) Adv. Immunol. 55: 181-220).Activation of this heteromeric receptorcomplex occurs when TGF-beta. binds toTbetaRII, which then recruits andphosphorylates TbetaRI. Activated TbetaRIthen propagates the signal to downstreamtargets (Chen, F. and Weinberg. R. A. (1995)PNA892: 1565-1569; Wrana, J. L. et al. (1994)Nature 370: 341.Anti-TGF betaGB2305921Members of the TGF-beta family of proteinsThe effect of TGF betas on signaling in the presence ofUseful for control offamily antibodiesinitiate cell signaling by binding to heteromerican anti-TGF beta antibody, can be assayed by treatingfibrosis, immune, andreceptor complexes of type I (TbetaRI) andPrimary BAECs transfected with a construct calledinflammatory disease.type II (TbetaRII) serine/threonine kinasep3TP-Lux, containing a TGF-beta responsive promoterreceptors (reviewed by Massague, J. et al.fused to a reporter gene, and measuring luciferase gene(1994) Trends Cell Biol. 4: 172 178; Miyazono, K.expression (Wrana et al., 1994, Nature 370: 341-347).et al. (1994) Adv. Immunol. 55: 181-220).Activation of this heteromeric receptorcomplex occurs when TGF-beta. binds toTbetaRII, which then recruits andphosphorylates TbetaRI. Activated TbetaRIthen propagates the signal to downstreamtargets (Chen, F. and Weinberg. R. A. (1995)PNA892: 1565-1569; Wrana, J. L. et al. (1994)Nature 370: 341.Latent TGF betaGeneSeqWO0012551Members of the TGF-beta family of proteinsThe effect of TGF betas on signaling in the presence ofUseful for inhibitingbinding protein IIAccessioninitiate cell signaling by binding to heteromerica TGF beta binding protein, can be assayed by treatingtissue or tumor growth.Y70552receptor complexes of type I (TbetaRI) andPrimary BAECs transfected with a construct calledtype II (TbetaRII) serine/threonine kinasep3TP-Lux, containing a TGF-beta responsive promoterreceptors (reviewed by Massague, J. et al.fused to a reporter gene, and measuring luciferase gene(1994) Trends Cell Biol. 4: 172 178; Miyazono, K.expression (Wrana et al., 1994, Nature 370: 341-347).et al. (1994) Adv. Immunol. 55: 181-220).Activation of this heteromeric receptorcomplex occurs when TGF-beta. binds toTbetaRII, which then recruits andphosphorylates TbetaRI. Activated TbetaRIthen propagates the signal to downstreamtargets (Chen, F. and Weinberg. R. A. (1995)PNA892: 1565-1569; Wrana, J. L. et al. (1994)Nature 370: 341.MP52GeneSeqWO9741250Members of the TGF-beta family of proteinsThe effect of TGF betas on signaling can be assayed byBone formation orAccessioninitiate cell signaling by binding to heteromerictreating Primary BAECs transfected with a constructRegenerationW36100receptor complexes of type I (TbetaRI) andcalled p3TP-Lux, containing a TGF-beta responsiveAbnormalitiestype II (TbetaRII) serine/threonine kinasepromoter fused to a reporter gene, and measuringreceptors (reviewed by Massague, J. et al.luciferase gene expression (Wrana et al., 1994, Nature(1994) Trends Cell Biol. 4: 172 178; Miyazono, K.370: 341-347).et al. (1994) Adv. Immunol. 55: 181-220).Activation of this heteromeric receptorcomplex occurs when TGF-beta. binds toTbetaRII, which then recruits andphosphorylates TbetaRI. Activated TbetaRIthen propagates the signal to downstreamtargets (Chen, F. and Weinberg. R. A. (1995)PNA892: 1565-1569; Wrana, J. L. et al. (1994)Nature 370: 341.b57 ProteinGeneSeqWO9837195BMPs are involved in the induction of boneBMP activity, in the presence of b57 protein, can beBMP Antagonist usefulAccessionformation. Specific antagonists are useful isdetermined using the following assays known in thefor Osteosarcoma,W69293preventing this activity from occurring.art: Nat Genet. 2001 Jan; 27(1): 84-8; Eur J Biochemabnormal bone growth.1996 Apr 1; 237(1): 295-302; J Biol Chem, Vol. 274,Issue 16, 1089-10902, Apr. 16, 1999; and Hogan, B. L. M.(1996) Genes Deve. 10, 1580-1594.ResistinGeneSeqWO0064920This gene belongs to the family defined byAbility of resistin to influence type II diabetes can beType II diabetes andAccessionmouse FIZZI and FIZZ3/Resistin genes. Thedetermined using assays known in the art: PontoglioSyndrome X.W69293characteristic feature of this family is the C-et al., J Clin Invest 1998 May 15; 101(10): 2215-22.terminal stretch of 10 cys residues with identicalspacing. The mouse homolog of this protein issecreted by adipocytes, may be the hormonepotantially linking obesity to type II diabetes.Galectin-4GeneSeqWO9703190Galectins are a family of carbohydrate-bindingAbility of Galectin-4 polypeptides to bind lactose canLactose intolerance.Accessionproteins characterized by an affinity for beta-be determined using assays known in the art: Wada, etW11841galactoside containing glycoconjugates.al., J Biol Chem 1997 Feb 28; 272(9): 6078-86.APM-I; ACRP-30;GeneSeqW00026363ACPR30 gene is exclusively expressed inAbility of ACRP30 polypeptides to influence obesityObesity, MetabolicFamoxinAccessionadipose tissue. ACRP30 is thought to increaseand fat oxidation can be determined using assaysdisorders, LipidY71035fatty acid oxidation by muscle tissue.known in the art: Fruebis et al., Proc Nat'l Acad SciMetabolism; HormoneUSA 2001 Feb 13; 98(4): 2005-10.Secretion.ACRP-30GeneSeqWO0063376ACPR30 gene is exclusively expressed inAbility of ACRP30 homologue polypeptides toObesity, MetabolicHomologue;Accessionadipose tissue. ACRP30 is thought to increaseinfluence obesity and fat oxidation can be determineddisorders, LipidComplementB30234fatty acid oxidation by muscle tissue.using assays known in the art: Fruebis et al., ProcMetabolism; HormoneComponent Clq CNat'l Acad Sci USA 2001 Feb 13; 98(4): 2005-10.Secretion.Calpain-10aGeneSeqWO0023603Calpain is believed to play a role in insulinAbility of Calpain-10 to influence type II diabetes canDiabetes mellitus;Accessionsecretion and insulin activity, and therefore maybe determined using assays known in the art:Regulation of InsulinY79567be useful in the treatment of type II diabetes.Pontoglio et al., J Clin Invest 1998 May 15;secretory response;101(10): 2215-22.Insulin mediated glucosetransport disorders.Calpain-10bGeneSeqWO0023603Calpain is believed to play a role in insulinAbility of Calpain-10 to influence type II diabetes canDiabetes mellitus;Accessionsecretion and insulin activity, and therefore maybe determined using assays known in the art:Regulation of InsulinY79568be useful in the treatment of type II diabetes.Pontoglio et al., J Clin Invest 1998 May 15;secretory response;101(10): 2215-22.Insulin mediated glucosetransport disorders.Calpain-10cGeneSeqWO0023603Calpain is believed to play a role in insulinAbility of Calpain-10 to influence type II diabetes canDiabetes mellitus;Accessionsecretion and insulin activity, and therefore maybe determined using assays known in the art:Regulation of InsulinY79569be useful in the treatment of type II diabetes.Pontoglio et al., J Clin Invest 1998 May 15;secretory response;101(10): 2215-22.Insulin mediated glucosetransport disorders.PDGF-DGeneSeqWO0027879Vascular Endothelial Growth Factor.Proliferation assay using NR6R-3T3 cells (RizzinoWound Healing;Accession1988 Cancer Res. 48: 4266).Atherosclermis.Y71130FasLGeneSeqWO9936079Activities associated with apoptosis andActivity can be determined using Apoptosis assaysApoptosis-relatedAccessionimmune system functions.known in the art: Walczak et al. (1996) EMBOJ 16:disorders; AutoimmuneY285945386-5397.disorders; Graft v-Hostdisorders.Chondro modulin-GeneSeqW00029579Chondromodulin proteins are cartilage proteinsAbility of Chondromodulin-like protein to inhibitAntianglogenic agent;like proteinAccessionthought to confer resistance to anglogeneis, andvascularization can be determined using assaysOsteoblast proliferationY71262thus are useful as anti-angiogenic agents thatknown in the art: Hirakie et al., J Biol Chem 1997stimulator; preventsmay have utility in combating cancer.Dec 19; 272(51): 32419-26.vascularization ofcartilage tissue; Usefulto treat cancer.PatchedGeneSeqUS5837538Patched is a tumour-suppressor receptor forAbility of soluble Patched to bind to and inhibit theReceptor for HedgehogAccessionSonic hedgehog (shh), which is a protein thatactivities of shh can be determined using assayscellular proliferationW72969controls developmental patterning and growth.known in the art: Stone et al., Nature 1996 Nov 14;signaling molecule.384(6605): 129-34.This receptor is useful asa means of preventingcellular proliferation viathe shh signalingpathway, thus useful forcancers.Patched-2GeneSeqWO9953058Patched is a tumour-suppressor receptor forAbility of soluble Patched to bind to and inhibit theReceptor for HedgehogAccessionSonic hedgehog (shh), which is a protein thatactivities of shh can be determined using assayscellular proliferationY43261controls developmental patterning and growth.known in the art: Stone et al., Nature 1996 Nov 14;signaling molecule.384(6605): 129-34.This receptor is useful asa means of preventingcellular proliferation viathe shh signalingpathway, thus useful forcancers.Maspin; ProteaseGeneSeqWO9405804Maspin is a member of the serpin family ofThe inhibitory effects of Maspin and other proteaseTumor suppressor whichInhibitor 5Accessionserine protease inhibitors that is thought toinhibitors can be assayed using methods known in theis down-regulated inR50938suppress tumor metastasis.art such as a labeled protease substrate, for example,breast cancers. TheUniversal Protease Substrate (casein, resorufin-maspin protein haslabeled): Roche Molecular Biochemicals, Cat. No.tumour suppressing and1080733.invasion suppressingactivity.EndostatinGeneSeqWO0064946Endostatin is believed to inhibit effects ofThe inhibitory effects of endostatin can be assayedAnti-angiogenic activity.Accessioncapillary endothelial cell proliferation.using assays disclosed by Cao et al. (1996) J. Biol.Useful in the preventionB28399Chem. 271 29461-29467.and/or treatment ofcancers.aFGF; FGF-1GeneSeqEP298723Fibroblast Growth FactorProliferation assay using NR6R-3T3 cells (RizzinoPromotion of growth andAccession1988 Cancer Res. 48: 4266); Examples 23 and 39proliferation of cells,P94037disclosed herein.such as epithelial cellsand keratinocytes.Antagonists may beuseful as anti-canceragents.bFGF; FGF-2GeneSeqFR2642086Fibroblast Growth FactorProliferation assay using NR6R-3T3 cells (RizzinoPromotion of growth andAccession1988 Cancer Res. 48: 4266); Examples 23 and 39proliferation of cells,R06685disclosed herein.such as epithelial cellsand keratinocytes.Antagonists may beuseful as anti-canceragents.FGF-3; INT-2GeneSeqWO9503831Fibroblast Growth FactorProliferation assay using NR6R-3T3 cells (RizzinoPromotion of growth andAccession1988 Cancer Res. 48: 4266); Examples 23 and 39proliferation of cells,R07824disclosed herein.such as epithelial cellsand keratinocytes.Antagonists may beuseful as anti-canceragents.FGF-4; HST-1;GeneSeqWO9503831Fibroblast Growth FactorProliferation assay using NR6R-3T3 cells (RizzinoPromotion of growth andHBGF-4Accession1988 Cancer Res. 48: 4266); Examples 23 and 39proliferation of cells,R07825disclosed herein.such as epithelial cellsand keratinocytes.Antagonists may beuseful as anti-canceragents.FGF-5GeneSeqWO9730155Fibroblast Growth FactorProliferation assay using NR6R-3T3 cells (RizzinoPromotion of growth andAccession1988 Cancer Res. 48: 4266); Examples 23 and 39proliferation of cells,W22600disclosed herein.such as epithelial cellsand keratinocytes.Antagonists may beuseful as anti-canceragents.FGF-6, HeparinGeneSeqEP613946Fibroblast Growth FactorProliferation assay using NR6R-3T3 cells (RizzinoPromotion of growth andbinding secretedAccession1988 Cancer Res. 48: 4266); Examples 23 and 39proliferation of cells,transformingR58555disclosed herein.such as epithelial cellsfactor-2and keratinocytes.Antagonists may beuseful as anti-canceragents.FGF-8GeneSeqWO9524928Fibroblast Growth FactorProliferation assay using NR6R-3T3 cells (RizzinoPromotion of growth andAccession1988 Cancer Res. 48: 4266); Examples 23 and 39proliferation of cells,R80783disclosed herein.such as epithelial cellsand keratinocytes.Antagonists may beuseful as anti-canceragents.FGF-9; GilaGeneSeqWO9503831Fibroblast Growth FactorProliferation assay using NR6R-3T3 cells (RizzinoPromotion of growth andactivating factorAccession1988 Cancer Res. 48: 4266); Examples 23 and 39proliferation of cells,R70822disclosed herein.such as epithelial cellsand keratinocytes.Antagonists may beuseful as anti-canceragents.FGF-12;GeneSeqWO9635708Fibroblast Growth FactorProliferation assay using NR6R-3T3 cells (RizzinoPromotion of growth andFibroblast growthAccession1988 Cancer Res. 48: 4266); Examples 23 and 39proliferation of cells,factor homologousW06309disclosed herein.such as epithelial cellsfactor-1and keratinocytes.Antagonists may beuseful as anti-canceragents.FGF-15GeneSeqWO9927100Fibroblast Growth FactorProliferation assay using NR6R-3T3 cells (RizzinoPromotion of growth andAccession1988 Cancer Res. 48: 4266); Examples 23 and 39proliferation of cells,Y08582disclosed herein.such as epithelial cellsand keratinocytes.Antagonists may beuseful as anti-canceragents.FGF-16GeneSeqWO9918128Fibroblast Growth FactorProliferation assay using NR6R-3T3 cells (RizzinoPromotion of growth andAccession1988 Cancer Res. 48: 4266); Examples 23 and 39proliferation of cells,Y05474disclosed herein.such as epithelial cellsand keratinocytes.Antagonists may beuseful as anti-canceragents.FGF-18GeneSeqWO9927100Fibroblast Growth FactorProliferation assay using NR6R-3T3 cells (RizzinoPromotion of growth andAccession1988 Cancer Res. 48: 4266); Examples 23 and 39proliferation of cells,Y08590disclosed herein.such as epithelial cellsand keratinocytes.Antagonists may beuseful as anti-canceragents.fit-3 ligandGeneSeqEP627487Stem Cell ProgenitorChemokine activities can be determined using assaysPromotion of immuneAccessionknown in the art: Methods in Molecular Biology,cell growth and/orR675412000, vol. 138: Chemokine Protocols. Edited by:differentiation.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Humana Press Inc., Totowa, NJ.VEGF-110GeneSeqWO0013702Promotes the growth and/or proliferation ofVEGF activity can be determined using assays knownPromotion of growth andAccessionendothelial cells.in the art, such as those disclosed in Internationalproliferation of cells,Y69417Publication No. WO0045835, for example.such as vascularendothelial cells.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancer.VEGB-121GeneSeqWO0071713Promotes the growth and/or proliferation ofVEGF activity can be determined using assays knownPromotion of growth andAccessionendothelial cells.in the art, such as those disclosed in Internationalproliferation of cells,B50432Publication No. WO0045835, for example.such as vascularendothelial cells.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancer.VEGF-138GeneSeqWO9940197Promotes the growth and/or proliferation ofVEGF activity can be determined using assays knownPromotion of growth andAccessionendothelial cells.in the art, such as those disclosed in Internationalproliferation of cells,Y43483Publication No. WO0045835, for example.such as vascularendothelial cells.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancer.VEGF-145GeneSeqWO0013702Promotes the growth and/or proliferation ofVEGF activity can be determined using assays knownPromotion of growth andAccessionendothelial cells.in the art, such as those disclosed in Internationalproliferation of cells,Y69413Publication No. WO0045835, for example.such as vascularendothelial cells.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancer.VEGF-162GeneSeqW09940197Promotes the growth and/or proliferation ofVEGF activity can be determined using assays knownPromotion of growth andAccessionendothelial cells.in the art, such as those disclosed in Internationalproliferation of cells,Y43484Publication No. WO0045835, for example.such as vascularendothelial cells.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancer.VEGF-165GeneSeqWO0013702Promotes the growth and/or proliferation ofVEGF activity can be determined using assays knownPromotion of growth andAccessionendothelial cells.in the art, such as those disclosed in Internationalproliferation of cells,Y69414Publication No. WO0045835, for example.such as vascularendothelial cells.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancer.VEGF-182GeneSeqW09940197Promotes the growth and/or proliferation ofVEGF activity can be determined using assays knownPromotion of growth andAccessionendothelial cells.in the art, such as those disclosed in Internationalproliferation of cells,Y43483Publication No. WO0045835, for example.such as vascularendothelial cells.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancer.VEGF-189GeneSeqWO0013702Promotes the growth and/or proliferation ofVEGF activity can be determined using assays knownPromotion of growth andAccessionendothelial cells.in the art, such as those disclosed in Internationalproliferation of cells,Y69415Publication No. WO0045835, for example.such as vascularendothelial cells.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancer.VEGF-206GeneSeqW00013702Promotes the growth and/or proliferation ofVEGF activity can be determined using assays knownPromotion of growth andAccessionendothelial cells.in the art, such as those disclosed in Internationalproliferation of cells,Y69416Publication No. WO0045835, for example.such as vascularendothelial cells.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancer.VEGF-DGeneSeqWO9807832Promotes the growth and/or proliferation ofVEGF activity can be determined using assays knownPromotion of growth andAccessionendothelial cells.in the art, such as those disclosed in Internationalproliferation of cells,W53240Publication No. WO0045835, for example.such as vascularendothelial cells.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancer.VEGF-E; VEGF-XGeneSeqW09947677Promotes the growth and/or proliferation ofVEGF activity can be determined using assays knownPromotion of growth andAccessionendothelial cells.in the art, such as those disclosed in Internationalproliferation of cells,Y33679Publication No. WO0045835, for example.such as vascularendothelial cells.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancer.VEGF Receptor;GeneSeqWO9831794Receptor for VEGF polypeptidesVEGF activity, in the presence of flk-1 polypeptides,VEGF Receptor. FusionKDR; flk-1Accessioncan be determined using assays known in the art, suchprotein with theW69679as those disclosed in International Publication No.extracellular domain isWO0045835, for example.useful as an anti-angiogenic agent.Antagonists may beuseful in the promotion ofangiogenesis.Soluble VEGFGeneSeqUS5712380Receptor for VEGF polypeptidesVEGF activity, in the presence of VEGF ReceptorVEGF Receptor. FusionReceptorAccessionpolypeptides, can be determined using assays knownprotein with theW47037in the art, such as those disclosed in Internationalextracellular domain isPublication No. WO0045835, for example.useful as an anti-angiogenic agent.Antagonists may beuseful in the promotion ofangiogenesis.flt-1GeneSeqWO0021560Receptor for VEGF polypeptidesVEGF activity, in the presence of flt-1 polypeptides,VEGF Receptor. FusionAccessioncan be determined using assays known in the art, suchprotein with theY70751as those disclosed in International Publication No.extracellular domain isWO0045835, for example.useful as an anti-angiogenic agent.Antagonists may beuseful in the promotion ofangiogenesis.VEGF R-3; flt-4GeneSeqWO0058511Receptor for VEGF polypeptidesVEGF activity, in the presence of flt-4 polypeptides,VEGF Receptor. FusionAccessioncan be determined using assays known in the art, suchprotein with theB29047as those disclosed in International Publication No.extracellular domain isWO0045835, for example.useful as an anti-angiogenic agent.Antagonists may beuseful in the promotion ofangiogenesis.Neuropilin-1GeneSeqWO9929858Vascular Endothelial Growth FactorVEGF activity can be determined using assays knownPromotion of growth andAccessionin the art, such as those disclosed in Internationalproliferation of cells,Y06319Publication No. WO0045835, for example.such as vascularendothelial cells.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancer.Neuropilin-2GeneSeqWO9929858Vascular Endothelial Growth FactorVEGF activity can be determined using assays knownPromotion of growth andAccessionin the art, such as those disclosed in Internationalproliferation of cells,Y03618Publication No. WO0045835, for example.such as vascularendothelial cells.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancer.Human fast twitchGeneSeqW09730085Troponins are contractile proteins that areAbility of soluble Troponins to inhibit anglogenesisAnti-angiogenesisskeletal muscleAccessionthought to inhibit angiogenesis. High levelscan be determined using assays known in the art:.troponin CW22597may contribute to the difficulty encountered inProc Natl Acad Sci USA 1999 Mar 16; 96(6): 2645-50.revascularizing the ischemic myocardium aftercardiovascular injury.Human fast twitchGeneSeqW09730085Troponins are contractile proteins that areAbility of soluble Troponins to inhibit anglogenesisAnti-angiogenesisskeletal muscleAccessionthought to inhibit angiogenesis. High levelscan be determined using assays known in the art:.troponin IW18054may contribute to the difficulty encountered inProc Natl Acad Sci USA 1999 Mar 16; 96(6): 2645-50.revascularizing the ischemic myocardium aftercardiovascular injury.Human fast twitchGeneSeqW09730085Troponins are contractile proteins that areAbility of soluble Troponins to inhibit anglogenesisAnti-angiogenesisskeletal muscleAccessionthought to inhibit angiogenesis. High levelscan be determined using assays known in the art:.troponin TW22599may contribute to the difficulty encountered inProc Natl Acad Sci USA 1999 Mar 16; 96(6): 2645-50.revascularizing the ischemic myocardium aftercardiovascular injury.fragment.GeneSeqW09719955Troponins are contractile proteins that areAbility of soluble Troponins to inhibit anglogenesisAnti-angiogenesismyofibrillarAccessionthought to inhibit angiogenesis. High levelscan be determined using assays known in the art:.protein troponin IW18053may contribute to the difficulty encountered inProc Natl Acad Sci USA 1999 Mar 16; 96(6): 2645-50.revascularizing the ischemic myocardium aftercardiovascular injury.myofibrillarGeneSeqW09719955Troponins are contractile proteins that areAbility of soluble Troponins to inhibit anglogenesisAnti-angiogenesisprotein troponin IAccessionthought to inhibit angiogenesis. High levelscan be determined using assays known in the art:.W18054may contribute to the difficulty encountered inProc Natl Acad Sci USA 1999 Mar 16; 96(6): 2645-50.revascularizing the ischemic myocardium aftercardiovascular injury.Troponin peptidesGeneSeqWO9933874Troponins are contractile proteins that areAbility of soluble Troponins to inhibit anglogenesisAnti-angiogenesisAccessionsthought to inhibit angiogenesis. High levelscan be determined using assays known in the art:.Y29581, Y29582,may contribute to the difficulty encountered inProc Natl Acad Sci USA 1999 Mar 16; 96(6): 2645-50.Y29583, Y29584,revascularizing the ischemic myocardium afterY29585, andcardiovascular injury.Y29586Human fast twitchGeneSeqWO0054770Troponins are contractile proteins that areAbility of soluble Troponins to inhibit anglogenesisAnti-angiogenesisskeletal muscleAccessionthought to inhibit angiogenesis. High levelscan be determined using assays known in the art:.Troponin subunit CB00134may contribute to the difficulty encountered inProc Natl Acad Sci USA 1999 Mar 16; 96(6): 2645-50.revascularizing the ischemic myocardium aftercardiovascular injury.Human fast twitchGeneSeqWO0054770Troponins are contractile proteins that areAbility of soluble Troponins to inhibit anglogenesisAnti-angiogenesisskeletal muscleAccessionthought to inhibit angiogenesis. High levelscan be determined using assays known in the art:.Troponin subunit IB00135may contribute to the difficulty encountered inProc Natl Acad Sci USA 1999 Mar 16; 96(6): 2645-50.Proteinrevascularizing the ischemic myocardium aftercardiovascular injury.Human fast twitchGeneSeqWO0054770Troponins are contractile proteins that areAbility of soluble Troponins to inhibit anglogenesisAnti-angiogenesisskeletal muscleAccessionthought to inhibit angiogenesis. High levelscan be determined using assays known in the art:.Troponin subunit TB00136may contribute to the difficulty encountered inProc Natl Acad Sci USA 1999 Mar 16; 96(6): 2645-50.revascularizing the ischemic myocardium aftercardiovascular injury.ActivatorGeneSeqWO9013648PAIs are believed to play a role in cancer, andMethods that measure plasminogen activator inhibitorAnti-angiogenesis; blood-Inhibitor-1; PAI-1Accessioncardiovascular disease and blood-clotting(PA1) activity are known in the art, for example, assayclotting disorders.R08411disorders.the ability of PA1 to inhibit tissue plasminogenactivator (tPA) or urokinase (uPA): J BiochemBiophys Methods 2000 Sep 11; 45(2): 127-40, BreastCancer Res Treat 1996; 41(2): 141-6. Methods thatmeasure anti-angiogenesis activity are known in theart, for example, Proc Natl Acad Sci USA 1999Mar 16; 96(6): 2645-50.PlasminogenGeneSeqDE3722673PAIs are believed to play a role in cancer, andMethods that measure plasminogen activator inhibitorAnti-angiogenesis; blood-ActivatorAccessioncardiovascular disease and blood-clotting(PA1) activity are known in the art, for example, assayclotting disorders.Inhibitor-2; PAI-2P94160disorders.the ability of PA1 to inhibit tissue plasminogenactivator (tPA) or urokinase (uPA): J BiochemBiophys Methods 2000 Sep 11; 45(2): 127-40, BreastCancer Res Treat 1996; 41(2): 141-6. Methods thatmeasure anti-angiogenesis activity are known in theart, for example, Proc Natl Acad Sci USA 1999Mar 16; 96(6): 2645-50.ActivatorGeneSeqWO9102057PAIs are believed to play a role in cancer, andMethods that measure plasminogen activator inhibitorAnti-angiogenesis; blood-Inhibitor-2; PAI-2Accessioncardiovascular disease and blood-clotting(PA1) activity are known in the art, for example, assayclotting disorders.R10921disorders.the ability of PA1 to inhibit tissue plasminogenactivator (tPA) or urokinase (uPA): J BiochemBiophys Methods 2000 Sep 11; 45(2): 127-40, BreastCancer Res Treat 1996; 41(2): 141-6. Methods thatmeasure anti-angiogenesis activity are known in theart, for example, Proc Natl Acad Sci USA 1999Mar 16; 96(6): 2645-50.Human PAI-1GeneSeqWO9105048PAIs are believed to play a role in cancer, andMethods that measure plasminogen activator inhibitorAnti-angiogenesis; blood-mutantsAccessionscardiovascular disease and blood-clotting(PA1) activity are known in the art, for example, assayclotting disorders.R11755, R11756,disorders.the ability of PA1 to inhibit tissue plasminogenR11757, R11758,activator (tPA) or urokinase (uPA): J BiochemR11759, R11760,Biophys Methods 2000 Sep 11; 45(2): 127-40, BreastR11761, R11762Cancer Res Treat 1996; 41(2): 141-6. Methods thatand R11763measure anti-angiogenesis activity are known in theart, for example, Proc Natl Acad Sci USA 1999Mar 16; 96(6): 2645-50.CXCR3; CXCGeneSeqWO0018431Chemokines are a family of related small,Chemokine activities can be determined using assaysSoluble CXCR3Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,polypeptides may beY79372processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:useful for inhibitingangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©chemokine activities andMembers of this family are involved in aHumana Press Inc., Totowa, NJ.viral infection.similarly diverse range of pathologies includinginflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a family of seventransmembrane G-protein coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.Modified RantesGeneSeqWO9737005Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders.Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,W38129processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJ.similarly diverse range of pathologies includinginflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a family of seventransmembrane G-protein coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.RANTESGeneSeqEP905240Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders.Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Y05299processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJ.similarly diverse range of pathologies includinginflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a family of seventransmembrane G-protein coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.MCI-1aGeneSeqWO9509232Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders.Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,R73914processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJ.similarly diverse range of pathologies includinginflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a family of seventransmembrane G-protein coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.MCP-1bGeneSeqWO9929728Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders.Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Y26176processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJ.similarly diverse range of pathologies includinginflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a family of seventransmembrane G-protein coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.MCP-1 receptorGeneSeqWO9519436Chemokines are a family of related small,Chemokine activities can be determined using assaysSoluble MCP-1 ReceptorAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,polypeptides may beR79165processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:useful for inhibitingangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©chemokine activities andMembers of this family are involved in aHumana Press Inc., Totowa, NJ.viral infection.similarly diverse range of pathologies includinginflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a family of seventransmembrane G-protein coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.MCP-3GeneSeqWO9509232Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders.Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,R73915processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJ.similarly diverse range of pathologies includinginflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a family of seventransmembrane G-protein coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.MCP-4 receptorGeneSeqW09809171Chemokines are a family of related small,Chemokine activities can be determined using assaysSoluble MCP-4 ReceptorAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,polypeptides may beW56689processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:useful for inhibitingangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©chemokine activities andMembers of this family are involved in aHumana Press Inc., Totowa, NJ.viral infection.similarly diverse range of pathologies includinginflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a family of seventransmembrane G-protein coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.RANTES receptorGeneSeqUS5652133Chemokines are a family of related small,Chemokine activities can be determined using assaysSoluble RANTESAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Receptor polypeptidesW29588processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:may be useful forangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©inhibiting chemokineMembers of this family are involved in aHumana Press Inc., Totowa, NJ.activities and viralsimilarly diverse range of pathologies includinginfection.inflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a family of seventransmembrane G-protein coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.CCR5 variantGeneSeqWO9854317Chemokines are a family of related small,Chemokine activities can be determined using assaysSoluble CCR5Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,polypeptides may beW88238processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:useful for inhibitingangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©chemokine activities andMembers of this family are involved in aHumana Press Inc., Totowa, NJ.viral infection.similarly diverse range of pathologies includinginflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a family of seventransmembrane G-protein coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.CCR7GeneSeqUS6153441Chemokines are a family of related small,Chemokine activities can be determined using assaysSoluble CCR7Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,polypeptides may beB50859processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:useful for inhibitingangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©chemokine activities andMembers of this family are involved in aHumana Press Inc., Totowa, NJ.viral infection.similarly diverse range of pathologies includinginflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a family of seventransmembrane G-protein coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.CXC3GeneSeqWO9727299Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders.Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,W23345processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJ.similarly diverse range of pathologies includinginflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a family of seventransmembrane G-protein coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.EotaxinGeneSeqWO9700960Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders.Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,W10099processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJ.similarly diverse range of pathologies includinginflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a family of seventransmembrane G-protein coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.NeurotactinGeneSeqUS6013257Neurotactin may play a role in chemotacticChemotactic leukocyte migration assays are known inImmune disorders.AccessionsWO9742224leukocyte migration and brain inflammationthe art, for example: J. Immunol. Methods 33,Y77537, W34307,processes.((1980)); Nature 1997 Jun 5; 387(6633): 611-7.Y53259, and,Y77539Human CKbeta-9GeneSeqUS6153441Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders.Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,B50860processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJ.similarly diverse range of pathologies includinginflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a family of seventransmembrane G-protein coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.LymphotactinGeneSeqWO0073320Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders.Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,B50052processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJ.similarly diverse range of pathologies includinginflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a family of seventransmembrane G.MIP-3 alphaGeneSeqWO9801557Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders.Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,W44398processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJ.similarly diverse range of pathologies includinginflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a family of seventransmembrane G.MIP-3 betaGeneSeqWO9801557Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders.Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,W44399processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJ.similarly diverse range of pathologies includinginflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a family of seventransmembrane G.MIP-GammaGeneSeqWO9504158Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders.Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,R70798processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJ.similarly diverse range of pathologies includinginflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a family of seventransmembrane G.Stem CellGeneSeqWO9104274Chemokines are a family of related small,Chemokine activities can be determined using assaysHematopoietic growthInhibitoryAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,factors.FactorR11553processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJ.similarly diverse range of pathologies includinginflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a family of seventransmembrane G.thrombopoietinGeneSeqWO9521920Thrombopoietin is involved in the regulation ofThrombopoietin (TPO) can be assayed to determineHematopoietic growthAccessionthe growth and differentiation ofregulation of growth and differentiation offactors.R79905megakaryocytes and preceptors thereof.megakaryocytes. Mol Cell Biol 2001 Apr;21(8): 2659-70; Exp Hematol 2001 Jan; 29(1): 51-8and within.c-kit ligand;GeneSeqEP992579 andC-kit ligan is thought to stimulate theChemokine activities can be determined using assaysHematopoietic growthSCF; Mast cellAccessionEP676470proliferation of mast cells, and is able toknown in the art: Methods in Molecular Biology,factors.growth factor;Y53284, R83978augment the proliferation of both myeloid and2000, vol. 138: Chemokine Protocols. Edited by:MGF;and R83977lymphoid hematopoietic progenitors in boneA. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Fibrosarcoma-marrow culture. C-kit ligand is also though toHumana Press Inc., Totowa, NJ.derived stemact synergistically with other cytokines.cell factorPlatelet derivedGeneSeq AccessionWO0066736Vascular Endothelial Growth FactorVEGF activity can be determined using assays knownPromotion of growth andgrowth factorB48653in the art, such as those disclosed in Internationalproliferation of cells,Publication No. WO0045835, for example.such as vascularendothelial cells.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancer.MelanomaGeneSeqWO9503328Melanoma inhibiting protein has melanoma-Tumor suppressor activity of melanoma inhibitingCancer, melanomainhibiting proteinAccession R69811inhibiting activity and can be used to treatprotein can be determined using assays known in thecancer (melanoma, glioblastoma,art: Matzuk et al., Nature 1992 Novneuroblastoma, small cell lung cancer,26; 360(6402): 313-9.neuroectodermal tumors) or as animmunosuppressant (it inhibits IL-2 orphytohaemagglutinin induced proliferation ofperipheral blood lymphocytes.Glioma-derivedGeneSeqEP399816Vascular Endothelial Growth FactorVEGF activity can be determined using assays knownPromotion of growth andgrowth factorAccession R08120in the art, such as those disclosed in Internationalproliferation of cells,Publication No. WO0045835, for example.such as vascularendothelial cells.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancer.Platelet derivedGeneSeqEP682110Vascular Endothelial Growth FactorVEGF activity can be determined using assays knownPromotion of growth andgrowth factorAccession R84759in the art, such as those disclosed in Internationalproliferation of cells,precursor APublication No. WO0045835, for example.such as vascularendothelial cells.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancer.Platelet derivedGeneSeqEP682110Vascular Endothelial Growth FactorVEGF activity can be determined using assays knownPromotion of growth andgrowth factorAccession R84760in the art, such as those disclosed in Internationalproliferation of cells,precursor BPublication No. WO0045835, for example.such as vascularendothelial cells.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancer.Platelet derivedGeneSeqEP282317Vascular Endothelial Growth FactorVEGF activity can be determined using assays knownPromotion of growth andgrowth factor Bv-Accession P80595in the art, such as those disclosed in Internationalproliferation of cells,sisand P80596Publication No. WO0045835, for example.such as vascularendothelial cells.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancer.Placental GrowthGeneSeqWO9206194Vascular Endothelial Growth FactorVEGF activity can be determined using assays knownPromotion of growth andFactorAccessions R23059in the art, such as those disclosed in Internationalproliferation of cells,and R23060Publication No. WO0045835, for example.such as vascularendothelial cells.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancer.Placental GrowthGeneSeq AccessionDE19748734Vascular Endothelial Growth FactorVEGF activity can be determined using assays knownPromotion of growth andFactor-2Y08289in the art, such as those disclosed in Internationalproliferation of cells,Publication No. WO0045835, for example.such as vascularendothelial cells.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancer.ThrombopoietinGeneSeq AccessionWO0000612Thrombopoietin is involved in the regulation ofThrombopoietin (TPO) can be assayed to determineThrombocytopenia,detivative1Y77244the growth and differentiation ofregulation of growth and differentiation ofcancer.megakaryocytes and preceptors thereof.megakaryocytes. Mol Cell Biol 2001 Apr;21(8): 2659-70; Exp Hematol 2001 Jan; 29(1): 51-8and within.ThrombopoietinGeneSeq AccessionWO0000612Thrombopoietin is involved in the regulation ofThrombopoietin (TPO) can be assayed to determineThrombocytopenia,derivative2Y77255the growth and differentiation ofregulation of growth and differentiation ofcancer.megakaryocytes and preceptors thereof.megakaryocytes. Mol Cell Biol 2001 Apr;21(8): 2659-70; Exp Hematol 2001 Jan; 29(1): 51-8and within.ThrombopoietinGeneSeq AccessionWO0000612Thrombopoietin is involved in the regulation ofThrombopoietin (TPO) can be assayed to determineThrombocytopenia,derivative3Y77262the growth and differentiation ofregulation of growth and differentiation ofcancer.megakaryocytes and preceptors thereof.megakaryocytes. Mol Cell Biol 2001 Apr;21(8): 2659-70; Exp Hematol 2001 Jan; 29(1): 51-8and within.ThrombopoietinGeneSeq AccessionWO0000612Thrombopoietin is involved in the regulation ofThrombopoietin (TPO) can be assayed to determineThrombocytopenia,derivative4Y77267the growth and differentiation ofregulation of growth and differentiation ofcancer.megakaryocytes and preceptors thereof.megakaryocytes. Mol Cell Biol 2001 Apr;21(8): 2659-70; Exp Hematol 2001 Jan; 29(1): 51-8and within.ThrombopoietinGeneSeq AccessionWO0000612Thrombopoietin is involved in the regulation ofThrombopoietin (TPO) can be assayed to determineThrombocytopenia,derivative5Y77246the growth and differentiation ofregulation of growth and differentiation ofcancer.megakaryocytes and preceptors thereof.megakaryocytes. Mol Cell Biol 2001 Apr;21(8): 2659-70; Exp Hematol 2001 Jan; 29(1): 51-8and within.ThrombopoietinGeneSeq AccessionWO0000612Thrombopoietin is involved in the regulation ofThrombopoietin (TPO) can be assayed to determineThrombocytopenia,derivative6Y77253the growth and differentiation ofregulation of growth and differentiation ofcancer.megakaryocytes and preceptors thereof.megakaryocytes. Mol Cell Biol 2001 Apr;21(8): 2659-70; Exp Hematol 2001 Jan; 29(1): 51-8and within.ThrombopoietinGeneSeq AccessionWO0000612Thrombopoietin is involved in the regulation ofThrombopoietin (TPO) can be assayed to determineThrombocytopenia,derivative7Y77256the growth and differentiation ofregulation of growth and differentiation ofcancer.megakaryocytes and preceptors thereof.megakaryocytes. Mol Cell Biol 2001 Apr;21(8): 2659-70; Exp Hematol 2001 Jan; 29(1): 51-8and within.FractalkineGeneSeq AccessionUS6043086Fractalkine is believed to play a role inFractalkine activity can be determined usingImmune disorders.Y53255chemotactic leukocyte migration andChemotactic leukocyte migration assays known in theneurological disorders.art, for example: J. Immunol. Methods 33, ((1980));Nature 1997 Jun 5; 387(6633): 611-7.CXC3GeneSeqWO9757599Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders.Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,W23345processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJ.similarly diverse range of pathologies includinginflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a family of seventransmembrane G-protein coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.CCR7GeneSeqUS6153441Chemokines are a family of related small,Chemokine activities can be determined using assaysSoluble CCR7Accession B50859secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,polypeptides may beprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:useful for inhibitingangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©chemokine activities andMembers of this family are involved in aHumana Press Inc., Totowa, NJ.viral infection.similarly diverse range of pathologies includinginflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a family of seventransmembrane G-protein coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.Nerve GrowthGeneSeqEP414151Nerve Growth FactorProliferation assay using NR6R-3T3 cells (RizzinoNeurological disorders,Factor-betaAccession R114741988 Cancer Res. 48: 4266)cancerNerve GrowthGeneSeqEP859056Nerve Growth FactorProliferation assay using NR6R 3T3 cells (RizzinoNeurological disorders,Factor-beta2Accession1988 Cancer Res. 48: 4266cancerW69725Neurotrophin-3GeneSeqWO9821234Neurotrophins regulate neuronal cell survivalTrk tyrosine kinase activation assays known in the artNeurological disorders,Accessionand synaptic plasticity.can be used to assay for neurotrophin activity, forcancerW8889example, Proc Natl Acad Sci USA 2001 Mar13; 98(6): 3555-3560.Neurotrophin-3GeneSeq AccessionWO9325684Neurotrophins regulate neuronal cell survivalTrk tyrosine kinase activation assays known in the artNeurological disorders,R47100and synaptic plasticity.can be used to assay for neurotrophin activity, forcancerexample, Proc Natl Acad Sci USA 2001 Mar13; 98(6): 3555-3560.Neurotrophin-4aGeneSeq AccessionWO9325684Neurotrophins regulate neuronal cell survivalTrk tyrosine kinase activation assays known in the artNeurological disorders,R47101and synaptic plasticity.can be used to assay for neurotrophin activity, forcancerexample, Proc Natl Acad Sci USA 2001 Mar13; 98(6): 3555-3560. 13; 98(6): 3555-3560Neurotrophin-4bGeneSeq AccessionWO9325684Neurotrophins regulate neuronal cell survivalTrk tyrosine kinase activation assays known in the artNeurological disorders,R47102and synaptic plasticity.can be used to assay for neurotrophin activity, forcancertyrosine kinases.example, Proc Natl Acad Sci USA 2001 Mar13; 98(6): 3555-3560.Neurotrophin-4cGeneSeq AccessionWO9325684Neurotrophins regulate neuronal cell survivalTrk tyrosine kinase activation assays known in the artNeurological disorders,R47103and synaptic plasticity.can be used to assay for neurotrophin activity, forcancertyrosine kinases.example, Proc Natl Acad Sci USA 2001 Mar13; 98(6): 3555-3560.Neurotrophin-4dGeneSeq AccessionWO9325684Neurotrophins regulate neuronal cell survivalTrk tyrosine kinase activation assays known in the artNeurological disorders,R47102and synaptic plasticity.can be used to assay for neurotrophin activity, forcancertyrosine kinases.example, Proc Natl Acad Sci USA 2001 Mar13; 98(6): 3555-3560.Platelet-DerivedGeneSeq AccessionUS5219739Vascular Endothelial Growth FactorVEGF activity can be determined using assays knownPromotion of growth andGrowth FactorR38918in the art, such as those disclosed in Internationalproliferation of cells,A chainPublication No. W00045835, for example.such as vascularendothelial cells.Hematopoietic andimmune disorders.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancerPlatelet-DerivedGeneSeq AccessionUS5219739Vascular Endothelial Growth FactorVEGF activity can be determined using assays knownPromotion of growth andGrowth FactorR38919in the art, such as those disclosed in Internationalproliferation of cells,B chainPublication No. W00045835, for example.such as vascularendothelial cells.Hematopoietic andimmune disorders.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancerStromal DerivedGeneSeqWO9948528Stromal Growth FactorProliferation assay using NR6R-3T3 cells (RizzinoHematopoietic, immuneFactor-1 alphaAccession1988 Cancer Res. 48: 4266)disorders, cancerY39995Stromal DerivedGeneSeqCA2117953Stromal Growth FactorProliferation assay using NR6R-3T3 cells (RizzinoHematopoietic, immuneFactor-1 betaAccession1988 Cancer Res. 48: 4266)disorders, cancerR75420TarcGeneSeqWO9711969Chemotactic for T lymphocytes. May play aChemotactic leukocyte migration assays are known inAntiinflammatory.Accessionrole in T-cell development. Thought to bindthe art, for example: J. Immunol. Methods 33 ((1980))Immune disorders, cancerW14917CCR8 and CCR4ProlactinGeneSeqWO9521625Prolactin is involved in immune cellImmune coil proliferation and suppression of apoptosisReproductive systemAccession R78691proliferation and apoptosis.by prolactin can be assayed by methods well-known indisorders, cancer.the art, for example, Buckley, AR and Buckley DJ,Ann N Y Acad Sci 2000; 917: 522-33, and within.Prolactin2GeneSeqUS5955346Prolactin is involved in immune cellImmune coil proliferation and suppression of apoptosisReproductive systemAccessionproliferation and apoptosis.by prolactin can be assayed by methods well-known indisorders, cancer.Y31764the art, for example, Buckley, AR and Buckley DJ,Ann N Y Acad Sci 2000; 917: 522-33, and within.FollicleGeneSeqEP974359FSH stimulates secretion of interleukin-1 byFSH activities can be determined using assays knownReproductive systemstimulatingAccessioncells isolated from women in the follicularin the art; J Gend Specif Med 1999 Nov-Dec; 2(6): 30-4;disorders, cancer.hormone AlphaY54160phaseMol Cell Endocrinol. 1997 Nov 15; 134(2): 109-18.subunitFollicleGeneSeqEP974359FSH stimulates secretion of interleukin-1 byFSH activities can be determined using assays knownReproductive systemstimulatingAccessioncells isolated from women in the follicularin the art; J Gend Specif Med 1999 Nov-Dec; 2(6): 30-4;disorders, cancer.hormone BetaY54161phaseMol Cell Endocrinol. 1997 Nov 15; 134(2): 109-18.subunitSubstance PGeneSeqWO0054053Substance P is associated withImmuneregulation and bone marrow, cell proliferationdiabetes mellitus,(tachykinin)Accessionimmunoregulation.by substance P can be assayed by methods well-knownhypertension, cancerB23027in the art, for example, Lai et al. Proc Natl Acad SciUSA 2001 Mar 27; 98(7): 3970-5; Jallat-Daloz et al.Allergy Asthma Proc 2001 Jan-Feb; 22(1): 17-23;Kahler et al. Exp Lung Res 2001 Jan-Feb; 27(1): 25-46;and Adamus MA and Dabrowski ZJ. J Cell Biochem2001; 81(3)499-506.OcytocinGeneSeqWO0053755Oxytocin is involved in the induction ofOxytocin and prostaglandin E(2) release and Ocytocininflammatory disorders(Neurophysin I)Accessionprostaglandin (E2) release as well as an(Ca2+) increase can be assayed by methods well-immunologic disorders,B24085 andincreased amount of calcium release by smoothknown in the art, for example, Pavan et al., AM JcancerB24086muscle cells.Obset Gynecol 2000 Jul; 183(1): 76-82 and Holda etal., Cell Calcium 1996 Jul; 20(1): 43 51.VasopressinGeneSeqWO0053755Vasopressinis believed to have a directVasopressin activity can be determined using assaysinflammatory disorders(Neurophysin II)Accessionantidiuretic action on the kidney, and it isknown in the art, for example, Endoer Regul 1996immunologic disorders,B24085 andthought to cause vasoconstriction of theMar; 30(1): 13-17.cancerB24086peripheral vessels.IL-1GeneSeqEP165654Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,P60326monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Orencole & Dinarclio (1989) Cytokine 1, 14-20.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.IL-1 matureGeneSeqEP456332Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R14855monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Orencole & Dinarclio (1989) Cytokine 1, 14-20.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.IL-1 betaGeneSeqWO9922763Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,Y08322monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Orencole & Dinarclio (1989) Cytokine 1, 14-20.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.IL-3 variantsGeneSeqWO8806161Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,P80382, P80383,monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerP80384, andfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andP80381immune cells (e.g., T helper cells, B cells,Kitamura et al (1989) J Cell Physiol. 140 323-334.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.IL-4GeneSeqWO8702990Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,P70615monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Siegel & Mostowski (1990) J Immunol Methodseosinophils, and lymphocytes), chemotaxis of132, 287-295.neutrophils and T lymphocytes, and/orinhibition of interferons.IL-4 muteinsGeneSeqWO9747744Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,W52151monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerW52152functions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andW52153immune cells (e.g., T helper cells, B cells,Siegel & Mostowski (1990) J Immunol MethodsW52154eosinophils, and lymphocytes), chemotaxis of132, 287-295.W52155neutrophils and T lymphocytes, and/orW52156inhibition of interferons.W52157W52158W52159W52160W52161W52162W52163W52164and W52165IL-1 alphaGeneSeqEP324447Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,P90108monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Orencole & Dinarello (1989) Cytokine 1, 14-20.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.IL-3 variantsGeneSeqWO9307171Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R38561, R38562,monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerR38563, R38564,functions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andR38565, R38566,immune cells (e.g., T helper cells, B cells,Aarden et al (1987) Eur. J. Immunol 17, 1411-16.R38567, R38568,eosinophils, and lymphocytes), chemotaxis ofR38569, R38570,neutrophils and T lymphocytes, and/orR38571, andinhibition of interferons.R38572IL-6GeneSeqWO9402512Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R45717 andmonocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerR45718functions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Aarden et al (1987) Eur. J. Immunol 17, 1411-16.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.IL-13GeneSeqWO9404680Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R48624monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Boutelier et al (1995) J. Immunol. Methods 181, 29.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.IL-4 muteinGeneSeqDE4137333Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R47182monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Siegel & Mostowski (1990) J Immunol Methodseosinophils, and lymphocytes), chemotaxis of132, 287-295.neutrophils and T lymphocytes, and/orinhibition of interferons.IL-4 muteinGeneSeqDE4137333Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Y124XAccessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R47183monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Siegel & Mostowski (1990) J Immunol Methodseosinophils, and lymphocytes), chemotaxis of132, 287-295.neutrophils and T lymphocytes, and/orinhibition of interferons.IL-4 muteinGeneSeqDE4137333Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Y124GAccessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R47184monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Siegel & Mostowski (1990) J Immunol Methodseosinophils, and lymphocytes), chemotaxis of132, 287-295.neutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqWO9317698Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Interleukin-10Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,(precursor)R41664monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Thompson-Snipes et al (1991) J. Exp. Med. 173,eosinophils, and lymphocytes), chemotaxis of507-510.neutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqWO9318783-AInterleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Interleukin-10Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R42642monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Thompson-Snipes et al (1991) J. Exp. Med. 173,eosinophils, and lymphocytes), chemotaxis of507-510.neutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqEP569042Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,interleukin-1Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,beta precursor.R42447monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Orencole & Dinarello (1989) Cytokine 1, 14-20.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Interleukin-GeneSeqEP578278Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,1alphaAccessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R45364monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225.immune cells (e.g., T helper cells, B cells,eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqJP04063595Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,interleukin-3Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,variantR22814monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Kitamura et al (1989) J Cell Physiol. 140 323-334.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.IL-1i fragmentsGeneSeqEP541920Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R35484 andmonocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerR35485functions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Orencole & Dinarclio (1989) Cytokine 1, 14-20.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.IL-1 inhibitorGeneSeqEPS541920Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,(IL-1i)Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R35486 andmonocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerR35484functions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Orencole & Dinarclio (1989) Cytokine 1, 14-20.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.ICE 22 kD subunit.GeneSeqEP533350Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R33780monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225.immune cells (e.g., T helper cells, B cells,eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.ICE 20 kD subunit.GeneSeqEP533350Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R33781monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225.immune cells (e.g., T helper cells, B cells,eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.ICE 10 kDGeneSeqEP533350Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,subunitAccessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R33782monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225.immune cells (e.g., T helper cells, B cells,eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqWO9317698Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Interleukin-10Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,(precursor)R41664monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Thompson-Snipes et al (1991) J. Exp. Med. 173,eosinophils, and lymphocytes), chemotaxis of507-510.neutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqWO9318783Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Interleukin-10Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R42642monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Thompson-Snipes et al (1991) J. Exp. Med. 173,eosinophils, and lymphocytes), chemotaxis of507-510.neutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqEP569042Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Interleukin-1Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,beta precursorR42447monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Kitamura et al (1989) J Cell Physiol. 140 323-334.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqWO9403492Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,interleukin-6Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R49041monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Aarden et al (1987) Eur. J. Immunol 17, 1411-16.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Mutant Interleukin 6GeneSeqWO9411402Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,S176RAccessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R54990monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Aarden et al (1987) Eur. J. Immunol 17, 1411-16.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Interleukin 6GeneSeqJP06145063Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R55256monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Aarden et al (1987) Eur. J. Immunol 17, 1411-16.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Interleukin 8GeneSeqJP06100595Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-8 receptor(IL-8) receptorAccessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may beR53932monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,useful for inhibitingfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andinterleukin activities.immune cells (e.g., T helper cells, B cells,Holmes et al (1991) Science 253, 1278-80.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqUS5328988Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,interleukin-7Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R59919monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Park et al (1990) J. Exp. Med. 171, 1073-79.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.IL-3 containingGeneSeqWO9521254Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,fusion protein.Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R79342 andmonocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerR79344functions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Kitamura et al (1989) J Cell Physiol. 140 323-334.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.IL-3 mutantGeneSeqZA9402636Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,proteinsAccessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R79254, R79255,monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerR79256, R79257,functions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andR79258, R79259,immune cells (e.g., T helper cells, B cells,Giri et al (1994) EMBO J. 13 2822-2830.R79260, R79261,eosinophils, and lymphocytes), chemotaxis ofR79262, R79263,neutrophils and T lymphocytes, and/orR79264, R79265,inhibition of interferons.R79266, R79267,R79268, R79269,R79270, R79271,R79272, R79273,R79274, R79275,R79276, R79277,R79278, R79279,R79280, R79281,R79282, R79283,R79284, andR79285IL-12 p40GeneSeqAU9466072Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,subunit.Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R63018monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225.immune cells (e.g., T helper cells, B cells,eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.AGFGeneSeqWO9429344Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R64240monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225.immune cells (e.g., T helper cells, B cells,eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqWO9519786Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,interlaukin-12 40 kDAccessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,subunitR79187monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Hori et al (1987), Blood 70, 1069-1078.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqWO9530695Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-8 receptorinterleukin-15Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may bereceptor fromR90843monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,useful for inhibitingclone P1functions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andinterleukin activities.immune cells (e.g., T helper cells, B cells,Giri et al (1994) EMBO J. 13 2822-2830.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqWO9604306Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,interleukin-7Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R92796monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Park et al (1990) J. Exp. Med. 171, 1073-79.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.interleukin-9GeneSeqWO9604306Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R92797monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Yang et al (1989) Blood 74, 1880-84.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.interleukin-3GeneSeqWO9604306Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R92801monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Kitamura et al (1989) J Cell Physiol. 140 323-334.eosinophils, and lymphocytes). chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqWO9604306Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,interleukin-5Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,R92802monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Kitamura et al (1989) J Cell Physiol. 140 323-334.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.RecombinantGeneSeqDE19617202Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,interleukin-16Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,W33373monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Lim et al (1996) J. Immunol. 156, 2566-70.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Human IL-16GeneSeqDE19617202Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,proteinAccessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,W33234monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Lim et al (1996) J. Immunol. 156, 2566-70.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Thrl 17 humanGeneSeqWO9708321Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,interleukin 9Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,W27521monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225.immune cells (e.g., T helper cells, B cells,eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Metl 17 humanGeneSeqWO9708321Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,interleukin 9Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,W27522monocytes, and macrophages. KnownInterferens: A Practical Approach. Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Yang et al (1989) Blood 74, 1880-84.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqEP86-4585Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,intracellular IL-1Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,receptorW77158monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerantagonist.functions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Orencole & Dinarello (1989) Cytokine 1, 14-20.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqEP864585Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,interleukin-18Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,protein (IL-18)W77158monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,USHIO et al (1996) J. Immunol. 156, 4274-79.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqEP861663Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,interleukin-18Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,W77077monocytes, and macrophages. KnownInterferens: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,USHIO et al (1996) J. Immunol. 156, 4274-79.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Human interleukinGeneSeqEP861663Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,18 derivativesAccessionscytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,W77083,monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerW77084,functions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andW77085,immune cells (e.g., T helper cells, B cells,Ushio et al (1996) J. Immunol, 156, 4274-79.W77086,eosinophils, and lymphocytes), chemotaxis ofW77087,neutrophils and T lymphocytes, and/orW77088, andinhibition of interferons.W77089Interleukin-9GeneSeq AccessionWO9827997Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,(IL-9) matureW68158cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,protein (Thrl17monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerversion).functions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Yang et al (1989) Blood 74, 1880-84.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.IL-9 matureGenSeq AccessionWO9827997Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,protein variantW68157cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,(Metl 17 version)monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Yang et al (1989) Blood 74, 1880-84.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Human IL-9GeneSeq AccessionWO9824904Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,receptor proteinW64058cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,variant #3.monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Yang et al (1989) Blood 74, 1880-84.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Human IL-9GenSeq AccessionWO9824904Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-9 receptorreceptor proteinW64060cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may bevariant fragmentmonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,useful for inhibitingfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andinterleukin activities.immune cells (e.g., T helper cells, B cells,Yang et al (1989) Blood 74, 1880-84.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Human IL-9GeneSeq AccessionWO9824904Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-9 receptorreceptor proteinW64061cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may bevariant #3.monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,useful for inhibitingfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andinterleukin activities.immune cells (e.g., T helper cells, B cells,Yang et al (1989) Blood 74, 1880-84.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeq AccessionWO9817689Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Interleukin-12 p40W51311cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,proteinmonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Hori et al (1987), Blood 70, 1069-1078.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeq AccessionWO9817689Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Interleukin-12 p35W51312cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,proteinmonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Hori et al (1987), Blood 70, 1069-1078.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Human proteinGeneSeq AccessionDE19649233-Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,with IL-16 activityW63753cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens at al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Lim et al (1996) J. Immunol. 156, 2566-70.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Human proteinGeneSeq AccessionDE19649233-Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,with IL-16 activityW59425cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Lim et al (1996) J. Immunol. 156, 2566-70.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeq AccessionUS5747024Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,interleukin-15W53878cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Giri et al (1994) EMBO J. 13 2822-2830.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Human wild-typeGeneSeq AccessionWO9747744Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,interleukin-4 (hIL-W52149cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,4) proteinmonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Siegel & Mostowski (1990) J Immunol Methodseosinophils, and lymphocytes), chemotaxis of132, 287-295.neutrophils and T lymphocytes, and/orinhibition of interferons.interleukin-4GeneSeqWO9747744Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,muteinsAccessionscytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,W52150,monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerW52151,functions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andW52153,immune cells (e.g., T helper cells, B cells,Siegel & Mostowski (1990) J Immunol MethodsW52154,eosinophils, and lymphocytes), chemotaxis of132, 287-295.W52155,neutrophils and T lymphocytes, and/orW52156,inhibition of interferons.W52157,W52158,W52159,W52160,W52161,W52162,W52163,W52164,W52165,W52166, andW52167Human interleukinGeneSeq AccessionWO9935268Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,1 deltaY28408cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Orencole & Dinarello (1989) Cytokine 1, 14-20.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeq AccessionWO9935268Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,interleukin-1Y24395cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,receptor antagonistmonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerbetafunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Orencole & Dinarello (1989) Cytokine 1, 14-20.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Human EDIRF IIGeneSeq AccessionWO9932632Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,protein sequenceY22199cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225.immune cells (e.g., T helper cells, B cells,eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Human EDIRF IGeneSeq AccessionWO9932632Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,protein sequenceY22197cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225.immune cells (e.g., T helper cells, B cells,eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Human IL-1RD10GeneSeq AccessionWO9919480Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-1RD10protein sequenceY14131cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andreceptor polypeptidesmonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,may be useful forfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andinhibiting interleukinimmune cells (e.g., T helper cells, B cells,Orencole & Dinarello (1989) Cytokine 1, 14-20.activities.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Human IL-1RD9GeneSeq AccessionWO9919480Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-1RD10Y14122cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andreceptor polypeptidesmonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,may be useful forfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andinhibiting interleukinimmune cells (e.g., T helper cells, B cells,Orencole & Dinarello (1989) Cytokine 1, 14-20.activities.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Human DNAXGeneSeq AccessionWO9919491Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,interleukin-40Y09196cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225.immune cells (e.g., T helper cells, B cells,eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.(DIL-40)GeneSeq AccessionWO9919491Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,alternativeY09197cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,sequencemonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225.immune cells (e.g., T helper cells, B cells,eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.IL-11GeneSeq AccessionWO9405318Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,R50176cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Lu et al (1994) J immunol. Methods 173, 19.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeq AccessionEP566410Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,adipogenesisR43260cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,inhibitory factormonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225.immune cells (e.g., T helper cells, B cells,eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.IL-11GeneSeq AccessionJP08127539Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,W02202cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Lu et al (1994) J immunol. Methods 173, 19.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.IL-14GeneSeq AccessionWO9416074Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,R55800cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Ambrus et al (1993) PNAS 90, 63330-34.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.IL-17 receptorGeneSeq AccessionUS6072033Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-7 receptorB03807cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptide may bemonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,useful for inhibitingfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andinterleukin activities.immune cells (e.g., T helper cells, B cells,Yao et al (1995) J. Immunol. 155, 5483-86.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.IL-17GeneSeq AccessionWO9518826Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,R76573cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Yao et al (1995) J. Immunol. 155, 5483-86.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.CTLA-8GeneSeq AccessionWO9704097Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,W13651cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225.immune cells (e.g., T helper cells, B cells,eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.IL-19GeneSeq AccessionWO9808870Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,W37935cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Gallagher et al (2000) Genes Immun. 1, 442-50.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.IL-21 (TIF)GeneSeq AccessionWO0024758Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysinflammatory disorders,Y92879cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,cancerfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andimmune cells (e.g., T helper cells, B cells,Parrish-Novak et al (2000) Nature 408, 57-63.cosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.IL-8 receptorGeneSeq AccessionWO9306229Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-8 receptorR33420cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may bemonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,useful for inhibitingfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andinterleukin activities.immune cells (e.g., T helper cells, B cells,Holmes et al (1991) Science 253, 1278-80..eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Human type IIGeneSeq AccessionUS5464937Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble type IIinterleukin-1R85480cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andinterleukin-1 receptorreceptormonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,polypeptides may befunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; anduseful for inhibitingimmune cells (e.g., T helper cells, B cells,Orencole & Dinarello (1989) Cytokine 1, 14-20.interleukin activities.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeq AccessionEP638644Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-12 receptorinterleukin-12R69632cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may bereceptormonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,useful for inhibitingfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andinterleukin activities.immune cells (e.g., T helper cells, B cells,Hori et al (1987), Blood 70, 1069-1078.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Interleukin 8GeneSeq AccessionUS5440021Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-8 receptor Breceptor BR80758cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may bemonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,useful for inhibitingfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andinterleukin activities.immune cells (e.g., T helper cells, B cells,Holmes et al (1991) Science 253, 1278-80.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Human IL-8GeneSeq AccessionJP08103276Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-8 receptor Areceptor proteinB09989cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may behIL8RAmonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al., eds,useful for inhibitingfunctions include stimulating proliferation ofIRL Press, Washington, D.C. 1987, pp. 221-225; andinterleukin activities.immune cells (e.g., T helper cells, B cells,Holmes et al (1991) Science 253, 1278-80.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Human IL-8GeneSeqJP08103276Interleukins are a group of multifunctionalInterleukin activity can be determined using asaysSoluble IL-8 receptorreceptor proteinAccession B09990cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may behIL8Rmonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,useful for inhibitingfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225;interleukin activities.immune cells (e.g., T helper cells, B cells,and Holmes et al (1991) Science 253, 1278-80.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Interleukin-2GeneSeqWO9621732-Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-2 receptorreceptor associatedAccession R97569cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may beprotein p43monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,useful for inhibitingfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225;interleukin activities.immune cells (e.g., T helper cells, B cells,and Gillis et al (1978) J. Immunol. 120, 2027.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqWO9629408Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-17 receptorinterleukin-17Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may bereceptorW04185monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,useful for inhibitingfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225;interleukin activities.immune cells (e.g., T helper cells, B cells,and Yao et al (1995) J. Immunol. 155, 5483-86.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqWO9619574Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-11 receptorinterleukin-11Accession R99090cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may bereceptormonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,useful for inhibitingfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225;interleukin activities.immune cells (e.g., T helper cells, B cells,and Lu et al (1994) J immunol. Methods 173, 19.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqWO9623067Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysInflammatory disorders,interleukin-1Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,receptor accessoryW01911monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,cancerproteinfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225;immune cells (e.g., T helper cells, B cells,and Orencole & Dinarello (1989) Cytokine 1, 14-20.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.AGF ProteinGeneSeqUS5488032Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysInflammatory disorders,Accession R92749cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andimmunologic disorders,monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,cancerfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225.immune cells (e.g., T helper cells, B cells,eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqW09607739Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-type-3interleukin-1 type-Accession R91064cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andreceptor polypeptides3 receptormonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,may be useful forfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225;inhibiting interleukinimmune cells (e.g., T helper cells, B cells,and Orencole & Dinarello (1989) Cytokine 1, 14-20.activitieseosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqWO9720926Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-13 betainterleukin-13 betaAccessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andreceptor polypeptidesreceptorW24972monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,may be useful forfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225;inhibiting interleukinimmune cells (e.g., T helper cells, B cells,and Boutelier et al (1995) J. Immunol. Methodsactivities.eosinophils, and lymphocytes), chemotaxis of181, 29.neutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqWO9720926Interleukins area group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-13 alphainterleukin-13Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andreceptor polypeptidesalpha receptorW24973monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,may be useful forfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225;inhibiting interleukinimmune cells (e.g., T helper cells, B cells,and Boutelier et al (1995) J. Immunol. Methodsactivities.eosinophils, and lymphocytes), chemotaxis of181, 29.neutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqUS5599905Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-4 receptorinterleukin-4Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may bereceptorW13499monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,useful for inhibitingfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225;interleukin activities.immune cells (e.g., T helper cells, B cells,and Siegel & Mostowski (1990) J Immunol Methodseosinophils, and lymphocytes), chemotaxis of132, 287-295.neutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqEP759466Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-12 beta-2interleukin-12Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andreceptor polypeptidesbeta-2 receptorW12771monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,may be useful forfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225;inhibiting interleukinimmune cells (e.g., T helper cells, B cells,and Hori et al (1987), Blood 70, 1069-1078.activities.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqEP759466Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-12 beta-1interleukin-12Accessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andreceptor polypeptidesbeta-1 receptor.W12772monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,may be useful forfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225;inhibiting interleukinimmune cells (e.g., T helper cells, B cells,and Hori et al (1987), Blood 70, 1069-1078.activities.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Human IL-9GeneSeqWO9824904Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-9 receptorreceptor proteinAccessionscytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may beW64055, W64056,monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,useful for inhibitingand W64057functions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225;interleukin activities.immune cells (e.g., T helper cells, B cells,and Yang et al (1989), Blood 74, 1880-84..eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.IL-10 receptorGeneSeqUS5716804Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-10 receptorAccessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may beW41804monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,useful for inhibitingfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225;interleukin activities.immune cells (e.g., T helper cells, B cells,and Thompson-Snipes et al (1991) J. Exp. Med. 173,eosinophils, and lymphocytes), chemotaxis of507-510.neutrophils and T lymphocytes, and/orinhibition of interferons.Human IL-6GeneSeqJP11196867Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-6 receptorreceptorAccession Y30938cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may bemonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,useful for inhibitingfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225;interleukin activities.immune cells (e.g., T helper cells, B cells,and Aarden et al (1987) Eur. J. Immunol 17, 1411-16.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Il-17 receptorGeneSeqUS6096305Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-17 receptorAccession Y97181cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may bemonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,useful for inhibitingfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225;interleukin activities.immune cells (e.g., T helper cells, B cells,and Yao et al (1995) J. Immunol. 155, 5483-86.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Il-17 receptorGeneSeqUS6100235Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-17 receptorAccession Y97131cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may bemonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,useful for inhibitingfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225;interleukin activities.immune cells (e.g., T helper cells, B cells,and Yao et al (1995) J. Immunol. 155, 5483-86.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.HumanGeneSeqEP509826Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-3 receptorinterleukin-3Accession R25300cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may bereceptormonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,useful for inhibitingfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225;interleukin activities.immune cells (e.g., T helper cells, B cells,and Kitamura et al (1989) J Cell Physiol. 140 323-334.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Human GM-CSFGeneSeqWO9102063Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble GM-CSFreceptorAccession R10919cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andreceptor polypeptidesmonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,may be useful forfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225.inhibiting interleukinimmune cells (e.g., T helper cells, B cells,activities.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Human IL-5GeneSeqEP492214Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-5 receptorreceptor alphaAccession R25064cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andalpha polypeptides maychainmonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,be useful for inhibitingfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225;interleukin activities.immune cells (e.g., T helper cells, B cells,and Kitamura et al (1989) J Cell Physiol. 140, 323-334.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Il-5 receptorGeneSeqWO9847923Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-5 receptorAccessioncytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may beW82842monocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,useflul for inhibitingfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225;interleukin activities.immune cells (e.g., T helper cells, B cells,and Kitamura et al (1989) J Cell Physiol. 140, 323-334.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Il-6 receptorGeneSeqJP05091892Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-6 receptorAccession R37215cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may bemonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,useful for inhibitingfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225;interleukin activities.immune cells (e.g., T helper cells, B cells,and Aarden et al (1987) Eur. J. Immunol 17, 1411-16.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.Human B cellGeneSeqAU8928720Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble B cellstimulating factor-Accession P90525cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andstimulating factor-22 receptormonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,receptor polypeptidesfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225.may be useful forimmune cells (e.g., T helper cells, B cells,inhibiting interleukineosinophils, and lymphocytes), chemotaxis ofactivities.neutrophils and T lymphocytes, and/orinhibition of interferons.IL-7 receptorGeneSeqEP403114Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-7 receptorcloneAccession R08330cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may bemonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,useful for inhibitingfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225;interleukin activities.immune cells (e.g., T helper cells, B cells,and Park et al (1990) J. Exp. Med. 171, 1073-79.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.EPO receptor;GeneSeqWO9008822EPO Receptor is involved in the proliferationEPO Receptor activity can be determined using assaysInflammatory disorders,EPORAccession R06512and differentiation of erythroblasts.known in the art, such as, J Biol Chem 2001 Marimmunologic disorders,23; 276(12: 8995-9002; JAK2 protein tyrosine kinasecancer, erythroblastactivity: Blood 1994 Sep 1; 84(5): 1501-7 and Mol Cellproliferation andBiol. 1994 Oct; 14(10: 6506-14.differentiationIL-15 receptorGeneSeqWO9530695Interleukins are a group of multifunctionalInterleukin activity can be determined using assaysSoluble IL-15 receptorAccession R90843cytokines synthesized by lymphocytes,known in the art: Matthews et al., in Lymphokines andpolypeptides may bemonocytes, and macrophages. KnownInterferons: A Practical Approach, Clemens et al.,useful for inhibitingfunctions include stimulating proliferation ofeds, IRL Press, Washington, D.C. 1987, pp. 221-225;interleukin activities.immune cells (e.g., T helper cells, B cells,and Giri et al (1994) EMBO J. 13 2822-2830.eosinophils, and lymphocytes), chemotaxis ofneutrophils and T lymphocytes, and/orinhibition of interferons.CD137; 4-1BBGeneSeqWO9507984Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and TSoluble 4-1BB receptorReceptor ProteinAccession R70977activation, and co-stimulation of immune cellscell co-stimulation can be determined using assayspolypeptides may besuch as T and B cells.known in the art: Moore et al., 1999, Science,useful for inhibiting285(5425): 260-3; Song HY et al., 1997 Proc Natlapoptosis, NF-kBAcad Sci USA 94(18): 9792-6; Epsevik and Nissen-activation, and/or co-Meyer, 1986, J. Immunol. Methods.stimulation of immunecells such as B and Tcells.BCMAGeneSeqWO0068378Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and TSoluble BCMA receptorAccession Y71979activation, and co-stimulation of immune cellscell co-stimulation can be determined using assayspolypeptides may besuch as T and B cells.known in the art: Moore et al., 1999, Science,useful for inhibiting285(5425): 260-3; Song HY et al., 1997 Proc Natlapoptosis, NF-kBAcad Sci USA 94(18): 9792-6; Epsevik and Nissen-activation, and/or co-Meyer, 1986, J. Immunol. Methods.stimulation of immunecells such as B and Tcells.CD27GeneSeqWO9201049Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and TSoluble CD27Accession R20814activation, and co-stimulation of immune cellscell co-stimulation can be determined using assayspolypeptides may besuch as T and B cells.known in the art: Moore et al., 1999, Science,useful for inhibiting285(5425): 260-3; Song HY et al., 1997 Proc Natlapoptosis, NF-kBAcad Sci USA 94(18): 9792-6; Epsevik and Nissen-activation, and/or co-Meyer, 1986, J. Immunol. Methods.stimulation of immunecells such as B and Tcells.CD30GeneSeqDE4200043Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and TSoluble CD30Accession R35478activation, and co-stimulation of immune cellscell co-stimulation can be determined using assayspolypeptides may besuch as T and B cells.known in the art: Moore et al., 1999, Science,useful for inhibiting285(5425): 260-3; Song HY et al., 1997 Proc Natlapoptosis, NF-kBAcad Sci USA 94(18): 9792-6; Epsevik and Nissen-activation, and/or co-Meyer, 1986, J. Immunol. Methods.stimulation of immunecells such as B and Tcells.CD40GeneSeqWO9945944Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and TSoluble CD40Accessionactivation, and co-stimulation of immune cellscell co-stimulation can be determined using assayspolypeptides may beY33499such as T and B cells.known in the art: Moore et al., 1999, Scienceuseful for inhibiting285(5425): 260-3; Song HY et al., 1997 Proc Natlapoptosis, NF-kBAcad Sci USA 94(18): 9792-6; Epsevik andactivation, and/or co-Nissen-Meyer, 1986, J. Immunol. Methods.stimulation of immunecells such as B and Tcells.EDARGenbankActivities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and T cellImmune Disorders,Accessionactivation, and co-stimulation of immune cellsco-stimulation can be determined using assays knownLymphomas, X-linkedAAD50077such as T and B cells.in the art: Moore et al., 1999, Science,hypohidrotic ectodermal285(5425): 260-3; Song HY et al., 1997 Proc Natl AcaddysplasiaSci USA 94(18): 9792-6; Epsevik and Nissen-Meyer,1986, J. Immunol. Methods.OX40; ACT-4GeneSeqWO9512673Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and T cellImmune Disorders,Accession R74737activation, and co-stimulation of immune cellsco-stimulation can be determined using assays knownLymphomas, T cellsuch as T and B cells.in the art: Moore et al., 1999, Science,disorders285(5425): 260-3; Song HY et al., 1997 Proc Natl AcadSci USA 94(18): 9792-6; Epsevik and Nissen-Meyer,1986, J. Immunol. Methods.TACIGeneSeqWO9839361Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and T cellSoluble TACI receptorAccessionactivation, and co-stimulation of immune cellsco-stimulation can be determined using assays knownpolypeptides may beW75783such as T and B cells.in the art: Moore et al., 1999, Science,useful for inhibiting285(5425): 260-3; Song HY et al., 1997 Proc Natl Acadapoptosis, NF-kBSci USA 94(18): 9792-6; Epsevik and Nissen-Meyer,activation, and/or co-1986, J. Immunol. Methods.stimulation of immunecells such as B and Tcells.TNF-RGeneSeqAU9058976Activities associates with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and T cellSoluble TNF-R receptorAccession R10986activation, and co-stimulation of immune cellsco-stimulation can be determined using assays knownpolypeptides may besuch as T and B cells.in the art: Moore at al., 1999, Science,useful for inhibiting285(5425): 260-3; Song HY et al., 1997 Proc Natl Acadapoptosis, NF-kBSci USA 94(18): 9792-6; Epsevik and Nissen-Meyer,activation, and/or co-1986, J. Immunol. Methods.stimulation of immunecells such as B and Tcells.TNF-RII; TNFGeneSeqEP418014Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and T cellSoluble TNFR-IIp75 receptor;Accession R11141activation, and co-stimulation of immune cellsco-stimulation can be determined using assays knownreceptor polypeptidesDeath Receptorsuch as T and B cells.in the art: Moore et al., 1999, Science,may be useful for285(5425): 260-3; Song HY et al., 1997 Proc Natl Acadinhibiting apoptosis,Sci USA 94(18)9792-6; Epsevik and Nissen-Meyer,NF-kB activation,1986, J. Immunol. Methods.and/or co-stimulation ofimmune cells such as Band T cells.hAPO-4; TROYGeneSeqWO9911791Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and T cellImmune Disorders,Accessionactivation, and co-stimulation of immune cellsco-stimulation can be determined using assays knownCancersW93581such as T and B cells.in the art: Moore et al., 1999, Science,285(5425): 260-3; Song HY et al., 1997 Proc Natl AcadSci USA 94(18): 9792-6; Epsevik and Nissen-Meyer,1986, J. Immunol. Methods.TNF-alphaGeneSeqEP205038Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and T cellInflammatory disorders,precursorAccession P60074activation, and co-stimulation of immune cellsco-stimulation can be determined using assays knownimmunologic disorders,such as T and B cells.in the art: Moore et al., 1999, Science,cancer285(5425): 260-3; Song HY et al., 1997 Proc Natl AcadSci USA 94(18): 9792-6; Epsevik and Nissen-Meyer,1986, J. Immunol. Methods.Human TNF-GeneSeqEP619372Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and T cellInflammatory disorders,alphaAccession R62463activation, and co-stimulation of immune cellsco-stimulation can be determined using assays knownimmunologic disorders,such as T and B cellsin the art: Moore et al., 1999, Science,cancer285(5425): 260-3; Song HY et al., 1997 Proc Natl AcadSci USA 94(18): 9792-6; Epsevik and Nissen-Meyer,1986, J. Immunol. Methods.Human TNF-GeneSeqEP563714Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and T cellInflammatory disorders,alphaAccession R42679activation, and co-stimulation of immune cellsco-stimulation can be determined using assays knownimmunologic disorders,such as T and B cells.in the art: Moore et al., 1999, Science,cancer285(5425): 260-3; Song HY et al., 1997 Proc Natl AcadSci USA 94(18): 9792-6; Epsevik and Nissen-Meyer,1986, J. Immunol. Methods.Human TNF-GeneSeqWO0064479Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and T cellInflammatory disorders,beta (LT-alpha)Accession B37799activation, and co-stimulation of immune cellsco-stimulation can be determined using assays knownimmunologic disorders,such as T and B cells.in the art: Moore et al., 1999, Science,cancer285(5425): 260-3; Song HY et al., 1997 Proc Natl AcadSci USA 94(18): 9792-6; Epsevik and Nissen-Meyer,1986, J. Immunol. Methods.LT-alphaGeneSeqEP250000Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and T cellInflammatory disorders,Accession P70107activation, and co-stimulation of immune cellsco-stimulation can be determined using assays knownimmunologic disorders,such as T and B cells.in the art: Moore et al., 1999, Science,cancer285(5425): 260-3; Song HY et al., 1997 Proc Natl AcadSci USA 94(18): 9792-6; Epsevik and Nissen-Meyer,1986, J. Immunol. Methods.LT-betaGeneSeqWO9413808Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and T cellInflammatory disorders,Accession R56869activation, and co-stimulation of immune cellsco-stimulation can be determined using assays knownimmunologic disorders,such as T and B cells.in the art: Moore et al., 1999, Science,cancer285(5425): 260-3; Song HY et al., 1997 Proc Natl AcadSci USA 94(18)9792-6; Epsevik and Nissen-Meyer,1986, J. Immunol. Methods.OPGLGeneSeqWO9846751Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and T cellInflammatory disorders,Accessionactivation, and co-stimulation of immune cellsco-stimulation can be determined using assays knownimmunologic disorders,W83195such as T and B cells.in the art: Moore et al., 1999, Science,cancer, loss of bone285(5425): 260-3; Song HY et al., 1997 Proc Natl AcadmassSci USA 94(18)9792-6; Epsevik and Nissen-Meyer,1986, J. Immunol. Methods.FasLGeneSeqWO9903999Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and T cellInflammatory disorders,Accessionactivation, and co-stimulation of immune cellsco-stimulation can be determined using assays knownimmunologic disorders,W98071such as T and B cells.in the art: Moore et al., 1999, Science,cancer285(5425): 260-3; Song HY et al., 1997 Proc Natl AcadSci USA 94(18)9792-6; Epsevik and Nissen-Meyer,1986, J. Immunol. Methods.FasLGeneSeqWO9903998Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and T cellInflammatory disorders,Accessionactivation, and co-stimulation of immune cellsco-stimulation can be determined using assays knownimunologic disorders,W95041such as T and B cells.in the art: Moore et al., 1999, Science,cancer285(5425): 260-3; Song HY et al., 1997 Proc Natl AcadSci USA 94(18): 9792-6; Epsevik and Nissen-Meyer,1986, J. Immunol. Methods.CD27LGeneSeqWO9405691Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and T cellInflammatory disorders,Accession R50121activation, and co-stimulation of immune cellsco-stimulation can be determined using assays knownimmunologic disorders,such as T and B cells.in the art: Moore et al., 1999, Science,cancer285(5425): 260-3; Song HY et al., 1997 Proc Natl AcadSci USA 94(18): 9792-6; Epsevik and Nissen-Meyer,1986, J. Immunol. Methods.CD30 ligandGeneSeqWO9324135Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and T cellInflammatory disorders,Accession R45007activation, and co-stimulation of immune cellsco-stimulation can be determined using assays knownimmunologic disorders,such as T and B cells.in the art: Moore et al., 1999, Science,cancer285(5425): 260-3; Song HY et al., 1997 Proc Natl AcadSci USA 94(18): 9792-6; Epsevik and Nissen-Meyer,1986, J. Immunol. Methods.CD40LGeneSeqWO9529935Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and T cellInflammatory disorders,Accession R85486activation, and co-stimulation of immune cellsco-stimulation can be determined using assays knownimmunologic disorders,such as T and B cells.in the art: Moore et al., 1999, Science,cancer285(5425): 260-3; Song HY et al., 1997 Proc Natl AcadSci USA 94(18): 9792-6; Epsevik and Nissen-Meyer,1986, J. Immunol. Methods.4-1BB ligandGeneSeqUS5674704Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and T cellInflammatory disorders,Accessionactivation, and co-stimulation of immune cellsco-stimulation can be determined using assays knownimmunologic disorders,W26657such as T and B cells.in the art: Moore et al., 1999, Science,cancer285(5425): 260-3; Song HY et al., 1997 Proc Natl AcadSci USA 94(18): 9792-6; Epsevik and Nissen-Meyer,1986, J. Immunol. Methods.FAS LigandGeneSeqWO0058465Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and T cellSoluble DcR3InhibitoryAccession B19335activation, and co-stimulation of immune cellsco-stimulation can be determined using assays knownpolypeptides may beProtein (DcR3)such as T and B cells.in the art: Moore et al., 1999, Science,useful for inhibiting285(5425): 260-3; Song HY et al., 1997 Proc Natl Acadapoptosis, NF-kBSci USA 94(18): 9792-6; Epsevik and Nissen-Meyer,activation, and/or co-1986, J. Immunol. Methodsstimulation of immunecells such as B and Tcells.OX40LGeneSeqWO9521915Activities associated with apoptosis, NF-kBApoptosis activity, NF-kB activation, and B and T cellInflammatory disorders,Accession R79903activation, and co-stimulation of immune cellsco-stimulation can be determined using assays knownimmunologic disorders,such as T and B cells.in the art: Moore et al., 1999, Science,cancer285(5425): 260-3; Song HY et al., 1997 Proc Natl AcadSci USA 94(18): 9792-6; Epsevik and Nissen-Meyer,1986, J. Immunol. Methods.ProteaseGeneSeqWO9106561Peptides that inhibit the function/binding ofHIV protease activities are known in the art: HIVHIV, inflammatoryinhibitorAccessionsHIVprotease assays: EP0387231. One can modify thedisorders, immunologicpeptidesR12435, R12436,assay to look for inhibition using any of the discloseddisorders, cancer, viralR12437, R12438,protease inhibitor polypeptides.infectionsR12439, R12440,and R1244Retroviral proteaseGeneSeqEP387231Peptides that inhibit the function/binding ofHIV protease activities are known in the art: HIVHIV, inflammatoryinhibitorsAccessionsHIVprotease assays: EP0387231. One can modify thedisorders, immunologicR06660, R06661,assay to look for inhibition using any of the discloseddisorders, cancer, viralR06662, R06663,protease inhibitor polypeptides.infectionsR06664, R06665,R06666, R06667,R06668, R06669,R06670, R06671,R06672, R06673,R06674, R06675,and R06676HIV proteaseGeneSeqWO9301828Peptides that inhibit the function/binding ofHIV protease activities are known in the art: HIVHIV, inflammatoryinhibitingAccessionsHIVprotease assays: EP0387231. One can modify thedisorders, immunologicpeptidesR59293, R59294,assay to look for inhibition using any of the discloseddisorders, cancer, viralR59295, R59296,protease inhibitor polypeptides.infectionsR59297,R59298, R59299,R592300, R59301,R59302, R59301,R59302, R59303,R59304, R59305,R59306, R59307,R59308, R59309,R59310, R59311,R59312, R59313,R59314, R59315,R59316, R59317R59318, R59319,R59320, R59321,R59322, R59323,R59324, R59325,R59326, R59327,R59328, R59329,R59330, R59331,R59332, R59333,R59334, R59335,R59336, R59337,R59338, R59339,R59340, R59341,R59342, R59343,R59344, R59345,R59346, R59347,R59348, R59349,and R59350HIV-1 proteaseGeneSeqDE4412174Peptides that inhibit the function/binding ofHIV protease activities are known in the art: HIVHIV, inflammatoryhinibitorsAccessionsHIVprotease assays: EP0387231. One can modify thedisorders, immunologicR86326, R86327,assay to look for inhibition using any of the discloseddisorders, cancer, viralR86328, R86329,protease inhibitor polypeptides.infectionsR86330, R86331,R86332, R86333,R86334, R86335,R86336, R86337,R86338, R86339,R86340, R86341,R86342, R86343,R86344, R86345,R86346, R86347,R86348, R86349,R86350, R86351,R86352, R86353,R86354, R86355,R86356, R86357,R86358, R86359,R86360, R86361,R86362, R86363,R86364, R86365,R86366, R86367,R86368, R86369,R86370, andR86371HIV InhibitorGeneSeqWO9959615Peptides that inhibit the function/binding ofHIV protease activities are known in the art: HIVHIV, inflammatoryPeptideAccessionHIVprotease assays: EP0387231. One can modify thedisorders, immunologicY89687assay to look for inhibition using any of the discloseddisorders, cancer, viralprotease inhibitor polypeptides.infectionsHIV InhibitorGenSeq AccessionWO9948513Peptides that inhibit the function/binding ofHIV Protease activities are known in the art; HIVHIV, inflammatoryPeptideY31955HIVprotease assays: EP0387231. One can modify thedisorders, immunologicassay to look for inhibition using any of the discloseddisorders, cancer, viralprotease inhibitor polypeptides.infections.HIV Inhibitorwww.sciencexpress.Peptides that inhibit the function/binding ofHIV protease activities are known in the art: HIVHIV, inflammatoryPeptideorg; PublishedHIVprotease assays: EP0387231. One can modify thedisorders, immunologiconline 12 Januaryassay to look for inhibition using any of the discloseddisorders, cancer, viral2001;protease inhibitor polypeptides.infections10.1126/science.1057453Human monocyteGeneSeqWO9509232Chemokines are a family of small, secretedChemokine activities can be determined using assaysImmune disorders,chemoattractantAccession R73915proteins involved in biological processesknown in the art: Methods in Molecular Biology,particularly useful forfactor hMCP-3ranging from hematopoiesis, angiogenesis, and2000, vol. 138: Chemokine Protocols, Edited by:treating bacterial and/orleukocyte trafficking. Members of this familyA. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©viral menigitisare involved in a similarly diverse range ofHumana Press Inc., Totowa, NJpathologies including inflammation, allergy,tissue rejection, viral infection, and tumorbiology. The chemokines exert their effects byacting on a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human monocyteGeneSeqWO9509232Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders,chemoattractantAccession R73914secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,particularly useful forfactor hMCP-1processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:treating bacterial and/orangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©viral menigitisMembers of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human gro-betaGeneSeqWO9429341Chemokines are a family of small, secretedChemokine activities can be determined using assaysImmune disorders,chemokineAccessionsproteins involved in biological processesknown in the art: Methods in Molecular Biology,inflammatory disorders,R66699 andranging from hematopoiesis, angiogenesis, and2000, vol. 138: Chemokine Protocols. Edited by:blood-related disorders,W17671leukocyte trafficking. Members of this familyA. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©stem cellare involved in a similarly diverse range ofHumana Press Inc., Totowa, NJtransplantation, cancerpathologies including inflammation, allergy,tissue rejection, viral infection, and tumorbiology. The chemokines exert their effects byacting on a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human gro-GeneSeqWO9429341Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders,gamma chemokineAccessionssecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,inflammatory disorders,R66700 andprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:blood-related disorders,W17672angiogenesis, and leukocyte trafficking.A. E. I. Proutfoot, T. N. C. Wells, and C. A. Power. ©stem cellMembers of this family are involved in aHumana Press Inc., Totowa, NJtransplantation, cancersimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identifiedHuman gro-alphaGeneSeqWO9429341Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders,chemokineAccessionssecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,inflammatory disorders,R66698 andprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:blood-related disorders,W18024angiogenesis, and leukocyle trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©stem cellMembers of this family are involved in aHumana Press Inc., Totowa, NJtransplantation, cancersimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identifiedHumanGeneSeqWO9632481Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders,eosinophil-Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,particularly treatment ofexpressedW05186processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:eosinophilia,chemokine (EEC)angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©inflammation, allergies,Members of this family are involved in aHumana Press Inc., Totowa, NJasthma, leukaemia andsimilarly diverse range of pathologieslymphomaincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identifiedChemokine-likeGeneSeqWO9613587Chemokines are a family of related small,Chemokine activities can be determined using assaysCancer and blood-protein PF4-414Accessionssecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,related disorders,Full-Length andR92318 andprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:particularlyMatureR99809angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©myelosuppressionMembers of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identifiedChemokine-likeGeneSeqWO9613587Chemokines are a family of related small,Chemokine activities can be determined using assaysCancer and blood-protein IL-8M3Accession R99812secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,related disorders,processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:particularlyangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©myelosuppressionMembers of this family are involved in aHumana Press Inc., Totowa, NJ; and Holmes et alsimilarly diverse range of pathologies(1991) Science 253, 1278-80.including inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identifiedHumanGeneSeqWO9613587Chemokines are a family of related small,Chemokine activities can be determined using assaysCancer and blood-interleukin-8 (IL-Accession R99814secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,related disorders,8)processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:particularlyangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©myelosuppressionMembers of this family are involved in aHumana Press Inc., Totowa, NJ; and Holmes et alsimilarly diverse range of pathologies(1991) Science 253, 1278-80.including inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identifiedChemokine-likeGeneSeqWO9613587Chemokines are a family of related small,Chemokine activities can be determined using assaysCancer and blood-protein IL-8M1Accessionssecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,related disorders,Full-Length andR99815 andprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:particularlyMatureR99803angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©myelosuppressionMembers of this family are involved in aHumana Press Inc., Totowa, NJ; and Holmes et alsimilarly diverse range of pathologies(1991) Science 253, 1278-80.including inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identifiedChemokine-likeGeneSeqWO9613587Chemokines are a family of related small,Chemokine activities can be determined using assasysCancer and blood-protein IL-8M8Accessionssecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,related disorders,Full-Length andR99816 andprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:particularlyMatureR99805angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot; T. N. C. Wells, and C. A. Power. ©myelosuppression.Members of this family are involved in aHumana Press Inc., Totowa, NJ; and Holmes et alsimilarly diverse range of pathologies(1991) Science 253, 1278-80.including inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Chemokine-likeGeneSeqWO9613587Chemokines are a family of related small,Chemokine activities can be determined using assasysCancer and blood-protein IL-8M8Accessionssecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,related disorders,Full-Length andR99817 andprocesses ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot;particularlyMatureR99806angiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © Humanamyelosuppression.Members of this family are involved in aPress Inc., Totowa, NJ; and Holmes et al (1991)similarly diverse range of pathologiesScience 253, 1278-80.including inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Chemokine-likeGeneSeqWO9613587Chemokines are a family of related small,Chemokine activities can be determined using assasysCancer and blood-protein IL-8M8Accessions R99818secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,related disorders,Full-Length andand R99804processes ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot;particularlyMatureangiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © Humanamyelosuppression.Members of this family are involved in aPress Inc., Totowa, NJ; and Holmes et al (1991)similarly diverse range of pathologiesScience 253, 1278-80.including inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Chemokine-likeGeneSeqWO9613587Chemokines are a family of related small,Chemokine activities can be determined using assasysCancer and blood-protein IL-8M8Accessions R99819secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,related disorders,Full-Length andand R99807processes ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot;particularlyMatureangiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © Humanamyelosuppression.Members of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Chemokine-likeGeneSeqWO9613587Chemokines are a family of related small,Chemokine activities can be determined using assasysCancer and blood-protein IL-8M8Accessions R99822secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,related disorders,Full-Length andand R9807processes ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot;particularlyMatureangiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © Humanamyelosuppression.Members of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human foetalGeneSeq AccessionWO9622374Chemokines are a family of related small,Chemokine activities can be determined using assasysImmune disordersspleen expressedR98499secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,chemokine, FSECprocesses ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot;angiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Liver expressedGeneSeq AccessionWO9616979Chemokines are a family of related small,Chemokine activities can be determined using assasysInflammation of thechemokine-R95689secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,liver1(LVEC-1)processes ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot;angiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Liver expressedGeneSeq AccessionWO9616979Chemokines are a family of related small,Chemokine activities can be determined using assasysInflammation of thechemokine-R95690secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,liver2(LVEC-2)processes ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot;angiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Pituitary expressedGeneSeq AccessionWO9616979Chemokines are a family of related small,Chemokine activities can be determined using assasysInflammation,chemokineR95691secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,particularly of the liver(PGEC)processes ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot;angiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Adenoid-GeneSeq AccessionWO9617868Chemokines are a family of related small,Chemokine activities can be determined using assasysInflammation,expressedR97664secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,angiogenesis,chemokineprocesses ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot;tumorigenesis,(ADEC)angiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanamusculoskeletalMembers of this family are involved in aPress Inc., Totowa, NJdisorderssimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.HumanGeneSeqWO9741230Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders, cellchemokineCC-2Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,migration, proliferation,W38170processes ranging from hematopoiesis,2000, vol. 138; Chemokine protocols. Edited by:and differentiationangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©disordersMembers of this family are involved in aHumana Press Inc. Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.HumanGeneSeqWO9741230Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders, cellchemokineAccessionsecreted proteins involved in biologicalknown in the art: Methods in molecular Biology 2000,migration, proliferation,HCC-1W38171processes ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by A. E. I. Proudfoot,and differentiationanglogenesis, and leukocyte trafficking.T. N. C. Wells and C. A. Power © HumanadisordersMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembraneG-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.HumanGeneSeqWO9741230Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders, cellchemokine CC-3Accessionsecreted proteins involved in biologicalknown in the art: Methods in molecular Biology,migration, proliferation.W38172processes ranging from hemotopoiesis,2000, vol. 138: Chemokine Protocols, Edited by A. E. I. Proudfoot,and differentiationanglogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power © HumanadisordersMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.NovelGeneSeqWO9739126Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders,betachemokineAccessionsecreted proteins involved in biologicalknown in the art: Methods in molecular Biology,vascular disorders,designated PTECW27271processes ranging from hemotopoiesis,2000, vol. 138: Chemokine Protocols, Edited by A. E. I. Proudfoot,canceranglogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human CX3CGeneSeqWO9727299Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders,111 amino acidAccessionsecreted proteins involved in biologicalknown in the art: Methods in molecular Biology,inflammatory diseases,chemokineW23344processes ranging from hemotopoiesis,2000, vol. 138: Chemokine Protocols, Edited by A. E. I. Proudfoot,abnormal proliferation,anglogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power © Humanaregeneration,Members of this family are involved in aPress Inc., Totowa, NJdegeneration, andsimilarly diverse range of pathologiesatrophyincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human CCF18GeneSeqWO9721812Chemokines are a family of related small,Chemokine activities can be determined using assaysAbnormal physiologychemokineAccessionsecreted proteins involved in biologicalknown in the art: Methods in molecular Biology,and developmentW25942processes ranging from hemotopoiesis,2000, vol. 138: Chemokine Protocols, Edited by A. E. I. Proudfoot,disorders, can also beanglogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power © Humanaused as an anti-viralMembers of this family are involved in aPress Inc., Totowa, NJagentsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human beta-GeneSeqWO9725427Chemokines are a family of related small,Chemokine activities can be determined using assaysChemotaxis,chemokineAccessionsecreted protein involved in biologicalknown in the art: Methods in molecular Biology,blood-related disorders,H1305 (MCP-2)W26655processes ranging from hemotopoiesis,2000, vol. 138: Chemokine Protocols, Edited by A. E. I. Proudfoot,viral infection, HIV,anglogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power © Humanawound healing, cancerMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.HumanGeneSeqWO9712914Chemokines are a family of related small,Chemokine activities can be determined using assaysInflammatory andeosinocyte CCAccessionsecreted proteins involved in biologicalknown in the art: Methods in molecular Biology,immune disorderstype chemokineW14990processes ranging from hemotopoiesis,2000, vol. 138: Chemokine Protocols, Edited by A. E. I. Proudfoot,eotaxinanglogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human thymusGeneSeqWO9711969Chemokines are a family of related small,Chemokine activities can be determined using assaysInflammatory andand activationAccessionsecreted proteins involved in biologicalknown in the art: Methods in molecular Biology,immune disordersregulatedW14018processes ranging from hemotopoiesis,2000, vol. 138: Chemokine Protocols, Edited by A. E. I. Proudfoot,cytokineanglogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power © Humana(TARC)Members of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.HumanGeneSeqWO9712041Chemokines are a family of related small,Chemokine activities can be determined using assaysCancer, would healing,chemokine beta-Accessionsecreted proteins involved in biologicalknown in the art: Methods in molecular Biology,immune disorders8 short formsW16315processes ranging from hemotopoiesis,2000, vol. 138: Chemokine Protocols, Edited by A. E. I. Proudfoot,anglogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.MicrophageGeneSeqWO9640923Chemokines are a family of related small,Chemokine activities can be determined using assaysInflammatory diseases,derivedAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,wound healin,chemokine, MDCW20058processes ranging from hermaatopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesisangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power.Members of this family are involved in a© Humana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeqWO9844117Chemokines are a family of related small,Chemokine activities can be determined using assaysInflammatory andZSIG-35Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,immune diseasesW30565processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power.Members of this family are involved in a© Humana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Primate CCGeneSeqWO98328658Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune andchemokineAccesssionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,inflammatory disorders,“ILINCK”W69990processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:abnormal proliferation,angiogenesis, and leukocyte trafficking.A. E. I. Prodfoot, T. N. C. Wells, and C. A. Power.regeneration, generation© Humana Press Inc., Totowa, NJand atrophy disordersPrimate CXCGeneSeqWO9832858Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune andchemokineAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,inflammatory disorders,“IBICK”W69989processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Editd by:abnormal proliferation,angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power.regeneration, generationMembers of this family are involved in a© Humana Press Inc., Totowa, NJand atrophy disorderssimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human CC-typeGeneSeqWO9831809Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune, inflammatory,chemokine proteinAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,and infectious disorders,designated SLCW69163processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:cancer(secondaryangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power.lymphoidMembers of this family are involved in a© Humana Press Inc., Totowa, NJchemokine)similarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human CCGeneSeqWO9826071Chemokines are a family of related small,Chemokine activities can be determined using assaysCancer and infectiouschemokine ELCAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,diseases, particularlyproteinW62542processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:herpes virusangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human DVic-1GeneSeqWo9823750Chemokines are a family of related small,Chemokine activities can be determined using assaysAbnormal proliferation,C-C chemokineAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,regeneration,W60649processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:degeneration, andangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©atrophy disorders,Members of this family are involved in aHumana Press Inc., Totowa, NJincluding cancersimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human C-CGeneSeqWO9823750Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders, cellchemokineAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,proliferation disorders,DGWCCW60650processes ranging from hematophoiesis,2000, vol. 138: Chemokine Protocols. Edited by:cancerangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identifed.Human STCP-1GeneSeqWO9824907Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders,Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,particularly T cellW62783processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:related disorders, viralangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©infection, andMembers of this family are involved in aHumana Press Inc., Totowa, NJinflammation, especiallysimilarly diverse range of pathologiesjointincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Exodua proteinGeneSeqWO9821330Chamokines are a family of related small,Chemokine activities can be determined using assaysImmune andAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,inflammatory disorders,W61279processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, cancer,angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©and proliferationMembers of this family are involved in aHumana Press Inc., Totowa, NJdisorders, particularlysimilarly diverse range of pathologiesmyeloproliferativeincluding inflammation, allergy, tissuediseasesrejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.HumanGeneSeqWO9814581Chemokines are a family of related small,Chemokine activities can be determined using assaysCancer and degenerativeChr19KineAcessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,disordersproteinW50887processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols, Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human T cellGeneSeqUS5780268Chemokines area family of related small,Chemokine activities can be determined using assaysImmune, inflammatory,mixedAccessionsecreted proteins involved in biologicalknown in the art: Mehtods of Molecular Biology,and infectious disorders,lymphocyteW58703processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:cancerreactionangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power ©expressedMembers of this family are involved in aHumana Press Inc., Totowa, NJchemokinesimilarly diverse range of pathologies(TMEC)including inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human 6CKineGeneSeqW09814581Chemokines area family of related small,Chemokine activities can be determined using assaysCancer and degenerativeproteinAccessionsecreted proteins involved in biologicalknown in the art: Mehtods of Molecular Biology,disordersW50885processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.human liver andGeneSeqWO9817800Chemokines area family of related small,Chemokine activities can be determined using assaysImmune, inflammatory,activationAccessionsecreted proteins involved in biologicalknown in the art: Mehtods of Molecular Biology,and infectious disorders,regulatedW57475processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:cancerchemokineangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power ©(LARC)Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.RANTESGeneSeqWO9744462Chemokines area family of related small,Chemokine activities can be determined using assaysInfectious diseases,peptideAccessionsecreted proteins involved in biologicalknown in the art: Mehtods of Molecular Biology,particularly HIVW29538processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.RANTES 8-68GeneSeqWO9744462Chemokines area family of related small,Chemokine activities can be determined using assaysInfectious diseases,Accessionsecreted proteins involved in biologicalknown in the art: Mehtods of Molecular Biology,particularly HIVW29529processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.RANTES 9-68GeneSeqWO9744462Chemokines area family of related small,Chemokine activities can be determined using assaysInfectious diseases,Accessionsecreted proteins involved in biologicalknown in the art: Mehtods of Molecular Biology,particularly HIVW29528processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.HumanGeneSeqWO9811226Chemokines area family of related small,Chemokine activities can be determined using assaysAbnormal proliferation,chemokineAccessionsecreted proteins involved in biologicalknown in the art: Mehtods of Molecular Biology,regeneration,protein 331D5W59433processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:degeneration or atrophy,angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power ©including cancerMembers of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.HumanGeneSeqWO9811226Chemokines area family of related small,Chemokine activities can be determined using assaysAbnormal proliferation,chemokineAccessionsecreted proteins involved in biologicalknown in the art: Mehtods of Molecular Biology,regeneration,protein 61164W59430processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:degeneration or atrophy,angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power ©including cancerMembers of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.ChemokineGeneSeqWO9809171Chemokines area family of related small,Chemokine activities can be determined using assaysImmune, Inflammatory,MCP-4Accessionsecreted proteins involved in biologicalknown in the art: Mehtods of Molecular Biology,and infectious diseasesW56690processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human stromalGeneSeqFR2751658Chemokines are a family of related small,Chemokine activities can be determined using assaysHIV infectionscell-derivedAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,chemokine, SDF-1W50766processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Thymus expressedGeneSeq AccessionWO9801557Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune andchemokineW44397secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,inflammatory disorders(TECK)processes ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot,angiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeq AccessionWO9801557Chemokines are a family of related small.Chemokine activities can be determined using assaysImmune andMIP-3alphaW44398secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,inflammatory disordersprocesses ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot,angiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeq AccessionWO9801557Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune andMIP-3betaW44399secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,inflammatory disordersprocesses ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot,angiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection; viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human monocyteGeneSeq AccessionWO9802459Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders,chemotacticW42072secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,respiratory disorders,proproteinprocesses ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot,cancer(MCPP) sequenceangiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Macrophage-GeneSeqUS5688927/Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune, andderived chemokineAccessions W40811US5932703secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,inflammatory disorders,(MDC)and Y24414processes ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot,cancerangiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.MacrophageGeneSeq AccessionUS5932703Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune andderived chemokineY24416secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,inflammatory disordersanalogue MDC-processes ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot,eyfyangiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.MacrophageGeneSeq AccessionUS5932703Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune andderived chemokineY24413secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,inflammatory disordersanalogue MDCprocesses ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot,(n + 1)angiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.MacrophageGeneSeq AccessionUS5932703Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune andderived chemokineY24415secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,inflammatory disordersanalogue MDC-ylprocesses ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot,angiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human type CCGeneSeq AccessionJP11243960Chemokines are a family of related small,Chemokine activities can be determined using assaysAllergic diseases andchemokine eotaxinY43178secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,HIV infection3 protein sequenceprocesses ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot,angiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human MCP-3GeneSeq AcessionWO9946392Chemokines are a family of related small,Chemokine activities can be determined using assaysCancer and immuneand human Muc-1Y29893secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,disorders, particularlycore epitopeprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:HIV infection(VNT) fusionangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©proteinMembers of this family are involved in aHumana Press Inc., Totowa, NJsimilarily diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, whichbind to ˜17 receptors thus far identified.Human IP-10 andGeneSeqWO9946392Chemokines are a family of related small,Chemokine activities can be determined using assaysCancer and immunehuman Muc-1 coreAccession Y29894secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,disorders, particularlyepitope (VNT)processes ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot,HIV infectionfusion proteinangiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarily diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, whichbind to ˜17 receptors thus far identified.Human IP-10 andGeneSeqW09946392Chemokines are a family of related small,Chemokine activities can be determined using assaysCancer and immuneHIV-1 gp 120Accession Y29897secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,disorders, particularlyhypervariableprocesses ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot,HIV infectionregion fusionangiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaproteinMembers of this family are involved in aPress Inc., Totowa, NJsimilarily diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, whichbind to ˜17 receptors thus far identified.Human mammaryGeneSeqWO9936540Chemokines are a family of related small,Chemokine activities can be determined using assaysBreast disease, includingassociatedAccessionssecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,cancerchemokineY29092 andprocesses ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot,(MACK) proteinY29093angiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaFull-Length andMembers of this family are involved in aPress Inc., Totowa, NJMaturesimilarily diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, whichbind to ˜17 receptors thus far identified.Tim-1 proteinGeneSeqWO9933990Chemokines are a family of related small,Chemokine activities can be determined using assaysInflammation due toAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,stimuli such as heartY28290processes ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot,attacks and stroke,angiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © Humanainfection, physicalMembers of this family are involved in aPress Inc., Totowa, NJtrauma, UV or ionizingsimilarily diverse range of pathologiesradiation, burns,including inflammation, allergy, tissuefrostbite or corrosiverejection, viral infection, and tumor biology.chemicalsThe chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, whichbind to ˜17 receptors thus far identified.Human Lkn-1GeneSeqWO9928473 andChemokines are a family of related small,Chemokine activities can be determined using assaysHIV infection andFull-Length andAccessionsWO9928472secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,cancer, particularlyMature proteinY17280, Y17274,processes ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot,leukemiaY17281, andangiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaY17275Members of this family are involved in aPress Inc., Totowa, NJsimilarily diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, whichbind to ˜17 receptors thus far identified.N-terminalGeneSeq AccessionWO9920759Chemokines are a family of related small,Chemokine activities can be determined using assaysInhibit or stimulatemodifiedY05818secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,angiogenesis, inhibit thechemokine met-processes ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot,binding of HIVhSDF-1 alphaangiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarily diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, whichbind to ˜17 receptors thus far identified.N-terminalGeneSeq AccessionWO9920759Chemokines are a family of related small,Chemokine activities can be determined using assaysInhibit or stimulatemodifiedY05819secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,angiogenesis, inhibit thechemokine met-processes ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot,binding of HIV,hSDF-1 betaangiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © Humanaantiinflammatory;Members of this family are involved in aPress Inc., Totowa, NJimmunosuppressantsimilarily diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, whichbind to ˜17 receptors thus far identified.N-terminalGeneSeq AccessionWO9920759Chemokines are a family of related small,Chemokine activities can be determined using assaysInhibit or stimulatemodifiedY05820secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,angiogenesis, inhibit thechemokineprocesses ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot,binding of HIV,GroHEK/hSDF-angiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © Humanaantiinflammatory;1alphaMembers of this family are involved in aPress Inc., Totowa, NJimmunosuppressantsimilarily diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, whichbind to ˜17 receptors thus far identified.N-terminalGeneSeq AccessionWO9920759Chemokines are a family of related small,Chemokine activities can be determined using assaysInhibit or stimulatemodifiedY05821secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,angiogenesis, inhibit thechemokineprocesses ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot,binding of HIV,GroHEK/hSDF-angiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © Humanaantiinflammatory;1beta.Members of this family are involved in aPress Inc., Totowa, NJimmunosuppressantsimilarily diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, whichbind to ˜17 receptors thus far identified.ChemokineGeneSeqWO9912968Chemokines are a family of related small,Chemokine activities can be determined using assaysIncrease or enhance anEotaxinAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Bilogy,inflammatory response,Y14230processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:an immune responseagiogenesis, and leukocye trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©orhaematopoietic cell-Members of this family are involved in aHumana Press Inc., Totowa, NJassociated activity; treatsimilarly diverse range of pathologiesa vascular indication;including inflammation, allergy, tissueCancer; enhance woundrejection, viralk infection, and tumor biology.healing, to prevent orThe chemokines exert their effects by actingtreat asthma, organon a family of seven transmembrane G-transplant rejction,protein-coupled receptors. Over 40 humanrheumatoid arthritis orchemokines have been described, which bindallergyto ˜17 receptors thus far identified.ChemokineGeneSeqWO9912968Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders,hMCP1aAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Bilogy,Vascular disorders,Y14225processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Wound healing, cancer,agiogenesis, and leukocye trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©prevent organ transplantMembers of this family are involved in aHumana Press Inc., Totowa, NJrejection, Increase orsimilarly diverse range of pathologiesenhance anincluding inflammation, allergy, tissueinflammatory response,rejection, viralk infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.ChemokineGeneSeqWO9912968Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders,hMCP1bAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Bilogy,Vascular disorders,Y14226processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Wound healing, cancer,agiogenesis, and leukocye trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©prevent organ transplantMembers of this family are involved in aHumana Press Inc., Totowa, NJrejection, Increase orsimilarly diverse range of pathologiesenhance anincluding inflammation, allergy, tissueinflammatory response,rejection, viralk infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.ChemokineGeneSeqWO9912968Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders,hSDF1bAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Bilogy,Vascular disorders,Y14228processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Wound healing, cancer,agiogenesis, and leukocye trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©prevent organ transplantMembers of this family are involved in aHumana Press Inc., Totowa, NJrejection, Increase orsimilarly diverse range of pathologiesenhance anincluding inflammation, allergy, tissueinflammatory response,rejection, viralk infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.ChemokineGeneSeqWO9912968Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders,hIL-8Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Bilogy,Vascular disorders,Y14229processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Wound healing, cancer,agiogenesis, and leukocye trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©prevent organ transplantMembers of this family are involved in aHumana Press Inc., Totowa, NJ; and Holmes et alrejection, Increase orsimilarly diverse range of pathologies(1991) Science 253, 1278-80.enhance anincluding inflammation, allergy, tissueinflammatory response,rejection, viralk infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.ChemokineGeneSeqWO9912968Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders,hMCP1Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Bilogy,Vascular disorders,Y14222processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot,Wound healing, cancer,agiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. ©prevent organ transplantMembers of this family are involved in aHumana Press Inc., Totowa, NJrejection, Increase orsimilarly diverse range of pathologiesenhance anincluding inflammation, allergy, tissueinflammatory response,rejection, viralk infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.ChemokineGeneSeqWO9912968Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders,hMCP2Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Bilogy,Vascular disorders,Y14223processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot,Wound healing, cancer,agiogenesis, and leukocye trafficking.T. N. C. Wells, and C. A. Power. ©prevent organ transplantMembers of this family are involved in aHumana Press Inc., Totowa, NJrejection, Increase orsimilarly diverse range of pathologiesenhance anincluding inflammation, allergy, tissueinflammatory response,rejection, viralk infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.ChemokineGeneSeqWO9912968Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders,hMCP3Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Bilogy,Vascular disorders,Y14224processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot,Wound healing, cancer,agiogenesis, and leukocye trafficking.T. N. C. Wells, and C. A. Power. ©prevent organ transplantMembers of this family are involved in aHumana Press Inc., Totowa, NJrejection, Increase orsimilarly diverse range of pathologiesenhance anincluding inflammation, allergy, tissueinflammatory response,rejection, viralk infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.C-C chemokine,GeneSeqEP905240Chemokines are a family of related small,Chemokine activities can be determined using assaysInflammatory, ImmuneMCP2Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Bilogy,and infectious diseases;Y05300processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:pulmonary diseases andagiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©skin disorders; tumours,Members of this family are involved in aHumana Press Inc., Totowa, NJand angiogenesis-andsimilarly diverse range of pathologieshaematopoiesis-relatedincluding inflammation, allergy, tissuediseasesrejection, viralk infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Wild typeGeneSeqEP906954Chemokines are a family of related small,Chemokine activities can be determined using assaysInflammatory, ImmunemonocyteAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Bilogy,and infectious diseases;chemotacticY07233processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:pulmonary diseases andprotein 2agiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©skin disorders; tumours,Members of this family are involved in aHumana Press Inc., Totowa, NJand angiogenesis-andsimilarly diverse range of pathologieshaematopoiesis-relatedincluding inflammation, allergy, tissuediseasesrejection, viralk infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.TruncatedGeneSeqEP906954Chemokines are a family of related small,Chemokines activities can be determined using assaysInflammatory, immunemonocyteAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,and infectious diseases;chemotacticY07234processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:pulmonary diseases andprotein 2 (6-76)angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power,skin disorders; tumours,Members of this family are involved in aHumana Press Inc., Totowa, NJand angiogenesis-andsimilarly diverse range of pathologies includinghaematopoiesis-relatedinflammation, allergy, tissue rejection, viraldiseasesinfection, and tumor biology. The chemokinesexert their effects by acting on a family of seventransmembrane G-protein-coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.TruncatedGeneSeqEP905241;Chemokines area family of related small,Chemokines activities can be determined using assaysInflammatory, immuneRANTESAccessionsEP906954secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,and infectious diseases;protein (3-68)Y07236 andprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:pulmonry diseases andY07232angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power,skin disorders; tumours,Members of this family are involved in aHumana Press Inc., Totowa, NJand angiogenesis-andsimilarly diverse range of pathologies includinghaematopoiesis-relatedinflammation, allergy, tissue rejection, viraldiseasesinfection, and tumor biology. The chemokinesexert their effects by acting on a fmaily of seventransmembrane G-protein-coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.Wild typeGeneSeqEP905241Chemokines area family of related small,Chemokines activities can be determined using assaysInflammatory, immunemonocyteAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,and infectious diseases;chemotacticY07237processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:pulmonry diseases andprotein 2angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power,skin disorders; tumours,Members of this family are involved in aHumana Press Inc., Totowa, NJand angiogenesis-andsimilarly diverse range of pathologies includinghaematopoiesis-relatedinflammation, allergy, tissue rejection, viraldiseasesinfection, and tumor biology. The chemokinesexert their effects by acting on a fmaily of seventransmembrane G-protein-coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.TruncatedGeneSeqEP905241Chemokines area family of related small,Chemokines activities can be determined using assaysInflammatory, immunemonocyteAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,and infectious diseases;chemotacticY07238processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:pulmonry diseases andprotein 2 (6-76)angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power,skin disorders; tumours,Members of this family are involved in aHumana Press Inc., Totowa, NJand angiogenesis-andsimilarly diverse range of pathologies includinghaematopoiesis-relatedinflammation, allergy, tissue rejection, viraldiseasesinfection, and tumor biology. The chemokinesexert their effects by acting on a fmaily of seventransmembrane G-protein-coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.A partialGeneSeqEP897980Chemokines area family of related small,Chemokines activities can be determined using assaysSoluble CXCR4BCXCR4BAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,receptor polypeptidesproteinW97363processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:may be useful forangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power,inhibiting chemokineMembers of this family are involved in aHumana Press Inc., Totowa, NJactivities and viralsimilarly diverse range of pathologies includinginfection.inflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a fmaily of seventransmembrane G-protein-coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.InterferonGeneSeqUS5871723Chemokines area family of related small,Chemokines activities can be determined using assaysAngiogenesis, Cancer,gamma-Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Inflammatory andinducibleW96709processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Immune disorders,protein (IP-10)angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power,Cardio-VascularMembers of this family are involved in aHumana Press Inc., Totowa, NJdiscorders, Musco-similarly diverse range of pathologies includingskeletal disordersinflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a fmaily of seventransmembrane G-protein-coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.A monokineGeneSeqUS5871723Chemokines area family of related small,Chemokines activities can be determined using assaysAngiogenesis, Cancer,induced byAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Inflammatory andgamma-W96710processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Immune disorders,interferonangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power,Cardio-Vascular(MIG)Members of this family are involved in aHumana Press Inc., Totowa, NJdiscorders, Musco-similarly diverse range of pathologies includingskeletal disordersinflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a fmaily of seventransmembrane G-protein-coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.Interleukin-8GeneSeqUS5871723Chemokines area family of related small,Chemokines activities can be determined using assaysAngiogenesis, Cancer,(IL-8) protein.Accessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Inflammatory andW96711processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Immune disorders,angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power,Cardio-VascularMembers of this family are involved in aHumana Press Inc., Totowa, NJ; and Holmes et aldiscorders, Musco-similarly diverse range of pathologies including(1991) Science 253, 1278-80.skeletal disordersinflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a fmaily of seventransmembrane G-protein-coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.EpithelialGeneSeqUS5871723Chemokines area family of related small,Chemokines activities can be determined using assaysAngiogenesis, Cancer,neutrophilAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Inflammatory andactivatingW96712processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Immune disorders,protein-78angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power,Cardio-Vascular(ENA-78)Members of this family are involved in aHumana Press Inc., Totowa, NJdiscorders, Musco-similarly diverse range of pathologies includingskeletal disordersinflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a fmaily of seventransmembrane G-protein-coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.Growth relatedGeneSeqUS5871723Chemokines area family of related small,Chemokines activities can be determined using assaysAngiogenesis, Cancer,oncogene-alphaAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Inflammatory and(GRO-alpha).W96713processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Immune disorders,angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power,Cardio-VascularMembers of this family are involved in aHumana Press Inc., Totowa, NJdiscorders, Musco-similarly diverse range of pathologies includingskeletal disordersinflammation, allergy, tissue rejection, viralinfection, and tumor biology. The chemokinesexert their effects by acting on a fmaily of seventransmembrane G-protein-coupled receptors.Over 40 human chemokines have beendescribed, which bind to ˜17 receptors thus faridentified.Growth relatedGeneSeqUS5871723Chemokines are a family of related small,Chemokine activities can be determined using assaysAngiogenesis, Cancer,oncogene-betaAccessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Inflammatory and(GRO-beta).W96714processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Immune disorders,angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power, ©Cardio-VascularMembers of this family are involved in aHumana Press Inc., Totowa, NJdisorders, Musco-similarly diverse range of pathologiesskeletal disordersincluding inflammation, allergy, tissuerejection, viral infection and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identifiedGrowth relatedGeneSeq AccessionUS5871723Chemokines are a family of related small,Chemokine activities can be determined using assaysAngiogenesis, Cancer,oncogene-gammaW96715secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Inflammatory and(GRO-gamma)processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Immune disorders,angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power, ©Cardio-VascularMembers of this family are involved in aHumana Press Inc., Totowa, NJdisorders, Musco-similarly diverse range of pathologiesskeletal disordersincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.A platelet basicGeneSeq AccessionUS5871723Chemokines are a family of related small,Chemokine activities can be determined using assaysAngiogenesis, Cancer,protein (PBP)W96716secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Inflammatory andprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Immune disorders,angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power, ©Cardio-VascularMembers of this family are involved in aHumana Press Inc., Totowa, NJdisorders, Musco-similarly diverse range of pathologiesskeletal disordersincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Connective tissueGeneSeqAccessionUS5871723Chemokines are a family of related small,Chemokine activities can be determined using assaysAngiogenesis, Cancer,activating protein-S96717secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Inflammatory andIII (CTAP-III)processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Immune disorders,angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power, ©Cardio-VascularMembers of this family are involved in aHumana Press Inc., Totowa, NJdisorders, Musco-similarly diverse range of pathologiesskeletal disordersincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Beta-GeneSeq AccessionUS5871723Chemokines are a family of related small,Chemokine activities can be determined using assaysAngiogenesis, Cancer,thromboglobulinW96718secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Inflammatory andprotein (beta-TG)processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Immune disorders,angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power, ©Cardio-VascularMembers of this family are involved in aHumana Press Inc., Totowa, NJdisorders, Musco-similarly diverse range of pathologiesskeletal disordersincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.NeutrophilGeneSeq AccessionUS5871723Chemokines are a family of related small,Chemokine activities can be determined using assaysAngiogenesis, Cancer,activating peptide-W96719secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Inflammatory and2 (NAP-2)processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Immune disorders,angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power, ©Cardio-VascularMembers of this family are involved in aHumana Press Inc., Totowa, NJdisorders, Musco-similarly diverse range of pathologiesskeletal disordersincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.GranulocyteGeneSeq AccessionUS5871723Chemokines are a family of related small,Chemokine activities can be determined using assaysAngiogenesis, Cancer,chemotacticW96720secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Inflammatory andprotein-2 (GCP-2)processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Immune disorders,angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power, ©Cardio-VascularMembers of this family are involved in aHumana Press Inc., Totowa, NJdisorders, Musco-similarly diverse range of pathologiesskeletal disordersincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeq AccessionEP887409Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders, viral,MIG-beta proteinW90124secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,parasitic, fungal orprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:bacterial infections,angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power, ©Cancer; autoimmuneMembers of this family are involved in aHumana Press Inc., Totowa, NJdiseases or transplantsimilarly diverse range of pathologiesrejectionincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.HumanGeneSeq AccessionWO9854326Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders,ZCHEMO-8W82716secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,cancer, myelopoieticprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:disorders, autoimmuneangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power, ©disorders andMembers of this family are involved in aHumana Press Inc., Totowa, NJimmunodeficiencies,similarly diverse range of pathologiesInflammatory andincluding inflammation, allergy, tissueinfectious diseases,rejection, viral infection, and tumor biology.Vascular disorders,The chemokines exert their effects by actingwound healingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human Act-2GeneSeq AccessionWO9854326Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders,proteinW82717secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,cancer, myelopoieticprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:disorders, autoimmuneangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power, ©disorders andMembers of this family are involved in aHumana Press Inc., Totowa, NJimmunodeficiencies,similarly diverse range of pathologiesInflammatory andincluding inflammation, allergy, tissueinfectious diseases,rejection, viral infection, and tumor biology.Vascular disorders,The chemokines exert their effects by actingwound healingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human SISDGeneSeqWO9854326Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune disorders,proteinAcessionsecreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,cancer, myelopoieticW82720processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols, Edited by:disorders, autoimmuneangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©disorders andMembers of this family are involved in aHumana Press Inc., Totowa, NJimmunodeficiencies,similarly diverse range of pathologiesInflammatory andincluding inflammation, allergy, tissueinfectious diseases,rejection, viral infection, and tumor biology.Vascular disorders,The chemokines exert their effects by actingwound healingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human M110GeneSeqWO9854326Chemokines area family of related small,Chemokine activities can be determined using assaysImmune disorders,proteinAccessionsecreted proteins involved in biologicalknown in the art: Mehtods of Molecular Biology,cancer, myelopoieticW82721processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:disorders, autoimmuneangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power ©disorders andMembers of this family are involved in aHumana Press Inc., Totowa, NJimmunodeficiencies,similarly diverse range of pathologiesInflammatory andincluding inflammation, allergy, tissueinfectious diseases,rejection, viral infection, and tumor biology.Vascular disorders,The chemokines exert their effects by actingwound healingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human M11AGeneSeqW09854326Chemokines area family of related small,Chemokine activities can be determined using assaysImmune disorders,proteinAccessionsecreted proteins involved in biologicalknown in the art: Mehtods of Molecular Biology,cancer, myelopoieticW82722processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:disorders, autoimmuneangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power ©disorders andMembers of this family are involved in aHumana Press Inc., Totowa, NJimmunodeficiencies,similarly diverse range of pathologiesInflammatory andincluding inflammation, allergy, tissueinfectious diseases,rejection, viral infection, and tumor biology.Vascular disorders,The chemokines exert their effects by actingwound healingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human CCC3GeneSeqWO9854326Chemokines area family of related small,Chemokine activities can be determined using assaysImmune disorders,proteinAccessionsecreted proteins involved in biologicalknown in the art: Mehtods of Molecular Biology,cancer, myelopoieticW82723processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:disorders, autoimmuneangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power ©disorders andMembers of this family are involved in aHumana Press Inc., Totowa, NJimmunodeficiencies,similarly diverse range of pathologiesInflammatory andincluding inflammation, allergy, tissueinfectious diseases,rejection, viral infection, and tumor biology.Vascular disorders,The chemokines exert their effects by actingwound healingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.A human L105GeneSeqWO9856818Chemokines area family of related small,Chemokine activities can be determined using assaysCancer, wound healingchemokineAccessionsecreted proteins involved in biologicalknown in the art: Mehtods of Molecular Biology,designatedW87588processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:huL105_3.angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bind10 ˜17 receptors thus far identified.A human L105GeneSeqWO9856818Chemokines area family of related small,Chemokine activities can be determined using assaysCancer, wound healingchemokineAccessionsecreted proteins involved in biologicalknown in the art: Mehtods of Molecular Biology,designatedW87589processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:huL105_7.angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human matureGeneSeqWO9848828Chemokines area family of related small,Chemokine activities can be determined using assaysInfectious diseases,gro-alphaAccessionsecreted proteins involved in biologicalknown in the art: Mehtods of Molecular Biology,sepsispolypeptideW81498processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:used to treatangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power ©sepsisMembers of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human matureGeneSeqWO9848828Chemokines area family of related small,Chemokine activities can be determined using assaysInfectious diseases,gro-gammaAccessionsecreted proteins involved in biologicalknown in the art: Mehtods of Molecular Biology,sepsispolypeptideW81500processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:used to treatangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power ©sepsisMembers of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human thymusGeneSeqWO0053635Chemokines area family of related small,Chemokine activities can be determined using assaysInflammatory disorders,expressedAccessionssecreted proteins involved in biologicalknown in the art: Mehtods of Molecular Biology,cancer, Immune andchemokineB19607 andprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:vascular disordersTECK andB19608angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power ©TECK variantMembers of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.HumanGeneSeqWO0042071Chemokines area family of related small,Chemokine activities can be determined using assaysAutoimmune disorders,chemokineAccession B15791secreted proteins involved in biologicalknown in the art: Mehtods of Molecular Biology,Immune, Vascular andSDF1alphaprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Inflammatory disordersangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeqWO0042071Chemokines are a family of related small,Chemokine activities can be determined using assasysAutoimmune disorders,GROalphaAccession B15793secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Immune, Vascular andprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Inflammatory diordersangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot; T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeqWO0042071Chemokines are a family of related small,Chemokine activities can be determined using assasysAutoimmune disorders,eotaxinAccession B15794secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,Immune, Vascular andprocesses ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot;Inflammatory disordersangiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeq AccessionWO0042071Chemokines are a family of related small,Chemokine activities can be determined using assasysAutoimmune disorders,MIGB15803secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,Immune, Vascular andprocesses ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot;inflammatory disordersangiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeq AccessionWO0042071Chemokines are a family of related small,Chemokine activities can be determined using assasysAutoimmune disorders,PF4B15804secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,Immune, Vascular andprocesses ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot;inflammatory disordersangiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeq AccessionWO0042071Chemokines are a family of related small,Chemokine activities can be determined using assasysAutoimmune disorders,I-309B15805secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,Immune, Vascular andprocesses ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot;Inflammatory disordersangiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeq AccessionWO0042071Chemokines are a family of related small,Chemokine activities call be determined using assasysAutoimmune disorders,HCC-1B15806secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,Immune, Vascular andprocesses ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot;Inflammatory disordersangiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeq AccessionWO0042071Chemokines are a family of related small,Chemokine activities can be determined using assasysAutoimmune disorders,C10B15807secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,Immune, Vascular andprocesses ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot;Inflammatory disordersangiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeq AccessionWO0042071Chemokines are a family of related small,Chemokine activities can be determined using assasysAutoimmune disorders,CCR-2B15808secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,Immune, Vascular andprocesses ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot;Inflammatory disordersangiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeq AccessionWO0042071Chemokines are a family of related small,Chemokine activities can be determined using assasysAutoimmune disorders,ENA-78B15809secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,Immune, Vascular andprocesses ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot;Inflammatory disordersangiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeq AccessionWO0042071Chemokines are a family of related small,Chemokine activities can be determined using assasysAutoimmune disorders,GRObetaB15810secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology, 2000,Immune, Vascular andprocesses ranging from hematopoiesis,vol. 138: Chemokine Protocols. Edited by: A. E. I. Proudfoot;Inflammatory disordersangiogenesis, and leukocyte trafficking.T. N. C. Wells, and C. A. Power. © HumanaMembers of this family are involved in aPress Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeqWO0042071Chemokines are a family of related small,Chemokine activities can be determined using assaysAutoimmune disorders,IP-10Accession B15811secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Immune, Vascular andprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Inflammatory disordersangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeq AccessionWO0042071Chemokines are a family of related small,Chemokine activities can be determined using assaysAutoimmune disorders,SDF1betaB15812secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Immune, Vascular andprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Inflammatory disordersangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeq AccessionWO0042071Chemokines are a family of related small,Chemokine activities can be determined using assaysAutoimmune disorders,GRO alphaB15813secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Immune, Vascular andprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Inflammatory disordersangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeq AccessionWO0042071Chemokines are a family of related small,Chemokine activities can be determined using assaysAutoimmune disorders,MIP1betaB15831secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Immune, Vascular andprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Inflammatory disordersangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.A human C-CGeneSeq AccessionUS6096300Chemokines are a family of related small,Chemokine activities can be determined using assaysCancerchemokineB07939secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,designated exodusprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeq AccessionUS6084071Chemokines are a family of related small,Chemokine activities can be determined using assaysChemotaxis, GeneL105_7Y96922secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Therapy, Wound healingprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeq AccessionUS6084071Chemokines are a family of related small,Chemokine activities can be determined using assaysChemotaxis, GeneL105_3Y96923secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Therapy, Wound healingprocesses ranging from hematopoiesis,2000. vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human secondaryGeneSeq AccessionWO0038706Chemokines are a family of related small,Chemokine activities can be determined using assaysCancer, Vascular andlymphoidB01434secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Immune disorderschemokine (SLC)processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human non-ELRGeneSeq AccessionWO0029439Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune andCXC chemokineY96310secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Inflammatory disorders,H174processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Cancer, Haemostaticangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©and thrombolyticMembers of this family are involved in aHumana Press Inc., Totowa, NJactivitysimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human non-ELRGeneSeq AccessionWO0029439Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune andCXC chemokineY96311secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Inflammatory disorders,IP10processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Cancer, haemostatic andangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©thrombolytic activityMembers of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human non-ELRGeneSeqWO0029439Chemokines are a family of related small,Chemokine activities can be determined using assaysImmune andCXC chemokineAccession Y96313secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Inflammatory disorders,Migprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:Cancer, haemostatic andangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©thrombolytic activityMembers of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeqWO0028035Chemokines are a family of related small,Chemokine activities can be determined using assaysCancer, wound healing,Ckbeta-7Accession Y96280secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,inflammatory andprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:immunoregulatoryangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©disordersMembers of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeqWO0028035Chemokines are a family of related small,Chemokine activities can be determined using assaysCancer, wound healing,MIP-1alphaAccession Y96281secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,inflammatory andprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:immunoregulatoryangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©disordersMembers of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human matureGenSeq AccessionWO0028035Chemokines are a family of related small,Chemokine activities can be determined using assaysCancer, wound healing,chemokineY96282secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,inflammatory andCkbeta-7processes ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:immunoregulatory(optionallyangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©disorderstruncated)Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human chemokineGeneSeqWO0018431Chemokines are a family of related small,Chemokine activities can be determined using assaysSoluble CXCR3receptor CXCR3Accession Y79372secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,polypeptides may beprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:useful for inhibitingangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©chemokine activities andMembers of this family are involved in aHumana Press Inc., Totowa, NJviral infection.similarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.HumanGeneSeqUS6043086Chemokines are a family of related small,Chemokine activities can be determined using assaysNeurological disorders,neurotactinAccession Y53259secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,Immune and respiratorychemokine likeprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:disordersdomainangiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identified.Human CC typeGeneSeqJP11302298Chemokines are a family of related small,Chemokine activities can be determined using assaysCancer and infectiouschemokineAccession Y57771secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,diseasesinterleukin Cprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Members of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identifiedHuman CKbeta-9GeneSeqUS6153441Chemokines are a family of related small,Chemokine activities can be determined using assaysCancer, Auto-immuneAccession B50860secreted proteins involved in biologicalknown in the art: Methods in Molecular Biology,and inflammatoryprocesses ranging from hematopoiesis,2000, vol. 138: Chemokine Protocols. Edited by:disorders,angiogenesis, and leukocyte trafficking.A. E. I. Proudfoot, T. N. C. Wells, and C. A. Power. ©Cardiovascular disordersMembers of this family are involved in aHumana Press Inc., Totowa, NJsimilarly diverse range of pathologiesincluding inflammation, allergy, tissuerejection, viral infection, and tumor biology.The chemokines exert their effects by actingon a family of seven transmembrane G-protein-coupled receptors. Over 40 humanchemokines have been described, which bindto ˜17 receptors thus far identifiedPreproapolipoproteinGeneSeqWO9637608Apoa-1 participates in the reverse transport ofLipid binding activity can be determined using assaysUseful for“paris” variantAccessioncholesterol from tissues to the liver forknown in the art, such as, for example, thecardiovascular disorders,W08602excretion by promoting cholesterol efflux fromCholesterol Efflux Assays of Takahaski et al.,cholesterol disorders,tissues and by acting as a cofactor for theP.N.A.S., Vol. 96, Issue 20, 11358-11363, Sep.and Hyperlipidaemialecithin cholesterol acyltransferase (lcat).28, 1999.Preproapolipoprotein5,721,114Apoa-1 participates in the reverse transport ofLipid binding activity can be determined using assaysUseful for“milano”cholesterol from tissues to the liver forknown in the art, such as, for example, thecardiovascular disorders,variantexcretion by promoting cholesterol efflux fromCholesterol Efflux Assays of Takahaski et al.,cholesterol disorders,tissues and by acting as a cofactor for theP.N.A.S., Vol. 96, Issue 20, 11358-11363, Sep.and Hyperlipidaemialecithin cholesterol acyltransferase (lcat).28, 1999.Glycodelin-A;GeneSeqWO9628169Naturally produced female contraceptive thatGlycodelin-A activity can be determined using theNaturally derivedProgesterone-Accessionis removed rapidly from the body following 2-hemizona assay as described in Oehninger, S.,contraceptive useful forassociatedW002893 days production. Uses include contraceptionCoddington, C. C., Hodgen, G. D., and Seppala, Mthe prevention ofendometrial(1995) Fertil. Steril. 63, 377-383.pregnancy.proteinNOGO-AGenbankNOGO polypeptides are potent inhibitors ofInhibition of Neurite outgrowth. Antagonists toNOGO-A polypeptideAccessionneurite growth.NOGO polypeptides may promote the outgrowth ofantagonists are usefulCAB99248neurites, thus inducing regeneration of neurons.for the promotion ofneural growth, whichcould be useful in thetreatment of neuraldisorders anddysfunction due todegenerative diseases ortrauma; useful in thetreatment of neoplasticdiseases of the CNS;induce regeneration ofneurons or to promotethe structural plasticityof the CNS.NOGO-BGenbankNOGO polypeptides are potent inhibitors ofInhibition of Neurite outgrowth. Antagonists toNOGO-B polypeptideAccessionneurite growth.NOGO polypeptides may promote the outgrowth ofantagonists are usefulCAB99249neurites, thus inducing regeneration of neurons.for the promotion ofneural growth, whichcould be useful in thetreatment of neuraldisorders anddysfunction due todegenerative diseases ortrauma; useful in thetreatment of neoplasticdiseases of the CNS;induce regeneration ofneurons or to promotethe structural plasticityof the CNS.NOGO-CGenbankNOGO polypeptides are potent inhibitors ofInhibition of Neurite outgrowth. Antagonists toNOGO-C polypeptideAccessionneurite growth.NOGO polypeptides may promote the outgrowth ofantagonists are usefulCAB99250neurites, thus inducing regeneration of neurons.for the promotion ofneural growth, whichcould be useful in thetreatment of neuraldisorders anddysfunction due todegenerative diseases ortrauma; useful in thetreatment of neoplasticdiseases of the CNS;induce regeneration ofneurons or to promotethe structural plasticityof the CNS.NOGO-66GenbankNOGO polypeptides are potent inhibitors ofInhibition of Neurite outgrowth by mediating theNOGO-66 receptorReceptorAccessionneurite growth, and are thought to mediatebiological effects of NOGO polypeptides. Solublepolypeptides are usefulAAG53612their effects through the NOGO-66 Receptor.NOGO-66 receptor polypeptides may promote thefor the promotion ofoutgrowth of neurites, thus inducing regeneration ofneural growth, whichneurons.could be useful in thetreatment of neuraldisorders anddysfunction due todegenerative diseases ortrauma; useful in thetreatment of neoplasticdiseases of the CNS;induce regeneration ofneurons or to promotethe structural plasticityof the CNS.AntibodiesUS5416197These antibodies are useful for the promotionCollapsin activity, which is thought to inhibit theUseful for the promotionspecific forof neurite outgrowthoutgrowth of neurites, can be assayed in the presenceof neural growth, whichcollapsinof antibodies specific for collapsing using assayscould be useful in theknown in the art, such as, for example, the collapsetreatment of neuralassay disclosed by Luo et al., Cell 1993 Octdisorders and22; 75(2): 217-27dysfunction due todegenerative diseases ortrauma.Humanized Anti-WO9845331These agents have anti-inflammatory and anti-VEGF activity can be determined using assays knownPromotion of growthVEGF Antibodies,cancer applicationsin the art, such as those disclosed in Internationaland proliferation ofand fragmentsPublication No. WO0045835, for example.cells, such as vascularthereofendothelial cells.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancerHumanized Anti-WO0029584These agents have anti-inflammatory and anti-VEGF activity can be determined using assays knownPromotion of growthVEGF Antibodies,cancer applicationsin the art, such as those disclosed in Internationaland proliferation ofand fragmentsPublication No. WO0045835, for example.cells, such as vascularthereofendothelial cells.Antagonists may beuseful as anti-angiogenicagents, and may beapplicable for cancerMembrane boundGeneSeq.WO9963088Cancer, Immune DisordersThese proteins can be used for linking bioactiveActivities can beproteinsAccessionmolecules to cells and for modulating biologicaldetermined using assayY66631-Y66765activities of cells, using the polypeptides for specificknown in the art, suchas,targeting. The polypeptide targeting can be used tofor example, the assayskill the target cells, e.g. for the treatment of cancers.disclosed inThese proteins are useful for the treatment of immuneInternational Publicationsystem disorders.No. WO0121658.Secreted andGenSeq AccessionWO0053756Cancer, Immune DisordersThese proteins can be used for linking bioactiveActivities can beTransmembraneB44241-B44334molecules to cells and for modulating biologicaldetermined using assaypolypeptidesactivities of cells, using the polypeptides for specificknown in the art, suchas,targeting. The polypeptide targeting can be used tofor example, the assayskill the target cells, e.g. for the treatment of cancers.disclosed inThese proteins are useful for the treatment of immuneInternational Publicationsystem disorders.No. WO0121658Secreted andGeneSeqWO9946281Cancer, Immune DisordersThese proteins can be used for linking bioactiveActivities can beTransmembraneAccessionmolecules to cells and for modulating biologicaldetermined using assaypolypeptidesY41685-Y41774activities of cells, using the polypeptides for specificknown in the art, suchas,targeting. The polypeptide targeting can be used tofor example, the assayskill the target cells, e.g. for the treatment of cancers.disclosed inThese proteins are useful for the treatment of immuneInternational Publicationsystem disorders.No. WO0121658

Delivery of a Drug or Therapeutic Protein to the Inside of a Cell and/or Across the Blood Brain Barrier (BBB)

Within the scope of the invention, the modified transferrin fusion proteins comprising at least one function C domain may be used as a carrier to deliver a molecule or small molecule therapeutic complexed to the ferric ion of transferrin to the inside of a cell or across the blood brain barrier. In these embodiments, the Tf fusion protein will typically be engineered or modified to inhibit, prevent or remove glycosylation to extend the serum half-life of the fusion protein and/or therapeutic protein portion. The addition of a targeting peptide or, for example, a single chain antibody is specifically contemplated to further target the Tf fusion protein to a particular cell type, e.g., a cancer cell.

In one embodiment, the iron-containing, anti-anemic drug, ferric-sorbitol-citrate complex is loaded onto a modified Tf fusion protein of the invention. Ferric-sorbitol-citrate (SC) has been shown to inhibit proliferation of various murine cancer cells in vitro and cause tumor regression in vivo, while not having any effect on proliferation of non-malignant cells (Poljak-Blazi et al. (June 2000) Cancer Biotherapy and Radiopharmaceuticals (United States), 15/3:285-293).

In another embodiment, the antineoplastic drug Adriamycin® (doxorubicin) and/or the chemotherapeutic drug bleomycin, both of which are known to form complexes with ferric ion, is loaded onto a trans-body of the invention. In other embodiments, a salt of a drug, for instance, a citrate or carbonate salt, may be prepared and complexed with the ferric iron that is then bound to Tf. As tumor cells often display a higher turnover rate for iron; transferrin modified to carry at least one anti-tumor agent may provide a means of increasing agent exposure or load to the tumor cells. (Demant, E. J., (1983) Eur. J. Biochem. 137:113-118; Padbury et al. (1985) J. Biol. Chem. 260:7820-7823).

Pharmaceutical Formulations and Treatment Methods

The modified fusion proteins of the invention may be administered to a patient in need thereof using standard administration protocols. For instance, the modified Tf fusion proteins of the present invention can be provided alone, or in combination, or in sequential combination with other agents that modulate a particular pathological process. As used herein, two agents are said to be administered in combination when the two agents are administered simultaneously or are administered independently in a fashion such that the agents will act at the same or near the same time.

The agents of the present invention can be administered via parenteral, subcutaneous, intravenous, intramuscular, intraperitoneal, transdermal and buccal routes. For example, an agent may be administered locally to a site of injury via microinfusion. Alternatively, or concurrently, administration may be noninvasive by either the oral, inhalation, nasal, or pulmonary route. The dosage administered will be dependent upon the age, health, and weight of the recipient, kind of concurrent treatment, if any, frequency of treatment, and the nature of the effect desired.

The present invention further provides compositions containing one or more transbodies of the invention. While individual needs vary, determination of optimal ranges of effective amounts of each component is within the skill of the art. Typical dosages comprise about 1 pg/kg to about 100 mg/kg body weight. The preferred dosages for systemic administration comprise about 100 ng/kg to about 100 mg/kg body weight. The preferred dosages for direct administration to a target site via microinfusion comprise about 1 ng/kg to about 1 mg/kg body weight. When administered via direct injection or microinfusion, modified fusion proteins of the invention may be engineered to exhibit reduced or no binding of iron to prevent, in part, localized iron toxicity.

In addition to the pharmacologically active fusion protein, the compositions of the present invention may contain suitable pharmaceutically acceptable carriers comprising excipients and auxiliaries that facilitate processing of the active compounds into preparations which can be used pharmaceutically for delivery to the site of action. Suitable formulations for parenteral administration include aqueous solutions of the active compounds in water-soluble form, for example, water-soluble salts. In addition, suspensions of the active compounds as appropriate oily injection suspensions may be administered. Suitable lipophilic solvents or vehicles include fatty oils, for example, sesame oil, or synthetic fatty acid esters, for example, ethyl oleate or triglycerides. Aqueous injection suspensions may contain substances which increase the viscosity of the suspension and include, for example, sodium carboxymethyl cellulose, sorbitol and dextran. Optionally, the suspension may also contain stabilizers. Liposomes can also be used to encapsulate the agent for delivery into the cell.

The pharmaceutical formulation for systemic administration according to the invention may be formulated for enteral, parenteral or topical administration. Indeed, all three types of formulations may be used simultaneously to achieve systemic administration of the active ingredient. Suitable formulations for oral administration include hard or soft gelatin capsules, pills, tablets, including coated tablets, elixirs, suspensions, syrups or inhalations and controlled release forms thereof.

In practicing the methods of this invention, the agents of this invention may be used alone or in combination, or in combination with other therapeutic or diagnostic agents. In certain preferred embodiments, the compounds of this invention may be co-administered along with other compounds typically prescribed for these conditions according to generally accepted medical practice. The compounds of this invention can be utilized in vivo, ordinarily in mammals, such as humans, sheep, horses, cattle, pigs, dogs, cats, rats and mice, ex vivo or in vitro.

Modified fusion proteins of the present invention may be used in the diagnosis, prognosis, prevention and/or treatment of diseases and/or disorders relating to diseases and disorders of the endocrine system, the nervous system, the immune system, respiratory system, cardiovascular system, reproductive system, digestive system, diseases and/or disorders relating to cell proliferation, and/or diseases or disorders relating to the blood.

In yet other embodiments of the invention, modified Tf fusion proteins may be used in the diagnosis, prognosis, prevention and/or treatment of diseases and/or disorders relating to diseases and disorders known to be associated with or treatable by therapeutic protein moieties as known in the art and exemplified by PCT Patent Publication Nos. WO 01/79258, WO 01/77137, WO 01/79442, WO 01/79443, WO 01/79444 and WO 01/79480, all of which are herein incorporated by reference in their entirety. Accordingly, the present invention encompasses a method of treating a disease or disorder listed in the “Preferred Indication Y” column of Table 1 comprising administering to a patient in which such treatment, prevention or amelioration is desired a modified transferrin fusion protein of the invention that comprises a therapeutic protein portion corresponding to a therapeutic protein disclosed in the “Therapeutic Protein X” column of Table 1 in an amount effective to treat, prevent or ameliorate the disease or disorder.

In certain embodiments, a transferrin fusion protein of the present invention may be used to diagnose and/or prognose diseases and/or disorders.

Modified transferrin fusion proteins of the invention and polynucleotides encoding transferrin fusion proteins of the invention may be useful in treating, preventing, diagnosing and/or prognosing diseases, disorders, and/or conditions of the immune system. Moreover, fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention can be used as a marker or detector of a particular immune system disease or disorder.

In a preferred embodiment, fusion proteins of the invention and/or polynucleotides encoding modified transferrin fusion proteins of the invention could be used as an agent to boost immunoresponsiveness among imnmunodeficient individuals. In specific embodiments, fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention could be used as an agent to boost immunoresponsiveness among B cell and/or T cell immunodeficient individuals.

The modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be useful in treating, preventing, diagnosing, and/or prognosing autoimmune disorders. Many autoimmune disorders result from inappropriate recognition of self as foreign material by immune cells. This inappropriate recognition results in an immune response leading to the destruction of the host tissue. Therefore, the administration of fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention, that can inhibit an immune response, particularly the proliferation, differentiation, or chemotaxis of T-cells, may be an effective therapy in preventing autoimmune disorders.

Modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be useful in treating, preventing, prognosing, and/or diagnosing diseases, disorders, and/or conditions of hematopoietic cells. Transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention could be used to increase differentiation and proliferation of hematopoietic cells, including the pluripotent stem cells, in an effort to treat or prevent those diseases, disorders, and/or conditions associated with a decrease in certain (or many) types hematopoietic cells, including but not limited to, leukopenia, neutropenia, anemia, and thrombocytopenia.

Alternatively, modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention could be used to increase differentiation and proliferation of hematopoietic cells, including the pluripotent stem cells, in an effort to treat or prevent those diseases, disorders, and/or conditions associated with an increase in certain (or many) types of hematopoietic cells, including but not limited to, histiocytosis.

Allergic reactions and conditions, such as asthma (particularly allergic asthma) or other respiratory problems, may also be treated, prevented, diagnosed and/or prognosing and using modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention. Moreover, these molecules can be used to treat, prevent, prognose, and/or diagnose anaphylaxis, hypersensitivity to an antigenic molecule, or blood group incompatibility.

Additionally, modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention, may be used to treat, prevent, diagnose and/or prognose IgE-mediated allergic reactions. Such allergic reactions include, but are not limited to, asthma, rhinitis, and eczema. In specific embodiments, fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be used to modulate IgE concentrations in vitro or in vivo.

Moreover, modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention have uses in the diagnosis, prognosis, prevention, and/or treatment of inflammatory conditions. For example, since fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may inhibit the activation, proliferation, and/or differentiation of cells involved in an inflammatory response, these molecules can be used to prevent and/or treat chronic and acute inflammatory conditions. Such inflammatory conditions include, but are not limited to, for example, inflammation associated with infection (e.g., septic shock, sepsis, or systemic inflammatory response syndrome), ischemia-reperfusion injury, endotoxin lethality, complement-mediated hyperacute rejection, nephritis, cytokine or chemokine induced lung injury, inflammatory bowel disease, Crohn's disease, over production of cytokines (e.g., TNF or IL-1), respiratory disorders (e.g., asthma and allergy); gastrointestinal disorders (e.g., inflammatory bowel disease); cancers (e.g., gastric, ovarian, lung, bladder, liver, and breast); CNS disorders (e.g., multiple sclerosis; ischemic brain injury and/or stroke, traumatic brain injury; neurodegenerative disorders (e.g., Parkinson's disease and Alzheizmer's disease); AIDS-related dementia; and prion disease); cardiovascular disorders (e.g., atherosclerosis, myocarditis, cardiovascular disease, and cardiopulmonary bypass complications); as well as many additional diseases, conditions, and disorders that are characterized by inflammation (e.g., hepatitis, rheumatoid arthritis, gout, trauma, pancreatitis, sarcoidosis, dermatitis, renal ischemia-reperfusion injury, Grave's disease, systemic lupus erythematosus, diabetes mellitus, and allogenic transplant rejection).

Because inflammation is a fundamental defense mechanism, inflammatory disorders can affect virtually any tissue of the body. Accordingly, modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention, have uses in the treatment of tissue-specific inflammatory disorders, including, but not limited to, adrenalitis, alveolitis, angiocholecystitis, appendicitis, balanitis, blepharitis, bronchitis, bursitis, carditis, cellulitis, cervicitis, cholecystitis, chorditis, colitis, conjunctivitis, cystitis, dermatitis, diverticulitis, encephalitis, endocarditis, esophagitis, eustachitis, fibrositis, folliculitis, gastritis, gastroenteritis, gingivitis, glossitis, hepatosplenitis, keratitis, labyrinthitis, laryngitis, lymphangitis, mastitis, media otitis, meningitis, metritis, mucitis, myocarditis, myosititis, myringitis, nephritis, neuritis, orchitis, osteochondritis, otitis, pericarditis, peritendonitis, peritonitis, pharyngitis, phlebitis, poliomyelitis, prostatititis, Pulpitis, retinitis, rhinitis, salpingitis, scleritis, sclerochoroiditis, scrotitis, sinusitis, spondylitis, steatitis, stomatitis, synovitis, syringitis, tendonitis, tonsillitis, urethritis, and vaginitis.

In specific embodiments, modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention, are useful to diagnose, prognose, prevent, and/or treat organ transplant rejections and graft-versus-host disease (GVHD). Organ rejection occurs by host immune cell destruction of the transplanted tissue through an immune response. Similarly, an immune response is also involved in GVHD, but, in this case, the foreign transplanted immune cells destroy the host tissues. Polypeptides, antibodies, or polynucleotides of the invention, and/or agonists or antagonists thereof, that inhibit an immune response, particularly the activation, proliferation, differentiation, or chemotaxis of T-cells, may be an effective therapy in preventing organ rejection or GVHD.

In another specific embodiment, modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention are used as an adjuvant to enhance anti-viral immune responses. Anti-viral immune responses that may be enhanced using the compositions of the invention as an adjuvant, include virus and virus associated diseases or symptoms described herein or otherwise known in the art. In specific embodiments, the compositions of the invention are used as an adjuvant to enhance an immune response to a virus, disease, or symptom selected from the group consisting of AIDS, meningitis, Dengue, EBV, and hepatitis (e.g., hepatitis B). In another specific embodiment, the compositions of the invention are used as an adjuvant to enhance an immune response to a virus, disease, or symptom selected from the group consisting of: HIV/AIDS, respiratory syncytial virus, Dengue, rotavirus, Japanese B encephalitis, influenza A and B, parainfluenza, measles, cytomegalovirus, rabies, Junin, Chikungunya, Rift Valley Fever, herpes simplex, and yellow fever.

In another specific embodiment, the compositions of the invention are used as an adjuvant to enhance an immune response to a bacterium or fungus, disease, or symptom selected from the group consisting of Vibrio cholerae, Mycobacterium leprae, Salmonellatyphi, Salmonella paratyphi, Neisseria meningitidis, Streptococcus pneumoniae, Group B Streptococcus, Shigella spp., Enterotoxigenic Escherichia coli, Enterohemorrhagic E. coli, Borrelia burgdorferi and Candida.

In another specific embodiment, modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may also be employed to treat infections diseases including silicosis, sarcoidosis, and idiopathic pulmonary fibrosis; for example, by preventing the recruitment and activation of mononuclear phagocytes.

In one embodiment, modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention are administered to an animal (e.g., mouse, rat, rabbit, hamster, guinea pig, pigs, micro-pig, chicken, camel, goat, horse, cow, sheep, dog, cat non-human primate, and human, most preferably human) to boost the immune system to produce increased quantities, of one or more antibodies (e.g., IgG, IgA, IgM, and IgE), to induce higher affinity antibody production and immunoglobulin class switching (e.g., IgG, IgA, IgM, and IgE), and/or to increase an immune response.

In another embodiment, modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention are used in one or more of the applications described herein, as they may apply to veterinary medicine.

In another specific embodiment, modified transferrin fusion proteins of the invention, and/or polynucleotides encoding transferrin fusion proteins of the invention are used as a means of blocking various aspects of immune responses to foreign agents or self. Examples of diseases or conditions in which blocking of certain aspects of immune responses may be desired include autoimmune disorders such as lupus, and arthritis, as well as immunoresponsiveness to skin allergies, inflammation, bowel disease, injury, and diseases/disorders associated with pathogens.

In another specific embodiment, modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention are used as a therapy for preventing the B cell proliferation and Ig secretion associated with autoimmune diseases such as idiopathic thrombocytopenic purpura, systemic lupus erythematosus and multiple sclerosis.

In another specific embodiment, modified transferrin fusion proteins or polynucleotides encoding transferrin fusion proteins of the invention are used as an inhibitor of B and/or T cell activation in endothelial cells. This activity disrupts tissue architecture or cognate responses and is useful, for example in disrupting immune responses, and blocking sepsis.

In another specific embodiment, modified transferrin fusion proteins of the invention, and/or polynucleotides encoding transferrin fusion proteins of the invention are used as a therapy for chronic hypergammaglobulinemia evident in such diseases as monoclonal gammopathy of undetermined significance (MGUS), Waldenstrom's disease, related idiopathic monoclonal gammopathies, and plasmacytomas.

Another specific embodiment, modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be employed for instance to inhibit polypeptide chemotaxis and activation of macrophages and their precursors, and of neutrophils, basophils, B lymphocytes and some T-cell subsets, e.g., activated and CD8 cytotoxic T cells and natural killer cells, in certain autoimmune and chronic inflammatory and infective diseases. Examples of autoimmune diseases are described herein and include multiple sclerosis, and insulin-dependent diabetes.

In another specific embodiment, modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion protein of the invention may also be employed for treating atherosclerosis, for example, by preventing monocyte infiltration in the artery wall.

In another specific embodiment, modified transferrin fusion proteins of the invention and/or-polynucleotides encoding transferrin fusion proteins of the invention may be employed to treat adult respiratory distress syndrome (ARDS).

In another specific embodiment, modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be useful for stimulating wound and tissue repair, stimulating angiogenesis, and/or stimulating the repair of vascular or lymphatic diseases or disorders. Additionally, fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be used to stimulate the regeneration of mucosal surfaces.

In a specific embodiment, modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention are used to diagnose, prognose, treat, and/or prevent a disorder characterized by primary or acquired immunodeficiency, deficient serum immunoglobulin production, recurrent infections, and/or immune system dysfunction. Moreover, modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be used to treat or prevent infections of the joints, bones, skin, and/or parotid glands, blood-borne infections (e.g., sepsis, meningitis, septic arthritis, and/or osteomyelitis), autoimmune diseases (e.g., those disclosed herein), inflammatory disorders, and malignancies, and/or any disease or disorder or condition associated with these infections, diseases, disorders and/or malignancies) including, but not limited to, Common Variable Immunodeficiency (CVID), other primary immune deficiencies, HIV disease, Chronic Lymphocytic Leukemia (CLL), recurrent bronchitis, sinusitis, otitis media, conjunctivitis, pneumonia, hepatitis, meningitis, herpes zoster (e.g., severe herpes zoster), and/or pneumocystis carnii. Other diseases and disorders that may be prevented, diagnosed, prognosed, and/or treated with fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention include, but are not limited to, HIV infection, HTLV-BLV infection, lymphopenia, phagocyte bactericidal dysfunction anemia, thrombocytopenia, and hemoglobinuria.

In a specific embodiment, modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be used to diagnose, prognose, prevent, and/or treat cancers or neoplasms including immune cell or immune tissue-related cancers or neoplasms. Examples of cancers or neoplasms that may be prevented, diagnosed, or treated by fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention include, but are not limited to, acute myelogenous leukemia, chronic myelogenous leukemia, Hodgkin's disease, non-Hodgkin's lymphoma, acute lymphocytic leukemia (ALL) chronic lymphocyte leukemia, plasmacytomas, multiple myeloma, Burkitt's lymphoma, EBV transformed diseases, and/or diseases and disorders described in the section entitled “Hyperproliferative Disorders” elsewhere herein.

In specific embodiments, the compositions of the invention are used as an agent to boost immunoresponsiveness among B cell immunodeficient individuals, such as, for example, an individual who has undergone a partial or complete splenectomy.

The modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be used to modulate hemostatic (the stopping of bleeding) or thrombolytic (clot dissolving) activity. For example, by increasing hemostatic or thrombolytic activity, fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention could be used to treat or prevent blood coagulation diseases, disorders, and/or conditions (e.g., afibrinogenemia, factor deficiencies, hemophilia), blood platelet diseases, disorders, and/or conditions (e.g. thrombocytopenia), or wounds resulting from trauma, surgery, or other causes. Alternatively, fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention that can decrease hemostatic or thrombolytic activity could be used to inhibit or dissolve clotting. These molecules could be important in the treatment or prevention of heart attacks (infarction), strokes, or scarring.

In specific embodiments, the modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be used to prevent diagnose, prognose, and/or treat thrombosis, arterial thrombosis, venous thrombosis, thromboembolism, pulmonary embolism, atherosclerosis, myocardial infarction, transient ischemic attack, unstable angina. In specific embodiments, the transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention maybe used for the prevention of occulsion of saphenous grafts, for reducing the risk of periprocedural thrombosis as might accompany angioplasty procedures, for reducing the risk of stroke in patients with atrial fibrillation including nonrheumatic atria fibrillation, for reducing the risk of embolism associated with mechanical heart valves and/or mitral valves disease. Other uses for the modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention, include, but are not limited to, the prevention of occlusions in extracorporeal devices (e.g., intravascular canals, vascular access shunts in hemodialysis patients, hemodialysis machines, and cardiopulmonary bypass machines).

In another embodiment, modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention, may be used to prevent, diagnose, prognose, and/or treat diseases and disorders of the blood and/or blood forming organs associated with the tissue(s) in which the polypeptide of the invention is expressed.

The modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be used to modulate hematopoietic activity (the formation of blood cells). For example, the transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be used to increase the quantity of all or subsets of blood cells, such as, for example, erythrocytes, lymphocytes (B or T cells), myeloid cells (e.g., basophils, eosinophils, neutrophils, mast cells, macrophages) and platelets. The ability to decrease the quantity of blood cells or subsets of blood cells may be useful in the prevention, detection, diagnosis, and/or treatment of anemias and leukopenias described below. Alternatively, the modified transferrin fusion proteins, of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be used to decrease the quantity of all or subsets of blood cells, such as, for example, erythrocytes, lymphocytes (B or T cells), myeloid cells (e.g., basophils, eosinophils, neutrophils, mast cells, macrophages) and platelets. The ability to decrease the quantity of blood cells or subsets of blood cells may be useful in the prevention, detection, diagnosis, and/or treatment of leukocytoses, such as, for example eosinophilia. The modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be used to prevent, treat, or diagnose blood dyscrasia.

Anemias are conditions in which the number of red blood cells or amount of hemoglobin (the protein that carries oxygen) in them is below normal. Anemia may be caused by excessive bleeding, decreased red blood cell production, or increased red blood cell destruction (hemolysis). The modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be useful in treating, preventing, and/or diagnosing anemias. Anemias that may be treated prevented or diagnosed by the transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention include iron deficiency anemia, hypochromic anemia, microcytic anemia, chlorosis, hereditary sideroblastic anemia, idiopathic acquired sideroblastic anemia, red cell aplasia, megaloblastic anemia (e.g., pernicious anemia, (vitamin B12 deficiency) and folic acid deficiency anemia), aplastic anemia, hemolytic anemias (e.g., autoimmune hemolytic anemia, microangiopathic hemolytic anemia, and paroxysmal nocturnal hemoglobinuria). The modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be useful in treating, preventing, and/or diagnosing anemias associated with diseases including but not limited to, anemias associated with systemic lupus erythematosus, cancers, lymphomas, chronic renal disease, and enlarged spleen. The transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be useful in treating, preventing, and/or diagnosing anemia arising from drug treatments such as anemias associated with methyldopa, dapsone, and/or sulfa drugs. Additionally, modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention maybe useful in treating, preventing, and/or diagnosing anemias associated with abnormal red blood cell architecture including but not limited to, hereditary spherocytosis, hereditary elliptocytosis, glucose-6-phosphate dehydrogenase deficiency, and sickle cell anemia.

The modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be useful in treating, preventing, and/or diagnosing hemoglobin abnormalities, (e.g., those associated with sickle cell anemia, hemoglobin C disease, hemoglobin S-C disease, and hemoglobin E disease). Additionally, the transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be useful in diagnosing, preventing, and/or prognosing in treating thalassemias, including, but not limited to, major and minor forms of alpha-thalassemia and beta-thalassemia.

In another embodiment, the modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be useful in diagnosing, prognosing, preventing, and/or treating bleeding disorders including, but not limited to, thrombocytopenia (e.g., idiopathic thrombocytopenic purpura, and thrombotic thrombocytopenic purpura), Von Willebrand's disease, hereditary platelet disorders (e.g., storage pool disease such as Chediak-Higashi and Hermansky-Pudlak syndromes, thromboxane A2 dysfunction, thromboasthenia, and Bernard-Soulier syndrome), hemolyticuremic syndrome, hemophilias such as hemophilia A or Factor V-II deficiency and Christmas disease or Factor IX deficiency, Hereditary Hemorhhagic Telangiectsia, also known as Rendu-Osler-Webe syndrome, allergic purpura (Henoch Schonlein purpura) and disseminated intravascular coagulation.

In other embodiments, the modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be useful as an agent to increase cytokine production.

In certain embodiments, fusion proteins of the invention, and/or polynucleotides encoding transferrin fusion proteins of the invention can be used to treat or detect hyperproliferative disorders, including neoplasms. Transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may inhibit the proliferation of the disorder through direct or indirect interactions. Alternatively, fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may cause proliferation of other cells which can inhibit the hyperproliferative disorder.

For example, by increasing an immune response, particularly increasing antigenic qualities of the hyperproliferative disorder or by proliferating, differentiating, or mobilizing T-cells, hyperproliferative disorders can be treated. This immune response may be increased by either enhancing an existing immune response, or by initiating a new immune response. Alternatively, decreasing an immune response may also be a method of treating hyperproliferative disorders, such as a chemotherapeutic agent.

Examples of hyperproliferative disorders that can be treated or detected by modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention include, but are not limited to neoplasms located in the colon, abdomen, bone, breast, digestive system, liver, pancreas, peritoneum, endocrine glands (adrenal, parathyroid, pituitary, testicles, ovary, thymus, thyroid), eye, head and neck, nervous (central and peripheral), lymphatic system, pelvis, skin, soft tissue, spleen, thorax, and urogenital tract.

Similarly, other hyperproliferative disorders can also be treated or detected by modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention. Examples of such hyperproliferative disorders include, but are not limited to Acute Childhood Lymphoblastic Leukemia; Acute Lymphoblastic Leukemia, Acute Lymphocytic Leukemia, Acute Myeloid Leukemia, Adrenocortical Carcinoma, Adult (Primary) Hepatocellular Cancer, Adult (Primary) Liver Cancer, Adult Acute Lymphocytic Leukemia, Adult Acute Myeloid Leukemia, Adult Hodgkin's Disease, Adult Hodgkin's Lymphoma, Adult Lymphocytic Leukemia, Adult Non-Hodgkin's Lymphoma, Adult Primary Liver Cancer, Adult Soft Tissue Sarcoma, AIDS-Related Lymphoma, AIDS-Related Malignancies, Anal Cancer, Astrocytoma, Bile Duct Cancer, Bladder Cancer, Bone Cancer, Brain Stem Glioma, Brain Tumors, Breast Cancer, Cancer of the Renal Pelvis and Ureter, Central Nervous System Lymphoma, Central Nervous System Lymphorria, Cerebellar Astrocytoma, Cerebral Astrocytoma, Cervical Cancer, Childhood (Primary) Hepatocellular Cancer, Childhood (Primary) Liver Cancer, Childhood Acute Lymphoblastic Leukemia, Childhood Acute Myeloid Leukemia, Childhood Brain Stem Glioma, Childhood Cerebellar Astrocytoma, Childhood Cerebral Astrocytoma, Childhood Extracranial Germ Cell Tumors, Childhood Hodgkin's Disease, Childhood Hodgkin's Lymphoma, Childhood Hypothalamic and Visual Pathway Glioma, Childhood Lymphoblastic Leukemia, Childhood Medulloblastoma, Childhood Non-Hodgkin's Lymphoma, Childhood Pineal and Supratentorial Primitive Neuroectodermal Tumors, Childhood Primary Liver Cancer, Childhood Rhabdomyosarcoma, Childhood Soft Tissue Sarcoma, Childhood Visual Pathway and Hypothalamic Glioma, Chronic Lymphocytic Leukemia, Chronic Myelogenous Leukemia, Colon Cancer, Cutaneous T-Cell Lymphoma, Endocrine Pancreas Islet Cell Carcinoma. Endometrial Cancer, Ependymoma, Epithelial Cancer, Esophageal Cancer, Ewing's Sarcoma and Related Tumors, Exocrine Pancreatic Cancer, Extracranial Germ Cell Tumor, Extragonadal Germ Cell Tumor, Extrahepatic Bile Duct Cancer, Eye Cancer, Female Breast Cancer, Gaucher's Disease, Gallbladder Cancer, Gastric Cancer, Gastrointestinal Carcinoid Tumor, Gastrointestinal Tumors, Germ Cell Tumors, Gestational Trophoblastic Tumor, Hairy Cell Leukemia, Head and Neck Cancer, Hepatocellular Cancer, Hodgkin's Disease, Hodgkin's Lymphoma, Hypergammaglobulinemia, Hypopharyngeal Cancer, Intestinal Cancers, Intraocular Melanoma, Islet Cell Carcinoma, Islet Cell Pancreatic Cancer, Kaposi's Sarcoma, Kidney Cancer, Laryngeal Cancer, Lip and Oral Cavity Cancer, Liver Cancer, Lung Cancer, Lympho proliferative Disorders, Macroglobulinemia, Male Breast Cancer, Malignant Mesothelioma, Malignant Thymoma, Medulloblastomia, Melanoma, Mesothelioma, Metastatic Occult Primary Squamous Neck Cancer, Metastatic Primary Squamous Neck Cancer, Metastatic Squamous Neck Cancer, Multiple Myeloma, Multiple Myeloma/Plasma Cell Neoplasm, Myelodysplastic Syndrome, Myelogenous Leukemia, Myeloid Leukemia, Myeloproliferative Disorders, Nasal Cavity and Paranasal Sinus Cancer, Nasopharyngeal Cancer, Neuroblastoma, Non-Hodgkin's Lymphoma During Pregnancy, Nonmelanoma Skin Cancer, Non-Small Cell Lung Cancer, Occult Primary Metastatic Squamous Neck Cancer, Oropharyngeal Cancer, Osteo/Malignant Fibrous Sarcoma, Osteosarcoma/Malignant Fibrous Histiocytoma, Osteosarcoma/Malignant Fibrous Histiocytoma of Bone, Ovarian Epithelial Cancer, Ovarian Germ Cell Tumor, Ovarian Low Malignant Potential Tumor, Pancreatic Cancer, Paraproteinemias, Purpura, Parathyroid, Cancer, Penile Cancer, Pheochromocytoma, Pituitary Tumor, Plasma Cell Neoplasm/Multiple Myeloma, Primary Central Nervous System Lymphoma, Primary Liver Cancer, Prostate Cancer, Rectal Cancer, Renal Cell Cancer, Renal Pelvis and Ureter Cancer, Retinoblastoma, Rhabdomyosarcoma, Salivary Gland Cancer, Sarcoidosis Sarcomas, Sezary Syndrome, Skin Cancer, Small Cell Lung Cancer, Small Intestine Cancer, Soft Tissue Sarcoma, Squamous Neck Cancer, Stomach Cancer, Supratentorial Primitive Neuroectodermal and Pineal Tumors, T-Cell Lymphoma, Testicular Cancer, Thymoma, Thyroid Cancer, Transitional Cell Cancer of the Renal Pelvis and Ureter, Transitional Renal Pelvis and Ureter Cancer, Trophoblastic Tumors, Ureter and Renal Pelvis Cell Cancer, Urethral Cancer, Uterine Cancer, Uterine Sarcoma, Vaginal Cancer, Visual Pathway and Hypothalamic Glioma, Vulvar Cancer, Waldenstrom's Macroglobulinemia, Wilm's Tumor, and any other hyperproliferative disease, besides neoplasia, located in an organ system listed above.

In another preferred embodiment, modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention are used to diagnose, prognose, prevent, and/or treat premalignant conditions and to prevent progression to a neoplastic or malignant state, including but not limited to those disorders described above. Such uses are indicated in conditions known or suspected of preceding progression to neoplasia or cancer, in particular, where non-neoplastic cell growth is consisting of hyperplasia, metaplasia, or most particularly, dysplasia has occurred (for review of such abnormal growth conditions, see Robbins. and Angell, 1976, Basic Pathology, 2d Ed. W. B. Saunders Co., Philadelphia, pp. 68-79).

Hyperplasia is a form of controlled cell proliferation, involving an increase in cell number in a tissue or organ, without significant alteration in structure or function. Hyperplastic disorders which can be diagnosed, prognosed, prevented, and/or treated with fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention include, but are not limited to, angiofollicular mediastinal lymph node hyperplasia, angiolymphoid hyperplasia with eosinophilia, atypical melanocytic hyperplasia, basal cell hyperplasia, benign giant lymph node hyperplasia, cementum hyperplasia, congenital adrenal hyperplasia, congenital sebaceous hyperplasia, cystic hyperplasia, cystic hyperplasia of the breast, denture hyperplasia, ductal hyperplasia, endometrial hyperplasia, fibromuscular hyperplasia, foca epithelial hyperplasia, gingival hyperplasia, inflammatory fibrous hyperplasia, inflammatory papillary hyperplasia, intravascular papillary endothelial hyperplasia, nodular hyperplasia of prostate, nodular regenerative hyperplasia, pseudoepitheliomatous hyperplasia, senile sebaceous hyperplasia, and verrucous hyperplasia.

In another embodiment, modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention conjugated to a toxin or a radio-active isotope, as described herein, may be used to treat cancers and neoplasms, including, but not limited to, those described herein. In a further preferred embodiment, transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention conjugated to a toxin or a radioactive isotope, as described herein, may be used to treat acute myelogenous leukemia.

Additionally, modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may affect apoptosis, and therefore, would be useful in treating a number of diseases associated with increased cell survival or the inhibition of apoptosis. For example, diseases associated with increased cell survival or the inhibition of apoptosis that could be diagnosed, prognosed, prevented, and/or treated by polynucleotides, polypeptides, and/or agonists or antagonists of the invention, include cancers (such as follicular-lymphomas, carcinomas with p53 mutations, and hormone-dependent tumors, including, but not limited to, colon cancer, cardiac tumors, pancreatic cancer, melanoma, retinoblastoma, glioblastoma, lung cancer, intestinal cancer, testicular cancer, stomach cancer, neuroblastoma, myxoma, myoma, lymphoma, endothelioma, osteoblastoma, osteoclastoma, osteosarcoma, chondrosarcoma, adenoma, breast cancer, prostrate cancer, Kaposi's sarcoma and ovarian cancer); autoimmune disorders such as, multiple sclerosis, Sjogren's syndrome, Hashimoto's thyroiditis, biliary cirrhosis, Behcet's disease, Crohn's disease, polymyositis, systemic lupus erythematosus and immune-related glomrerulonephritis and rheumatoid arthritis) and viral infections (such as herpes viruses, pox viruses and adenoviruses), inflammation, graft v. host disease, acute graft rejection, and chronic graft rejection.

In preferred embodiments, modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention are used to inhibit growth, progression, and/or metastasis of cancers, in particular those listed above.

Additional diseases or conditions associated with increased cell survival that could be diagnosed, prognosed, prevented, and/or treated by modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention, include but are not limited to, progression and/or metastases of malignancies and related disorders such as leukemia (including acute leukemia (e.g., acute lymphocytic leukemia, acute myelocytic leukemia (including myeloblastic, promyelocytic, mylomonocytic, monocytic, and erythroleukemia)) and chronic leukemia (e.g., chronic myelocytic (granulocytic) leukemia and chronic lymphocytic leukemia)), polycythemia vera, lymphomas (e.g., Hodgkin's disease and non-Hodgkin's disease), multiple myeloma, Waldenstrom's macroglobulinemia, heavy chain disease, and solid tumors including, but not limited to, sarcomas and, carcinomas such as fibrosarcoma, myxosarcoma, fiposarcoma, chondrosarcoma, osteogenic sarcoma, chordoma, angiosarcoma, endotheliosarcoma, lymphangiosarcoma, lymphangioendotheliosarcoma, synovioma, mesothelioma, Ewing's tumor, leiomyosarcoma, rhabdomyosarcoma, colon carcinoma, pancreatic cancer, breast cancer, ovarian cancer, prostate cancer, squamous cell carcinoma, basal cell carcinoma, adenocarcinoma, sweat gland carcinoma, sebaceous gland carcinoma, papillary carcinoma, papillary adenocarcinomas, cystadenocarcinoma, medullary carcinoma, bronchogenic carcinoma, renal cell carcinoma, hepatoma, bile duct carcinoma, choriocarcinoma, seminoma, embryonal carcinoma, Wilm's tumor, cervical cancer, testicular tumor, lung carcinoma, small cell lung carcinoma, bladder carcinoma, epithelial carcinoma, glioma, astrocytoma, medulloblastoma, craniopharyngioma, ependymoma, pinealoma, emangioblastoma, acoustic neuroma, oligodendrogliomia, menangioma, melanoma, neuroblastoma, and retinoblastoma.

Diseases associated with increased apoptosis that could be diagnosed, prognosed, prevented, and/or treated by modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention, include AIDS; neurodegenerative disorders (such as Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, retinitis pigmentosa, cerebral degeneration and brain tumor or prion associated disease); autoimmune disorders (such as, multiple sclerosis, Sjogren's syndrome, Hashimoto's thyroiditis, biliary cirrhosis, Behcet's disease, Crohn's disease, polymyositis, systemic lupus erythematosus and immune-related glomerulonephritis and rheumatoid arthritis) myelodysplastic syndromes (such as aplastic anemia), graft Y host disease, ischemic injury (such as that caused by myocardial infarction, stroke and repercussion injury), liver injury (e.g., hepatitis related liver injury, ischemia/reperfusion injury, cholestosis (bile duct injury) and liver cancer); toxin-induced liver disease (such as that caused by alcohol), septic shock, cachexia and anorexia.

Another preferred embodiment utilizes polynucleotides encoding modified transferrin fusion proteins of the invention to inhibit aberrant cellular division, by gene therapy using the present invention, and/or protein fusions or fragments thereof.

Thus, the present invention provides a method for treating cell proliferative disorders by inserting into an abnormally proliferating cell a polynucleotide encoding modified transferrin fusion protein of the present invention, wherein said polynucleotide represses said expression.

Another embodiment of the present invention provides a method of treating cell proliferative disorders in individuals comprising administration of one or more active gene copies of the present invention to an abnormally proliferating cell or cells.

The polynucleotides of the present invention may be delivered directly to cell proliferative disorderly disease sites in internal organs, body cavities, and the like by use of imaging devices used to guide an injecting needle directly to the disease site. The polynucleotides of the present invention may also be administered to disease sites at the time of surgical intervention.

By cell proliferative disease is meant any human or animal disease or disorder, affecting any one or any combination of organs, cavities, or body parts, which is characterized by single or multiple local abnormal proliferations of cells, groups of cells, or tissues, whether benign or malignant.

Any amount of the polynucleotides of the present invention may be administered as long as it has a biologically inhibiting effect on the proliferation of the treated cells.

Moreover, it is possible to administer more than one of the polynucleotides of the present invention simultaneously to the same site. By “biologically inhibiting” is meant partial or total growth inhibition as well as decreases in the rate of proliferation or growth of the cells.

Modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention are useful in inhibiting the metastasis of proliferative cells or tissues. Inhibition may occur as a direct result of administering these transferrin fusion proteins and/or polynucleotides, or indirectly, such as activating the expression of proteins known to inhibit metastasis, for example alpha, integrins, (See, e.g., Curr. Top. Mirobiol. Immunol. 1998; 231:1 41, which is hereby incorporated by reference). Such therapeutic affects of the present invention may be achieved either alone, or in combination with small molecule drugs or adjuvants.

In another embodiment, the invention provides a method of delivering compositions containing the transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention to targeted cells expressing the polypeptide bound by, that binds to, or associates with a modified transferrin fusion protein of the invention. Transferrin fusion proteins of the invention may be associated with heterologous polypeptides, heterologous nucleic acids, toxins, or prodrugs via hydrophobic, hydrophilic, ionic and/or covalent interactions.

Kidney diseases which can be diagnosed, prognosed, prevented, and/or treated with compositions of the invention include, but are not limited to, acute kidney failure, chronic kidney failure, atheroembolic renal failure, end-stage renal disease, inflammatory diseases of the kidney (e.g., acute glomerulonephritis, post infectious glomerulonephritis, rapidly progressive glomerulonephritis, nephritic syndrome, membranous glomerulonephritis, familial nephritic syndrome, membrane proliferative glomerulonephritis and mesangial proliferative glomerulonephritis, chronic glomerulonephritis, acute tubulo interstitial nephritis, chronic tubulointerstitial nephritis, acute post-streptococcal glomerulonephritis(PSGN), pyelonephritis, lupus nephritis, chronic nephritis, interstitial nephritis, and post streptococcal glomerulonephritis), blood vessel disorders of the kidneys (e.g., kidney infarction, atherombolic kidney disease, cortical necrosis, malignant nephrosclerosis, renal vein thrombosis, renal under perfusion, renal retinopathy, renal ischemia-reperfusion, renal artery embolism and renal artery stenosis), and kidney disorders resulting form urinary tract disease (e.g., pyelonephritis, hydronephrosis, urolithiasis (renal lithiasis, nephrolithiasis), reflux nephropathy, urinary tract infections, urinary retention, and acute or chronic unilateral obstructive uropathy). In addition, compositions of the invention can be used to diagnose, prognose, prevent, and/or treat metabolic and congenital disorders of the kidney (e.g., uremia, renal amyloidosis, renal osteodystrophy, renal tubular acidosis, renal glycosuria, nephrogenic diabetes insipidus, cystinuria, Fanconi's syndrome, renal fibrocystic osteosis (renal rickets), Hartnup disease, Bartter's syndrome, Liddle's syndrome, polycystic kidney disease, medullary cystic disease, medullary sponge kidney, Alport's syndrome, nail-patella syndrome, congenital nephritic syndrome, CRUSH syndrome, horseshoe kidney, diabetic nephropathy, nephrogenic diabetes insipidus, analgesic nephropathy, kidney stones, and membranous nephropathy), and autoimmune disorders of the kidney (e.g., systemic lupus erythematosus (SLE), Good-pasture syndrome, IgA nephropathy, and ICFM mesangial proliferative glomerulonephritis).

Compositions of the invention can also be used to diagnose, prognose, prevent, and/or treat sclerotic or lecrotic disorders of the kidney (e.g., glomerulosclerosis, diabeticnephropathy, focal segmental glomerulo sclerosis (FSGS), narcotizing glomerulonephritis, and renal papillary necrosis), cancers of the kidney (e.g., nephroma, hypernephroma, nephroblastoma, renal cell cancer, transitional cell cancer, renal adenocarcinoma, squamous cell cancer, and Wilm's tumor), and electrolyte imbalances (e.g., nephrocalcinosis, pyuria, edema, hydronephritis, proteinuria, hyponatremia, hypernatremia, hypokalemia, hyperkalemia, hypocalcemia, hypercalcemia, hypophosphatemia, and hyperphosphatemia).

Compositions of the invention may be administered using any method known in the art, including, but not limited to, direct needle injection at the delivery site, intravenous injection, topical administration, catheter infusion, biolistic injectors, particle accelerators, gel foam sponge depots, other commercially available depot materials, osmotic pumps, oral or suppositorial solid pharmaceutical formulations, decanting or topical applications during surgery, aerosol delivery. Such methods are known in the art. Compositions of the invention may be administered as part of a Therapeutic, described in more detail below.

Cardiovascular disorders, includes, but is not limited to, cardiovascular abnormalities, such as arterio arterial fistula, arteriovenous fistula, cerebral arteriovenous malformations, congenital heart defects, pulmonary atresia, and Scimitar Syndrome.

Congenital heart defects include, but are not limited to, aortic coarctation, cortriatriatum, coronary vessel anomalies, crisscross heart, dextrocardia, patent ductus arteriosus, Ebstein's anomaly, Eisenmenger complex, hypoplastic left heart syndrome, levocardia, tetralogy of fallot, transposition of great vessels, double outlet right ventricle, tricuspidatresia, persistent truncus arteriosus, and heart septal defects, such as aortopulmonary septald defect, endocardial cushion defects, Lutembacher's Syndrome, trilogy of Fallot, ventricular heart septal defects.

Cardiovascular disorders also include, but are not limited to, heart disease, such arrhythmias, carcinoid heart disease, high cardiac output, low cardiac output, cardiactamponade, endocarditis (including bacteria), heart aneurysm, cardiac arrest, congestive heart failure, congestive cardiomyopathy, paroxysmal dyspnea, cardiac edema, heart hypertrophy, congestive cardiomyopathy left ventricular hypertrophy, right ventricularhypertrophy, post-infarction heart rupture, ventricular septal rupture, heart valve diseases myocardial diseases, myocardial ischemia, pericardial effusion, pericarditis (including constrictive and tuberculous), pricumopericardium, post pericardiotomy syndrome, pulmonary heart disease, rheumatic heart disease, ventricular dysfunction, hyperemia, cardiovascular pregnancy complications, Scimitar Syndrome, cardiovascular syphilis, and cardiovascular tuberculosis.

Arrhythmias include, but are not limited to, sinus arrhythmia, atrial fibrillation, atrial flutter, bradycardia, extrasystole, Adams-Stokes Syndrome, bundle-branch block, sinoatrial block, long QT syndrome, parasystole, Lown-Ganong-Levine Syndrome, Mahaim-type pre-excitation syndrome, Wolff-Parkinson-White syndrome, sick sinus syndrome, itachycardias, and ventricular fibrillation. Tachycardias include paroxysmal tachycardia, suprayentriculai tachycardia, accelerated idioventricular rhythm, atrioventricular nodal reentry tachycardia, ectopic atrial tachycardia, ectopic junctional tachycardia, sinoattial nodalreenthy tachycardia, sinus tachycardia, Torsades de Pointes, and ventricular tachycardia.

Heart valve diseases include, but are not limited to, aortic valve insufficiency aorticvalve stenosis, heart murmurs, aortic valve prolapse, neutral valve prolapse, tricuspid valve prolapse, mitral valve insufficiency, mitral valve stenosis, pulmonary atresia, pulmonary valve insufficiency, pulmonary valve stenosis, tricuspid atresia, tricuspid valve insufficiency, and tricuspid valve stenosis.

Myocardial diseases include, but are not limited to, alcoholic cardiomyopathy, congestive cardiomyopathy, hypertrophic cardiomyopathy, aortic subvalvular stenosis, pulmonary subvalvular stenosis, restrictive cardiomyopathy, Chagas cardiomyopathy, endocardial fibroelastosis, endomyocardial fibrosis, Kearns Syndrome, myocardial reperfusion injury, and myocarditis.

Myocardial ischemias include, but are not limited to, coronary disease, such as angina pectoris, coronary aneurysm, coronary arteriosclerosis, coronary thrombosis, coronary vasospasm, myocardial infarction, and myocardial stunning.

Cardiovascular diseases also include vascular diseases such as aneurysms, angiodysplasia, angiomatosis, bacillary angiomiatosis, Hippel-Lindau Disease, Klippel Trenaunay Weber Syndrome, Sturge Weber Syndrome, angioneurotic edema, aortic diseases, Takayasu's Arthritis, aortitis, Leriche's Syndrome, arterial occlusive diseases, arthritis, enarteritis, polyarteritis nodosa, cerebrovascular disorders, diabetic angiopathies, diabetic retinopathy, embolisms, thrombosis, erythromelalgia, hemorrhoids, hepatic veno-occlusive disease, hypertension, hypotension, ischemia, peripheral vascular diseases, phlebitis, pulmonary veno-occlusive disease, Raynaud's disease, CREST syndrome, retinal vein occlusion, Scimitar syndrome, superior vena cava syndrome, telangiectasia, ataxia telangiectasia, hereditary hemorrhagic telangiectasia, varicocele, varicose veins, varicoseulcer, vasculitis, and venous insufficiency.

Cerebrovascular disorders include, but are not limited to, cardio artery diseases but includes respiratory disorders. Transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be used to treat, prevent, diagnose, and/or prognose diseases and/or disorders of the respiratory system.

Diseases and disorders of the respiratory system include, but are not limited to, nasalvestibulitis, nonallergic rhinitis (e.g., acute rhinitis, chronic rhinitis, atrophic rhinitis, vasomotor rhinitis), nasal polyps, and sinusitis, juvenile angiofibromas, cancer of the nose and juvenile papillomas, vocal cord polyps, nodules (singer's nodules), contact ulcers, vocal cord paralysis, laryngoceles, pharyngitis (e.g., viral and bacterial), tonsillitis, tonsillar cellulitis, parapharyngeal abscess, laryngitis, laryngoceles, and throat cancers (e.g., cancer of the nasopharynx, tonsil cancer, larynx cancer), lung cancer (e.g., squamous cell carcinoma, small cell (oat cell) carcinoma, large cell carcinoma, and adenocarcinoma), allergic disorders (eosinophilic pneumonia, hypersensitivity pneumonitis (e.g., extrinsicallergic alveolitis, allergic interstitial pneumonitis, organic dust pneumoconiosis, allergic bronchopulmonary aspergillosis, asthma, Wegener's granulomatosis (granulomatous vasculitis), Goodpasture's syndrome), pneumonia (e.g., bacterial pneumonia (e.g., Streptococcus pneumoniae (pneumoncoccal pneumonia), Staphylococcus aureus (staphylococeal pneumonia), Gram negative bacteria pneumonia (caused by, e.g., Klebsiella and Pseudomonas spp.), Mycoplasma pneumoniae pneumonia, Hemophilus influenza pneumonia, Legionella pneumophila (Legionnaires' disease), and Chlamydia psittaci (Psittacosis)), and viral pneumonia (e.g., influenza, chickenpox (varicella).

Additional diseases and disorders of the respiratory system include, but are not limited to bronchiolitis, polio (poliomyelitis), croup, respiratory syncytial viral infection, mumps, erythema infectiosum (fifth disease), roseola infantum, progressive rubellapanencephalitis, German measles, and subacute sclerosing panencephalitis), fungal pneumonia (e.g., Histoplasmosis, Coccidioidomycosis, Blastomycosis, fungal infections in people with severely suppressed immune systems (e.g., cryptococcosis, caused by Cryptococcus neoformans; aspergillosis, caused by Aspergillus spp.) candidiasis, caused by Candida; and mucormycosis)), Pneumocystis carinii (pneumocystis pneumonia), atypicalpneumonias (e.g., Mycoplasma and Chlamydia spp.), opportunistic infection pneumonia, nosocomial pneumonia, chemical pneumonitis, and aspiration pneumonia, pleural disorders (e.g., pleurisy, pleural effusion, and pneumothorax (e.g., simple spontaneous pneumothorax, complicated spontaneous pneumothorax, tension pneumothorax)),obstructive airway diseases (e.g., asthma, chronic obstructive pulmonary disease (COPD), emphysema, chronic or acute bronchitis), occupational lung diseases (e.g., silicosis, blacklung (coal workers' pneumoconiosis, asbestosis, berylliosis, occupational asthma, and byssinosis), Infiltrative Lung Disease (e.g., pulmonary fibrosis (e.g., usual interstitial pneumonia), idiopathic pulmonary fibrosis, desquamative interstitial pneumonia, lymphoid interstitial pneumonia, histiocytosis (e.g., Letterer-Siwe disease, Hand-Schüller-Christian disease, eosinophilic granuloma), idiopathic pulmonary hemosiderosis, sarcoidosis and pulmonary, alveolar proteinosis), Acute respiratory distress syndrome (also called, e.g., adult respiratory distress syndrome), edema, pulmonary embolism, bronchitis (e.g., viral, bacterial), bronchiectasis, atelectasis, lung abscess (caused by, e.g., Staphylococcus aureus or Legionella pneumophila), and cystic fibrosis.

Cancers which may be treated with modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention include, but are not limited to solid tumors, including prostate, lung, breast, ovarian, stomach, pancreas, larynx, esophagus, liver, parotid, biliary tract, colon, rectum, cervix, uterus, 1 endometrium, kidney, bladder, thyroid cancer; primary tumors and metastases; melanomas; glioblastoma; Kaposi's sarcoma; leiomyosarcoma; non-small cell lung cancer; colorectal cancer; advanced malignancies; and blood born tumors such as leukemia. For example, fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be delivered topically, in order to treat cancers such as skin cancer, head and neck tumors, breast tumors, and Kaposi's sarcoma.

Modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be useful, in treating other disorders, besides cancers, which involve angiogenesis. These disorders include, but are not limited to: benign tumors, for example hemangiomas, acoustic neuromas, neurofibromas, trachomas, and pyogenicgranulomas; artherosclerotic plaques; ocular angiogenic diseases, for example, diabetic retinopathy, retinopathy of prematurity, macular degeneration, corneal graft rejection, neovascular glaucoma, retrolental fibroplasia, rubeosis, retinoblastoma, uvietis and Pterygiaab normal blood vessel growth) of the eye; rheumatoid arthritis; psoriasis; delayed wound healing; endometriosis; vasculogenesis; granulations; hypertrophic scars (keloids); nonunion fractures; scleroderma; trachoma; vascular adhesions; myocardial angiogenesis; coronary collaterals; cerebral collaterals; arteriovenous malformations; ischemic limb angiogenesis; Osler-Webber Syndrome; plaque neovascularization; telangiectasia; hemophiliac joints; angiofibroima; fibromuscular dysplasia; wound granulation; Crohn's disease; and atherosclerosis.

Thus, within one aspect of the present invention methods are provided for treating neovascular diseases of the eye.

Additionally, disorders which can be treated with modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention include, but are not limited to, hemangioma, arthritis, psoriasis, angiofibroma, atherosclerotic plaques, delayed wound healing, granulations, hemophilic joints hypertrophic scars, nonunion fractures, Osler-Weber syndrome, pyogenic granuloma, scleroderma, trachoma; and vascular adhesions.

Moreover, disorders and/or states, which can be treated, prevented, diagnosed, and/or prognosed with the modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention include, but are not limited to, solid tumors, blood born tumors such as leukemia, tumor metastasis, Kaposi's sarcoma, benign tumors, for example hemangiomas, acoustic neuromas, neurofibromas, trachomas, and pyogenic granulomas, rheumatoid arthritis, psoriasis, ocularangiogenic diseases, for example, diabetic retinopathy, retinopathy of prematurity, macular degeneration, corneal graft rejection, neovascular glaucoma, retrolental fibroplasia, rubeosis, refinoblastoma, and uvietis, delayed wound healing, endometriosis, vasculogenesis, granulations, hypertrophic scars (keloids, nonunion fractures, scleroderma, trachoma, vascular adhesions, myocardial angiogenesis, coronary collaterals, cerebral collaterals, arteriovenous malformations, ischemic limb angiogenesis, Osler-Webber Syndrome, plaque neovascularization, telangiectasia, hemophiliac joints, angiofibroma fibromuscular dysplasia, wound granulation, Crohn's disease, atherosclerosis, birth control agent by preventing vascularization required for embryo, implantation controlling menstruation, diseases that have angiogenesis as a pathologic consequence such as cat scratch disease (Rochele nunalia quintosa), ulcers (Helicobacter pylori), Bartonellosis and baculary angiomatosis.

In one aspect of the birth control method, an amount of the compound sufficient to block embryo implantation is administered before or after intercourse and fertilization have occurred, thus providing an effective method of birth control, possibly a “morning after” method. Modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may also be used in controlling menstruation or administered as either a peritoneal lavage fluid or for peritoneal implantation in the treatment of endometriosis.

Modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be utilized in a wide variety of surgical procedures.

Diseases associated with increased cell survival or the inhibition of apoptosis that could be treated, prevented, diagnosed, and/or prognosed using modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention, include cancers (such as follicular lymphomas, carcinomas with mutations, and hormone-dependent tumors, including, but not limited to colon cancer, cardiac tumors, pancreatic cancer, melanoma, retinoblastoma, glioblastoma, lung cancer, intestinal cancer, testicular cancer, stomach cancer, neuroblastoma, myxoma, myoma, lymphoma, endothelioma, osteoblastoma, osteoclastoma, osteosarcoma, chondrosarcoma, adenoma, breast cancer, prostate cancer, Kaposi's sarcoma and ovarian cancer); autoimmune disorders (such as, multiple sclerosis, Sjogren's syndrome, Hashimoto's thyroiditis, biliary cirrhosis, Behcet's disease, Crohn's disease, polymyositis, systemic lupus thematosus and immune-related ryglomerulonephritis and rheumatoid arthritis) and viral infections (such as herpes viruses, pox viruses and adenoviruses), inflammation, graft v. host disease, acute graft rejection, and chronic graft rejection.

Additional diseases or conditions associated with increased cell survival that could be treated or detected by modified fusion proteins of the invention and/or polynucleotides encoding, transferrin fusion proteins of the invention include, but are not limited to, progression, and/or metastases of malignances and related disorders such as leukemia (including acute leukemia (e.g., acute lymphocytic leukemia, acute myelocytic leukemia (including myeloblastic, promyelocytic, myelomonocytic, monocytic, and erythroleukemia)) and chronic leukemia (e.g., chronic myelocytic (granulocytic) leukemia and chroniclymphocytic leukemia)), polycytemia vera, lymphomas (e.g., Hodgkin's disease and non-Hodgkin's disease), multiple myeloma, Waldenstrom's macroglobulinemia, heavy chain disease, and solid tumors including, but not limited to, Sarcomas and carcinomas such as fibrosarcoma, myxosarcoma, liposarcoma, chondrosarcoma, osteogenic sarcoma, chordoma, angiosarcoma, endotheliosarcoma, lymphangiosarcoma, lymphangioendotheliosarcoma, synovioma, mesothelioma, Ewing's tumor, leiomyosarcoma, rhabdomyosarcoma, colon carcinoma, pancreatic cancer, breast cancer, ovarian cancer, prostate cancer, squamous cell carcinoma, basa cell carcinoma, adenocarcinoma, sweat gland carcinoma, sebaceous aland carcinoma, papillary carcinoma, papillary adenocarcinomas, cystadenocarcinoma, medullary carcinoma, bronchogenic carcinoma, renal cell carcinoma, hepatoma, bile duct carcinoma, choriocarcinoma, seminoma, embryonal carcinoma, Wilm's tumor, cervical cancer, testicular tumor, Jung carcinoma, small cell lung carcinoma, bladder carcinoma, epithelial carcinoma, glioma, astrocytoma, medulloblastoma, craniopharyngioma, ependymoma, pinealoma, hemangioblastoma, acoustic neuroma, oligodendroglioma, menangioma, melanoma neuroblastoma, and retinoblastoma.

Diseases associated with increased apoptosis that could be treated, prevented, diagnosed, and/or prognosed using modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention, include, but are not limited to, AIDS; neurodegenerative disorders (such as Alzheimer's disease, Parkinson's disease, Amyotrophic lateral sclerosis, Retinitis pigmentosa, Cerebellar degeneration and brain tumor or prion associated disease); autoimmune disorders (such as, multiple sclerosis, Sjogren's syndrome, Hashimoto's thyroiditis, biliary cimhosis, Behcet's disease, Crohn's' disease, polymyositis, systemic lupus erythematosus and immune-related glomerulonephritis and rheumatoid arthritis) Myelodysplastic syndromes (such as aplasiic anemia), graft v. host disease, ischemic injury (such as that caused, by myocardial. infarction, stroke and reperfusion injury), liver injury (e.g., hepatitis related liver injury, ischemia/reperfusion injury, cholestosis (bile duct injury) and liver cancer); toxin-induced liver disease (such as that caused by alcohol), septic shock, cachexia and anorexia.

In addition, modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention could be, used to treat or prevent the onset of diabetes mellitus. In patients with newly diagnosed Types I and II diabetes, where some islet cell function remains, fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention, could be used to maintain the islet function so as to alleviate, delay or prevent permanent manifestation of the disease. Also, fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention could be used as an auxiliary in islet cell transplantation to improve or promote islet cell function.

The modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be used for the diagnosis and/or treatment of diseases, disorders, damage or injury of the brain and/or nervous system. Nervous system disorders that can be treated with the compositions of the invention (e.g., fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention), limited to nervous systems include, but are not limited injuries, and diseases or disorders which result in either a disconnection of axons, a diminution or degeneration of neurons, or demyelination. Nervous system lesions which may be treated in a patient (including human and non-human mammalian patients) according to the methods of the invention, include but are not limited to, the following lesions of either the central (including spinal cord, brain) or peripheral nervous systems: (1) ischemic lesions, in which a lack of oxygen in a portion of the nervous system results in neuronal injury or death, including cerebral infarction or ischemia, or spinal cord infarction or ischemia; (2) traumatic lesions, including lesions caused by physical injury or associated with surgery, for example, lesions which sever a portion of the nervous system, or compression injuries; (3) malignant lesions, in which a portion of the nervous system is destroyed or injured by malignant tissue which is either a nervous system associated malignancy or a malignancy derived from nervous system tissue; (4) infectious lesions in which a portion of the nervous system is destroyed or injured as a result of infection, for example, by an abscess or associated with infection by human immunodeficiency virus, herpes zoster, or herpes simplex virus or with Lyme disease, tuberculosis, or syphilis; (5) degenerative lesions, in which a portion of the nervous system is destroyed or injured as a result of a degenerative process including but not limited to, degeneration associated with Parkinson's disease, Alzheimer's disease, Huntington's chorea, or amyotrophic lateral sclerosis (ALS); (6) lesions associated with nutritional diseases or disorders, in which a portion of the nervous system is destroyed or injured by a nutritional disorder or disorder of metabolism including, but not limited to vitamin B-12 deficiency, folic acid deficiency, Wernicke disease, tobacco-alcohol amblyopic, Marchiafava-Blanami disease (primary degeneration of the corpus callosum), and alcoholic cerebral degeneration; (7) neurological lesions associated with systemic diseases including, but not limited to diabetes (diabetic neuropathy, Bell's palsy), systemic lupus erythematosus, carcinoma, or sarcoidoisis; (8) lesions caused by toxic substances including alcohol, lead, or particular, neurotoxins; and (9) demyelinated lesions in which a portion of the nervous system is destroyed or injured by a demyelinating disease including, but not limited to, multiple sclerosis, human immunodeficiency virus-associated myelopathy, transverse myelopathy or various etiologies, progressive multifocal leukoencephalopathy, and central pontine myelinolysis.

In one embodiment, the modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention are used to protect neural cells from the damaging effects of hypoxia. In a further preferred embodiment, the modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention are used to protect neural cells from the damaging effects of cerebral hypoxia.

In specific embodiments, motor neuron disorders that may be treated according to the invention include, but are not limited to, disorders such as infarction, infection, exposure to toxin, trauma, surgical damage, degenerative disease or malignancy that may affect motor neurons as well as other components of the nervous system, as well as disorders that selectively affect neurons such as amyotrophic lateral sclerosis, and including, but not limited to, progressive spinal muscular atrophy, progressive bulbar palsy, primary lateral sclerosis, infantile and juvenile muscular atrophy, progressive bulbar paralysis of childhood (Fazio-Londe syndrome), poliomyelitis and the post polio syndrome, and Hereditary Motor sensory Neuropathy (Charcot-Marie-Tooth Disease).

Further, modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may play a role in neuronal survival; synapse formation; conductance; neural differentiation, etc. Thus, compositions of the invention (including fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention) may be used to diagnose and/or treat or prevent diseases or disorders associated with these roles, including, but not limited to, learning and/or cognition disorders. The compositions of the invention may also be useful in the treatment or prevention of neurodegenerative disease states and/or behavioral disorders. Such neurodegenerative disease states and/or behavioral disorders include, but are not limited to, Alzheimer's Disease, Parkinson's Disease, Huntington's Disease, Tourette Syndrome, schizophrenia, mania, dementia, paranoia, obsessive compulsive disorder, panic disorder, learning disabilities, ALS, psychoses, autism, and altered behaviors, including disorders in feeding, sleep patterns, balance, and perception.

Examples of neurologic diseases which can be treated or detected with modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention include, brain diseases, such as metabolic brain diseases which includes phenylketonuria such as maternal phenylketonuria, pyruvate carboxylase deficiency, pyruvate dehydrogenase complex deficiency, Wernicke's Encephalopathy, brain edema, brain neoplasms such as cerebellar neoplasms which include infratentorial neoplasms, cerebral ventricle neoplasms such as choroid plexus neoplasms, hypothalmic neoplasms, supratentorial neoplasms, canavan disease, cerebellar diseases such as cerebellar ataxia which include spinocerebellar degeneration such as ataxia telangiectasia, cerebellar dyssynergia, Friederich's Ataxia, Machado-Joseph Disease, olivopontocerebellar atrophy, cerebellar neoplasms such as infratentorial neoplasms, diffuse cerebral sclerosis such as encephalitis periaxialis, globoid cell leukodystrophy, metachromatic leukodystrophy and subacute sclerosing panencephalitis.

Additional neurologic diseases which can be treated or detected with modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention include cerebrovascular disorders (such as carotid artery diseases which include carotid artery thrombosis, carotid stenosis and Moyamoya Disease), cerebral amyloid angiopathy, cerebral aneurysm, cerebral anoxia, cerebral arteriosclerosis, cerebral arteriovenous malformations, cerebral artery diseases, cerebral embolism and thrombosis such as carotid artery thrombosis, sinus thrombosis and Wallenberg's Syndrome, cerebral hemorrhage such as epidermal hematoma, subdural hematoma and subarachnoid hemorrhage, cerebral infarction, cerebral ischemia such as transient cerebral ischemia, Subclavian Steal Syndrome and vertebrobasilar insufficiency, vascular dementia such as multi-infarct dementia, periventricular leukomalacia, vascular headache such as cluster headache and migraine.

Additional neurologic diseases which can be treated or detected with modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention include dementia such as AIDS Dementia Complex, presenile dementia such as Alzheimer's Disease and Creutzfeldt-Jakob Syndrome, senile dementia such as Alzheimer's Disease and progressive supranuclear palsy, vascular dementia such as multi-infarct dementia, encephalitis which include encephalitis periaxialis, viral encephalitis such as epidemicencephalitis, Japanese Encephalitis, St. Louis Encephalitis, tick-borne encephalitis and West Nile Fever, acute disseminated encephalomyelitis, meningoencephalitis such as uveomeningoencephalitic syndrome, Postencephalitic Parkinson Disease and subacute sclerosing panencephalitis, encephalomalacia such as periventricular leukomalacia, epilepsy such as generalized epilepsy, which includes infantile spasms, absence epilepsy, myoclonic epilepsy which includes MERRF Syndrome, tonic-clonic epilepsy, partial epilepsy such as complex partial epilepsy, frontal lobe epilepsy and temporal lobe epilepsy, post-traumatic epilepsy, status epilepticus such as Epilepsia Partialis Continua, and Hallervorden-Spatz Syndrome.

Additional neurologic diseases which can be treated or detected with modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention include hydrocephalus such as Dandy-Walker Syndrome and normal pressure hydrocephalus, hypothalamic diseases such as hypothalamic neoplasms, cerebral malaria, narcolepsy which includes cataplexy, bulbar poliomyelitis, cerebripseudo tumor, Rett Syndrome, Reye's Syndrome, thalamic diseases, cerebral toxoplasmosis, intracranialtuberculoma and Zellweger Syndrome, central nervous system infections such as AIDS, Dementia Complex, Brain Abscess, subdural empyema, encephalomyelitis such as Equine Encephalomyelitis, Venezuelan Equine Encephalomyelitis, Necrotizing Hemorrhabaic Encephalomyelitis, Visna, and cerebral malaria.

Additional neurologic diseases which can be treated or detected with modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention include meningitis such as arachnoiditis, aseptic meningitis such as viral meningitis which includes lymphocytic chronic meningitis, Bacterial meningitis which includes Haemophilus Meningitis, Listeria Meningitis, Meningococcal Meningitis such as Waterhouse-Fridericlisen Syndrome, Pneumococcal Meningitis and meningeal tuberculosis, fungal meningitis such as Cryptococcal Meningitis, subdural effusion, meningencephalitis, myelitis such as transverse myelitis, neurosyphilis such as tabes dorsalis, poliomyelitis which includes bulbar poliomyelitis and post poliomyelitis syndrome, prion diseases (such as Creutzfeldt-Jakob Syndrome, Bovine Spongiform Encephalopathy, Gerstmann-Straussler Syndrome, Kuru, Scrapie), and cerebral toxoplasmosis.

Additional neurologic diseases which can be treated or detected with modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention include central nervous system neoplasms such as brain neoplasms that include cerebellarneoplasms such as infratentorial neoplasms, cerebral ventricle neoplasms such as choroids plexus neoplasms, hypothalamic neoplasms and supratentorial neoplasms, meningealneoplasms, spinal cord neoplasms which include epidural neoplasms, demyelinating diseases such as Canavan Diseases, diffuse cerebral sculleries which include sadrenoleukodystrophy, encephalitis periaxialis, globoid cell leukodystrophy, diffuse cerebral sclerosis such as metachromatic leukodystrophy, allergic encephalomyelitis, necrotizing hemorrhagic encephalomyelitis, progressive multifocal leukoencephalopathy, in multiple sclerosis, central pontine myelinolysis, transverse myelitis, neuromyelitis optica, Scrapie, Swayback, Chronic Fatigue Syndrome, Visna, High Pressure Nervous Syndrome, Meningism, spinal cord diseases such as amyotonia congenita, amyotrophic lateral-sclerosis, spinal muscular atrophy such as Werdnig-Hoffmann Disease, spinal cord compression, spinal cord neoplasms such as epidural neoplasms, syringomyelia, Tabes Dorsalis, Stiff-Man Syndrome, mental retardation such as Angelman Syndrome, Cri-du-Chat Syndrome, De Lange's Syndrome, Down Syndrome, Gangliosidoses such as gangliosidoses G(MI), Sandhoff Disease, Tay-Sachs Disease, Hartnup Disease, homocystinuria, Laurence-Moon-Bied Syndrome, Lesch-Nylian Syndrome, Maple Syrup Urine Disease, mucolipidosis such as fucosidosis, neuronal ceroid-lipofuscinosis, oculocerebrorenal syndrome, phenylketonuria such as maternal phenylketonuria, Prader-Willi Syndrome, Rett Syndrome, Rubinstein-Taybi Syndrome, Tuberous Sclerosis, WAGR Syndrome, nervous system abnormalities such as holoprosencephaly, neural tube defects such as anencephaly which includes hydrangencephaly, Arnold-Chairi Deformity, encephalocele, meningocele, meningomyelocele, spinal dysraphism such as Spina bifida cystica and spina bifida occulta.

Endocrine system and/or hormone imbalance and/or diseases encompass disorders of uterine motility including, but not limited to complications with pregnancy and labor (e.g., pre-term labor, post-term pregnancy, spontaneous abortion, and slow or stopped labor); and disorders and/or diseases of the menstrual cycle, (e.g., dysmenorrhea and endometriosis).

Endocrine system and/or hormone imbalance disorders and/or diseases include disorders and/or diseases of the pancreas, such as, for example, diabetes mellitus, diabetes insipidus, congenital pancreatic agenesis, pheochromocytoma islet cell tumor syndrome; disorders and/or diseases of the adrenal glands such as, for example, Addison's Disease, corticosteroid deficiency, virilizing disease, hirsutism, Cushing's Syndrome, hyperaldosterlonism, pheochromocytoma; disorders and/or diseases of the pituitary gland, such as, for example, hyperpituitarism, hypopituitarism, pituitary dwarfism, pituitary adenoma, panhypopituitarism, acromegaly, gigantism; disorders and/or diseases of the thyroid, including but not limited to, hyperthyroidism, hypothyroidism, Plummer's disease, Graves' disease (toxic diffuse goiter), toxic nodular goiter, thyroiditis (Hashimoto's thyroiditis, subacute granulomatous thyroiditis, and silent lymphocytic thyroiditis), Pendred's syndrome, myxedema, cretinism, thyrotoxicosis, thyroid hormone coupling defect, thymic aplasia, Hurthle cell tumors of the thyroid, thyroid cancer, thyroid carcinoma, Medullary thyroid carcinoma; disorders and/or diseases of the parathyroid, such as, for example, hyperparathyroidism, hypoparathyroidism; disorders and/or diseases of the hypothalamus.

In addition, endocrine system and/or hormone imbalance disorders and/or diseases may also include disorders and/or diseases of the testes or ovaries, including cancer. Other disorders and/or diseases of the testes or ovaries further include, for example, ovarian cancer, polycystic ovary syndrome, Klinefelter's syndrome, vanishing testes syndrome (bilateral anorchia), congenital absence of Leydig's cells, cryptorchidism, Noonan's syndrome, myotonic dystrophy, capillary haemangioma of the testis (benign), neoplasias of the testis and neotestis.

Moreover, endocrine system and/or hormone imbalance disorders and/or diseases may also include disorders and/or diseases such as, for example, polyglandular deficiency syndromes, pheochromocytoma, neuroblastoma, multiple Endocrine neoplasia, and disorders and/or cancers of endocrine tissues.

The modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be used for the diagnosis, treatment, or prevention of diseases and/or disorders of the reproductive system. Reproductive system disorders that can be treated by the compositions of the invention, include, but are not limited to, reproductive system injuries, infections, neoplastic disorders, congenital defects, and diseases or disorders will result in infertility, complications with pregnancy, labor, or parturition, and postpartum difficulties.

Reproductive system disorders and/or diseases include diseases and/or disorders, of the testes, including testicular atrophy, testicular feminization, cryptorchism (unilateral and bilateral), anorchia, ectopic testis, epididymitis and orchitis (typically resulting from infections such as, for example, gonorrhea, mumps, tuberculosis, and syphilis), testiculartorsiori, vasitis nodosa, germ cell tumors (e.g., seminomas, embryonal cell carcinomas, teratocarcinomas, choriocarcinomas, yolk sac tumors, and teratomas), stromal tumors (e.g., Leydig cell tumors), hydrocele, hematocele, varicocele, spermatocele, inguinal hemia, and disorders of sperm production (e.g., immotile cilia syndrome, spermia, asthenozoospermia, azoospermia, oligospermia, and teratozoospermia).

Reproductive system disorders also include disorders of the prostate gland, such as acute non-bacterial prostatitis, chronic non-bacterial prostatitis, acute bacterial prostatitis, chronic bacterial prostatitis, postatodystonia, prostatosis, granulomatotis prostatitis, malacoplakia, benign prostatic hypertrophy or hyperplasia, and prostate neoplastic disorders, including adenocarcinomas, transitional cell carcinomas, ductal carcinomas, and squamous cell carcinomas.

Additionally, the compositions of the invention may be useful in the diagnosis, treatment, and/or prevention of disorders or diseases of the penis and urethra, including inflammatory disorders, such as balanoposthitis, balanitis xerotica obliterans, phimosis, paraphmosis, syphilis, herpes simplex virus, gonorrhea, non-gonococcal urethritis, chlamydia, mycoplasma, trichomonas, HIV, AIDS, Reiter's syndrome, condyloma acuminatum, condyloma latum, and pearly penile papules, urethral abnormalities, such as hypospadias, epispadias, and phimosis, premalignant lesions, including Erythroplasia of Queyrat, Bowen's disease, Bowenoid paplosis, criant condyloma of Buscke-Lowenstein, and varrucous carcinoma; penile cancers, including squamous cell carcinomas, carcinoma in situ, verrucous carcinoma, and disseminated penile carcinoma; urethral neoplastic disorders, including penile urethial carcinoma, bulbomembranotis urethial carcinoma, and prostaticurethral carcinoma; and erectile disorders, such as priapism, Peyronie's disease, erectile dysfunction, and impotence.

Moreover, diseases and/or disorders of the vas deferens include vasculititis and CBAVD (congenital bilateral absence of the vas deferens); additionally, the transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be used in the diagnosis, treatment, and/or prevention of diseases and/or disorders of the seminal vesicles, including hydatid disease, congenital chloride diarrhea, and polycystic kidney disease.

Other disorders and/or diseases of the male reproductive system include, for example, Klinefelters syndrome, Young's syndrome, premature ejaculation, diabetes mellitus, cystic fibrosis, Kartagener's syndrome, high fever, multiple sclerosis, and gynecomastia.

Further, the polynucleotides, modified fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be used in the diagnosis treatment and/or prevention of diseases and/or disorders of the vagina and vulva, including bacterial vaginosis, candida vaginitis, herpes simplex virus, chancroid, granuloma inguinale, lymphogranuloma venereum, scabies, human papillomavirus, vaginal trauma, vulvartrauma, adenosis, chlamydia vaginitis, gonorrhea, trichomonas vaginitis, condylomaacuminatum, syphilis, molluscum contagiosum, atrophic vaginitis, Paaet's disease, lichensclerosus, lichen planus, vulvodynia, toxic shock syndrome, vaginismus, vulvovaginitis, vulvar vestibulitis, and neoplastic disorders, such as squamous cell hyperplasia, clear cell carcinoma, basal cell carcinoma, melanomas, cancer of Bartholin's gland, and vulvarintraepaelial neoplasia.

Disorders and/or diseases of the uterus include dysmenorrhea, retroverted uterus, endometriosis, fibroids, adenomyosis, anovulatory bleeding, amenorrhea, Cushiner's syndrome, hydatidiform moles, Asherman's syndrome, premature menopause, precocious puberty, uterine polyps, dysfunctional uterine bleeding (e.g., due to aberrant hormonal signals), and neoplastic disorders, such as adenocarcinomas, keiomyosarcomas, and sarcomas. Additionally, the transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may be useful as a marker or detector of, as well as, in the diagnosis, treatment, and/or prevention of congenital uterine abnormalities, such as bicomuate uterus, septate uterus, simple unicomuate uterus, unicomuate uterus with a noncavitary rudimentary horn, unicorriuate uterus with a non-communicating cavitary rudimentary horn, unicomuate uterus with a communicating cavitary horn, arcuate uterus, uterine didelfus, and T-shaped uterus.

Ovarian diseases and/or disorders include an ovulation, polycystic ovary syndrome (Stein-Leventhal syndrome), ovarian cysts, ovarian hypofunction, ovarian insensitivity to gonadotropins, ovarian over production of androgens, right ovarian vein syndrome, in amenorrhea, hirutism, and ovarian cancer (including, but not limited to, primary and secondary cancerous growth, Sertoli-Leydig tumors, endometriod carcinoma of the ovary, ovarian papillary serous adenocarcinoma, ovarian mucinous adenocarcinoma, and Ovarian Krukenberg tumors).

Cervical diseases and/or disorders include cervicitis, chronic cervicitis, mucopurulent cervicitis, and cervical dysplasia, cervical polyps, Nabothian cysts, cervical erosion, cervical incompetence, and cervical neoplasms (including, for example, cervical carcinoma, squamous metaplasia, squamous cell carcinoma, adenosquamous cell neoplasia, and columnar cell neoplasia).

Modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention can be used to treat or detect infectious agents. For example, by increasing the immune response, particularly increasing the proliferation and differentiation of B and/or T cells, infectious diseases may be treated. The immune response may be increased by either enhancing an existing immune response, or by fusion proteins of the invention and/or initiating a new immune response. Alternatively, polynucleotides encoding transferrin fusion proteins of the invention may also directly inhibit infectious agent, without necessarily eliciting an immune response.

Viruses are one example of an infectious agent that can cause disease or symptoms that can be treated or detected by transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention. Examples of viruses, include, but are not limited to the following DNA and RNA viruses and viral families: Arbovirus, Adenoviridae, Arenaviridae, Arterivirus, Bimaviridae, Bunyaviridae, Caliciviridae, Circoviridae, Coronaviridae, Dengue, EBV, HIV, Flaviviridae, Hepadnaviridae Hepatitis, Herpesviridae (such as, Cytomegalovirus, Herpes Simplex, Herpes Zoster), Mononegavirus (e.g., Paramyxoviridae, Morbillivirus, Rhabdoviridae), Orthomyxoviridae (e.g., Influenza A, Influenza B, and parainfluenza), Papilloma virus, Papovaviridae, Parvoviridae, Picomaviridae, Poxviridae (such as Smallpox or Vaccinia), Reoviridae (e.g., Rotavirus), Retroviridae (HTLV-I, HTLV-11, -Lentivirus), and Togaviridae (e.g., Rubivirus).

Similarly, bacterial and fungal agents that can cause disease or symptoms that can be treated or detected by transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention include, but not limited to, the following Gram-negative and Gram-positive bacteria, bacterial families, and fungi: Actinomyces (e.g., Norcardia), Acinetobacter, Cryptococcus neoformans, Aspergillus, Bacillaceae (e.g., Bacillus anthrasis), Bacteroides (e.g., Bacteroides fragilis), Blastoinycosis, Bordetella, Borrelia (e.g., Borrelia burgdorferi), Brucella, Candidia, Campyobacter, Chlamydia, Clostridiuffi (e.g., Clostridium botulinum, Clostridium dificile, Clostridium perfringens, Clostridiumtetani), Coccidioides, Corynebacterium (e.g., Corynebacterium-diptheriae), Cryptococcus, Dermatocycoses, E. coli (e.g., Enterotoxigenic E. coli and Enterohemorrhagic E. coli), Enterobacter (e.g. Enterobacter aerogenes), Enterobacteriaceae (Klebsiella, Salmonella (e.g., Salmonella typhi, Salmonella enteritidis, Salmonella typhi), Serratia, Yersinia, Shigella), Erysipelothrix, Haemophilus (e.g., Haemophlilus influenza type B), Helicobacter, Legionella (e.g., Legionella pneumophila), Leptospira, Listeria (e.g., Listeria monocytogenes), Mycoplasma, Mycobacterium (e.g., Mycobacterium leprae and Mycobacterium tuberculosis), Vibrio (e.g., Vibrio cholerae), Neisseriaceae (e.g., Neisseriagonorrhea, Neisseria meningitidis), Pasteurellaceae, Proteus, Pseudomonas (e.g., Pseudomionas aeruginosa), Rickettsiaceae, Spirochetes (e.g., Treponema. spp., Leptospira spp., Borrielia spp.), Shigella spp., Staphlylococcus (e.g., Staphylococcus aureus), Meningiococcus, Pneumnococcus and Streptococcus (e.g., Streptococcus pneumoniae and Groups A, B, and C Streptococci), and Ureaplasmas.

Moreover, parasitic agents causing disease or that can be treated, prevented, and/or diagnosed by fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention include, but not limited to, the following families or class: Amebiasis, Babesiosis, Coccidiosis, Cryptosporidiosis, Dientamoebiasis, Dourine, Ectoparasitic, Giardias, Helminthiasis, Leishmaniasis, Schistisoma, Theileriasis, Toxoplasmosis, Trypanosomiasis, and Trichomonas and Sporozoans (e.g., Plasmodium vivax, Plasmodium falciparium, Plasmodium malariae and Plasmodium ovale).

Modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention can be used to differentiate, proliferate, and attract cells, pleading to the regeneration of tissues. (See, Science 276:59-87 (1997)). The regeneration of tissues could be used to repair, replace, or protect tissue damaged by congenital defects, trauma (wounds, burns, incisions, or ulcers), age, disease (e.g. osteoporosis, osteocarthritis, periodontal disease, liver failure), surgery, including cosmetic plastic surgery, fibrosis, reperfusion injury, or systemic cytokine damage.

Tissues that could be regenerated using the present invention include organs (e.g., pancreas, liver, intestine, kidney, skin, endothelium), muscle (smooth, skeletal or cardiac), vasculature (including vascular and lymphatics), nervous, hematopoietic, and skeletal (bone, cartilage, tendon, and ligament) tissue. Preferably, regeneration occurs without or decreased scarring. Regeneration also may include angiogenesis.

Modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention, may be used to treat, prevent, diagnose, and/or prognose gastrointestinal disorders, including inflammatory diseases and/or conditions, infections, cancers (e.g., intestinal neoplasms (carcinoid tumor of the small intestine, non-Hodgkin's lymphoma of the small intestine, small bowel lymphoma), and ulcers, such as peptic ulcers.

Gastrointestinal disorders include dysphagia, odynophagia, inflammation of the esophagus, peptic esophagitis, gastric reflux, submucosal fibrosis and structuring, Mallory-Weiss lesions, lipomas, epidermal cancers, adeoncarcinomas, gastric retention disorders, gastroenteritis, gastric atrophy, gastric/stomach cancers, polyps of the stomach, autoimmune disorders such as pemicious anemia, pyloric stenosis, gastritis (bacterial, viral, eosinophilic, stress-induced, chronic erosive, atrophic, plasma cell, and Menetrier's), and peritoneal diseases (e.g., chylo perioneum, hemoperitoneum, mesenteric cyst, mesentericlymphadenitis, mesenteric vascular occlusion, panniculiti, neoplasms, peritonitis, pneumoperitoneum, bubphrenic abscess.

Gastrointestinal disorders also include disorders associated with the small intestine, such as malabsorption syndrome's, distension, irritable bowel syndrome, sugar intolerance, celiac disease, duodenal ulcers, duodenitis, tropical sprue, Whipple's disease, intestinal lymphangiectasia, Crohn's disease, appendicitis, obstructions of the ileum, Meckel's diverticulum, multiple diverticula, failure of complete rotation of the small and large intestine, lymphoma, and bacterial and parasitic diseases (such as Traveler's diarrhea, typhoid and paratyphoid, cholera, infection by Roundworms (Ascariasis lumbricoides), Hookworms (Ancylostoina duodenale), Threadworms (Enterobius vermicularis), Tapeworms Taenia saginata, Echinococcus granulosus, Diphyllobothriumn spp. and T. solium).

Liver diseases and/or disorders include intrahepatic cholestasis (Alagille syndrome, biliary liver cirrhosis), fatty, liver (alcoholic fatty liver, Reye's syndrome), hepatic veiri, thrombosis, hepatolentricular degeneration, hepatomegaly, hepatopulmonary syndrome, hepatorenal, syndrome, portal hypertension (esophageal and gastric varices), liver abscess (amebic liver abscess), liver cirrhosis (alcoholic, biliary and experimental), alcoholic liver diseases (fatty liver, hepatitis, cirrhosis), parasitic (hepatic echinococcosis, fascioliasis, amebic liver abscess), jaundice (hemolytic, hepatocellular, and cholestatic), cholestasis, portal hypertension, liver, enlargement, ascites, hepatitis (alcoholic hepatitis, intra-familial hepatitis, chronic hepatitis (autoimmune, hepatitis B, hepatitis C, hepatitis D, drug induced), toxic hepatitis, viral human hepatitis (hepatitis A, hepatitis B, hepatitis C, hepatitis D, hepatitis E), Wilson's disease, granulomatous hepatitis, secondary biliary cirrhosis, hepaticencephalopathy, portal hypertension, varices, hepatic encephalopathy, primary biliary hemangiomas, bilecirrhosis, primary sclerosing cholangitis, hepatocellular adenoma, stones, liver failure (hepatic encephalopathy, acute liver failure), and liver neoplasms (ancriomyolipoma, calcified liver metastases, cystic liver metastases, epithelial tumors, fibro lamellar hepatocarcinoma, focal nodular hyperplasia, hepatic adenoma, hepatobiliarycystadenoma, hepatoblastoma, hepatocellular carcinoma, hepatoma, liver cancer, liver hemangioendothelioma, mesenchymal hamartoma, mesenchymal tumors of liver, nodular regenerative hyperplasia, benign liver tumors (Hepatic cysts, Simple cysts, Polycystic liver disease, Hepatobiliary cystadenoma, Choledochal cysts, Mesenchymal tumors, Mesenchymal hamartoma, Infantile hemangioendothelioma, Hemangioma, Peliosis hepatis, Lipomas, Inflammatory pseudo tumor, Miscellaneous Epithelial tumors, Bile duct epithelium (Bile duct hamartoma, Bile duct adenoma), Hepatocyte (Adenoma, Focal nodular hyperplasia, Nodular regenerative hyperplasia), malignant liver tumors (hepatocellular, hepatoblastoma, hepatocellular carcinoma, cholangiocellular, cholangiocarcinoma, cystadenocarcinoma, tumors of blood vessels, anaiosarcoma, Karposi's sarcoma, hemangioendothelioma, other tumors, embryonal sarcorria, fibrosarcoma, rhabdomyosarcoma, carcinosarcoma, teratoma, carcinoid, squamous carcinoma, primarylymphorria)), peliosis hepatis, erythrohepatic porphyria, hepatic porphyria (acute interirtittentporphyria, polphyria cutanea tarda), Zelli Neger syndrome).

Pancreatic diseases and/or disorders include acute pancreatitis, chronic pancreatitis (acute necrotizing pancreatitis, alcoholic pancreatitis), neoplasms (adenocarcinoma of the pancreas, cystadenocarcinoma, insulinoma, gastrinoma, and glucacronoma, cysticcitmeoplasms, islet-cell tumors, pancreoblastoma), and other pancreatic diseases (e.g., cysticfibrosis, cyst (pancreatic pseudocyst, pancreatic fistula, insufficiency)).

Gallbladder diseases include gallstones (cholelithiasis and choledocholithiasis), postcholeeystectomy syndrome, diverticulosis of the gallbladder, acute cholecystitis, chronic cholecystitis, bile duct tumors, and mucocele.

Diseases and/or disorders of the large intestine include antibiotic-associated colitis, diverticulitis, ulcerative colitis, acquired megacolon, abscesses, fungal and bacterial infections, anorectal disorders (e.g., fissures, hemorrhoids), colonic diseases (colitis, colonic neoplastris, colon cancer, adenomatous colon polyps (e.g., villous adenoma), coloncarcinoma, colorectal cancer, colonic diverticulitis, colonic diverticulosis, megacolon, Hirschsprung disease, toxic inegacolon, sigmoid diseases proctocolitis, sigmoinneoplasmsj, constipation, Crohn's disease, diarrhea (infantile diarrhea, dysentery), duodenal diseases (duodenal neoplasins, duodenal obstruction, duodenal ulcer, duodenitis), enteritis (enterocolitis), HIV enteropathy, leal diseases (leal neoplasins, ileitis), immunoproliferative small intestinal disease, inflammatory bowel disease (ulcerative colitis, Crohn's disease), intestinal atresia, parasitic diseases (anisakiasis, balantidiasis, blastocystis infections, cryptosporidiosis, dientamoebiasis, amebic dysentery, giardiasis), intestinal fistula (rectal fistula), intestinal neoplasms (cecal neoplasms, colonic neoplasms, duodenalpneoplasms, leal neoplasms, intestinal polyps, jejunal neoplasins, rectal neoplasms), intestinal obstruction (afferent loop syndrome, duodenal obstruction, impacted feces, intestinal pseudo obstruction cecal volvulus, intussusception), intestinal perforation, intestinal polyps (colonic polyps, gardner syndrome, peutz-jeghers syndrome), jejunal diseases Oejunal neoplasms), mal absorption syndromes (blind loop syndrome, celiac disease, lactose intolerance, short bowl syndrome, tropical sprue, whipple's disease), mesenteric vascular occlusion, pneumatosis cystoides intestinalis, protein losing enteropathies (intestinal lymphagiectasis), rectal diseases (anus diseases, fecal incontinence, hemorrhoids, proctitis, rectal fistula, rectal prolapse, rectocele), peptic ulcer (duodenalulcer, peptic esophagitis, hemorrhage, perforation, stomach ulcer, Zollinger-Ellison syndrome), postgastrectomy syndromes (dumping syndrome), stomach diseases (e.g., achlorhydria, duodenogastric reflux (bile reflux), gastric antral vascular ectasia, gastricfistula, gastric outlet obstruction, gastritis (atrophic or hypertrophic), gastroparesis, stomach dilatation, stomach diverticulum, stomach neoplasms (gastric cancer, gastric polyps, gastric adenocarcinoma, hyperplastic gastric polyp), stomach rupture, stomach ulcer, stomach volvulus), tuberculosis, visceroptosis, vomiting (e.g., hematemesis, hyperemesisgravidarum, postoperative nausea- and vomiting) and hemorrhagic colitis.

Further diseases and/or disorders of the gastrointestinal system include biliary tract diseases, such as, gastroschisis, fistula (e.g., biliary fistula, esophageal fistula, gastricfistula, intestinal fistula, pancreatic fistula), neoplasms (e.g., biliary tract neoplasins, esophageal neoplasms, such as adenocarcinoma of the esophagus, esophageal squamous cell carcinoma, gastrointestinal neoplasms, pancreatic neoplasins, such as adenocarcinoma of the pancreas, mucinous cystic neoplasm of the pancreas, pancreatic eystic neoplasms, pancreatoblastoma, and peritoneal neoplasms), esophageal disease (e.g., bullous diseases, candidiasis, glycoaenie acanthosis, ulceration, barrett esophagus varices, atresia, cyst, diverticulum. (e.g., Zenker's diverticulum), fistula (e.g., tracheoesophageal fistula), motility disorders (e.g., CREST syndrome, deglutition disorders, achalasia, spasm, gastroesophageal reflux), neoplasms, perforation (e.g., Boerhaave syndrome, Mallory-Weiss syndrome), stenosis, esophagitis, diaphragmatic hernia (e.g., hiatal hernia); gastrointestinal diseases, such as, gastroenteritis (e.g., cholera morbus, norwalk virus infection), hemorrhage (e.g., hematemesis, melena, peptic ulcer hemorrhage), stomach neoplasms (gastric cancer, gastric polyps, gastric adenocarcinoma, stomach cancer)), hernia (e.g., congenital diaphragmatic hernia, femoral hernia, inguinal hernia, obturator hernia, umbilical hernia, ventral hernia), and intestinal diseases (e.g., cecal diseases (appendicitis, cecal neoplasms)).

Modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may have chemotaxis activity. A chemotaxic molecule attracts or mobilizes cells (e.g., monocytes, fibroblasts, neutrophils, T-cells, mast cells, eosinophils, epithelial and/or endothelial cells) to a particular site in the body, such as inflammation, infection, or site of hyperproliferation. The mobilized cells can then fight off and/or heal the particular trauma or abnormality.

Modified transferrin fusion proteins of the invention and/or polynucleotides encoding transferrin fusion proteins of the invention may increase chemotaxic activity of particular cells. These chemotactic molecules can then be used to treat inflammation, infection, hyperproliferative disorders, or any immune system disorder by increasing the number of cells targeted to a particular location in the body.

Transgenic Animals

The production of transgenic non-human animals that contain a modified transferrin fusion construct with increased serum half-life increased serum stability or increased bioavailability of the instant invention is contemplated in one embodiment of the present invention. In some embodiments, lactoferrin may be used as the Tf portion of the fusion protein so that the fusion protein is produced and secreted in milk. In other embodiments, the present invention includes producing Tf fusion proteins in milk.

The successful production of transgenic, non-human animals has been described in a number of patents and publications, such as, for example U.S. Pat. No. 6,291,740 (issued Sep. 18, 2001); U.S. Pat. No. 6,281,408 (issued Aug. 28, 2001); and U.S. Pat. No. 6,271,436 (issued Aug. 7, 2001) the contents of which are hereby incorporated by reference in their entireties.

The ability to alter the genetic make-up of animals, such as domesticated mammals including cows, pigs, goats, horses, cattle, and sheep, allows a number of commercial applications. These applications include the production of animals which express large quantities of exogenous proteins in an easily harvested form (e.g., expression into the milk or blood), the production of animals with increased weight gain, feed efficiency, carcass composition, milk production or content, disease resistance and resistance to infection by specific microorganisms and the production of animals having enhanced growth rates or reproductive performance. Animals which contain exogenous DNA sequences in their genome are referred to as transgenic animals.

The most widely used method for the production of transgenic animals is the microinjection of DNA into the pronuclei of fertilized embryos (Wall et al., J. Cell. Biochem. 49:113 [1992]). Other methods for the production of transgenic animals include the infection of embryos with retroviruses or with retroviral vectors. Infection of both pre- and post-implantation mouse embryos with either wild-type or recombinant retroviruses has been reported (Janenich, Proc. Natl. Acad. Sci. USA 73:1260 [1976]; Janenich et al, Cell 24:519 [1981]; Stuhlmann et al., Proc. Natl. Acad. Sci. USA 81:7151 [1984]; Jahner et al., Proc. Natl. Acad Sci. USA 82:6927 [1985]; Van der Putten et al., Proc. Natl. Acad Sci. USA 82:6148-6152 [1985]; Stewart et al., EMBO J. 6:383-388 [1987]).

An alternative means for infecting embryos with retroviruses is the injection of virus or virus-producing cells into the blastocoele of mouse embryos (Jahner, D. et al., Nature 298:623 [1982]). The introduction of transgenes into the germline of mice has been reported using intrauterine retroviral infection of the midgestation mouse embryo (Jahner et al., supra [1982]). Infection of bovine and ovine embryos with retroviruses or retroviral vectors to create transgenic animals has been reported. These protocols involve the micro-injection of retroviral particles or growth arrested (i.e., mitomycin C-treated) cells which shed retroviral particles into the perivitelline space of fertilized eggs or early embryos (PCT International Application WO 90/08832 [1990]; and Haskell and Bowen, Mol. Reprod. Dev., 40:386 [1995]. PCT International Application WO 90/08832 describes the injection of wild-type feline leukemia virus B into the perivitelline space of sheep embryos at the 2 to 8 cell stage. Fetuses derived from injected embryos were shown to contain multiple sites of integration.

U.S. Pat. No. 6,291,740 (issued Sep. 18, 2001) describes the production of transgenic animals by the introduction of exogenous DNA into pre-maturation oocytes and mature, unfertilized oocytes (i.e., pre-fertilization oocytes) using retroviral vectors which transduce dividing cells (e.g., vectors derived from murine leukemia virus [MLV]). This patent also describes methods and compositions for cytomegalovirus promoter-driven, as well as mouse mammary tumor LTR expression of various recombinant proteins.

U.S. Pat. No. 6,281,408 (issued Aug. 28, 2001) describes methods for producing transgenic animals using embryonic stem cells. Briefly, the embryonic stem cells are used in a mixed cell co-culture with a morula to generate transgenic animals. Foreign genetic material is introduced into the embryonic stem cells prior to co-culturing by, for example, electroporation, microinjection or retroviral delivery. ES cells transfected in this manner are selected for integrations of the gene via a selection marker such as neomycin.

U.S. Pat. No. 6,271,436 (issued Aug. 7, 2001) describes the production of transgenic animals using methods including isolation of primordial germ cells, culturing these cells to produce primordial germ cell-derived cell lines, transforming both the primordial germ cells and the cultured cell lines, and using these transformed cells and cell lines to generate transgenic animals. The efficiency at which transgenic animals are generated is greatly increased, thereby allowing the use of homologous recombination in producing transgenic non-rodent animal species.

Gene Therapy

The use of modified transferrin fusion constructs for gene therapy wherein a modified transferrin protein or transferrin domain is joined to a therapeutic protein or peptide is contemplated in one embodiment of this invention. The modified transferrin fusion constructs with increased serum half-life or serum stability of the instant invention are ideally suited to gene therapy treatments.

The successful use of gene therapy to express a soluble fusion protein has been described. Briefly, gene therapy via injection of an adenovirus vector containing a gene encoding a soluble fusion protein consisting of cytotoxic lymphocyte antigen 4 (CTLA4) and the Fc portion of human immunoglobulin G1 was recently shown in Ijima et al. (Human Gene Therapy (United States) 12/9:1063-77, 2001). In this application of gene therapy, a murine model of type II collagen-induced arthritis was successfully treated via intraarticular injection of the vector.

Gene therapy is also described in a number of U.S. patents including U.S. Pat. No. 6,225,290 (issued May 1, 2001); U.S. Pat. No. 6,187,305 (issued Feb. 13, 2001); and U.S. Pat. No. 6,140,111 (issued Oct. 31, 2000).

U.S. Pat. No. 6,225,290 provides methods and constructs whereby intestinal epithelial cells of a mammalian subject are genetically altered to operatively incorporate a gene which expresses a protein which has a desired therapeutic effect. Intestinal cell transformation is accomplished by administration of a formulation composed primarily of naked DNA, and the DNA may be administered orally. Oral or other intragastrointestinal routes of administration provide a simple method of administration, while the use of naked nucleic acid avoids the complications associated with use of viral vectors to accomplish gene therapy. The expressed protein is secreted directly into the gastrointestinal tract and/or blood stream to obtain therapeutic blood levels of the protein thereby treating the patient in need of the protein. The transformed intestinal epithelial cells provide short or long term therapeutic cures for diseases associated with a deficiency in a particular protein or which are amenable to treatment by overexpression of a protein.

U.S. Pat. No. 6,187,305 provides methods of gene or DNA targeting in cells of vertebrate, particularly mammalian, origin. Briefly, DNA is introduced into primary or secondary cells of vertebrate origin through homologous recombination or targeting of the DNA, which is introduced into genomic DNA of the primary or secondary cells at a preselected site.

U.S. Pat. No. 6,140,111 (issued Oct. 31, 2000) describes retroviral gene therapy vectors. The disclosed retroviral vectors include an insertion site for genes of interest and are capable of expressing high levels of the protein derived from the genes of interest in a wide variety of transfected cell types. Also disclosed are retroviral vectors lacking a selectable marker, thus rendering them suitable for human gene therapy in the treatment of a variety of disease states without the co-expression of a marker product, such as an antibiotic. These retroviral vectors are especially suited for use in certain packaging cell lines. The ability of retroviral vectors to insert into the genome of mammalian cells has made them particularly promising candidates for use in the genetic therapy of genetic diseases in humans and animals. Genetic therapy typically involves (1) adding new genetic material to patient cells in vivo, or (2) removing patient cells from the body, adding new genetic material to the cells and reintroducing them into the body, i.e., in vitro gene therapy. Discussions of how to perform gene therapy in a variety of cells using retroviral vectors can be found, for example, in U.S. Pat. No. 4,868,116, issued Sep. 19, 1989, and U.S. Pat. No. 4,980,286, issued Dec. 25, 1990 (epithelial cells), WO89/07136 published Aug. 10, 1989 (hepatocyte cells), EP 378,576 published Jul. 25, 1990 (fibroblast cells), and WO89/05345 published Jun. 15, 1989 and WO/90/06997, published Jun. 28, 1990 (endothelial cells), the disclosures of which are incorporated herein by reference.

Without further description, it is believed that a person of ordinary skill in the art can, using the preceding description and the following illustrative examples, make and utilize the present invention and practice the claimed methods. For example, a skilled artisan would readily be able to determine the biological activity, both in vitro and in vivo, for the fusion protein constructs of the present invention as compared with the comparable activity of the therapeutic moiety fused to transferrin. Similarly, a person skilled in the art could readily determine the serum half life and serum stability of constructs according to the present invention. The following working examples therefore, specifically point out the preferred embodiments of the present invention, and are not to be construed as limiting in any way the remainder of the disclosure.

EXAMPLES
Example 1
NC(N) Transferrin

The starting point for this variant is transferrin into which the regions around the N glycosylation sites of the C domain (N413-S415 and N611-T613 of SEQ ID NO: 3) are replaced by grafting over the structurally equivalent regions of the N domain.

N413

The region 413-427 (SEQ ID NO: 3) of the C domain is replaced with 86-96 (SEQ ID NO: 3) of the N domain. The exact region replaced can extent further at each side of the residues given to improve the remodeling should it be required. As can be seen below the sequence around the regions highlighted for replacement (boxed), the structure of the N and C domain is almost identical.
embedded image

As part of the remodeling of this region it is necessary to mutate C637 (SEQ ID NO: 3) to e.g. G637. C637 (SEQ ID NO: 3) forms a disulfide bond C418, which is replaced in this remodeling. If C637 were not mutated a free cysteine would remain.

N611

The region 610-620 (SEQ ID NO: 3) of the C domain is replaced with 276-283 (SEQ ID NO: 3) of the N domain. The exact region replaced can extend further at each side of the residues given to improve the remodeling should it be required. As can be seen below the sequence around the regions highlighted for replacement (boxed), the structure of the N and C domain is almost identical. The cysteines in this segment, C615 and C620 form a disulfide bond between themselves so no further changes are required to address this.
embedded image

Example 2
NN Transferrin

This variant(s) of transferrin comprises a duplication of the N domain. The sequence used is amino acids 4-330 with T5 mutated to P5 to provide the kink required in this region. To make such a variant the cDNA requires codon optimization for one or other of the two N domains to prevent homologous recombination in the expression vector.

The point at which the second N domain is attached can involve most, if not all, of the peptide linker (331-339). If all the linker were used then a free cysteine would be included as C339 normally forms a disulfide bond with C596 in the C domain for which there is no equivalent in the N domain. Two options exist here, mutate or delete C339 and leave the rest of the molecule as is or leave C339 and remove, mutate, or graft over the structurally equivalent region of the C domain.
embedded image

The C-terminus of the NN variant differs from that of the normal C-terminus of Tf in that it ends 13 amino acids shorter. There are a further two options, add the normal C-terminus onto the end of the second N domain or continue the end of the N domain by using the peptide linker in some form.
embedded image

Using the natural C-terminus (TSSLLEACTFRRP, amino acids 667 to 679 of SEQ ID NO: 3) of the C-domain would require mutation of C674 to e.g. G674 as this residue normally forms a disulfide bond with C402 of the C domain. This disulfide normally anchors the C-terminus and as such its deletion may render the C-terminus more accessible. Alternatively N74, the structural equivalent of C402, could be removed, mutated to a cysteine or the region grafted over with the similar region of the C domain.
embedded image

If the linker peptide (CPEAPTDEC, amino acids 331-339 of SEQ ID NO: 3) were included, with the deletion of the terminal cysteine, the C-terminus would be orientated differently due to being kinked in the opposite direction to the normal C-terminus. For a C-terminal fusion this may result in better bioavailability as it is more exposed. A disulfide bond could, potentially, anchor the peptide. In the C-terminus there is a disulfide bond formed between C474 and C655. This bond could be introduced by mutating G229 of the second N domain to a cysteine. Alternatively C331 may naturally form a bond with C474. If neither of these options occurs C474 would need to be mutated to prevent a free cysteine remaining. The modification to the duplicated N-domain could be taken further using more of the structurally equivalent regions of the C domain if this were to be deemed necessary.

A model for NN Transferrin was constructed by overlaying a second N domain (9-339), N′, onto the Hu Tf model, deleting the C domain of Hu Tf back to 344 and then ligating the two N-domains together. From there on changes were made as detailed above.
embedded image

Although the present invention has been described in detail with reference to examples above, it is understood that various modifications can be made without departing from the spirit of the invention. Accordingly, the invention is limited only by the following claims. All cited patents, patent applications and publications referred to in this application are herein incorporated by reference in their entirety.

Modified transferrin fusion proteins comprising duplicate transferrin amino or carboxy terminal domains

Information

Publication Number

Date Filed

Date Published

Inventors

CPC

US Classifications

International Classifications

Abstract

Description

Claims

RELATED APPLICATIONS

PCT Information

Provisional Applications (1)