Patent Grant
9315580
The present invention relates in general to the field of vaccines, and more particularly, to compositions and methods for targeting and delivering antigens to Langerhans cells for antigen presentation using high affinity anti-Langerin monoclonal antibodies and fusion proteins therewith.
None.
Without limiting the scope of the invention, its background is described in connection with antigen presentation.
Dendritic Cells (DCs) are professional antigen-presenting cells (APCs) that induce and sustain immune responses and are fundamental in establishing both tolerance and immunity. DCs capture and present antigens to CD4+ T cells, which then determine the quantity and quality of antigen-specific CD8+ T cells. There are subsets of DCs1,2, including both myeloid and plasmacytoid DCs (mDCs and pDCs, respectively).
Prior Langerin related agents include those taught in U.S. Pat. No. 6,878,528, issued to Duvert-Frances, et al., which include polynucleotides encoding a mammalian Langerhans cell antigen, including purified mammalian DC cell surface protein, designated Langerin, nucleic acids encoding Langerin, and antibodies which specifically bind Langerin.
Other anti-DC related agents are taught in, e.g., United States Patent Application Publication No. 20060257412, filed by Bowdish, et al., which includes a method of treating autoimmune disease by inducing antigen presentation by tolerance inducing antigen presenting cells. Briefly, this application teaches that antibodies to antigen presenting cells may be utilized to interfere with the interaction of the antigen presenting cell and immune cells, including T cells. Peptides may be linked to the antibodies thereby generating an immune response to such peptides, e.g., those peptides associated with autoimmunity.
In one embodiment, the present invention includes compositions and methods for activating T and B cell responses by targeting antigens to antigen presenting cells along with the proper activation of the APC to activate T cell and B cells responses. One embodiment is a vaccine comprising an isolated anti-Langerin antibody or binding fragment thereof and one or more antigenic peptides at the carboxy-terminus of the anti-Langerin antibody, wherein when two or more antigens are present, they are separated by one or more linker peptides that comprise at least one glycosylation site. In one aspect, the antibody binding fragment is selected from an Fv, Fab, Fab′, F(ab′)2, Fc, or a ScFv fragment. In another aspect, the antibody comprises one or more complementarity determining regions selected from:
or a direct equivalent thereof. In another aspect, the antigenic peptide is a cancer antigen selected from:
or binding fragments thereof. In another aspect, the antigenic peptide is a viral antigen selected from:
In another aspect, when two or more antigens are present, the antigens are separated by one or more peptide linkers are selected from:
In another aspect, the anti-Langerin antibody is selected from the following pairs of amino acid sequences SEQ ID NOS.: 2 and 4; 6 and 7; 52 and 54; 56 and 58; and 78 and 80 or binding fragments thereof. In another aspect, the anti-Langerin antibody is the expression product of the following pairs of nucleic acid sequences SEQ ID NOS.: 1 and 3; 5 and 6; 51 and 53; 55 and 57; and 77 and 79. In another aspect, the anti-Langerin antibody or binding fragment thereof is at least one of 15B10 having ATCC Accession No. PTA-9852, 2G3 having ATCC Accession No. PTA-9853, 91E7, 37C1, or 4C7 and humanized derivatives thereof. In another aspect, the anti-Langerin antibody or binding fragment thereof and the antigenic peptide are a fusion protein.
Another embodiment of the present invention includes an isolated nucleic acid vector that expresses an anti-Langerin antibody or binding fragment thereof and two or more antigenic peptides at the carboxy-terminus of the light chain, the heavy chain or both the light and heavy chains of the anti-Langerin antibody, wherein when two or more antigenic peptides are present, the antigenic peptides are separated by the one or more peptide linkers that comprise at least one glycosylation site. In one aspect, the antigenic peptides are cancer peptides selected from tumor associated antigens selected from CEA, prostate specific antigen (PSA), HER-2/neu, BAGE, GAGE, MAGE 1-4, 6 and 12, MUC (Mucin) (e.g., MUC-1, MUC-2, etc.), GM2 and GD2 gangliosides, ras, myc, tyrosinase, MART (melanoma antigen), MARCO-MART, cyclin B1, cyclin D, Pmel 17(gp100), GnT-V intron V sequence (N-acetylglucoaminyltransferase V intron V sequence), Prostate Ca psm, prostate serum antigen (PSA), PRAME (melanoma antigen), β-catenin, MUM-1-B (melanoma ubiquitous mutated gene product), GAGE (melanoma antigen) 1, BAGE (melanoma antigen) 2-10, c-ERB2 (Her2/neu), EBNA (Epstein-Barr Virus nuclear antigen) 1-6, gp75, human papilloma virus (HPV) E6 and E7, p53, lung resistance protein (LRP), Bcl-2, and Ki-67. In another aspect, the antigenic peptides are cancer peptides are selected from tumor associated antigens comprising antigens from leukemias and lymphomas, neurological tumors such as astrocytomas or glioblastomas, melanoma, breast cancer, lung cancer, head and neck cancer, gastrointestinal tumors, gastric cancer, colon cancer, liver cancer, pancreatic cancer, genitourinary tumors such cervix, uterus, ovarian cancer, vaginal cancer, testicular cancer, prostate cancer or penile cancer, bone tumors, vascular tumors, or cancers of the lip, nasopharynx, pharynx and oral cavity, esophagus, rectum, gall bladder, biliary tree, larynx, lung and bronchus, bladder, kidney, brain and other parts of the nervous system, thyroid, Hodgkin's disease, non-Hodgkin's lymphoma, multiple myeloma and leukemia. In another aspect, the antigenic peptides are selected from Influenza A Hemagglutinin HA-1 from a H1N1 Flu strain, HLA-A201-FluMP (58-66) peptide (GILGFVFTL (SEQ ID NO. 43)) tetramer, Avian Flu (HA5-1), dockerin domain from C. thermocellum (doc), HIV gag p24 (gag), or a string of HIV peptides (LipoS), PSA (KLQCVDLHV (SEQ ID NO. 44))-tetramer, or an HIVgag-derived p24-PLA. In another aspect, the anti-Langerin antibody is selected from the following pairs of amino acid sequences SEQ ID NOS.: 2 and 4; 6 and 8; 52 and 54; 56 and 58; and 78 and 80 or binding fragments thereof. In another aspect, the anti-Langerin antibody is the expression product of the following pairs of nucleic acid sequences SEQ ID NOS.: 1 and 3; 5 and 7; 51 and 53; 55 and 57; and 77 and 79. In another aspect, the anti-Langerin antibody or binding fragment thereof is at least one of 15B10 having ATCC Accession No. PTA-9852, 2G3 having ATCC Accession No. PTA-9853, 91E7, 37C1, or 4C7 and humanized derivatives thereof. In another aspect, the anti-Langerin antibody or binding fragment thereof and the antigenic peptide are a fusion protein.
Yet another embodiment of the present invention includes a method of enhancing T and B cell responses comprising: immunizing a subject in need of vaccination with an effective amount of a vaccine comprising an isolated fusion protein comprising an anti-Langerin antibody or binding portion thereof and one or more antigenic peptides linked to the carboxy-terminus of the anti-Langerin antibody. In one aspect, the antigenic peptides are cancer peptides selected from tumor associated antigens selected from CEA, prostate specific antigen (PSA), HER-2/neu, BAGE, GAGE, MAGE 1-4, 6 and 12, MUC (Mucin) (e.g., MUC-1, MUC-2, etc.), GM2 and GD2 gangliosides, ras, myc, tyrosinase, MART (melanoma antigen), MARCO-MART, cyclin B1, cyclin D, Pmel 17(gp100), GnT-V intron V sequence (N-acetylglucoaminyltransferase V intron V sequence), Prostate Ca psm, prostate serum antigen (PSA), PRAME (melanoma antigen), β-catenin, MUM-1-B (melanoma ubiquitous mutated gene product), GAGE (melanoma antigen) 1, BAGE (melanoma antigen) 2-10, c-ERB2 (Her2/neu), EBNA (Epstein-Ban Virus nuclear antigen) 1-6, gp75, human papilloma virus (HPV) E6 and E7, p53, lung resistance protein (LRP), Bcl-2, and Ki-67. In another aspect, the antigenic peptides are cancer peptides selected from tumor associated antigens comprising antigens from leukemias, lymphomas, neurological tumors such as astrocytomas or glioblastomas, melanoma, breast cancer, lung cancer, head and neck cancer, gastrointestinal tumors, gastric cancer, colon cancer, liver cancer, pancreatic cancer, genitourinary tumors such cervix, uterus, ovarian cancer, vaginal cancer, testicular cancer, prostate cancer or penile cancer, bone tumors, vascular tumors, or cancers of the lip, nasopharynx, pharynx and oral cavity, esophagus, rectum, gall bladder, biliary tree, larynx, lung and bronchus, bladder, kidney, brain and other parts of the nervous system, thyroid, Hodgkin's disease, non-Hodgkin's lymphoma, multiple myeloma and leukemia. In another aspect, the antigenic peptides are selected from Influenza A Hemagglutinin HA-1 from a H1N1 Flu strain, HLA-A201-FluMP (58-66) peptide (GILGFVFTL (SEQ ID NO. 43)) tetramer, Avian Flu (HA5-1), Influenza A Hemagglutinin HA-1 from a H1N1 Flu strain (HA1-1), dockerin domain from C. thermocellum (doc), HIV gag p24 (gag), or a string of HIV peptides (Hipo5), PSA (KLQCVDLHV (SEQ ID NO. 44))-tetramer, or an HIVgag-derived p24-PLA.
Yet another embodiment is a method of making an anti-Langerin-antigen fusion protein comprising: expressing an isolated fusion protein comprising an anti-Langerin antibody or binding fragment thereof in a host cell, the fusion protein comprising one or more antigenic peptides at the carboxy-terminus of the anti-Langerin antibody or binding fragment thereof, wherein when two or more cancer peptides are present, the cancer peptides are separated by one or more linkers, at least one linker comprising a glycosylation site; and isolating the fusion protein. In one aspect, fusion protein expressed in the host is further isolated and purified. In another aspect, the host is a eukaryotic cell. In another aspect, the antigenic peptides are cancer peptides selected from tumor associated antigens selected from CEA, prostate specific antigen (PSA), HER-2/neu, BAGE, GAGE, MAGE 1-4, 6 and 12, MUC-related protein (Mucin) (MUC-1, MUC-2, etc.), GM2 and GD2 gangliosides, ras, myc, tyrosinase, MART (melanoma antigen), MARCO-MART, cyclin B1, cyclin D, Pmel 17 (gp100), GnT-V intron V sequence (N-acetylglucoaminyltransferase V intron V sequence), Prostate Ca psm, prostate serum antigen (PSA), PRAME (melanoma antigen), β-catenin, MUM-1-B (melanoma ubiquitous mutated gene product), GAGE (melanoma antigen) 1, BAGE (melanoma antigen) 2-10, c-ERB2 (Her2/neu), EBNA (Epstein-Barr Virus nuclear antigen) 1-6, gp75, human papilloma virus (HPV) E6 and E7, p53, lung resistance protein (LRP), Bcl-2, and Ki-67. In another aspect, the antigenic peptides are cancer peptides selected from tumor associated antigens comprising antigens from leukemias and lymphomas, neurological tumors such as astrocytomas or glioblastomas, melanoma, breast cancer, lung cancer, head and neck cancer, gastrointestinal tumors, gastric cancer, colon cancer, liver cancer, pancreatic cancer, genitourinary tumors such cervix, uterus, ovarian cancer, vaginal cancer, testicular cancer, prostate cancer or penile cancer, bone tumors, vascular tumors, or cancers of the lip, nasopharynx, pharynx and oral cavity, esophagus, rectum, gall bladder, biliary tree, larynx, lung and bronchus, bladder, kidney, brain and other parts of the nervous system, thyroid, Hodgkin's disease, non-Hodgkin's lymphoma, multiple myeloma and leukemia. In another aspect, the cancer peptides are selected from at least one of:
or immunogenic fragments thereof.
In another embodiment, the invention includes a method of expanding antigen-specific T cells or B cells in vitro comprising: isolating peripheral blood mononuclear cells (PBMCs) from a cancer patient; incubating the isolated PBMCs with an immunogenic amount of an isolated anti-Langerin-(PL-Ag)x or anti-Langerin-(Ag-PL)x vaccine, wherein Ag is a tumor associated antigen and x is an integer 1 to 20; expanding the PBMCs in the presence of an effective amount of IL-2; harvesting the cells; and assessing the cytokine production by the cells to determine the presence of anti-cancer specific T cells or B cells.
In yet another embodiment, the invention includes a tumor associated antigen-specific T cell or B cell made by the method comprising: isolating peripheral blood mononuclear cells (PBMCs) from a cancer patient; incubating the isolated PBMCs with an immunogenic amount of an anti-Langerin-(PL-Ag)x or anti-Langerin-(Ag-PL)x vaccine, wherein Ag is a tumor associated antigen and x is an integer 1 to 20; expanding the PBMCs in the presence of an effective amount of IL-2; harvesting the cells; and assessing the cytokine production by the cells to determine the presence of tumor associated antigen-specific T cells or B cells.
Another embodiment of the invention includes a therapeutic vaccine comprising an isolated fusion protein comprising the formula: Ab-(PL-Ag)x; Ab-(Ag-PL)x; Ab-(PL-Ag-PL)x; Ab-(Ag-PL-Ag)x; Ab-(PL-Ag)x-PL; or Ab-(Ag-PL)x-Ag; wherein Ab is an anti-Langerin monoclonal antibody or binding fragment thereof; PL is at least one peptide linker comprising at least one glycosylation site; Ag is at least one infectious disease antigen; and x is an integer from 1 to 20.
Yet another embodiment includes a method of expanding antigen-specific T cells or B cells in vitro comprising: isolating peripheral blood mononuclear cells (PBMCs) from a patient suspected of having an infection; incubating the isolated PBMCs with an immunogenic amount of an isolated anti-Langerin-(PL-Ag)x or αLangerin-(Ag-PL)x vaccine, wherein Ag is an antigen of the infectious agent and x is an integer 1 to 20; expanding the PBMCs in the presence of an effective amount of one or more cytokines; harvesting the cells; and assessing the cytokine production by the cells to determine the presence of anti-infections agent specific T cells or B cells. Another embodiment is a viral associated antigen-specific T cell or B cell made by the method comprising: isolating peripheral blood mononuclear cells (PBMCs) from a patient suspected of having a viral infection; incubating the isolated PBMCs with an immunogenic amount of an isolated anti-Langerin-(PL-Ag)x or anti-Langerin-(Ag-PL)x vaccine, wherein Ag is a viral associated antigen and x is an integer 1 to 20; expanding the PBMCs in the presence of an effective amount of one or more cytokines; harvesting the cells; and assessing the cytokine production by the cells to determine the presence of viral associated antigen-specific T cells or B cells.
Another embodiment is a therapeutic vaccine comprising an isolated fusion protein comprising the formula: Ab-(PL-Ag)x; Ab-(Ag-PL)x; Ab-(PL-Ag-PL)x; Ab-(Ag-PL-Ag)x; Ab-(PL-Ag)x-PL; or Ab-(Ag-PL)x-Ag; wherein Ab is an anti-Langerin monoclonal antibody or binding fragment thereof; PL is at least one peptide linker comprising at least one glycosylation site; Ag is at least one viral antigen; and x is an integer from 1 to 20. In one example, the isolated antibody comprising one or more of complementarity determining regions selected from:
or a direct equivalent thereof. In one aspect, the antibody is humanized. In another aspect, the antibody is 15B10 having ATCC Accession No. PTA-9852 and humanized derivatives thereof. In another aspect, the antibody is 2G3 having ATCC Accession No. PTA-9853, 91E7, 37C1, or 4C7, and humanized derivatives thereof.
Yet another embodiment is an isolated nucleic acid that encodes a 15B10, 2G3, 91E7, 37C1, or 4C7 antibody, antibody binding fragment or a humanized derivative thereof. In one aspect, the anti-Langerin antibody is selected from the following pairs of amino acid sequences SEQ ID NOS.: 2 and 4; 6 and 7; 52 and 54; 56 and 58; and 78 and 80; or binding fragments thereof respectively. In another aspect, the anti-Langerin antibody is the expression product from the following pairs of nucleic acid sequences SEQ ID NOS.: 1 and 3; 5 and 6; 51 and 53; 55 and 57; and 77 and 79; or binding fragments thereof, which are the 15B10, 2G3, 91E7, 37C1, or 4C7 antibodies, respectively.
Yet another embodiment of the present invention is a pharmaceutical composition comprising an isolated anti-Langerin antibody or binding fragment thereof and one or more antigenic peptides attached to the anti-Langerin antibody, wherein when two or more antigens are present, they are separated by one or more linker peptides that comprise at least one glycosylation site. In one aspect, the antibody binding fragment is selected from an Fv, Fab, Fab′, F(ab′)2, Fc, or a ScFv fragment. In another aspect, the anti-Langerin antibody is selected from the following pairs of amino acid sequences SEQ ID NOS.: 2 and 4; 6 and 7; 52 and 54; 56 and 58; and 78 and 80 or binding fragments thereof. In another aspect, the anti-Langerin antibody is the expression product of the following pairs of nucleic acid sequences SEQ ID NOS.: 1 and 3; 5 and 6; 51 and 53; 55 and 57; and 77 and 79. In another aspect, the anti-Langerin antibody or binding fragment thereof is at least one of 15B10 having ATCC Accession No. PTA-9852, 2G3 having ATCC Accession No. PTA-9853, 91E7, 37C1, or 4C7 and humanized derivatives thereof. In another aspect, the anti-Langerin antibody or binding fragment thereof and the antigenic peptide are a fusion protein. In another aspect, the composition further comprises an adjuvant. In another aspect, the composition further comprises one or more pharmaceutical excipients.
Yet another embodiment of the present invention is a therapeutic vaccine comprising a fusion protein comprising the formula: Ab-(PL-Ag)x; Ab-(Ag-PL)x; Ab-(PL-Ag-PL)x; Ab-(Ag-PL-Ag)x; Ab-(PL-Ag)x-PL; or Ab-(Ag-PL)x-Ag; wherein Ab is an anti-Langerin monoclonal antibody or binding fragment thereof; PL is at least one peptide linker comprising at least one glycosylation site; Ag is at least one viral antigen; and x is an integer from 1 to 20.
The invention provides a Langerin binding antibody (15B10) that comprises at least one immunoglobulin light chain variable domain (VL) which comprises the amino acid and nucleic acid sequence encoding:
or and direct equivalent thereof.
Accordingly the invention provides a Langerin binding antibody (15B10) that comprises an antigen binding site comprising at least one immunoglobulin heavy chain variable domain (VH) which comprises the amino acid and nucleic acid sequence encoding:
and direct equivalents thereof.
The invention provides a Langerin binding antibody (2G3) that comprises at least one immunoglobulin light chain variable domain (VL) which comprises the amino acid and nucleic acid sequence encoding:
or and direct equivalent thereof.
Accordingly the invention provides a Langerin binding antibody (2G3) that comprises an antigen binding site comprising at least one immunoglobulin heavy chain variable domain (VH) which comprises the amino acid and nucleic acid sequence encoding:
and direct equivalents thereof.
In one aspect the invention provides a single domain Langerin antibody comprising an isolated immunoglobulin light chain comprising a heavy chain variable domain (VL) as defined above. In another aspect the invention provides a single domain Langrin binding molecule comprising an isolated immunoglobulin heavy chain comprising a heavy chain variable domain (VH) as defined above.
In another aspect the invention also provides a Langerin binding antibody comprising a light chain (VL) variable domains in which the Langerin binding antibody comprises at least one antigen binding site comprising: an antibody light chain variable domain (VL) which comprises in sequence hypervariable regions obtained from the amino acid and nucleic acid sequences encoding:
and direct equivalents thereof.
In another aspect the invention also provides a Langerin binding antibody comprising, the amino acid and nucleic acid sequences of heavy chain variable domain (VH) which comprises in sequence hypervariable regions obtained from:
and direct equivalents thereof.
mAnti-Langerin15B10K—Nucleotide and mature protein amino acid sequence of the light chain of the mouse anti-Langerin 15B10 antibody cDNA, respectively. The variable region residues are underlined.
ATGAAGTTGCCTGTTAGGCTGTTGGTGCTGATGTTCTGGATTCCTGC
SPKLLIYKVSNRFSGVPDRFSGSGSGTNFTLKISRVEAEDLGLYFCS
mAnti-Langerin15B10H-LV-hIgG4H-C—Nucleotide and mature protein amino acid sequence of the heavy chain variable region of the mouse anti-Langerin 15B10 antibody fused to human IgG4, respectively. The variable region residues are underlined.
ATGGAATGGAGGATCTTTCTCTTCATCCTGTCAGGAACTGCAGGTG
WIGDIYPGSGYSFYNENFKGKATLTADKSSTTAYMQLSSLTSEDSA
VYFCATYYNYPFAYWGQGTLVTVSAAKTTGPSVFPLAPCSRSTSES
mAnti-Langerin2G3L—Nucleotide and mature protein amino acid sequence of the light chain of the mouse anti-Langerin 2G3 antibody cDNA, respectively. The variable region residues are underlined.
ATGGCCTGGATTTCACTTATACTCTCTCTCCTGGCTCTCAGCTCAG
TGLIGGTNNRVSGVPARFSGSLIGDKAALTITGAQTEDEAIYFCAL
mAnti-Langerin2G3H—Nucleotide and mature protein amino acid sequence of the heavy chain of the mouse anti-Langerin 2G3 antibody cDNA, respectively. The variable region residues are underlined.
ATGACATTGAACATGCTGTTGGGGCTGAAGTGGGTTTTCTTTGTTGT
VARIRNKSNNYATYYADSVKDRFTISRDDSQSLLYLQMNNLKTEDTA
MYYCVGRDWFDYWGQGTLVTVSAAKTTPPSVYPLAPGSAAQTNSMVT
In another embodiment the invention includes an antibody comprising one or more of the complementarity determining regions selected from: ASISCRSSQSLVHSNGNTYLHWYLQKPGQSPKLLIYKVSNRFSGVPDRFSGSGSGTNFTLKISRVEAEDLGLYFCS (SEQ ID NO.: 45); SVKMSCKASGYTFTDYVISWVKQRTGQGLEWIGDIYPGSGYSFYNENFKGKATLTADKSSTTAYMQLSSLTSEDSAVYFCA (SEQ ID NO.: 46); VTLTCRSSTGAVTTSNYANWVQEKPDHLFTGLIGGTNNRVSGVPARFSGSLIGDKAALTITGAQTEDEAIYFCA (SEQ ID NO.: 47); SLKLSCAASGLTFNIYAMNWVRQAPGKGLEWVARIRNKSNNYATYYADSVKDRFTISRDDSQSLLYLQMNNLKTEDTAMYYC (SEQ ID NO.: 48); or a direct equivalent thereof. In one aspect, the antibody is humanized. In another aspect, the antibody is 15B10, 2G3 or humanized derivatives thereof. In another aspect, the invention includes nucleic acids that encode the 15B10, the 2G3 antibody or humanized derivatives thereof.
For a more complete understanding of the features and advantages of the present invention, reference is now made to the detailed description of the invention along with the accompanying figures and in which:
While the making and using of various embodiments of the present invention are discussed in detail below, it should be appreciated that the present invention provides many applicable inventive concepts that can be embodied in a wide variety of specific contexts. The specific embodiments discussed herein are merely illustrative of specific ways to make and use the invention and do not delimit the scope of the invention.
To facilitate the understanding of this invention, a number of terms are defined below. Terms defined herein have meanings as commonly understood by a person of ordinary skill in the areas relevant to the present invention. Terms such as “a”, “an” and “the” are not intended to refer to only a singular entity, but include the general class of which a specific example may be used for illustration. The terminology herein is used to describe specific embodiments of the invention, but their usage does not delimit the invention, except as outlined in the claims.
Subsets of Dendritic Cells (DCs). The present inventors have discovered that two main DC differentiation pathways exist. A myeloid pathway generates two subsets: Langerhans cells (LCs) found in stratified epithelia such as the skin, and interstitial DCs (intDCs) found in all other tissues. A plasmacytoid pathway generates plasmacytoid DCs (pDCs), which secrete large amounts of IFNαβ after viral infection3 and efficiently present viral antigens in a novel mechanism4 (
The invention includes also variants and other modification of an antibody (or “Ab”) of fragments thereof, e.g., anti-Langerin fusion protein (antibody is used interchangeably with the term “immunoglobulin”). As used herein, the term “antibodies or binding fragments thereof,” includes whole antibodies or binding fragments of an antibody, e.g., Fv, Fab, Fab′, F(ab′)2, Fc, and single chain Fv fragments (ScFv) or any biologically effective fragments of an immunoglobulins that binds specifically to, e.g., Langerin. Antibodies from human origin or humanized antibodies have lowered or no immunogenicity in humans and have a lower number or no immunogenic epitopes compared to non-human antibodies. Antibodies and their fragments will generally be selected to have a reduced level or no antigenicity in humans.
As used herein, the terms “Ag” or “antigen” refer to a substance capable of either binding to an antigen binding region of an immunoglobulin molecule or of eliciting an immune response, e.g., a T cell-mediated immune response by the presentation of the antigen on Major Histocompatibility Antigen (MHC) cellular proteins. As used herein, “antigen” includes, but is not limited to, antigenic determinants, haptens, and immunogens, which may be peptides, small molecules, carbohydrates, lipids, nucleic acids or combinations thereof. The skilled immunologist will recognize that when discussing antigens that are processed for presentation to T cells, the term “antigen” refers to those portions of the antigen (e.g., a peptide fragment) that is a T cell epitope presented by MHC to the T cell receptor. When used in the context of a B cell mediated immune response in the form of an antibody that is specific for an “antigen”, the portion of the antigen that binds to the complementarity determining regions of the variable domains of the antibody (light and heavy) the bound portion may be a linear or three-dimensional epitope. In the context of the present invention, the term antigen is used on both contexts, that is, the antibody is specific for a protein antigen (Langerin), but also carries one or more peptide epitopes for presentation by MHC to T cells. In certain cases, the antigens delivered by the vaccine or fusion protein of the present invention are internalized and processed by antigen presenting cells prior to presentation, e.g., by cleavage of one or more portions of the antibody or fusion protein.
As used herein, the term “antigenic peptide” refers to that portion of a polypeptide antigen that is specifically recognized by either B-cells or T-cells. B-cells respond to foreign antigenic determinants via antibody production, whereas T-lymphocytes are the mediate cellular immunity. Thus, antigenic peptides are those parts of an antigen that are recognized by antibodies, or in the context of an MHC, by T-cell receptors.
As used herein, the term “epitope” refers to any protein determinant capable of specific binding to an immunoglobulin or of being presented by a Major Histocompatibility Complex (MHC) protein (e.g., Class I or Class II) to a T-cell receptor. Epitopic determinants are generally short peptides 5-30 amino acids long that fit within the groove of the MHC molecule that presents certain amino acid side groups toward the T cell receptor and has certain other residues in the groove, e.g., due to specific charge characteristics of the groove, the peptide side groups and the T cell receptor. Generally, an antibody specifically binds to an antigen when the dissociation constant is 1 mM, 100 nM or even 10 nM.
As used herein, the term “vector” is used in two different contexts. When using the term “vector” with reference to a vaccine, a vector is used to describe a non-antigenic portion that is used to direct or deliver the antigenic portion of the vaccine. For example, an antibody or binding fragments thereof may be bound to or form a fusion protein with the antigen that elicits the immune response. For cellular vaccines, the vector for delivery and/or presentation of the antigen is the antigen presenting cell, which is delivered by the cell that is loaded with antigen. In certain cases, the cellular vector itself may also process and present the antigen(s) to T cells and activate an antigen-specific immune response. When used in the context of nucleic acids, a “vector” refers a construct that is capable of delivering, and preferably expressing, one or more genes or polynucleotide sequences of interest in a host cell. Examples of vectors include, but are not limited to, viral vectors, naked DNA or RNA expression vectors, DNA or RNA expression vectors associated with cationic condensing agents, DNA or RNA expression vectors encapsulated in liposomes, and certain eukaryotic cells, such as producer cells.
The compositions and methods of the present invention can be used with a wide variety of peptides and/or protein in which the antibody or binding fragment thereof and the peptide linker or “PL” create a protein that is stable and/or soluble.
As used herein, the compositions and methods use an anti-Langerin antigen delivery vector comprising the formula:
Ab-(PL-Ag)x or Ab-(Ag-PL)x;
wherein Ab is an anti-Langerin antibody or binding fragment thereof;
PL is at least one Peptide Linker comprising at least one glycosylation site;
Ag is at least one antigen; and
x is an integer from 1 to 20.
As used herein, the terms “stable” and “unstable” when referring to proteins is used to describe a peptide or protein that maintains its three-dimensional structure and/or activity (stable) or that loses immediately or over time its three-dimensional structure and/or activity (unstable). As used herein, the term “insoluble” refers to those proteins that when produced in a cell (e.g., a recombinant protein expressed in a eukaryotic or prokaryotic cell or in vitro) are not soluble in solution absent the use of denaturing conditions or agents (e.g., heat or chemical denaturants, respectively). The antibody or binding fragment thereof and the linkers taught herein have been found to convert antibody fusion proteins with the peptides from insoluble and/or unstable into proteins that are stable and/or soluble. Another example of stability versus instability is when the domain of the protein with a stable conformation has a higher melting temperature (Tm) than the unstable domain of the protein when measured in the same solution. A domain is stable compared to another domain when the difference in the Tm is at least about 2° C., more preferably about 4° C., still more preferably about 7° C., yet more preferably about 10° C., even more preferably about 15° C., still more preferably about 20° C., even still more preferably about 25° C., and most preferably about 30° C., when measured in the same solution.
As used herein, “polynucleotide” or “nucleic acid” refers to a strand of deoxyribonucleotides or ribonucleotides in either a single- or a double-stranded form (including known analogs of natural nucleotides). A double-stranded nucleic acid sequence will include the complementary sequence. The polynucleotide sequence may encode variable and/or constant region domains of immunoglobulin that are formed into a fusion protein with one or more linkers. For use with the present invention, multiple cloning sites (MCS) may be engineered into the locations at the carboxy-terminal end of the heavy and/or light chains of the antibodies to allow for in-frame insertion of peptide for expression between the linkers. As used herein, the term “isolated polynucleotide” refers to a polynucleotide of genomic, cDNA, or synthetic origin or some combination thereof. By virtue of its origin the “isolated polynucleotide” (1) is not associated with all or a portion of a polynucleotide in which the “isolated polynucleotides” are found in nature, (2) is operably linked to a polynucleotide which it is not linked to in nature, or (3) does not occur in nature as part of a larger sequence. The skilled artisan will recognize that to design and implement a vector having the formula Ab-(PL-Ag)x or Ab-(Ag-PL)x, can be manipulated at the nucleic acid level by using techniques known in the art, such as those taught in Current Protocols in Molecular Biology, 2007 by John Wiley and Sons, relevant portions incorporated herein by reference. Briefly, the Ab, Ag and PL encoding nucleic acid sequences can be inserted using polymerase chain reaction, enzymatic insertion of oligonucleotides or polymerase chain reaction fragments in a vector, which may be an expression vector. To facilitate the insertion of (PL-Ag)x or (Ag-PL)x at the carboxy terminus of the antibody light chain, the heavy chain, or both, a multiple cloning site (MCS) may be engineered in sequence with the antibody sequences.
As used herein, the term “polypeptide” refers to a polymer of amino acids and does not refer to a specific length of the product; thus, peptides, oligopeptides, and proteins are included within the definition of polypeptide. This term also does not refer to or exclude post expression modifications of the polypeptide, for example, glycosylations, acetylations, phosphorylations and the like. Included within the definition are, for example, polypeptides containing one or more analogs of an amino acid (including, for example, unnatural amino acids, etc.), polypeptides with substituted linkages, as well as other modifications known in the art, both naturally occurring and non-naturally occurring. The term “domain,” or “polypeptide domain” refers to that sequence of a polypeptide that folds into a single globular region in its native conformation, and that may exhibit discrete binding or functional properties. As used herein, the term “fusion protein” refers to a hybrid protein expressed by a nucleic acid molecule comprising nucleotide sequences of at least two genes into a protein. For example, a fusion protein can comprise at least part of anti-Langerin antibody or binding fragment thereof fused with one or more antigen and/or one or more linkers if more than one antigen is fused with the antibody or fragment thereof.
A polypeptide or amino acid sequence “derived from” a designated nucleic acid sequence refers to a polypeptide having an amino acid sequence identical to that of a polypeptide encoded in the sequence, or a portion thereof wherein the portion consists of at least 3-5 amino acids, preferably at least 4-7 amino acids, more preferably at least 8-10 amino acids, and even more preferably at least 11-15 amino acids, or which is immunologically identifiable with a polypeptide encoded in the sequence. This terminology also includes a polypeptide expressed from a designated nucleic acid sequence.
As used herein, “pharmaceutically acceptable carrier” refers to any material that when combined with an immunoglobulin (Ig) fusion protein of the present invention allows the Ig to retain biological activity and is generally non-reactive with the subject's immune system. Examples include, but are not limited to, standard pharmaceutical carriers such as a phosphate buffered saline solution, water, emulsions such as an oil/water emulsion, and various types of wetting agents. Certain diluents may be used with the present invention, e.g., for aerosol or parenteral administration, that may be phosphate buffered saline or normal (0.85%) saline.
The invention provides a Langerin binding antibody (15B10) that comprises at least one immunoglobulin light chain variable domain (VL) which comprises the amino acid and nucleic acid sequence encoding: ASISCRSSQSLVHSNGNTYLHWYLQKPGQSPKLLIYKVSNRFSGVPDRFSGSGSGTNFTLKISRVEAEDLGLYFCS (SEQ ID NO.: 45); or and direct equivalent thereof.
Accordingly the invention provides a Langerin binding antibody (15B10) that comprises an antigen binding site comprising at least one immunoglobulin heavy chain variable domain (VH) which comprises the amino acid and nucleic acid sequence encoding: SVKMSCKASGYTFTDYVISWVKQRTGQGLEWIGDIYPGSGYSFYNENFKGKATLTADKSSTTAYMQLSSLTSEDSAVYFCA (SEQ ID NO.: 46); and direct equivalents thereof.
The invention provides a Langerin binding antibody (2G3) that comprises at least one immunoglobulin light chain variable domain (VL) which comprises the amino acid and nucleic acid sequence encoding: VTLTCRSSTGAVTTSNYANWVQEKPDHLFTGLIGGTNNRVSGVPARFSGSLIGDKAALTITGAQTEDEAIYFCA (SEQ ID NO.: 47); or and direct equivalent thereof.
Accordingly the invention provides a Langerin binding antibody (2G3) that comprises an antigen binding site comprising at least one immunoglobulin heavy chain variable domain (VH) which comprises the amino acid and nucleic acid sequence encoding: SLKLSCAASGLTFNIYAMNWVRQAPGKGLEWVARIRNKSNNYATYYADSVKDRFTISRDDSQSLLYLQMNNLKTEDTAMYYC (SEQ ID NO.: 48); and direct equivalents thereof.
In one aspect the invention provides a single domain Langerin antibody comprising an isolated immunoglobulin light chain comprising a heavy chain variable domain (VL) as defined above. In another aspect the invention provides a single domain Langerin binding molecule comprising an isolated immunoglobulin heavy chain comprising a heavy chain variable domain (VH) as defined above.
In another aspect the invention also provides a Langerin binding antibody comprising a light chain (VL) variable domains in which the Langerin binding antibody comprises at least one antigen binding site comprising: an antibody light chain variable domain (VL) which comprises in sequence hypervariable regions obtained from the amino acid and nucleic acid sequences encoding: ASISCRSSQSLVHSNGNTYLHWYLQKPGQSPKLLIYKVSNRFSGVPDRFSGSGSGTNFTLKISRVEAEDLGLYFCS (SEQ ID NO.: 45); or VTLTCRSSTGAVTTSNYANWVQEKPDHLFTGLIGGTNNRVSGVPARFSGSLIGDKAALTITGAQTEDEAIYFCA (SEQ ID NO.: 47); and direct equivalents thereof.
In another aspect the invention also provides a Langerin binding antibody comprising, the amino acid and nucleic acid sequences of heavy chain variable domain (VH) which comprises in sequence hypervariable regions obtained from: SVKMSCKASGYTFTDYVISWVKQRTGQGLEWIGDIYPGSGYSFYNENFKGKATLTADKSSTTAYMQLSSLTSEDSAVYFCA (SEQ ID NO.: 46); or SLKLSCAASGLTFNIYAMNWVRQAPGKGLEWVARIRNKSNNYATYYADSVKDRFTISRDDSQSLLYLQMNNLKTEDTAMYYC (SEQ ID NO.: 48); and direct equivalents thereof.
Unless otherwise indicated, any polypeptide chain is herein described as having an amino acid sequence starting at the N-terminal end and ending at the C-terminal end. When the antigen binding site comprises both the VH and VL domains, these may be located on the same polypeptide molecule or, preferably, each domain may be on a different chain, the VH domain being part of an immunoglobulin heavy chain or binding fragment thereof and the VL being part of an immunoglobulin light chain or binding fragment thereof.
As used herein, the term “Langerin binding molecule” or “Langerin binding antibody” refer to any molecule capable of binding to the Langerin antigen either alone or associated with other molecules having one or more the VL and VH CDRs taught herein, in some cases 2, 3, 4, 5, or all 6 CDRs. The binding reaction may be shown by standard methods (qualitative assays) including, for example, a bioassay for determining by blocking the binding of other molecules to Langerin or any kind of binding or activity assays (e.g., activation, reduction or modulation of an immune response), with reference to a negative control test in which an antibody of unrelated specificity but of the same isotype, e.g., an anti-CD25 or anti-CD80 antibody, is used.
The present invention may also be made into a single chain antibody having the variable domains of the heavy and light chains of an antibody covalently bound by a peptide linker usually including from 10 to 30 amino acids, preferably from 15 to 25 amino acids. Therefore, such a structure does not include the constant part of the heavy and light chains and it is believed that the small peptide spacer should be less antigenic than a whole constant part.
As used herein, the term “chimeric antibody” refers to an antibody in which the constant regions of heavy or light chains or both are of human origin while the variable domains of both heavy and light chains are of non-human (e.g., mouse, hamster or rat) origin or of human origin but derived from a different human antibody.
As used herein, the term “CDR-grafted antibody” refers to an antibody in which the hypervariable complementarity determining regions (CDRs) are derived from a donor antibody, such as a non-human (e.g., mouse) antibody or a different human antibody, while all or substantially all the other parts of the immunoglobulin (e.g., the conserved regions of the variable domains, i.e., framework regions), are derived from an acceptor antibody (in the case of a humanized antibody—an antibody of human origin). A CDR-grafted antibody may include a few amino acids of the donor sequence in the framework regions, for instance in the parts of the framework regions adjacent to the hypervariable regions.
As used herein, the term “human antibody” refers to an antibody in which the constant and variable regions of both the heavy and light chains are all of human origin, or substantially identical to sequences of human origin, not necessarily from the same antibody and includes antibodies produced by mice in which the mouse, hamster or rat immunoglobulin variable and constant part genes have been replaced by their human counterparts, e.g. as described in general terms in EP 0546073 B1, U.S. Pat. No. 5,545,806, U.S. Pat. No. 5,569,825, U.S. Pat. No. 5,625,126, U.S. Pat. No. 5,633,425, U.S. Pat. No. 5,661,016, U.S. Pat. No. 5,770,429, EP Patent No. 0 438474 B1 and EP Patent No. 0 463151 B1, relevant portions incorporated herein by reference.
The Langerin binding antibodies of the invention include humanized antibodies that comprise the CDRs obtained from the anti-Langerin 15B10 or 2G3 antibody. One example of a chimeric antibody includes the variable domains of both heavy and light chains are of human origin, for instance those of the anti-Langerin 15B10 or 2G3 antibody. The constant region domains preferably also comprise suitable human constant region domains, for instance as described in “Sequences of Proteins of Immunological Interest”, Kabat E. A. et al, US Department of Health and Human Services, Public Health Service, National Institute of Health.
Hypervariable regions may be associated with any kind of framework regions, e.g., of human origin. Suitable framework regions were described Kabat E. A. One heavy chain framework is a heavy chain framework, for instance those of the anti-Langerin 15B10 or 2G3 antibody, includes sequences for the light chain framework regions: FR1L, FR2L, FR3L and FR4L regions. In a similar manner, the anti-Langerin 15B10 or 2G3 heavy chain framework that includes the sequence of FR1H, FR2H, FR3H and FR4H regions. The CDRs may be added to a human antibody framework, such as those described in U.S. Pat. No. 7,456,260, issued to Rybak, et al., which teach new human variable chain framework regions and humanized antibodies comprising the framework regions, relevant portions and framework sequences incorporated herein by reference. To accomplish the engraftment at a genetic level, the present invention also includes the underlying nucleic acid sequences for the VL AND VH regions as well as the complete antibodies and the humanized versions thereof. The nucleic acid sequences of the present invention include the anti-Langerin antibody light and the heavy chains, respectively, as well as those nucleic acid sequences that include variable codon usage for the same amino acid sequences and conservative variations thereof having 85, 90, 95 or 100% sequence identity at the nucleic or amino acid level. Likewise, the CDRs may have 85, 90, 95 or 100% sequence identity at the nucleic or amino acid level, individually, in groups or 2, 3, 4 or 5 or all together.
Monoclonal antibodies raised against a protein naturally found in all humans are typically developed in a non-human system e.g. in mice, and as such are typically non-human proteins. As a direct consequence of this, a xenogenic antibody as produced by a hybridoma, when administered to humans, elicits an undesirable immune response that is predominantly mediated by the constant part of the xenogenic immunoglobulin. Xenogeneic antibodies tend to elicit a host immune response, thereby limiting the use of such antibodies as they cannot be administered over a prolonged period of time. Therefore, it is particularly useful to use single chain, single domain, chimeric, CDR-grafted, or especially human antibodies that are not likely to elicit a substantial allogenic response when administered to humans. The present invention includes antibodies with minor changes in an amino acid sequence such as deletion, addition or substitution of one, a few or even several amino acids which are merely allelic forms of the original protein having substantially identical properties.
The inhibition of the binding of Langerin to its receptor may be conveniently tested in various assays including such assays are described hereinafter in the text. By the term “to the same extent” is meant that the reference and the equivalent molecules exhibit, on a statistical basis, essentially identical Langerin binding inhibition curves in one of the assays referred to above. For example, the assay used may be an assay of competitive inhibition of binding of Langerin by the binding molecules of the invention.
Generally, the human anti-Langerin antibody comprises at least: (a) one light chain which comprises a variable domain having an amino acid sequence substantially identical to the 15B10 or 2G3 antibody starting with the amino acid at position 1 and ending with the amino acid at position 107 and the constant part of a human light chain; and (b) one heavy chain which comprises a variable domain having an amino acid sequence substantially identical to the 15B10 or 2G3 antibody and the constant part of a human heavy chain. The constant part of a human heavy chain may be of the γ1, γ2, γ3, μ, β2, or δ or ε type, preferably of the γ-type, whereas the constant part of a human light chain may be of the κ or λ type (which includes the λ1, λ2 and λ3 subtypes) but is preferably of the κ type. The amino acid sequences of the general locations of the variable and constant domains are well known in the art and generally follow the Kabat nomenclature.
A Langerin binding molecule of the invention may be produced by recombinant DNA techniques. In view of this, one or more DNA molecules encoding the binding molecule must be constructed, placed under appropriate control sequences and transferred into a suitable host organism for expression.
In a very general manner, there are accordingly provided: (i) DNA molecules encoding a single domain Langerin binding molecule of the invention, a single chain Langerin binding molecule of the invention, a heavy or light chain or binding fragments thereof of a Langerin binding molecule of the invention; and (ii) the use of the DNA molecules of the invention for the production of a Langerin binding molecule of the invention by recombinant methods.
The present state of the art is such that the skilled worker in the art can synthesize the DNA molecules of the invention given the information provided herein, i.e., the amino acid sequences of the hypervariable regions and the DNA sequences coding for them. A method for constructing a variable domain gene is for example described in EPA 239 400, relevant portions incorporated herein by reference. Briefly, a gene encoding a variable domain of a MAb is cloned. The DNA segments encoding the framework and hypervariable regions are determined and the DNA segments encoding the hypervariable regions are removed so that the DNA segments encoding the framework regions are fused together with suitable restriction sites at the junctions. The restriction sites may be generated at the appropriate positions by mutagenesis of the DNA molecule by standard procedures. Double stranded synthetic CDR cassettes are prepared by DNA synthesis according to the sequences given in for 15B10 or 2G3 (amino acid and nucleic acid sequences, respectively). These cassettes are often provided with sticky ends so that they can be ligated at the junctions of the framework.
It is not necessary to have access to the mRNA from a producing hybridoma cell line in order to obtain a DNA construct coding for the Langerin binding molecules of the invention. For example, PCT application WO 90/07861 gives full instructions for the production of an antibody by recombinant DNA techniques given only written information as to the nucleotide sequence of the gene, relevant portions incorporated herein by reference. Briefly, the method comprises the synthesis of a number of oligonucleotides, their amplification by the PCR method, and their splicing to give the desired DNA sequence.
Expression vectors comprising a suitable promoter or genes encoding heavy and light chain constant parts are publicly available. Thus, once a DNA molecule of the invention is prepared it may be conveniently transferred in an appropriate expression vector. DNA molecules encoding single chain antibodies may also be prepared by standard methods, for example, as described in WO 88/1649. In view of the foregoing, no hybridoma or cell line deposit is necessary to comply with the criteria of sufficiency of description.
For example, first and second DNA constructs are made that bind specifically to Langerin. Briefly, a first DNA construct encodes a light chain of an antibody, CDRs or binding fragments thereof and comprises a) a first part which encodes a variable domain comprising alternatively framework and hypervariable regions, the hypervariable regions being in sequence CDR1L, CDR2L and CDR3L the amino acid sequences of which are found in SEQ ID NOs. 45-48; this first part starting with a codon encoding the first amino acid of the variable domain and ending with a codon encoding the last amino acid of the variable domain, and b) a second part encoding a light chain constant part or binding fragment thereof which starts with a codon encoding the first amino acid of the constant part of the heavy chain and ends with a codon encoding the last amino acid of the constant part or binding fragment thereof, followed by a stop codon.
The first part encodes a variable domain having an amino acid sequence substantially identical to the amino acid sequences of 15B10 or 2G3. A second part encodes the constant part of a human heavy chain, more preferably the constant part of the human γ1 chain. This second part may be a DNA fragment of genomic origin (comprising introns) or a cDNA fragment (without introns).
The second DNA construct encodes a heavy chain or binding fragment thereof and comprises a) a first part which encodes a variable domain comprising alternatively framework and hypervariable regions; the hypervariable regions being CDR1H and optionally CDR2H and CDR3H, the amino acid sequences of 15B10 or 2G3; this first part starting with a codon encoding the first amino acid of the variable domain and ending with a codon encoding the last amino acid of the variable domain, and b) a second part encoding a heavy chain constant part or binding fragment thereof which starts with a codon encoding the first amino acid of the constant part of the light chain and ends with a codon encoding the last amino acid of the constant part or binding fragment thereof followed by a stop codon.
The first part encodes a variable domain having an amino acid sequence substantially identical to the amino acid sequence of 15B10 or 2G3. The first part has the nucleotide sequence of the 15B10 or 2G3 antibodies starting with the nucleotide at position 1 and ending with the nucleotide at position 321. Also preferably the second part encodes the constant part of a human light chain, more preferably the constant part of the human κ chain.
The invention also includes Langerin binding molecules in which one or more of the residues of CDR1L, CDR2L, CDR3L, CDR1H, CDR2H or CDR3H or the frameworks, typically only a few (e.g. FR1-4L or H), are changed from the residues of the 15B10 or 2G3 antibodies; by, e.g., site directed mutagenesis of the corresponding DNA sequences. The invention includes the DNA sequences coding for such changed Langerin binding molecules. In particular the invention includes a Langerin binding molecules in which one or more residues of CDR1L, CDR2L and/or CDR3L have been changed from the residues of the 15B10 or 2G3 antibodies and one or more residues of CDR1H, CDR2H and/or CDR3H have been changed from the residues of the 15B10 or 2G3 antibodies.
Each of the DNA constructs are placed under the control of suitable control sequences, in particular under the control of a suitable promoter. Any kind of promoter may be used, provided that it is adapted to the host organism in which the DNA constructs will be transferred for expression. However, if expression is to take place in a mammalian cell, an immunoglobulin gene promoter may be used in B cells. The first and second parts may be separated by an intron, and, an enhancer may be conveniently located in the intron between the first and second parts. The presence of such an enhancer that is transcribed but not translated, may assist in efficient transcription. In particular embodiments the first and second DNA constructs comprise the enhancer of, e.g., a heavy chain human gene.
The antibody or binding fragments thereof can be isolated, purified, and stored using any method known in the art. The binding fragments retain the specific binding activity of the intact antibody, and can be used for any application that employs the intact antibody (e.g., therapeutics, diagnostic assays, competitive binding assays, etc.).
In another aspect, the invention provides an antibody or binding fragment generated by the above-described method, and may further include a half-life extending vehicle, such as those known to those skilled in the art. Such vehicles include, but are not limited to, linear polymers (e.g., polyethylene glycol (PEG), polylysine, dextran, etc.); branched-chain polymers (See, e.g., U.S. Pat. No. 4,289,872; U.S. Pat. No. 5,229,490; WO 93/21259); a lipid; a cholesterol group (such as a steroid); a carbohydrate or polysaccharide; or any natural or synthetic protein, polypeptide or peptide. Additionally, it will be appreciated that one or more Fc regions, can also be employed with the invention to increase half-life. It will be appreciated that the vehicle can be linked to the antibody or binding fragment by way of various techniques known in the art including, for example, covalent linkage.
The desired antibody may be produced in an animal as an ascites, in cell culture or in a transgenic animal. A suitable transgenic animal may be obtained according to standard methods that include micro injecting into eggs the first and second DNA constructs placed under suitable control sequences transferring the so prepared eggs into appropriate pseudo-pregnant females and selecting a descendant expressing the desired antibody.
The invention also provides an expression vector able to replicate in a prokaryotic or eukaryotic cell line, which comprises at least one of the DNA constructs above described. Each expression vector containing a DNA construct is then transferred into a suitable host organism. When the DNA constructs are separately inserted on two expression vectors, they may be transferred separately, i.e. one type of vector per cell, or co-transferred, this latter possibility being preferred. A suitable host organism may be a bacterium, a yeast or a mammalian cell line, this latter being preferred. More preferably, the mammalian cell line is of lymphoid origin, e.g., a myeloma, hybridoma or a normal immortalized B-cell, which conveniently does not express any endogenous antibody heavy or light chain.
When the antibody chains are produced in a cell culture, the DNA constructs must first be inserted into either a single expression vector or into two separate but compatible expression vectors, the latter possibility being preferred. For expression in mammalian cells it is preferred that the coding sequence of the Langerin binding molecule is integrated into the host cell DNA within a locus which permits or favors high level expression of the Langerin binding molecule.
In a further aspect of the invention there is provided a process for the product of a Langerin binding molecule that comprises: (i) culturing an organism which is transformed with an expression vector as defined above; and (ii) recovering the Langerin binding molecule from the culture.
In accordance with the present invention it has been found that the anti-Langerin antibodies 15B10, 2G3, 91E7, 37C1, or 4C7 and humanized derivatives thereof, appear to have binding specificity for the antigenic epitope of human Langerin. It is therefore most surprising that antibodies to this epitope, e.g. the anti-Langerin 15B10, 2G3, 91E7, 37C1, or 4C7 and humanized derivatives thereof, are capable of delivering antigen efficiently into dendritic cells (DCs). Antibodies, in particular chimeric and CDR-grafted antibodies and especially human antibodies, which have binding specificity for the antigenic epitope of mature human Langerin; and use of such antibodies for DC antigen loading are novel and are included within the scope of the present invention.
To use the anti-Langerin antibody of the present invention for treatment indications, the appropriate dosage will, of course, vary depending upon, for example, the antibody disclosed herein to be employed, the host, the mode of administration and the nature and severity of the condition being treated. However, in prophylactic use, satisfactory results are generally found at dosages from about 0.05 mg to about 10 mg per kilogram body weight more usually from about 0.1 mg to about 5 mg per kilogram body weight. The frequency of dosing for prophylactic uses will normally be in the range from about once per week up to about once every 3 months, more usually in the range from about once every 2 weeks up to about once every 10 weeks, e.g., once every 4 to 8 weeks. The anti-Langerin antibody of the present can be administered parenterally, intravenously, e.g., into the antecubital or other peripheral vein, intramuscularly, or subcutaneously.
Pharmaceutical compositions of the invention may be manufactured in conventional manner, e.g., in a lyophilized form. For immediate administration it is dissolved in a suitable aqueous carrier, for example sterile water for injection or sterile buffered physiological saline. If it is considered desirable to make up a solution of larger volume for administration by infusion rather as a bolus injection, it is advantageous to incorporate human serum albumin or the patient's own heparinized blood into the saline at the time of formulation. The presence of an excess of such physiologically inert protein prevents loss of antibody by adsorption onto the walls of the container and tubing used with the infusion solution. If albumin is used, a suitable concentration is from 0.5 to 4.5% by weight of the saline solution.
One embodiment of the present invention provides an immunoconjugate comprising a humanized antibody of the invention, e.g., a humanized anti-Langerin antibody, linked to one or more effector molecules, antigen(s) and/or a detectable label(s). Preferably, the effector molecule is a therapeutic molecule such as, for example, one or more peptides that comprise one or more T cell epitopes, a toxin, a small molecule, a cytokine or a chemokine, an enzyme, or a radiolabel.
Exemplary toxins include, but are not limited to, Pseudomonas exotoxin or diphtheria toxin. Examples of small molecules include, but are not limited to, chemotherapeutic compounds such as taxol, doxorubicin, etoposide, and bleiomycin. Exemplary cytokines include, but are not limited to, IL-1, IL-2, IL-4, IL-5, IL-6, and IL-12, IL-17, and IL-25. Exemplary enzymes include, but are not limited to, RNAses, DNAses, proteases, kinases, and caspases. Exemplary radioisotopes include, but are not limited to, 32P and 125I.
As used herein, the term “epitope” refers to a molecule or substance capable of stimulating an immune response. In one example, epitopes include but are not limited to a polypeptide and a nucleic acid encoding a polypeptide, wherein expression of the nucleic acid into a polypeptide is capable of stimulating an immune response when the polypeptide is processed and presented on a Major Histocompatibility Complex (MHC) molecule. Generally, epitopes include peptides presented on the surface of cells non-covalently bound to the binding groove of Class I or Class II MHC, such that they can interact with T cell receptors and the respective T cell accessory molecules.
Proteolytic Processing of Antigens. Epitopes that are displayed by MHC on antigen presenting cells are cleavage peptides or products of larger peptide or protein antigen precursors. For MHC I epitopes, protein antigens are often digested by proteasomes resident in the cell. Intracellular proteasomal digestion produces peptide fragments of about 3 to 23 amino acids in length that are then loaded onto the MHC protein. Additional proteolytic activities within the cell, or in the extracellular milieu, can trim and process these fragments further. Processing of MHC Class II epitopes generally occurs via intracellular proteases from the lysosomal/endosomal compartment. The present invention includes, in one embodiment, pre-processed peptides that are attached to the anti-Langerin antibody (or binding fragment thereof) that directs the peptides against which an enhanced immune response is sought directly to antigen presenting cells.
To identify epitopes potentially effective as immunogenic compounds, predictions of MHC binding alone are useful but often insufficient. The present invention includes methods for specifically identifying the epitopes within antigens most likely to lead to the immune response sought for the specific sources of antigen presenting cells and responder T cells.
The present invention allows for a rapid and easy assay for the identification of those epitopes that are most likely to produce the desired immune response using the patient's own antigen presenting cells and T cell repertoire. The compositions and methods of the present invention are applicable to any protein sequence, allowing the user to identify the epitopes that are capable of binding to MHC and are properly presented to T cells that will respond to the antigen. Accordingly, the invention is not limited to any particular target or medical condition, but instead encompasses and MHC epitope(s) from any useful source.
As used herein, the term “veneered” refers to a humanized antibody framework onto which antigen-binding sites or CDRs obtained from non-human antibodies (e.g., mouse, rat or hamster), are placed into human heavy and light chain conserved structural framework regions (FRs), for example, in a light chain or heavy chain polynucleotide to “graft” the specificity of the non-human antibody into a human framework from, e.g., SEQ ID NOS: 45-48 or the nucleic acids that encode those sequences, as will be readily apparent to the skilled artisan. The polynucleotide expression vector or vectors that express the veneered antibodies can be transfected mammalian cells for the expression of recombinant human antibodies which exhibit the antigen specificity of the non-human antibody and will undergo posttranslational modifications that will enhance their expression, stability, solubility, or combinations thereof.
Antigens.
Examples of viral antigens for use with the present invention include, but are not limited to, e.g., HIV, HCV, CMV, adenoviruses, retroviruses, picornaviruses, etc. Non-limiting example of retroviral antigens such as retroviral antigens from the human immunodeficiency virus (HIV) antigens such as gene products of the gag, pol, and env genes, the Nef protein, reverse transcriptase, and other HIV components; hepatitis viral antigens such as the S, M, and L proteins of hepatitis B virus, the pre-S antigen of hepatitis B virus, and other hepatitis, e.g., hepatitis A, B, and C, viral components such as hepatitis C viral RNA; influenza viral antigens such as hemagglutinin and neuraminidase and other influenza viral components; measles viral antigens such as the measles virus fusion protein and other measles virus components; rubella viral antigens such as proteins E1 and E2 and other rubella virus components; rotaviral antigens such as VP7sc and other rotaviral components; cytomegaloviral antigens such as envelope glycoprotein B and other cytomegaloviral antigen components; respiratory syncytial viral antigens such as the RSV fusion protein, the M2 protein and other respiratory syncytial viral antigen components; herpes simplex viral antigens such as immediate early proteins, glycoprotein D, and other herpes simplex viral antigen components; varicella zoster viral antigens such as gpI, gpII, and other varicella zoster viral antigen components; Japanese encephalitis viral antigens such as proteins E, M-E, M-E-NS1, NS1, NS1-NS2A, 80% E, and other Japanese encephalitis viral antigen components; rabies viral antigens such as rabies glycoprotein, rabies nucleoprotein and other rabies viral antigen components. See Fundamental Virology, Second Edition, eds. Fields, B. N. and Knipe, D. M. (Raven Press, New York, 1991) for additional examples of viral antigens. The at least one viral antigen may be peptides from an adenovirus, retrovirus, picornavirus, herpesvirus, rotaviruses, hantaviruses, coronavirus, togavirus, flavirvirus, rhabdovirus, paramyxovirus, orthomyxovirus, bunyavirus, arenavirus, reovirus, papilomavirus, parvovirus, poxvirus, hepadnavirus, or spongiform virus. In certain specific, non-limiting examples, the at least one viral antigen are peptides obtained from at least one of HIV, CMV, hepatitis A, B, and C, influenza, measles, polio, smallpox, rubella; respiratory syncytial, herpes simplex, varicella zoster, Epstein-Barr, Japanese encephalitis, rabies, flu, and/or cold viruses.
In one aspect, the one or more of the antigenic peptides are selected from at least one of: Nef (66-97): VGFPVTPQVPLRPMTYKAAVDLSHFLKEKGGL (SEQ ID NO.: 31); Nef (116-145): HTQGYFPDWQNYTPGPGVRYPLTFGWLYKL (SEQ ID NO.: 32); Gag p17 (17-35): EKIRLRPGGKKKYKLKHIV (SEQ ID NO.: 33); Gag p17-p24 (253-284): NPPIPVGEIYKRWIILGLNKIVRMYSPTSILD (SEQ ID NO.: 34); or Pol 325-355 (RT 158-188) is: AIFQSSMTKILEPFRKQNPDIVIYQYMDDLY (SEQ ID NO.: 35). In one aspect, the fusion protein peptides are separated by one or more linkers selected from:
Antigenic targets that may be delivered using the anti-Langerin-antigen vaccines of the present invention include genes encoding antigens such as viral antigens, bacterial antigens, fungal antigens or parasitic antigens. Pathogens include trypanosomes, tapeworms, roundworms, helminthes, malaria. Tumor markers, such as fetal antigen or prostate specific antigen, may be targeted in this manner. Other examples include: HIV env proteins and hepatitis B surface antigen. Administration of a vector according to the present invention for vaccination purposes would require that the vector-associated antigens be sufficiently non-immunogenic to enable long-term expression of the transgene, for which a strong immune response would be desired. In some cases, vaccination of an individual may only be required infrequently, such as yearly or biennially, and provide long-term immunologic protection against the infectious agent. Specific examples of organisms, allergens and nucleic and amino sequences for use in vectors and ultimately as antigens with the present invention may be found in U.S. Pat. No. 6,541,011, relevant portions incorporated herein by reference, in particular, the tables that match organisms and specific sequences that may be used with the present invention.
Bacterial antigens for use with the anti-Langerin-antigen vaccines disclosed herein include, but are not limited to, e.g., bacterial antigens such as pertussis toxin, filamentous hemagglutinin, pertactin, FIM2, FIM3, adenylate cyclase and other pertussis bacterial antigen components; diptheria bacterial antigens such as diptheria toxin or toxoid and other diptheria bacterial antigen components; tetanus bacterial antigens such as tetanus toxin or toxoid and other tetanus bacterial antigen components; streptococcal bacterial antigens such as M proteins and other streptococcal bacterial antigen components; gram-negative bacilli bacterial antigens such as lipopolysaccharides and other gram-negative bacterial antigen components, Mycobacterium tuberculosis bacterial antigens such as mycolic acid, heat shock protein 65 (HSP65), the 30 kDa major secreted protein, antigen 85A and other mycobacterial antigen components; Helicobacter pylori bacterial antigen components; pneumococcal bacterial antigens such as pneumolysin, pneumococcal capsular polysaccharides and other pneumococcal bacterial antigen components; haemophilus influenza bacterial antigens such as capsular polysaccharides and other haemophilus influenza bacterial antigen components; anthrax bacterial antigens such as anthrax protective antigen and other anthrax bacterial antigen components; rickettsiae bacterial antigens such as rompA and other rickettsiae bacterial antigen component. Also included with the bacterial antigens described herein are any other bacterial, mycobacterial, mycoplasmal, rickettsial, or chlamydial antigens. Partial or whole pathogens may also be: haemophilus influenza; Plasmodium falciparum; neisseria meningitidis; streptococcus pneumoniae; neisseria gonorrhoeae; salmonella serotype typhi; shigella; vibrio cholerae; Dengue Fever; Encephalitides; Japanese Encephalitis; lyme disease; Yersinia pestis; west nile virus; yellow fever; tularemia; hepatitis (viral; bacterial); RSV (respiratory syncytial virus); HPIV 1 and HPIV 3; adenovirus; small pox; allergies and cancers.
Fungal antigens for use with compositions and methods of the invention include, but are not limited to, e.g., candida fungal antigen components; histoplasma fungal antigens such as heat shock protein 60 (HSP60) and other histoplasma fungal antigen components; cryptococcal fungal antigens such as capsular polysaccharides and other cryptococcal fungal antigen components; coccidiodes fungal antigens such as spherule antigens and other coccidiodes fungal antigen components; and tinea fungal antigens such as trichophytin and other coccidiodes fungal antigen components.
Examples of protozoal and other parasitic antigens include, but are not limited to, e.g., plasmodium falciparum antigens such as merozoite surface antigens, sporozoite surface antigens, circumsporozoite antigens, gametocyte/gamete surface antigens, blood-stage antigen pf 155/RESA and other plasmodial antigen components; toxoplasma antigens such as SAG-1, p30 and other toxoplasmal antigen components; schistosomae antigens such as glutathione-S-transferase, paramyosin, and other schistosomal antigen components; leishmania major and other leishmaniae antigens such as gp63, lipophosphoglycan and its associated protein and other leishmanial antigen components; and trypanosoma cruzi antigens such as the 75-77 kDa antigen, the 56 kDa antigen and other trypanosomal antigen components.
Antigen that can be targeted using the anti-Langerin-antigen vaccines of the present invention will generally be selected based on a number of factors, including: likelihood of internalization, level of immune cell specificity, type of immune cell targeted, level of immune cell maturity and/or activation and the like. In this embodiment, the antibodies may be mono- or bi-specific antibodies that include one anti-Langerin binding domain and one binding domain against a second antigen, e.g., cell surface markers for dendritic cells such as, MHC class I, MHC Class II, B7-2, CD18, CD29, CD31, CD43, CD44, CD45, CD54, CD58, CD83, CD86, CMRF-44, CMRF-56, DCIR and/or Dectin-1 and the like; while in some cases also having the absence of CD2, CD3, CD4, CD8, CD14, CD15, CD16, CD 19, CD20, CD56, and/or CD57. Examples of cell surface markers for antigen presenting cells include, but are not limited to, MHC class I, MHC Class I, CD45, B7-1, B7-2, IFN-γ receptor and IL-2 receptor, ICAM-1 and/or Fcγ receptor. Examples of cell surface markers for T cells include, but are not limited to, CD3, CD4, CD8, CD 14, CD20, CD11b, CD16, CD45 and HLA-DR.
Target antigens on cell surfaces for delivery include those characteristic of tumor antigens typically will be derived from the cell surface, cytoplasm, nucleus, organelles and the like of cells of tumor tissue. Examples of tumor targets for the antibody portion of the present invention include, without limitation, hematological cancers such as leukemias and lymphomas, neurological tumors such as astrocytomas or glioblastomas, melanoma, breast cancer, lung cancer, head and neck cancer, gastrointestinal tumors such as gastric or colon cancer, liver cancer, pancreatic cancer, genitourinary tumors such cervix, uterus, ovarian cancer, vaginal cancer, testicular cancer, prostate cancer or penile cancer, bone tumors, vascular tumors, or cancers of the lip, nasopharynx, pharynx and oral cavity, esophagus, rectum, gall bladder, biliary tree, larynx, lung and bronchus, bladder, kidney, brain and other parts of the nervous system, thyroid, Hodgkin's disease, non-Hodgkin's lymphoma, multiple myeloma and leukemia.
Examples of antigens that may be delivered alone or in combination to immune cells for antigen presentation using the present invention includes tumor proteins, e.g., mutated oncogenes; viral proteins associated with tumors; and tumor mucins and glycolipids. The antigens may be viral proteins associated with tumors would be those from the classes of viruses noted above. Certain antigens may be characteristic of tumors (one subset being proteins not usually expressed by a tumor precursor cell), or may be a protein that is normally expressed in a tumor precursor cell, but having a mutation characteristic of a tumor. Other antigens include mutant variant(s) of the normal protein having an altered activity or subcellular distribution, e.g., mutations of genes giving rise to tumor antigens.
Specific non-limiting examples of tumor antigens for use in an anti-Langerin-fusion protein vaccine include, e.g., CEA, prostate specific antigen (PSA), HER-2/neu, BAGE, GAGE, MAGE 1-4, 6 and 12, MUC (Mucin) (e.g., MUC-1, MUC-2, etc.), GM2 and GD2 gangliosides, ras, myc, tyrosinase, MART (melanoma antigen), Pmel 17 (gp100), GnT-V intron V sequence (N-acetylglucoaminyltransferase V intron V sequence), Prostate Ca psm, PRAME (melanoma antigen), β-catenin, MUM-1-B (melanoma ubiquitous mutated gene product), GAGE (melanoma antigen) 1, MAGE, BAGE (melanoma antigen) 2-10, c-ERB2 (Her2/neu), DAGE, EBNA (Epstein-Barr Virus nuclear antigen) 1-6, gp75, human papilloma virus (HPV) E6 and E7, p53, lung resistance protein (LRP), Bcl-2, Ki-67, Cyclin B1, gp100, Survivin, and NYESO-1.
In addition, the immunogenic molecule can be an autoantigen involved in the initiation and/or propagation of an autoimmune disease, the pathology of which is largely due to the activity of antibodies specific for a molecule expressed by the relevant target organ, tissue, or cells, e.g., SLE or MG. In such diseases, it can be desirable to direct an ongoing antibody-mediated (i.e., a Th2-type) immune response to the relevant autoantigen towards a cellular (i.e., a Th1-type) immune response. Alternatively, it can be desirable to prevent onset of or decrease the level of a Th2 response to the autoantigen in a subject not having, but who is suspected of being susceptible to, the relevant autoimmune disease by prophylactically inducing a Th1 response to the appropriate autoantigen. Autoantigens of interest include, without limitation: (a) with respect to SLE, the Smith protein, RNP ribonucleoprotein, and the SS-A and SS-B proteins; and (b) with respect to MG, the acetylcholine receptor. Examples of other miscellaneous antigens involved in one or more types of autoimmune response include, e.g., endogenous hormones such as luteinizing hormone, follicular stimulating hormone, testosterone, growth hormone, prolactin, and other hormones.
Antigens involved in autoimmune diseases, allergy, and graft rejection can be used in the compositions and methods of the invention. For example, an antigen involved in any one or more of the following autoimmune diseases or disorders can be used in the present invention: diabetes, diabetes mellitus, arthritis (including rheumatoid arthritis, juvenile rheumatoid arthritis, osteoarthritis, psoriatic arthritis), multiple sclerosis, myasthenia gravis, systemic lupus erythematosis, autoimmune thyroiditis, dermatitis (including atopic dermatitis and eczematous dermatitis), psoriasis, Sjogren's Syndrome, including keratoconjunctivitis sicca secondary to Sjogren's Syndrome, alopecia areata, allergic responses due to arthropod bite reactions, Crohn's disease, aphthous ulcer, iritis, conjunctivitis, keratoconjunctivitis, ulcerative colitis, asthma, allergic asthma, cutaneous lupus erythematosus, scleroderma, vaginitis, proctitis, drug eruptions, leprosy reversal reactions, erythema nodosum leprosum, autoimmune uveitis, allergic encephalomyelitis, acute necrotizing hemorrhagic encephalopathy, idiopathic bilateral progressive sensorineural hearing loss, aplastic anemia, pure red cell anemia, idiopathic thrombocytopenia, polychondritis, Wegener's granulomatosis, chronic active hepatitis, Stevens-Johnson syndrome, idiopathic sprue, lichen planus, Crohn's disease, Graves ophthalmopathy, sarcoidosis, primary biliary cirrhosis, uveitis posterior, and interstitial lung fibrosis. Examples of antigens involved in autoimmune disease include glutamic acid decarboxylase 65 (GAD 65), native DNA, myelin basic protein, myelin proteolipid protein, acetylcholine receptor components, thyroglobulin, and the thyroid stimulating hormone (TSH) receptor.
Examples of antigens involved in allergy include pollen antigens such as Japanese cedar pollen antigens, ragweed pollen antigens, rye grass pollen antigens, animal derived antigens such as dust mite antigens and feline antigens, histocompatiblity antigens, and penicillin and other therapeutic drugs. Examples of antigens involved in graft rejection include antigenic components of the graft to be transplanted into the graft recipient such as heart, lung, liver, pancreas, kidney, and neural graft components. The antigen may be an altered peptide ligand useful in treating an autoimmune disease.
It will be appreciated by those of skill in the art that the sequence of any protein effector molecule may be altered in a manner that does not substantially affect the functional advantages of the effector protein. For example, glycine and alanine are typically considered to be interchangeable as are aspartic acid and glutamic acid and asparagine and glutamine. One of skill in the art will recognize that many different variations of effector sequences will encode effectors with roughly the same activity as the native effector. The effector molecule and the antibody may be conjugated by chemical or by recombinant means as described above. Chemical modifications include, for example, derivitization for the purpose of linking the effector molecule and the antibody to each other, either directly or through a linking compound, by methods that are well known in the art of protein chemistry. Both covalent and noncovalent attachment methods may be used with the humanized antibodies of the present invention.
The procedure for attaching an effector molecule to an antibody will vary according to the chemical structure of the moiety to be attached to the antibody. Polypeptides typically contain a variety of functional groups; e.g., carboxylic acid (COOH), free amine (—NH2) or sulfhydryl (—SH) groups, which are available for reaction with a suitable functional group on an antibody to result in the binding of the effector molecule. Alternatively, the antibody can be derivatized to expose or to attach additional reactive functional groups, e.g., by attachment of any of a number of linker molecules such as those available from Pierce Chemical Company, Rockford Ill.
The linker is capable of forming covalent bonds to both the antibody and to the effector molecule. Suitable linkers are well known to those of skill in the art and include, but are not limited to, straight or branched-chain carbon linkers, heterocyclic carbon linkers, or peptide linkers. Where the antibody and the effector molecule are polypeptides, the linkers may be joined to the constituent amino acids through their side groups (e.g., through a disulfide linkage to cysteine). However, in a preferred embodiment, the linkers will be joined to the alpha carbon amino and carboxyl groups of the terminal amino acids.
In some circumstances, it is desirable to free the effector molecule from the antibody when the immunoconjugate has reached its target site. Therefore, in these circumstances, immunoconjugates will comprise linkages that are cleavable in the vicinity of the target site. Cleavage of the linker to release the effector molecule from the antibody may be prompted by enzymatic activity or conditions to which the immunoconjugate is subjected either inside the target cell or in the vicinity of the target site. When the target site is a tumor, a linker that is cleavable under conditions present at the tumor site (e.g. when exposed to tumor-associated enzymes or acidic pH) may be used.
Exemplary chemical modifications of the effector molecule and the antibody of the present invention also include derivitization with polyethylene glycol (PEG) to extend time of residence in the circulatory system and reduce immunogenicity, according to well known methods (See for example, Lisi, et al., Applied Biochem. 4:19 (1982); Beauchamp, et al., Anal Biochem. 131:25 (1982); and Goodson, et al., Bio/Technology 8:343 (1990)).
The present invention contemplates vaccines for use in both active and passive immunization embodiments. Immunogenic compositions, proposed to be suitable for use as a vaccine, may be prepared most readily directly from immunogenic T-cell stimulating peptides prepared in a manner disclosed herein. The final vaccination material is dialyzed extensively to remove undesired small molecular weight molecules and/or lyophilized for more ready formulation into a desired vehicle. In certain embodiment of the present invention, the compositions and methods of the present invention are used to manufacture a cellular vaccine, e.g., the antigen-delivering anti-Langerin binding portion of the antibody is used to direct the antigen(s) to an antigen presenting cell, which then “loads” the antigen onto MHC proteins for presentation. The cellular vaccine is, therefore, the antigen presenting cell that has been loaded using the compositions of the present invention to generate antigen-loaded antigen presenting cells.
When the vaccine is the anti-Langerin binding protein itself, e.g., a complete antibody or binding fragments thereof, then these “active ingredients” can be made into vaccines using methods understood in the art, e.g., U.S. Pat. Nos. 4,608,251; 4,601,903; 4,599,231; 4,599,230; and 4,578,770, relevant portions incorporated herein by reference. Typically, such vaccines are prepared as injectables, e.g., as liquid solutions or suspensions or solid forms suitable for re-suspension in liquid prior to injection. The preparation may also be emulsified. The active immunogenic ingredient is often mixed with excipients which are pharmaceutically acceptable and compatible with the active ingredient. Suitable excipients are, for example, water, saline, dextrose, glycerol, ethanol, or the like and combinations thereof. In addition, if desired, the vaccine may contain minor amounts of auxiliary substances such as wetting or emulsifying agents, pH buffering agents, or adjuvants that enhance the effectiveness of the vaccines.
The vaccines are administered in a manner compatible with the dosage formulation, and in such amount as will be therapeutically effective and immunogenic. The quantity to be administered depends on the subject to be treated, including, e.g., the capacity of the individual's immune system to generate an immune response. Precise amounts of cells or active ingredient required to be administered depend on the judgment of the practitioner. However, suitable dosage ranges are of the order of a few thousand cells (to millions of cells) for cellular vaccines. For standard epitope or epitope delivery vaccines then the vaccine may be several hundred micrograms active ingredient per vaccination. Suitable regimes for initial administration and booster shots are also variable, but are typified by an initial administration followed by subsequent inoculations or other administrations.
The manner of application may vary widely, however, certain embodiments herein will most likely be delivered intravenously or at the site of a tumor or infection directly. Regardless, any of the conventional methods for administration of a vaccine are applicable. The dosage of the vaccine will depend on the route of administration and will vary according to the size of the host.
In many instances, it will be desirable to have multiple administrations of the vaccine, e.g., four to six vaccinations provided weekly or every other week. A normal vaccination regimen will often occur in two to twelve week intervals or from three to six week intervals. Periodic boosters at intervals of 1-5 years, usually three years, may be desirable to maintain protective levels of the immune response or upon a likelihood of a remission or re-infection. The course of the immunization may be followed by assays for, e.g., T cell activation, cytokine secretion or even antibody production, most commonly conducted in vitro. These immune response assays are well known and may be found in a wide variety of patents and as taught herein.
The vaccine of the present invention may be provided in one or more “unit doses” depending on whether the nucleic acid vectors are used, the final purified proteins, or the final vaccine form is used. Unit dose is defined as containing a predetermined-quantity of the therapeutic composition calculated to produce the desired responses in association with its administration, i.e., the appropriate route and treatment regimen. The quantity to be administered, and the particular route and formulation, are within the skill of those in the clinical arts. The subject to be treated may also be evaluated, in particular, the state of the subject's immune system and the protection desired. A unit dose need not be administered as a single injection but may include continuous infusion over a set period of time. Unit dose of the present invention may conveniently be described in terms of DNA/kg (or protein/Kg) body weight, with ranges between about 0.05, 0.10, 0.15, 0.20, 0.25, 0.5, 1, 10, 50, 100, 1,000 or more mg/DNA or protein/kg body weight are administered.
Likewise, the amount of anti-Langerin-antigen vaccine delivered can vary from about 0.2 to about 8.0 mg/kg body weight. Thus, in particular embodiments, 0.4 mg, 0.5 mg, 0.8 mg, 1.0 mg, 1.5 mg, 2.0 mg, 2.5 mg, 3.0 mg, 4.0 mg, 5.0 mg, 5.5 mg, 6.0 mg, 6.5 mg, 7.0 mg and 7.5 mg of the vaccine may be delivered to an individual in vivo. The dosage of vaccine to be administered depends to a great extent on the weight and physical condition of the subject being treated as well as the route of administration and the frequency of treatment. A pharmaceutical composition that includes a naked polynucleotide prebound to a liposomal or viral delivery vector may be administered in amounts ranging from 1 μg to 1 mg polynucleotide to 1 μg to 100 mg protein. Thus, particular compositions may include between about 1 μg, 5 μg, 10 μg, 20 μg, 30 μg, 40 μg, 50 μg, 60 μg, 70 μg, 80 μg, 100 μg, 150 μg, 200 μg, 250 μg, 500 μg, 600 μg, 700 μg, 800 μg, 900 μg or 1,000 μg polynucleotide or protein that is bound independently to 1 μg, 5 μg, 10 μg, 20 μg, 3.0 μg, 40 μg 50 μg, 60 μg, 70 μg, 80 μg, 100 μg, 150 μg, 200 μg, 250 μg, 500 μg, 600 μg, 700 μg, 800 μg, 900 μg, 1 mg, 1.5 mg, 5 mg, 10 mg, 20 mg, 30 mg, 40 mg, 50 mg, 60 mg, 70 mg, 80 mg, 90 mg or 100 mg vector.
Antibodies of the present invention may optionally be covalently or non-covalently linked to a detectable label. Detectable labels suitable for such use include any composition detectable by spectroscopic, photochemical, biochemical, immunochemical, electrical, optical or chemical methods. Useful labels in the present invention include magnetic beads (e.g. DYNABEADS™), fluorescent dyes (e.g., fluorescein isothiocyanate, Texas red, rhodamine, green fluorescent protein, and the like), radiolabels (e.g., 3H, 125I, 35S, 14C, or 32P), enzymes (e.g., horse radish peroxidase, alkaline phosphatase and others commonly used in an ELISA), and colorimetric labels such as colloidal gold or colored glass or plastic (e.g. polystyrene, polypropylene, latex, etc.) beads.
Methods of detecting such labels are well known to those of skill in the art. Thus, for example, radiolabels may be detected using photographic film or scintillation counters, fluorescent markers may be detected using a photodetector to detect emitted illumination. Enzymatic labels are typically detected by providing the enzyme with a substrate and detecting the reaction product produced by the action of the enzyme on the substrate, and colorimetric labels are detected by simply visualizing the colored label.
The antibody and/or immunoconjugate compositions of this invention are particularly useful for parenteral administration, such as intravenous administration or administration into a body cavity. The compositions for administration will commonly comprise a solution of the antibody and/or immunoconjugate dissolved in a pharmaceutically acceptable carrier, preferably an aqueous carrier. A variety of aqueous carriers can be used, e.g., buffered saline and the like. These solutions are sterile and generally free of undesirable matter. These compositions may be sterilized by conventional, well-known sterilization techniques. The compositions may contain pharmaceutically acceptable auxiliary substances as required to approximate physiological conditions such as pH adjusting and buffering agents, toxicity adjusting agents and the like, for example, sodium acetate, sodium chloride, potassium chloride, calcium chloride, sodium lactate and the like. The concentration of fusion protein in these formulations can vary widely, and will be selected primarily based on fluid volumes, viscosities, body weight and the like in accordance with the particular mode of administration selected and the patient's needs.
Thus, a typical pharmaceutical immunoconjugate composition of the present invention for intravenous administration would be about 0.1 to 10 mg per patient per day. Dosages from 0.1 up to about 100 mg per patient per day may be used. Actual methods for preparing administrable compositions will be known or apparent to those skilled in the art and are described in more detail in such publications as R
The compositions of the present invention can be administered for therapeutic treatments. In therapeutic applications, compositions are administered to a patient suffering from a disease, in an amount sufficient to cure or at least partially arrest the disease and its complications. An amount adequate to accomplish this is defined as a “therapeutically effective dose.” Amounts effective for this use will depend upon the severity of the disease and the general state of the patient's health. An effective amount of the compound is that which provides either subjective relief of a symptom(s) or an objectively identifiable improvement as noted by the clinician or other qualified observer.
Single or multiple administrations of the compositions are administered depending on the dosage and frequency as required and tolerated by the patient. In any event, the composition should provide a sufficient quantity of the proteins of this invention to effectively treat the patient. Preferably, the dosage is administered once but may be applied periodically until either a therapeutic result is achieved or until side effects warrant discontinuation of therapy. Generally, the dose is sufficient to treat or ameliorate symptoms or signs of disease without producing unacceptable toxicity to the patient.
Controlled release parenteral formulations of the immunoconjugate compositions of the present invention can be made as implants, oily injections, or as particulate systems. For a broad overview of protein delivery systems see, Banga, A. J., T
Polymers can be used for ion-controlled release of immunoconjugate compositions of the present invention. Various degradable and non-degradable polymeric matrices for use in controlled drug delivery are known in the art (Langer, R., Accounts Chem. Res. 26:537-542 (1993)). For example, the block copolymer, poloxamer 407® exists as a viscous yet mobile liquid at low temperatures but forms a semisolid gel at body temperature, hydroxyapatite has been used as a microcarrier for controlled release of proteins, and/or liposomes may be used for controlled release as well as drug targeting of the lipid-capsulated drug. Numerous additional systems for controlled delivery of therapeutic proteins are known. See, e.g., U.S. Pat. Nos. 5,055,303, 5,188,837, 4,235,871, 4,501,728, 4,837,028 4,957,735 and 5,019,369, 5,055,303; 5,514,670; 5,413,797; 5,268,164; 5,004,697; 4,902,505; 5,506,206, 5,271,961; 5,254,342 and 5,534,496, relevant portions of each of which are incorporated herein by reference.
Among various uses of the immunoconjugates of the invention are included a variety of disease conditions caused by specific human cells that may be eliminated by the toxic action of the fusion protein. For example, for the humanized Anti-Langerin antibodies, e.g., 15B10 having ATCC Accession No. PTA-9852, 2G3 having ATCC Accession No. PTA-9853, 91E7, 37C1, or 4C7 and binding fragments thereof, disclosed herein. For example, one application for immunoconjugates is the treatment of malignant cells expressing Langerin. Exemplary malignant cells include those of chronic lymphocytic leukemia and hairy cell leukemia.
In another embodiment, this invention provides kits for the delivery of antigens, e.g., Langerin or an immunoreactive fragment thereof, conjugated or in the form of a fusion protein with one or more T cell or B cell epitopes. A “biological sample” as used herein is a sample of biological tissue or fluid that contains the antigen. Such samples include, but are not limited to, tissue from biopsy, blood, and blood cells (e.g., white cells). Preferably, the cells are lymphocytes, e.g., dendritic cells. Biological samples also include sections of tissues, such as frozen sections taken for histological purposes. A biological sample is typically obtained from a multicellular eukaryote, preferably a mammal such as rat, mouse, cow, dog, guinea pig, or rabbit, and more preferably a primate, such as a macaque, chimpanzee, or human. Most preferably, the sample is from a human. The antibodies of the invention may also be used in vivo, for example, as a diagnostic tool for in vivo imaging.
Kits will typically comprise a nucleic acid sequence that encodes an antibody of the present invention (or binding fragment thereof) with one or more framework portions or multiple cloning sites at the carboxy-terminal end into which the coding sequences for one or more antigens may be inserted. In some embodiments, the antibody will be a humanized anti-Langerin Fv fragment, such as an scFv or dsFv fragment. In addition the kits will typically include instructional materials disclosing methods of use of an antibody of the present invention (e.g. for loading into dendritic cells prior to immunization with the dendritic cells, which can be autologous dendritic cells). The kits may also include additional components to facilitate the particular application for which the kit is designed. Thus, for example, the kit may additionally contain methods of detecting the label (e.g. enzyme substrates for enzymatic labels, filter sets to detect fluorescent labels, appropriate secondary labels such as a sheep anti-mouse-HRP, or the like). The kits may additionally include buffers and other reagents routinely used for the practice of a particular method. Such kits and appropriate contents are well known to those of skill in the art.
In another set of uses for the invention, immunoconjugates targeted by antibodies of the invention can be used to purge targeted cells from a population of cells in a culture. For example, if a specific population of T cells is preferred, the immunoconjugates of the present invention may be used to enrich a population of T cells having the opposite effect of the on-going immune response. Thus, for example, cells cultured from a patient having a cancer can be purged of cancer cells by providing the patient with dendritic cells that were antigen loaded using the antibodies of the invention as a targeting moiety for the antigens that will trigger an immune response against the cancer, virus or other pathogen. Likewise, the immunoconjugates can be used to increase the population of regulatory T cells or drive the immune response toward or away from a cytotoxic T cell response or even drive a B cell response.
Differential functions of DC subsets: The present inventors have demonstrated that LCs and intDCs derived from CD34+ hematopoietic progenitor cells differ in their capacity to activate lymphocytes (
DC subsets play an important role in determining CD4+ T cell responses. Either polarized DCs or distinct DC subsets provide T cells with different signals that determine the types of immune response (Type 1 versus Type 2)21. Thus, in mice, splenic CD8+ DCs prime naïve CD4+ T cells to make Th1 cytokines in a process involving IL-12, whereas splenic CD8+DCs prime naïve CD4+ T cells to make Th2 cytokines22,23. Furthermore, different signals from the same DCs can induce different T-cell polarization, as shown by the induction of IL-12 production and Th1-cell polarization when DCs are activated with Escherichia coli lipopolysaccharide (LPS), but no IL-12 production and Th2-cell polarization when DCs are exposed to LPS from Porphyromonas gingivalis24. CD40-ligand (CD40L)-activated DCs prime Th1 responses through an IL-12-dependent mechanism, whereas pDCs activated with IL-3 and CD40L have been shown to secrete negligible amounts of IL-12 and prime Th2 responses25. Soares, et al. also reported that two DC subsets that express different lectins have innate propensities to differentially affect the Th1/Th2 balance in vivo by distinct mechanisms. More interestingly, we have found that delivering the same antigens to the same type of DCs, but through different DC-receptors, induces a different quality of CD4+ T cell responses (see preliminary data). Thus, both DC subsets and activation signals to which DCs are exposed are important factors determining the nature of immune outcome.
This data shows that addition of antigen to the H-chain C-termini does not affect the binding of the antibody to cell surface Langerin and also demonstrates that these anti-Langerin antibodies serve as effective vehicles to bring antigen to the surface of cells bearing human Langerin.
These data show that an anti-Langerin vaccine bearing a cancer antigen can prime a potent antigen-specific anti-CD4+ T cell response in vitro using immune cells from a normal individual. In this in vitro culture system this agent is as potent as an anti-CD40 based vaccine—these DCs express both receptors. In vivo, an anti-Langerin-based vaccine would target antigen only to Langerhans cells (LCs), and based on recent research [Immunity, Volume 29, Issue 3, 497-510, 19 Sep. 2008] LCs preferentially induce the differentiation of CD4+ T cells secreting T helper 2 (Th2) cell cytokines and are particularly efficient at priming and cross priming naive CD8+ T cells—the latter characteristic is particularly desirable for evoking anti-cancer CTL responses. In contrast, anti-CD40 targeting agents would deliver antigen to a much broader array of APC in vivo.
These data show that an anti-Langerin vaccine bearing a cancer antigen can prime a potent antigen-specific anti-CD8+ T cell response in vitro using immune cells from a prostate cancer. In this in vitro culture system this agent is as potent as a anti-CD40 based vaccine—these DCs express both receptors. In vivo, an anti-Langerin-based vaccine would target antigen only to Langerhans cells (LCs), and based on recent research [Immunity, Volume 29, Issue 3, 497-510, 19 Sep. 2008] LCs preferentially induce the differentiation of CD4+ T cells secreting T helper 2 (Th2) cell cytokines and are particularly efficient at priming and cross priming naive CD8+ T cells—the latter characteristic is particularly desirable for evoking anti-cancer CTL responses. In contrast, anti-CD40 targeting agents would deliver antigen to a much broader array of APC in vivo.
The data in panel
Constructs.
mAnti-Langerin15B10K—Nucleotide and mature protein amino acid sequence of the light chain of the mouse anti-Langerin 15B10 antibody cDNA, respectively. The variable region residues are underlined.
ATGAAGTTGCCTGTTAGGCTGTTGGTGCTGATGTTCTGGATTCCTG
QSPKLLIYKVSNRFSGVPDRFSGSGSGTNFTLKISRVEAEDLGLYF
CSQSTHVPYTFGGGTKLEIKRADAAPTVSIFPPSSEQLTSGGASVV
mAnti-Langerin15B10H-LV-hIgG4H-C—Nucleotide and mature protein amino acid sequence of the heavy chain variable region of the mouse anti-Langerin 15B10 antibody fused to human IgG4, respectively. The variable region residues are underlined.
ATGGAATGGAGGATCTTTCTCTTCATCCTGTCAGGAACTGCAGGTGT
IGDIYPGSGYSFYNENFKGKATLTADKSSTTAYMQLSSLTSEDSAVY
FCATYYNYPFAYWGQGTLVTVSAAKTTGPSVFPLAPCSRSTSESTAA
mAnti-Langerin2G3L (produced by hybridoma ATCC Accession No. PTA-9853)—Nucleotide and mature protein amino acid sequence of the light chain of the mouse anti-Langerin 2G3 antibody cDNA, respectively. The variable region residues are underlined.
ATGGCCTGGATTTCACTTATACTCTCTCTCCTGGCTCTCAGCTCAG
GLIGGTNNRVSGVPARFSGSLIGDKAALTITGAQTEDEAIYFCALWY
mAnti-Langerin2G3H—Nucleotide and mature protein amino acid sequence of the heavy chain of the mouse anti-Langerin 2G3 antibody cDNA, respectively. The variable region residues are underlined.
ATGACATTGAACATGCTGTTGGGGCTGAAGTGGGTTTTCTTTGTTGT
VARIRNKSNNYATYYADSVKDRFTISRDDSQSLLYLQMNNLKTEDTA
MYYCVGRDWFDYWGQGTLVTVSAAKTTPPSVYPLAPGSAAQTNSMVT
C84 rAB-pIRES2 [mAnti-Langerin2G3H-LV-hIgG4H-C-Dockerin] The coding region for this H chain-dockerin fusion protein is shown below. Start and stop codons are in bold, as is the joining GCTAGC restriction site.
ATGACATTGAACATGCTGTTGGGGCTGAGGTGGGTTTTCTTTGTTGTTTT
ACGGAAAAGTAAACTCCACTGACTTGACTTTGTTAAAAAGATATGTTCTT
AAAGCCGTCTCAACTCTCCCTTCTTCCAAAGCTGAAAAGAACGCAGATGT
AAATCGTGACGGAAGAGTTAATTCCAGTGATGTCACAATACTTTCAAGAT
ATTTGATAAGGGTAATCGAGAAATTACCAATA
TAA
The mature H chain sequence for C84 heavy chain is shown below. Joining sequence AS is bold and dockerin is underlined.
NSTDLTLLKRYVLKAVSTLPSSKAEKNADVNRDGRVNSSDVTILSRYLIRVIEKLPI
C85 rAB-pIRES2 [mAnti-Langerin2G3H-LV-hIgG4H-C-Flex-FluHA1-1-6×His] The coding region for this H chain-Flu HA1-1 fusion protein is shown below. Start and stop codons are in bold, as is the joining GCTAGC restriction site.
ATGACATTGAACATGCTGTTGGGGCTGAGGTGGGTTTTCTTTGTTGTTTT
ACACAATATGTATAGGCTACCATGCGAACAATTCAACCGACACTGTTGAC
ACAGTACTCGAGAAGAATGTGACAGTGACACACTCTGTTAACCTGCTCGA
AGACAGCCACAACGGAAAACTATGTAGATTAAAAGGAATAGCCCCACTAC
AATTGGGGAAATGTAACATCGCCGGATGGCTCTTGGGAAACCCAGAATGC
GACCCACTGCTTCCAGTGAGATCATGGTCCTACATTGTAGAAACACCAAA
CTCTGAGAATGGAATATGTTATCCAGGAGATTTCATCGACTATGAGGAGC
TGAGGGAGCAATTGAGCTCAGTGTCATCATTCGAAAGATTCGAAATATTT
CCCAAAGAAAGCTCATGGCCCAACCACAACACAAACGGAGTAACGGCAGC
ATGCTCCCATGAGGGGAAAAGCAGTTTTTACAGAAATTTGCTATGGCTGA
CGGAGAAGGAGGGCTCATACCCAAAGCTGAAAAATTCTTATGTGAACAAA
AAAGGGAAAGAAGTCCTTGTACTGTGGGGTATTCATCACCCGCCTAACAG
TAAGGAACAACAGAATCTCTATCAGAATGAAAATGCTTATGTCTCTGTAG
TGACTTCAAATTATAACAGGAGATTTACCCCGGAAATAGCAGAAAGACCC
AAAGTAAGAGATCAAGCTGGGAGGATGAACTATTACTGGACCTTGCTAAA
ACCCGGAGACACAATAATATTTGAGGCAAATGGAAATCTAATAGCACCAA
TGTATGCTTTCGCACTGAGTAGAGGCTTTGGGTCCGGCATCATCACCTCA
AACGCATCAATGCATGAGTGTAACACGAAGTGTCAAACACCCCTGGGAGC
TATAAACAGCAGTCTCCCTTACCAGAATATACACCCAGTCACAATAGGAG
AGTGCCCAAAATACGTCAGGAGTGCCAAATTGAGGATGGTTCACCATCAC
CATCACCAT
TGA
The mature H chain sequence for C85 heavy chain is shown below. Joining sequence AS is bold and Flu HA1-1 is underlined. A flexible linker joining sequence is italicized.
HANNSTDTVDTVLEKNVTVTHSVNLLEDSHNGKLCRLKGIAPLQLGKCNIAGWLLGNP
ECDPLLPVRSWSYIVETPNSENGICYPGDFIDYEELREQLSSVSSFERFEIFPKESSWPNHN
TNGVTAACSHEGKSSFYRNLLWLTEKEGSYPKLKNSYVNKKGKEVLVLWGIHHPPNS
KEQQNLYQNENAYVSVVTSNYNRRFTPEIAERPKVRDQAGRMNYYWTLLKPGDTIIFE
ANGNLIAPMYAFALSRGFGSGIITSNASMHECNTKCQTPLGAINSSLPYQNIHPVTIGECP
KYVRSAKLRMVHHHHHH
C86 rAB-pIRES2 [mAnti-Langerin2G3H-LV-hIgG4H-C-Flex-FluHA5-1-6×His] The coding region for this H chain-Flu HA5-1 fusion protein is shown below. Start and stop codons are in bold, as is the joining GCTAGC restriction site.
ATGACATTGAACATGCTGTTGGGGCTGAGGTGGGTTTTCTTTGTTGTTTT
ATCAGATTTGCATTGGTTACCATGCAAACAACTCGACAGAGCAGGTTGAC
ACAATAATGGAAAAGAACGTTACTGTTACACATGCCCAAGACATACTGGA
AAAGAAACACAACGGGAAGCTCTGCGATCTAGATGGAGTGAAGCCTCTAA
TTTTGAGAGATTGTAGCGTAGCTGGATGGCTCCTCGGAAACCCAATGTGT
GACGAATTCATCAATGTGCCGGAATGGTCTTACATAGTGGAGAAGGCCAA
TCCAGTCAATGACCTCTGTTACCCAGGGGATTTCAATGACTATGAAGAAT
TGAAACACCTATTGAGCAGAATAAACCATTTTGAGAAAATTCAGATCATC
CCCAAAAGTTCTTGGTCCAGTCATGAAGCCTCATTAGGGGTGAGCTCAGC
ATGTCCATACCAGGGAAAGTCCTCCTTTTTCAGAAATGTGGTATGGCTTA
TCAAAAAGAACAGTACATACCCAACAATAAAGAGGAGCTACAATAATACC
AACCAAGAAGATCTTTTGGTACTGTGGGGGATTCACCATCCTAATGATGC
GGCAGAGCAGACAAAGCTCTATCAAAACCCAACCACCTATATTTCCGTTG
GGACATCAACACTAAACCAGAGATTGGTACCAAGAATAGCTACTAGATCC
AAAGTAAACGGGCAAAGTGGAAGGATGGAGTTCTTCTGGACAATTTTAAA
GCCGAATGATGCAATCAACTTCGAGAGTAATGGAAATTTCATTGCTCCAG
AATATGCATACAAAATTGTCAAGAAAGGGGACTCAACAATTATGAAAAGT
GAATTGGAATATGGTAACTGCAACACCAAGTGTCAAACTCCAATGGGGGC
GATAAACTCTAGCATGCCATTCCACAATATACACCCTCTCACCATTGGGG
AATGCCCCAAATATGTGAAATCAAACAGATTAGTCCTTGCGCACCATCAC
CATCACCAT
TGA
The mature H chain sequence for C86 heavy chain is shown below. Joining sequence AS is bold and Flu HA5-1 is underlined. A flexible linker joining sequence is italicized.
HANNSTEQVDTIMEKNVTVTHAQDILEKKHNGKLCDLDGVKPLILRDCSVAGWLLGN
PMCDEFINVPEWSYIVEKANPVNDLCYPGDFNDYEELKHLLSRINHFEKIQIIPKSSWSS
HEASLGVSSACPYQGKSSFFRNVVWLIKKNSTYPTIKRSYNNTNQEDLLVLWGIHHPND
AAEQTKLYQNPTTYISVGTSTLNQRLVPRIATRSKVNGQSGRMEFFWTILKPNDAINFES
NGNFIAPEYAYKIVKKGDSTIMKSELEYGNCNTKCQTPMGAINSSMPFHNIHPLTIGECP
KYVKSNRLVLAHHHHHH
C804 rAB-cetHS-puro [mAnti-Langerin2G3H-LV-hIgGK-C-Flex-hPSA] The coding region for this H chain-PSA fusion protein is shown below. Start and stop codons are in bold, as is the joining GCTAGC restriction site.
ATGACATTGAACATGCTGTTGGGGCTGAAGTGGGTTTTCTTTGTTGTTTT
CGACAACAACACTTCTAGCGCCCCTCATCCTGTCTCGGATTGTGGGAGGC
TGGGAGTGCGAGAAGCATTCCCAACCCTGGCAGGTGCTTGTGGCCTCTCG
TGGCAGGGCAGTCTGCGGCGGTGTTCTGGTGCACCCCCAGTGGGTCCTCA
CAGCTGCCCACTGCATCAGGAACAAAAGCGTGATCTTGCTGGGTCGGCAC
AGCCTGTTTCATCCTGAAGACACAGGCCAGGTATTTCAGGTCAGCCACAG
CTTCCCACACCCGCTCTACGATATGAGCCTCCTGAAGAATCGATTCCTCA
GGCCAGGTGATGACTCCAGCCACGACCTCATGCTGCTCCGCCTGTCAGAG
CCTGCCGAGCTCACGGATGCTGTGAAGGTCATGGACCTGCCCACCCAGGA
GCCAGCACTGGGGACCACCTGCTACGCCTCAGGCTGGGGCAGCATTGAAC
CAGAGGAGTTCTTGACCCCAAAGAAACTTCAGTGTGTGGACCTCCATGTT
ATTTCCAATGACGTGTGTGCGCAAGTTCACCCTCAGAAGGTGACCAAGTT
CATGCTGTGTGCTGGACGCTGGACAGGGGGCAAAAGCACCTGCTCGGGTG
ATTCTGGGGGCCCACTTGTCTGTAATGGTGTGCTTCAAGGTATCACGTCA
TGGGGCAGTGAACCATGTGCCCTGCCCGAAAGGCCTTCCCTGTACACCAA
GGTGGTGCATTACCGGAAGTGGATCAAGGACACCATCGTGGCCAACCCC
T
GA
The mature H chain sequence for C804 heavy chain is shown below. Joining sequence AS is bold and PSA is underlined. A flexible linker joining sequence is italicized.
LILSRIVGGWECEKHSQPWQVLVASRGRAVCGGVLVHPQWVLTAAHCIRNKSVILLGR
HSLFHPEDTGQVFQVSHSFPHPLYDMSLLKNRFLRPGDDSSHDLMLLRLSEPAELTDAV
KVMDLPTQEPALGTTCYASGWGSIEPEEFLTPKKLQCVDLHVISNDVCAQVHPQKVTK
FMLCAGRWTGGKSTCSGDSGGPLVCNGVLQGITSWGSEPCALPERPSLYTKVVHYRK
WIKDTIVANP
C87 rAB-pIRES2 [mAnti-Langerin15B10H-SLAML-V-hIgG4H-Flex-FluHA5-1-6×His] The coding region for this H chain-Flu HA5-1 fusion protein is shown below. Start and stop codons are in bold, as is the joining GCTAGC restriction site.
ATGGACCCCAAAGGCTCCCTTTCCTGGAGAATACTTCTGTTTCTCTCCCT
CAGATCAGATTTGCATTGGTTACCATGCAAACAACTCGACAGAGCAGGTT
GACACAATAATGGAAAAGAACGTTACTGTTACACATGCCCAAGACATACT
GGAAAAGAAACACAACGGGAAGCTCTGCGATCTAGATGGAGTGAAGCCTC
TAATTTTGAGAGATTGTAGCGTAGCTGGATGGCTCCTCGGAAACCCAATG
TGTGACGAATTCATCAATGTGCCGGAATGGTCTTACATAGTGGAGAAGGC
CAATCCAGTCAATGACCTCTGTTACCCAGGGGATTTCAATGACTATGAAG
AATTGAAACACCTATTGAGCAGAATAAACCATTTTGAGAAAATTCAGATC
ATCCCCAAAAGTTCTTGGTCCAGTCATGAAGCCTCATTAGGGGTGAGCTC
AGCATGTCCATACCAGGGAAAGTCCTCCTTTTTCAGAAATGTGGTATGGC
TTATCAAAAAGAACAGTACATACCCAACAATAAAGAGGAGCTACAATAAT
ACCAACCAAGAAGATCTTTTGGTACTGTGGGGGATTCACCATCCTAATGA
TGCGGCAGAGCAGACAAAGCTCTATCAAAACCCAACCACCTATATTTCCG
TTGGGACATCAACACTAAACCAGAGATTGGTACCAAGAATAGCTACTAGA
TCCAAAGTAAACGGGCAAAGTGGAAGGATGGAGTTCTTCTGGACAATTTT
AAAGCCGAATGATGCAATCAACTTCGAGAGTAATGGAAATTTCATTGCTC
CAGAATATGCATACAAAATTGTCAAGAAAGGGGACTCAACAATTATGAAA
AGTGAATTGGAATATGGTAACTGCAACACCAAGTGTCAAACTCCAATGGG
GGCGATAAACTCTAGCATGCCATTCCACAATATACACCCTCTCACCATTG
GGGAATGCCCCAAATATGTGAAATCAAACAGATTAGTCCTTGCGCACCAT
CACCATCACCAT
TGA
The mature H chain sequence for C87 heavy chain is shown below. Joining sequence AS is bold and Flu HA5-1 is underlined.
NSTEQVDTIMEKNVTVTHAQDILEKKHNGKLCDLDGVKPLILRDCSVAGWLLGNPMC
DEFINVPEWSYIVEKANPVNDLCYPGDFNDYEELKHLLSRINHFEKIQIIPKSSWSSHEAS
LGVSSACPYQGKSSFFRNVVWLIKKNSTYPTIKRSYNNTNQEDLLVLWGIHHPNDAAE
QTKLYQNPTTYISVGTSTLNQRLVPRIATRSKVNGQSGRMEFFWTILKPNDAINFESNGN
FIAPEYAYKIVKKGDSTIMKSELEYGNCNTKCQTPMGAINSSMPFHNIHPLTIGECPKYV
KSNRLVLAHHHHHH
C88 rAB-pIRES2 [mAnti-Langerin15B10H-SLAML-V-hIgG4H-C-Dockerin] The coding region for this H chain-dockerin fusion protein is shown below. Start and stop codons are in bold, as is the joining GCTAGC restriction site.
ATGGACCCCAAAGGCTCCCTTTCCTGGAGAATACTTCTGTTTCTCTCCCT
ATGACGGAAAAGTAAACTCCACTGACTTGACTTTGTTAAAAAGATATGTT
CTTAAAGCCGTCTCAACTCTCCCTTCTTCCAAAGCTGAAAAGAACGCAGA
TGTAAATCGTGACGGAAGAGTTAATTCCAGTGATGTCACAATACTTTCAA
GATATTTGATAAGGGTAATCGAGAAATTACCAATA
TAA
The mature H chain sequence for C88 heavy chain is shown below. Joining sequence AS is bold and dockerin is shaded grey. A flexible linker joining sequence is underlined.
LTLLKRYVLKAVSTLPSSKAEKNADVNRDGRVNSSDVTILSRYLIRVIEKLPI
C89 rAB-pIRES2[mAnti-Langerin15B10H-SLAML-V-hIgG4H-Flex-FluHA1-1-6×His] The coding region for this H chain-Flu HA1-1 fusion protein is shown below. Start and stop codons are in bold, as is the joining GCTAGC restriction site.
ATGGACCCCAAAGGCTCCCTTTCCTGGAGAATACTTCTGTTTCTCTCCCT
CAGACACAATATGTATAGGCTACCATGCGAACAATTCAACCGACACTGTT
GACACAGTACTCGAGAAGAATGTGACAGTGACACACTCTGTTAACCTGCT
CGAAGACAGCCACAACGGAAAACTATGTAGATTAAAAGGAATAGCCCCAC
TACAATTGGGGAAATGTAACATCGCCGGATGGCTCTTGGGAAACCCAGAA
TGCGACCCACTGCTTCCAGTGAGATCATGGTCCTACATTGTAGAAACACC
AAACTCTGAGAATGGAATATGTTATCCAGGAGATTTCATCGACTATGAGG
AGCTGAGGGAGCAATTGAGCTCAGTGTCATCATTCGAAAGATTCGAAATA
TTTCCCAAAGAAAGCTCATGGCCCAACCACAACACAAACGGAGTAACGGC
AGCATGCTCCCATGAGGGGAAAAGCAGTTTTTACAGAAATTTGCTATGGC
TGACGGAGAAGGAGGGCTCATACCCAAAGCTGAAAAATTCTTATGTGAAC
AAAAAAGGGAAAGAAGTCCTTGTACTGTGGGGTATTCATCACCCGCCTAA
CAGTAAGGAACAACAGAATCTCTATCAGAATGAAAATGCTTATGTCTCTG
TAGTGACTTCAAATTATAACAGGAGATTTACCCCGGAAATAGCAGAAAGA
CCCAAAGTAAGAGATCAAGCTGGGAGGATGAACTATTACTGGACCTTGCT
AAAACCCGGAGACACAATAATATTTGAGGCAAATGGAAATCTAATAGCAC
CAATGTATGCTTTCGCACTGAGTAGAGGCTTTGGGTCCGGCATCATCACC
TCAAACGCATCAATGCATGAGTGTAACACGAAGTGTCAAACACCCCTGGG
AGCTATAAACAGCAGTCTCCCTTACCAGAATATACACCCAGTCACAATAG
GAGAGTGCCCAAAATACGTCAGGAGTGCCAAATTGAGGATGGTTCACCAT
CACCATCACCAT
TGA
The mature H chain sequence for C89 heavy chain is shown below. Joining sequence AS is bold and Flu HA1-1 is underlined. A flexible linker joining sequence is italicized.
NSTDTVDTVLEKNVTVTHSVNLLEDSHNGKLCRLKGIAPLQLGKCNIAGWLLGNPECD
PLLPVRSWSYIVETPNSENGICYPGDFIDYEELREQLSSVSSFERFEIFPKESSWPNHNTN
GVTAACSHEGKSSFYRNLLWLTEKEGSYPKLKNSYVNKKGKEVLVLWGIHHPPNSKE
QQNLYQNENAYVSVVTSNYNRRFTPEIAERPKVRDQAGRMNYYWTLLKPGDTIIFEAN
GNLIAPMYAFALSRGEGSGIITSNASMHECNTKCQTPLGAINSSLPYQNIHPVTIGECPKY
VRSAKLRMVHHHHHH
C246 rAB-pIRES2[mAnti-Langerin15B10H-SLAML-V-hIgG4H-Viralgag] The coding region for this H chain-gag fusion protein is shown below. Start and stop codons are in bold, as is the joining GCTAGC restriction site.
ATGGACCCCAAAGGCTCCCTTTCCTGGAGAATACTTCTGTTTCTCTCCCT
TCGGTAGGCCTATAGTGCAGAACATCCAGGGGCAAATGGTACATCAGGCC
ATATCACCTAGAACTTTAAATGCATGGGTAAAAGTAGTAGAAGAGAAGGC
TTTCAGCCCAGAAGTAATACCCATGTTTTCAGCATTATCAGAAGGAGCCA
CCCCACAAGATTTAAACACCATGCTAAACACAGTGGGGGGACATCAAGCA
GCCATGCAAATGTTAAAAGAGACCATCAATGAGGAAGCTGCAGAATGGGA
TAGAGTACATCCAGTGCATGCAGGGCCTATTGCACCAGGCCAGATGAGAG
AACCAAGGGGAAGTGACATAGCAGGAACTACTAGTACCCTTCAGGAACAA
ATAGGATGGATGACAAATAATCCACCTATCCCAGTAGGAGAAATTTATAA
AAGATGGATAATCCTGGGATTAAATAAAATAGTAAGAATGTATAGCCCTA
CCAGCATTCTGGACATAAGACAAGGACCAAAAGAACCTTTTAGAGACTAT
GTAGACCGGTTCTATAAAACTCTAAGAGCCGAGCAAGCTTCACAGGAGGT
AAAAAATTGGATGACAGAAACCTTGTTGGTCCAAAATGCGAACCCAGATT
GTAAGACTATTTTAAAAGCATTGGGACCAGCGGCTACACTAGAAGAAATG
ATGACAGCATGTCAGGGAGTAGGAGGACCCGGCCATAAGGCAAGAGTTTT
G
TGA
The mature H chain sequence for C89 heavy chain is shown below. Joining sequence AS is bold and Gag p24 is underlined. A flexible linker joining sequence is italicized.
GQMVHQAISPRTLNAWVKVVEEKAFSPEVIPMFSALSEGATPQDLNTMLNTVGGHQA
AMQMLKETINEEAAEWDRVHPVHAGPIAPGQMREPRGSDIAGTTSTLQEQIGWMTNNP
PIPVGEIYKRWIILGLNKIVRMYSPTSILDIRQGPKEPFRDYVDRFYKTLRAEQASQEVKN
WMTETLLVQNANPDCKTILKALGPAATLEEMMTACQGVGGPGHKARVL
C742 rAB-cetHS-puro [mAnti-Langerin15B10H-LV-hIgG4H-C-Flex-hPSA] The coding region for this H chain-PSA fusion protein is shown below. Start and stop codons are in bold, as is the joining GCTAGC restriction site.
ATGGAATGGAGGATCTTTCTCTTCATCCTGTCAGGAACTGCAGGTGTCCA
AGAACCTGCAACACCTACAACACCTGTAACAACACCGACAACAACACTTC
TAGCGCCCCTCATCCTGTCTCGGATTGTGGGAGGCTGGGAGTGCGAGAAG
CATTCCCAACCCTGGCAGGTGCTTGTGGCCTCTCGTGGCAGGGCAGTCTG
CGGCGGTGTTCTGGTGCACCCCCAGTGGGTCCTCACAGCTGCCCACTGCA
TCAGGAACAAAAGCGTGATCTTGCTGGGTCGGCACAGCCTGTTTCATCCT
GAAGACACAGGCCAGGTATTTCAGGTCAGCCACAGCTTCCCACACCCGCT
CTACGATATGAGCCTCCTGAAGAATCGATTCCTCAGGCCAGGTGATGACT
CCAGCCACGACCTCATGCTGCTCCGCCTGTCAGAGCCTGCCGAGCTCACG
GATGCTGTGAAGGTCATGGACCTGCCCACCCAGGAGCCAGCACTGGGGAC
CACCTGCTACGCCTCAGGCTGGGGCAGCATTGAACCAGAGGAGTTCTTGA
CCCCAAAGAAACTTCAGTGTGTGGACCTCCATGTTATTTCCAATGACGTG
TGTGCGCAAGTTCACCCTCAGAAGGTGACCAAGTTCATGCTGTGTGCTGG
ACGCTGGACAGGGGGCAAAAGCACCTGCTCGGGTGATTCTGGGGGCCCAC
TTGTCTGTAATGGTGTGCTTCAAGGTATCACGTCATGGGGCAGTGAACCA
TGTGCCCTGCCCGAAAGGCCTTCCCTGTACACCAAGGTGGTGCATTACCG
GAAGTGGATCAAGGACACCATCGTGGCCAACCCC
TGA
The mature H chain sequence for C742 heavy chain is shown below. Joining sequence AS is bold and PSA is underlined. A flexible linker joining sequence is italicized.
RIVGGWECEKHSQPWQVLVASRGRAVCGGVLVHPQWVLTAAHCIRNKSVILLGRHSL
FHPEDTGQVFQVSHSFPHPLYDMSLLKNRFLRPGDDSSHDLMLLRLSEPAELTDAVKV
MDLPTQEPALGTTCYASGWGSIEPEEFLTPKKLQCVDLHVISNDVCAQVHPQKVTKFM
LCAGRWTGGKSTCSGDSGGPLVCNGVLQGITSWGSEPCALPERPSLYTKVVHYRKWIK
DTIVANP
C1011 rAB-cetHS-puro [mAnti-Langerin15B10H-LV-hIgG4H-C-Flex-v1-Pep-gag17-f1-gag253-2-nef116-f3-nef66-f4-pol158] a.k.a. Anti-Langerin15B10H-HIPO5. The coding region for this H chain-HIV peptides fusion protein is shown below. Start and stop codons are in bold, as is the joining GCTAGT restriction site.
ATGGAATGGAGGATCTTTCTCTTCATCCTGTCAGGAACTGCAGGTGTCCA
CACCAACACCATCAGCGTGACCCCCACCAACAACAGCACCCCCACCAACA
ACAGCAACCCCAAGCCCAACCCCGCTAGTGAGAAGATCCGGCTGCGGCCC
GGCGGCAAGAAGAAGTACAAGCTGAAGCACATCGTGGCTAGTAGCAGCGT
GAGCCCCACCACCAGCGTGCACCCCACCCCCACCAGCGTGCCCCCCACCC
CCACCAAGAGCAGCCCCGCTAGTAACCCCCCCATCCCCGTGGGCGAGATC
TACAAGCGGTGGATCATCCTGGGCCTGAACAAGATCGTGCGGATGTACAG
CCCCACCAGCATCCTGGACGCTAGTCCCACCAGCACCCCCGCCGACAGCA
GCACCATCACCCCCACCGCCACCCCCACCGCCACCCCCACCATCAAGGGC
GCTAGTCACACCCAGGGCTACTTCCCCGACTGGCAGAACTACACCCCCGG
CCCCGGCGTGCGGTACCCCCTGACCTTCGGCTGGCTGTACAAGCTGGCTA
GTACCGTGACCCCCACCGCCACCGCCACCCCCAGCGCCATCGTGACCACC
ATCACCCCCACCGCCACCACCAAGCCCGCTAGTGTGGGCTTCCCCGTGAC
CCCCCAGGTGCCCCTGCGGCCCATGACCTACAAGGCCGCCGTGGACCTGA
GCCACTTCCTGAAGGAGAAGGGCGGCCTGGCTAGTACCAACGGCAGCATC
ACCGTGGCCGCCACCGCCCCCACCGTGACCCCCACCGTGAACGCCACCCC
CAGCGCCGCCGCTAGTGCCATCTTCCAGAGCAGCATGACCAAGATCCTGG
AGCCCTTCCGGAAGCAGAACCCCGACATCGTGATCTACCAGTACATGGAC
GACCTGTACGCTAGC
TGA
The mature H chain sequence for C1011 heavy chain is shown below. Joining sequences AS are bold and HIV peptides are underlined. A flexible linker joining sequence is italicized.
NP
ASEKIRLRPGGKKKYKLKHIVASSSVSPTTSVHPTPTSVPPTPTKSSPASNPPIPVGEIYK
RWIILGLNKIVRMYSPTSILD
AS
PTSTPADSSTITPTATPTATPTIKG
AS
HTQGYFPDWQNY
TPGPGVRYPLTFGWLYKL
AS
TVTPTATATPSAIVTTITPTATTKP
AS
VGFPVTPQVPLRPMT
YKAAVDLSHFLKEKGGL
AS
TNGSITVAATAPTVTPTVNATPSAA
AS
AIFQSSMTKILEPFRK
QNPDIVIYQYMDDLY
AS
These data show that both anti-Langerin 15B10 and 2G3 recombinant antibodies or such antibodies linked to a cancer antigen retain significant binding to NHP Langerin—a very desirable property for commercial development of these antibodies as antigen-targeting vaccines [this enables mechanism-based preclinical testing of safety and efficacy in NHP models].
The 15B10.3 hydridoma has been deposited under the Budapest Treaty with the U.S. American Type Culture Collection and received Deposit No. PTA-9852; and the 2G3.6 hybridoma received Deposit No. PTA-9853.
mAnti-Langerin 91E7K Light Chain Sequence
mAnti-Langerin 91E7K Light Chain Sequence
mAnti-Langerin 91E7H [Mouse IgG2a] Heavy Chain
ATGAGATCACTGTTCTCTTTACAGTTACTGAGCACACAGGACCTCGCCATGG GATGGAGCTGTATCATCCTCTTCTTGGTAGCAACAGCTACAGGTGTCCACTCTCAGG TCCAACTGCAGCAGCCTGGGGCTGAACTTGTGAAGCCTGGGGCTTCAGTGAAGCTG TCCTGCAAGGCTTCTGGCTACACCTTCACCAGTTACTGGATGCAGTGGGTAAAGCA GAGGCCTGGACAGGGCCTTGAGTGGATCGGAGAGATTGATCCTTCTGATAGCTATA CTAACTACAATCAAAGGTTCAAGGGCAAGGCCACATTGACTGTGGACACATCCTCC AGCACAGCCTACATACAGCTCAGCAGCCTGACGTCTGAGGACTCTGCGGTCTGTTT CTGTGCAAGACGCTACTATGGTAACTACGATGGGTTTGCTTACTGGGGCCAAGGGA CTCTGGTCACTGTCTCTGCAGCCAAAACAACAGCCCCATCGGTCTATCCACTGGCCC CTGTGTGTGGAGGTACAACTGGCTCCTCGGTGACTCTAGGATGCCTGGTCAAGGGT TATTTCCCTGAGCCAGTGACCTTGACCTGGAACTCTGGATCCCTGTCCAGTGGTGTG CACACCTTCCCAGCTCTCCTGCAGTCTGGCCTCTACACCCTCAGCAGCTCAGTGACT GTAACCTCGAACACCTGGCCCAGCCAGACCATCACCTGCAATGTGGCCCACCCGGC AAGCAGCACCAAAGTGGACAAGAAAATTGAGCCCAGAGTGCCCATAACACAGAAC CCCTGTCCTCCACTCAAAGAGTGTCCCCCATGCGCAGCTCCAGACCTCTTGGGTGGA CCATCCGTCTTCATCTTCCCTCCAAAGATCAAGGATGTACTCATGATCTCCCCGAGC CCCATGGTCACATGTGTGGTGGTGGATGTGAGCGAGGATGACCCAGACGTCCAGAT CAGCTGGTTTGTGAACAACGTGGAAGTACACACAGCTCAGACACAAACCCATAGAG AGGATTACAACAGTACTCTCCGGGTGGTCAGTGCCCTCCCCATCCAGCACCAGGAC TGGATGAGTGGCAAGGAGTTCAAATGCAAGGTCAACAACAGAGCCCTCCCATCCCC CATCGAGAAAACCATCTCAAAACCCAGAGGGCCAGTAAGAGCTCCACAGGTATAT GTCTTGCCTCCACCAGCAGAAGAGATGACTAAGAAAGAGTTCAGTCTGACCTGCAT GATCACAGGCTTCTTACCTGCCGAAATTGCTGTGGACTGGACCAGCAATGGGCGTA CAGAGCAAAACTACAAGAACACCGCAACAGTCCTGGACTCTGATGGTTCTTACTTC ATGTACAGCAAGCTCAGAGTACAAAAGAGCACTTGGGAAAGAGGAAGTCTTTTCGC CTGCTCAGTGGTCCACGAGGGTCTGCACAATCACCTTACGACTAAGACCATCTCCC GGTCTCTGGGTAAAGCTAGCTGA [GCTAGC in bold is for the in-frame fusion of antigens at the H-chain C-terminus] (SEQ ID NO.: 53)
mAnti-Langerin 91E7H [Mouse IgG2a] Mature H Heavy Chain Sequence
mAnti-Langerin 37C1K Light Chain
mAnti-Langerin 37C1K Light Chain
mAnti-Langerin 37C1H [Mouse IgG2a] Heavy Chain
mAnti-Langerin 37C1H [Mouse IgG2a] Heavy Chain
mAnti-Langerin 4C7K (Light Chain)
mAnti-Langerin 4C7H [Mouse IgG2a] Heavy Chain
mAnti-Langerin 4C7H [Mouse IgG2a] Heavy Chain
It is contemplated that any embodiment discussed in this specification can be implemented with respect to any method, kit, reagent, or composition of the invention, and vice versa. Furthermore, compositions of the invention can be used to achieve methods of the invention.
It will be understood that particular embodiments described herein are shown by way of illustration and not as limitations of the invention. The principal features of this invention can be employed in various embodiments without departing from the scope of the invention. Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, numerous equivalents to the specific procedures described herein. Such equivalents are considered to be within the scope of this invention and are covered by the claims.
All publications and patent applications mentioned in the specification are indicative of the level of skill of those skilled in the art to which this invention pertains. All publications and patent applications are herein incorporated by reference to the same extent as if each individual publication or patent application was specifically and individually indicated to be incorporated by reference.
The use of the word “a” or “an” when used in conjunction with the term “comprising” in the claims and/or the specification may mean “one,” but it is also consistent with the meaning of “one or more,” “at least one,” and “one or more than one.” The use of the term “or” in the claims is used to mean “and/or” unless explicitly indicated to refer to alternatives only or the alternatives are mutually exclusive, although the disclosure supports a definition that refers to only alternatives and “and/or.” Throughout this application, the term “about” is used to indicate that a value includes the inherent variation of error for the device, the method being employed to determine the value, or the variation that exists among the study subjects.
As used in this specification and claim(s), the words “comprising” (and any form of comprising, such as “comprise” and “comprises”), “having” (and any form of having, such as “have” and “has”), “including” (and any form of including, such as “includes” and “include”) or “containing” (and any form of containing, such as “contains” and “contain”) are inclusive or open-ended and do not exclude additional, unrecited elements or method steps. As used herein, the phrase “consisting essentially of” limits the scope of a claim to the specified materials or steps and those that do not materially affect the basic and novel characteristic(s) of the claimed invention. As used herein, the phrase “consisting of” excludes any element, step, or ingredient not specified in the claim except for, e.g., impurities ordinarily associated with the element or limitation.
The term “or combinations thereof” as used herein refers to all permutations and combinations of the listed items preceding the term. For example, “A, B, C, or combinations thereof” is intended to include at least one of: A, B, C, AB, AC, BC, or ABC, and if order is important in a particular context, also BA, CA, CB, CBA, BCA, ACB, BAC, or CAB. Continuing with this example, expressly included are combinations that contain repeats of one or more item or term, such as BB, AAA, MB, BBC, AAABCCCC, CBBAAA, CABABB, and so forth. The skilled artisan will understand that typically there is no limit on the number of items or terms in any combination, unless otherwise apparent from the context.
As used herein, words of approximation such as, without limitation, “about”, “substantial” or “substantially” refers to a condition that when so modified is understood to not necessarily be absolute or perfect but would be considered close enough to those of ordinary skill in the art to warrant designating the condition as being present. The extent to which the description may vary will depend on how great a change can be instituted and still have one of ordinary skilled in the art recognize the modified feature as still having the required characteristics and capabilities of the unmodified feature. In general, but subject to the preceding discussion, a numerical value herein that is modified by a word of approximation such as “about” may vary from the stated value by at least ±1, 2, 3, 4, 5, 6, 7, 10, 12 or 15%.
All of the compositions and/or methods disclosed and claimed herein can be made and executed without undue experimentation in light of the present disclosure. While the compositions and methods of this invention have been described in terms of preferred embodiments, it will be apparent to those of skill in the art that variations may be applied to the compositions and/or methods and in the steps or in the sequence of steps of the method described herein without departing from the concept, spirit and scope of the invention. All such similar substitutes and modifications apparent to those skilled in the art are deemed to be within the spirit, scope and concept of the invention as defined by the appended claims.
This application is a continuation of U.S. patent application Ser. No. 12/882,052 now abandoned, which claims priority to U.S. Provisional Application Ser. No. 61/242,283, filed Sep. 14, 2009, the entire contents of which are incorporated herein by reference.
This invention was made with U.S. Government support under Contract No. 1U19AI057234-0100003 awarded by the NIH. The government has certain rights in this invention.
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| 1452636 | Oct 2003 | CN |
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| Number | Date | Country | |
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| 20140030264 A1 | Jan 2014 | US |
| Number | Date | Country | |
|---|---|---|---|
| 61242283 | Sep 2009 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 12882052 | Sep 2010 | US |
| Child | 13863131 | US |
