Patent Application
20100172917
Pursuant to 37 C.F.R. §1.52(e)(1)(ii), a compact disc containing an electronic version of the Sequence Listing has been submitted concomitant with this application, the contents of which are hereby incorporated by reference. A second compact disc is submitted and is an identical copy of the first compact disc. The discs are labeled “copy 1” and “copy 2,” respectively, and each disc contains one file entitled “2578-7586US seq listing.txt” which is 812 KB and created on Mar. 4, 2009.
In general, various embodiments of the invention relate to biotechnology and medicine. In particular, the invention relates to binding molecules capable of specifically binding to SARS-coronavirus (SARS-CoV). The binding molecules are useful in the diagnosis of SARS CoV and the prophylaxis and/or treatment of a condition resulting from SARS-CoV.
Recently, a new and in several cases deadly clinical syndrome was observed in the human population, which is now called “severe acute respiratory syndrome” (or “SARS”) (Holmes, 2003). The syndrome is caused by a coronavirus (Ksiazek et al., 2003), referred to as the SARS-CoV. The genome sequence of SARS-CoV has been determined (Rota et al., 2003; Marra et al., 2003). However, much remains to be learned about this virus.
Provided are means and methods for use in diagnostics, prevention and/or treatment of SARS-CoV.
Specifically provided are binding molecules capable of specifically binding to SARS-CoV. In a preferred embodiment, the binding molecules are human binding molecules. Furthermore, the invention pertains to nucleic acid molecules encoding at least the binding region of the binding molecules. The invention further provides for the use of the binding molecules described herein in the prophylaxis and/or treatment of a subject having, or at risk of developing, a condition resulting from SARS-CoV. Besides that, the invention pertains to the use of the binding molecules described herein in the diagnosis/detection of SARS-CoV.
Hereinbelow follow definitions of terms as used herein.
Amino acid sequence. The term “amino acid sequence,” as used herein, refers to naturally occurring or synthetic molecules and to a peptide, oligopeptide, polypeptide, or protein sequence.
Binding molecule. As used herein, the term “binding molecule” refers to an intact immunoglobulin including monoclonal antibodies, such as chimeric, humanized, or human monoclonal antibodies, or to an antigen-binding and/or variable domain comprising fragment of an immunoglobulin that competes with the intact immunoglobulin for specific binding to the binding partner of the immunoglobulin, e.g., the SARS-CoV. Regardless of structure, the antigen-binding fragment binds with the same antigen that is recognized by the intact immunoglobulin. An antigen-binding fragment can comprise a peptide or polypeptide comprising an amino acid sequence of at least two contiguous amino acid residues, at least five contiguous amino acid residues, at least ten contiguous amino acid residues, at least 15 contiguous amino acid residues, at least 20 contiguous amino acid residues, at least 25 contiguous amino acid residues, at least 30 contiguous amino acid residues, at least 35 contiguous amino acid residues, at least 40 contiguous amino acid residues, at least 50 contiguous amino acid residues, at least 60 contiguous amino residues, at least 70 contiguous amino acid residues, at least contiguous 80 amino acid residues, at least contiguous 90 amino acid residues, at least contiguous 100 amino acid residues, at least contiguous 125 amino acid residues, at least 150 contiguous amino acid residues, at least contiguous 175 amino acid residues, at least 200 contiguous amino acid residues, or at least contiguous 250 amino acid residues of the amino acid sequence of the binding molecule.
The term “binding molecule,” as used herein, includes all immunoglobulin classes and subclasses known in the art. Depending on the amino acid sequence of the constant domain of their heavy chains, binding molecules can be divided into the five major classes of intact antibodies: IgA, IgD, IgE, IgG, and IgM, and several of these may be further divided into subclasses (isotypes), e.g., IgA1, IgA2, IgG1, IgG2, IgG3 and IgG4.
Antigen-binding fragments include, inter alia, Fab, F(ab′), F(ab′)2, Fv, dAb, Fd, complementarity determining region (CDR) fragments, single-chain antibodies (scFv), bivalent single-chain antibodies, single-chain phage antibodies, diabodies, triabodies, tetrabodies, (poly)peptides that contain at least a fragment of an immunoglobulin that is sufficient to confer specific antigen binding to the (poly)peptide, etc. These fragments may be produced synthetically or by enzymatic or chemical cleavage of intact immunoglobulins or they may be genetically engineered by recombinant DNA techniques. The methods of production are well known in the art and are described, e.g., in Antibodies: A Laboratory Manual, Edited by: E. Harlow and D. Lane (1988), Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y., which is incorporated herein by reference. A binding molecule or antigen-binding fragment thereof may have one or more binding sites. If there is more than one binding site, the binding sites may be identical to one another or they may be different.
The binding molecule can be a naked or unconjugated binding molecule, but can also be part of an immunoconjugate. A naked or unconjugated binding molecule is intended to refer to a binding molecule that is not conjugated, operatively linked, or otherwise physically or functionally associated with an effector moiety or tag, such as, inter alia, a toxic substance, a radioactive substance, a liposome, an enzyme. It will be understood that naked or unconjugated binding molecules do not exclude binding molecules that have been stabilized, multimerized, humanized or in any other way manipulated, other than by the attachment of an effector moiety or tag. Accordingly, all post-translationally modified naked and unconjugated binding molecules are included herewith, including where the modifications are made in the natural binding molecule-producing cell environment, by a recombinant binding molecule-producing cell, and are introduced by the hand of man after initial binding molecule preparation. The term naked or unconjugated binding molecule does not exclude the ability of the binding molecule to form functional associations with effector cells and/or molecules after administration to the body, as some of such interactions are necessary in order to exert a biological effect. The lack of associated effector group or tag is, therefore, applied in definition to the naked or unconjugated binding molecule in vitro, not in vivo.
Biological sample. As used herein, the term “biological sample” encompasses a variety of sample types, including blood and other liquid samples of biological origin, solid tissue samples such as a biopsy specimen or tissue cultures, or cells derived therefrom and the progeny thereof. The term also includes samples that have been manipulated in any way after their procurement, such as by treatment with reagents, solubilization, or enrichment for certain components, such as proteins or polynucleotides. The term encompasses various kinds of clinical samples obtained from any species, and also includes cells in culture, cell supernatants, and cell lysates.
Complementary determining regions (CDR). The term “complementary determining regions,” as used herein, means sequences within the variable regions of binding molecules, such as immunoglobulins, that usually contribute to a large extent to the antigen binding site that is complementary in shape and charge distribution to the epitope recognized on the antigen. The CDR regions can be specific for linear epitopes, discontinuous epitopes, or conformational epitopes of proteins or protein fragments, either as present on the protein in its native conformation or, in some cases, as present on the proteins as denatured, e.g., by solubilization in SDS. Epitopes may also consist of posttranslational modifications of proteins.
Deletion. The term “deletion,” as used herein, denotes a change in either amino acid or nucleotide sequence in which one or more amino acid or nucleotide residues, respectively, are absent as compared to the parent, often the naturally occurring, molecule.
Expression-regulating nucleic acid sequence. The term “expression regulating nucleic acid sequence,” as used herein, refers to polynucleotide sequences necessary for and/or affecting the expression of an operably linked coding sequence in a particular host organism. The expression-regulating nucleic acid sequences, such as, inter alia, appropriate transcription initiation, termination, promoter, enhancer sequences; repressor or activator sequences; efficient RNA processing signals, such as splicing and polyadenylation signals; sequences that stabilize cytoplasmic mRNA; sequences that enhance translation efficiency (e.g., ribosome binding sites); sequences that enhance protein stability; and when desired, sequences that enhance protein secretion, can be any nucleic acid sequence showing activity in the host organism of choice and can be derived from genes encoding proteins that are either homologous or heterologous to the host organism.
Functional variant. The term “functional variant,” as used herein, refers to a binding molecule that comprises a nucleotide and/or amino acid sequence that is altered by one or more nucleotides and/or amino acids compared to the nucleotide and/or amino acid sequences of the parent binding molecule and that is still capable of competing for binding to the binding partner, e.g., SARS-CoV, with the parent binding molecule. In other words, the modifications in the amino acid and/or nucleotide sequence of the parent binding molecule do not significantly affect or alter the binding characteristics of the binding molecule encoded by the nucleotide sequence or containing the amino acid sequence, i.e., the binding molecule is still able to recognize and bind its target. The functional variant may have conservative sequence modifications including nucleotide and amino acid substitutions, additions and deletions. These modifications may be introduced by standard techniques known in the art, such as site-directed mutagenesis and random PCR-mediated mutagenesis, and may comprise natural as well as non-natural nucleotides and amino acids.
Conservative amino acid substitutions include the ones in which the amino acid residue is replaced with an amino acid residue having similar structural and/or chemical properties. Families of amino acid residues having similar side chains have been defined in the art. These families include amino acids with basic side chains (e.g., lysine, arginine, histidine), acidic side chains (e.g., aspartic acid, glutamic acid), uncharged polar side chains (e.g., glycine, asparagine, glutamine, serine, threonine, tyrosine, cysteine, tryptophan), nonpolar side chains (e.g., alanine, valine, leucine, isoleucine, proline, phenylalanine, methionine), beta-branched side chains (e.g., threonine, valine, isoleucine) and aromatic side chains (e.g., tyrosine, phenylalanine, tryptophan, histidine). It will be clear to the skilled artisan that other classifications of amino acid residue families than the one used above can also be employed. Furthermore, a variant may have non-conservative amino acid substitutions, e.g., replacement of an amino acid with an amino acid residue having different structural or chemical properties. Similar minor variations may also include amino acid deletions or insertions, or both. Guidance in determining which amino acid residues may be substituted, inserted, or deleted without abolishing immunological activity may be found using computer programs well known in the art.
A mutation in a nucleotide sequence can be a single alteration made at a locus (a point mutation), such as transition or transversion mutations, or alternatively, multiple nucleotides may be inserted, deleted or changed at a single locus. In addition, one or more alterations may be made at any number of loci within a nucleotide sequence. The mutations may be performed by any suitable method known in the art.
Host. The term “host,” as used herein, is intended to refer to an organism or a cell into which a vector such as a cloning vector or an expression vector has been introduced. The organism or cell can be prokaryotic or eukaryotic. It should be understood that this term is intended to refer not only to the particular subject organism or cell, but to the progeny of such an organism or cell as well. Because certain modifications may occur in succeeding generations due to either mutation or environmental influences, such progeny may not, in fact, be identical to the parent organism or cell, but are still included within the scope of the term “host” as used herein.
Human. The term “human,” when applied to binding molecules as defined herein, refers to molecules that are either directly derived from a human or based upon a human sequence. When a binding molecule is derived from or based on a human sequence and subsequently modified, it is still to be considered human as used throughout the specification. In other words, the term human, when applied to binding molecules is intended to include binding molecules having variable and constant regions derived from human germline immunoglobulin sequences based on variable or constant regions either or not occurring in a human or human lymphocyte or in modified form. Thus, the human binding molecules may include amino acid residues not encoded by human germline immunoglobulin sequences, comprise substitutions and/or deletions (e.g., mutations introduced by for instance random or site-specific mutagenesis in vitro or by somatic mutation in vivo). “Based on,” as used herein, refers to the situation that a nucleic acid sequence may be exactly copied from a template, or with minor mutations, such as by error-prone PCR methods, or synthetically made matching the template exactly or with minor modifications. Semisynthetic molecules based on human sequences are also considered to be human as used herein.
Insertion. The term “insertion,” also known as the term “addition,” denotes a change in an amino acid or nucleotide sequence resulting in the addition of one or more amino acid or nucleotide residues, respectively, as compared to the parent, often the naturally occurring, molecule.
Isolated. The term “isolated,” when applied to binding molecules as defined herein, refers to binding molecules that are substantially free of other proteins or polypeptides, particularly free of other binding molecules having different antigenic specificities, and are also substantially free of other cellular material and/or chemicals. For example, when the binding molecules are recombinantly produced, they are preferably substantially free of culture medium, and when the binding molecules are produced by chemical synthesis, they are preferably substantially free of chemical precursors or other chemicals, i.e., they are separated from chemical precursors or other chemicals which are involved in the synthesis of the protein. The term “isolated” when applied to nucleic acid molecules encoding binding molecules as defined herein, is intended to refer to nucleic acid molecules in which the nucleotide sequences encoding the binding molecules are free of other nucleotide sequences, particularly nucleotide sequences encoding binding molecules that bind binding partners other than SARS-CoV. Furthermore, the term “isolated” refers to nucleic acid molecules that are substantially separated from other cellular components that naturally accompany the native nucleic acid molecule in its natural host, e.g., ribosomes, polymerases, or genomic sequences with which it is naturally associated. Moreover, “isolated” nucleic acid molecules, such as cDNA molecules, can be substantially free of other cellular material, or culture medium when produced by recombinant techniques, or substantially free of chemical precursors or other chemicals when chemically synthesized.
Monoclonal antibody. The term “monoclonal antibody,” as used herein, refers to a preparation of antibody molecules of single molecular composition. A monoclonal antibody displays a single binding specificity and affinity for a particular epitope. Accordingly, the term “human monoclonal antibody” refers to an antibody displaying a single binding specificity which has variable and constant regions derived from or based on human germline immunoglobulin sequences or derived from completely synthetic sequences. The method of preparing the monoclonal antibody is not relevant.
Naturally occurring. The term “naturally occurring,” as used herein, as applied to an object refers to the fact that an object can be found in nature. For example, a polypeptide or polynucleotide sequence that is present in an organism that can be isolated from a source in nature and which has not been intentionally modified by man in the laboratory is naturally occurring.
Nucleic acid molecule. The term “nucleic acid molecule,” as used in the invention, refers to a polymeric form of nucleotides and includes both sense and antisense strands of RNA, cDNA, genomic DNA, and synthetic forms and mixed polymers of the above. A nucleotide refers to a ribonucleotide, deoxynucleotide or a modified form of either type of nucleotide. The term also includes single- and double-stranded forms of DNA. In addition, a polynucleotide may include either or both naturally occurring and modified nucleotides linked together by naturally occurring and/or non-naturally occurring nucleotide linkages. The nucleic acid molecules may be modified chemically or biochemically or may contain non-natural or derivatized nucleotide bases, as will be readily appreciated by those of skill in the art. Such modifications include, for example, labels, methylation, substitution of one or more of the naturally occurring nucleotides with an analog, internucleotide modifications such as uncharged linkages (e.g., methyl phosphonates, phosphotriesters, phosphoramidates, carbamates, etc.), charged linkages (e.g., phosphorothioates, phosphorodithioates, etc.), pendent moieties (e.g., polypeptides), intercalators (e.g., acridine, psoralen, etc.), chelators, alkylators, and modified linkages (e.g., alpha anomeric nucleic acids, etc.). The above term is also intended to include any topological conformation, including single-stranded, double-stranded, partially duplexed, triplex, hairpinned, circular and padlocked conformations. Also included are synthetic molecules that mimic polynucleotides in their ability to bind to a designated sequence via hydrogen bonding and other chemical interactions. Such molecules are known in the art and include, for example, those in which peptide linkages substitute for phosphate linkages in the backbone of the molecule. A reference to a nucleic acid sequence encompasses its complement unless otherwise specified. Thus, a reference to a nucleic acid molecule having a particular sequence should be understood to encompass its complementary strand, with its complementary sequence. The complementary strand is also useful, e.g., for antisense therapy, hybridization probes, and PCR primers.
Operably linked. The term “operably linked” refers to two or more nucleic acid sequence elements that are usually physically linked and are in a functional relationship with each other. For instance, a promoter is operably linked to a coding sequence if the promoter is able to initiate or regulate the transcription or expression of a coding sequence, in which case the coding sequence should be understood as being “under the control of” the promoter.
Pharmaceutically acceptable excipient. By “pharmaceutically acceptable excipient” is meant any inert substance that is combined with an active molecule such as a drug, agent, or binding molecule for preparing an agreeable or convenient dosage form. The “pharmaceutically acceptable excipient” is an excipient that is non-toxic to recipients at the dosages and concentrations employed and is compatible with other ingredients of the formulation comprising the drug, agent or binding molecule.
Specifically Binding. The term “specifically binding,” as used herein, in reference to the interaction of a binding molecule, e.g., an antibody, and its binding partner, e.g., an antigen, means that the interaction is dependent upon the presence of a particular structure, e.g., an antigenic determinant or epitope, on the binding partner. In other words, the antibody preferentially binds or recognizes the binding partner even when the binding partner is present in a mixture of other molecules or organisms. The binding may be mediated by covalent or non-covalent interactions or a combination of both. In yet other words, the term “specifically binding” means immunospecifically binding to an antigen or a fragment thereof and not immunospecifically binding to other antigens. A binding molecule that immunospecifically binds to an antigen may bind to other peptides or polypeptides with lower affinity as determined by, e.g., radioimmunoassays (RIA), enzyme-linked immunosorbent assays (ELISA), BIACORE®, or other assays known in the art. Binding molecules or fragments thereof that immunospecifically bind to an antigen may be cross-reactive with related antigens. Preferably, binding molecules or fragments thereof that immunospecifically bind to an antigen do not cross-react with other antigens.
Substitutions. A “substitution,” as used herein, denotes the replacement of one or more amino acids or nucleotides by different amino acids or nucleotides, respectively.
Therapeutically effective amount. The term “therapeutically effective amount” refers to an amount of the binding molecule as defined herein that is effective for preventing, ameliorating, and/or treating a condition resulting from infection with SARS-CoV.
Treatment. The term “treatment” refers to therapeutic treatment as well as to prophylactic or preventative measures to cure or halt or at least retard disease progress. Those in need of treatment include those already inflicted with a condition resulting from infection with SARS-CoV as well as those in which infection with SARS-CoV is to be prevented. Subjects partially or totally recovered form infection with SARS-CoV might also be in need of treatment. Prevention encompasses inhibiting or reducing the spread of SARS-CoV or inhibiting or reducing the onset, development or progression of one or more of the symptoms associated with infection with SARS-CoV.
Vector. The term “vector” denotes a nucleic acid molecule into which a second nucleic acid molecule can be inserted for introduction into a host where it will be replicated, and in some cases expressed. In other words, a vector is capable of transporting a nucleic acid molecule to which it has been linked. Cloning as well as expression vectors are contemplated by the term “vector,” as used herein. Vectors include, but are not limited to, plasmids, cosmids, bacterial artificial chromosomes (BAC) and yeast artificial chromosomes (YAC) and vectors derived from bacteriophages or plant or animal (including human) viruses. Vectors comprise an origin of replication recognized by the proposed host and in case of expression vectors, promoter and other regulatory regions recognized by the host. A vector containing a second nucleic acid molecule is introduced into a cell by transformation, transfection, or by making use of viral entry mechanisms. Certain vectors are capable of autonomous replication in a host into which they are introduced (e.g., vectors having a bacterial origin of replication can replicate in bacteria). Other vectors can be integrated into the genome of a host upon introduction into the host, and thereby are replicated along with the host genome.
In one aspect, the invention encompasses binding molecule capable of specifically binding to SARS-CoV. The binding molecules may be capable of specifically binding to SARS-CoV in activated or inactivated/attenuated form. Methods for inactivating/attenuating viruses are well known in the art and include, but are not limited to, heat inactivation, inactivation by UV irradiation, and/or inactivation by gamma irradiation. The binding molecules may also be capable of specifically binding to one or more fragments of the SARS-CoV such as, inter alia, a preparation of one or more proteins, peptides, and/or polypeptides derived from SARS-CoV. For methods of treatment and/or prevention of SARS, the binding molecules are preferably capable of specifically binding to surface accessible proteins, which include, but are not limited to, inner and outer membrane proteins, proteins adhering to the cell wall, and potential secreted proteins. Surface accessible proteins of SARS-CoV include, but are not limited to, the spike protein, the membrane (matrix) protein, the (small) envelope protein, Orf 3, Orf 4, Orf 7, Orf 8, Orf 9, Orf 10 and Orf 14. For diagnostical purposes the binding molecules may also be capable of specifically binding to proteins not present on the surface of SARS-CoV. Therefore, proteins including, but not limited to, the nucleocapsid (N) protein, ORF 11, and ORF 13 may be used. The amino acid sequence of proteins and potential proteins of various known strains of SARS-CoV can be found in the EMBL-database and/or other databases. For instance, the complete genome of the SARS coronavirus Urbani can be found in the EMBL-database under accession number AY278741, the complete genome of the SARS coronavirus HSR 1 can be found under accession number AY323977, the complete genome of the SARS coronavirus Frankfurt 1 can be found under accession number AY291315 and the complete genome of the SARS coronavirus TOR2 can be found under accession number AY274119. Preferably, the fragment at least comprises an antigenic determinant recognized by the binding molecules described herein. An “antigenic determinant,” as used herein, is a moiety, such as a SARS-CoV (poly)peptide, protein, glycoprotein, analog or fragment thereof, that is capable of binding to a binding molecule of the invention with sufficiently high affinity to form a detectable antigen-binding molecule complex.
The binding molecules described herein are preferably human binding molecules, preferably human monoclonal antibodies. They can be intact immunoglobulin molecules such as polyclonal or monoclonal antibodies, in particular human monoclonal antibodies, or the binding molecules can be antigen-binding fragments including, but not limited to, Fab, F(ab′), F(ab′)2, Fv, dAb, Fd, complementarity determining region (CDR) fragments, single-chain antibodies (scFv), bivalent single-chain antibodies, single-chain phage antibodies, diabodies, triabodies, tetrabodies, and (poly)peptides that contain at least a fragment of an immunoglobulin that is sufficient to confer specific antigen binding to the SARS-CoV or fragment thereof. The binding molecules described herein can be used in non-isolated or isolated form. Furthermore, the binding molecules described herein can be used alone or in a mixture comprising at least one binding molecule (or variant or fragment thereof). In other words, the binding molecules can be used in combination, e.g., as a pharmaceutical composition comprising two or more binding molecules, variants or fragments thereof. For example, binding molecules having different, but complementary, activities can be combined in a single therapy to achieve a desired prophylactic, therapeutic or diagnostic effect, but alternatively, binding molecules having identical activities can also be combined in a single therapy to achieve a desired prophylactic, therapeutic or diagnostic effect. The mixture may further comprise at least one other therapeutic agent. Preferably, the therapeutic agent is useful in the prophylaxis and/or treatment of a condition resulting from SARS-CoV.
Typically, binding molecules described herein can bind to their binding partners, i.e., SARS-CoV or fragments thereof, with an affinity constant (Kd-value) that is lower than 0.2*10−4 M, 1.0*10−5 M, 1.0*10−6 M, 1.0*10−7 M, preferably lower than 1.0*10−8 M, more preferably lower than 1.0*10−9 M, more preferably lower than 1.0*10−10 M, even more preferably lower than 1.0*10−11 M, and in particular lower than 1.0*10−12 M. The affinity constants can vary for antibody isotypes. For example, affinity binding for an IgM isotype refers to a binding affinity of at least about 1.0*10−7 M. Affinity constants can for instance be measured using surface plasmon resonance, i.e., an optical phenomenon that allows for the analysis of real-time biospecific interactions by detection of alterations in protein concentrations within a biosensor matrix, for example, using the BIACORE® system (Pharmacia Biosensor AB, Uppsala, Sweden).
The binding molecules described herein may bind to SARS-CoV in soluble form such as, for instance, in a sample or may bind to SARS-CoV bound or attached to a carrier or substrate, e.g., microtiter plates, membranes and beads, etc. Carriers or substrates may be made of glass, plastic (e.g., polystyrene), polysaccharides, nylon, nitrocellulose, or Teflon®, etc. The surface of such supports may be solid or porous and of any convenient shape. Furthermore, the binding molecules may bind to SARS-CoV in purified/isolated or non-purified/non-isolated form.
In certain embodiments, the binding molecules described herein neutralize SARS-CoV infectivity. This neutralization may be achieved by preventing the attachment of SARS-CoV to possible receptors on host cells or inhibition of the release of RNA into the cytoplasm of the cell or prevention of RNA transcription or translation. In a specific embodiment, the binding molecules described herein prevent SARS-CoV from infecting host cells by at least 99%, at least 95%, at least 90%, at least 85%, at least 80%, at least 75%, at least 70%, at least 60%, at least 50%, at least 45%, at least 40%, at least 45%, at least 35%, at least 30%, at least 25%, at least 20%, or at least 10% relative to infection of host cells by SARS-CoV in the absence of the binding molecules. Neutralization can for instance be measured as described herein.
The binding molecules described herein, those that do not prevent SARS-CoV from binding its host cell receptor, but inhibit or down-regulate SARS-CoV replication, can also be administered to a mammal to treat, prevent, or ameliorate one or more symptoms associated with a SARS-CoV infection. A binding molecule's ability to inhibit or down-regulate SARS-CoV replication may be determined by techniques known in the art, e.g., by the inhibition or down-regulation of SARS-CoV replication can be determined by detecting the SARS-CoV titer in a biological sample of a mammal, preferably a human. A binding molecule of the invention may inhibit or down-regulate SARS-CoV replication by at least 99%, at least 95%, at least 90%, at least 85%, at least 80%, at least 75%, at least 70%, at least 60%, at least 50%, at least 45%, at least 40%, at least 45%, at least 35%, at least 30%, at least 25%, at least 20%, or at least 10% relative to SARS-CoV replication in absence of the binding molecules. Furthermore, the binding molecules described herein may be complement fixing binding molecules capable of assisting in the lysis of enveloped SARS-CoV. The binding molecules described herein might also act as opsonins and augment phagocytosis of SARS-CoV either by promoting its uptake via Fc or C3b receptors or by agglutinating SARS-CoV to make it more easily phagocytosed.
In a preferred embodiment, the binding molecules described herein comprise at least a CDR3 region, preferably a heavy chain CDR3 region, comprising the amino acid sequence selected from the group consisting of SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, SEQ ID NO:7, SEQ ID NO:8, SEQ ID NO:9, SEQ ID NO:10, SEQ ID NO:11, SEQ ID NO:12, SEQ ID NO:13, SEQ ID NO:75, SEQ ID NO:76, SEQ ID NO:77, SEQ ID NO:78, SEQ ID NO:291, SEQ ID NO:292, SEQ ID NO:293, SEQ ID NO:294, SEQ ID NO:295, SEQ ID NO:296, SEQ ID NO:297, SEQ ID NO:298, SEQ ID NO:299, SEQ ID NO:300, and SEQ ID NO:301.
In yet another embodiment, the binding molecules described herein comprise a variable heavy chain comprising an amino acid sequence selected from the group consisting of SEQ ID NO:15, SEQ ID NO:17, SEQ ID NO:19, SEQ ID NO:21, SEQ ID NO:23, SEQ ID NO:25, SEQ ID NO:27, SEQ ID NO:29, SEQ ID NO:31, SEQ ID NO:33, SEQ ID NO:35, SEQ ID NO:37, SEQ ID NO:39, SEQ ID NO:80, SEQ ID NO:82, SEQ ID NO:84, SEQ ID NO:86, SEQ ID NO:303, SEQ ID NO:307, SEQ ID NO:311, SEQ ID NO:315, SEQ ID NO:319, SEQ ID NO:323, SEQ ID NO:327, SEQ ID NO:331, SEQ ID NO:335, SEQ ID NO:339, SEQ ID NO:343, SEQ ID NO:347, SEQ ID NO:351, SEQ ID NO:355, SEQ ID NO:359, SEQ ID NO:363, SEQ ID NO:367, SEQ ID NO:371, SEQ ID NO:375, SEQ ID NO:379, SEQ ID NO:383, SEQ ID NO:387, SEQ ID NO:391, SEQ ID NO:395, SEQ ID NO:399, SEQ ID NO:403, SEQ ID NO:407, SEQ ID NO:411, SEQ ID NO:415, SEQ ID NO:419, SEQ ID NO:423, SEQ ID NO:427, SEQ ID NO:431, SEQ ID NO:435, SEQ ID NO:439, SEQ ID NO:443, SEQ ID NO:447, SEQ ID NO:451, SEQ ID NO:455, and SEQ ID NO:459.
In a further embodiment, the binding molecules described herein comprise a variable heavy chain comprising the amino acid sequence of SEQ ID NO:15 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:17 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:19 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:21 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:23 and a variable light chain comprising the amino acid sequence of SEQ ID NO:43, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:25 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:27 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:29 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:31 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:33 and a variable light chain comprising the amino acid sequence of SEQ ID NO:45, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:35 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:37 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:39 and a variable light chain comprising the amino acid sequence of SEQ ID NO:45, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:80 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:82 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:84 and a variable light chain comprising the amino acid sequence of SEQ ID NO:88, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:86 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:303 and a variable light chain comprising the amino acid sequence of SEQ ID NO:305, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:307 and a variable light chain comprising the amino acid sequence of SEQ ID NO:309, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:311 and a variable light chain comprising the amino acid sequence of SEQ ID NO:313, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:315 and a variable light chain comprising the amino acid sequence of SEQ ID NO:317, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:319 and a variable light chain comprising the amino acid sequence of SEQ ID NO:321, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:323 and a variable light chain comprising the amino acid sequence of SEQ ID NO:325, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:327 and a variable light chain comprising the amino acid sequence of SEQ ID NO:329, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:331 and a variable light chain comprising the amino acid sequence of SEQ ID NO:333, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:335 and a variable light chain comprising the amino acid sequence of SEQ ID NO:337, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:339 and a variable light chain comprising the amino acid sequence of SEQ ID NO:341, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:343 and a variable light chain comprising the amino acid sequence of SEQ ID NO:345, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:347 and a variable light chain comprising the amino acid sequence of SEQ ID NO:349, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:351 and a variable light chain comprising the amino acid sequence of SEQ ID NO:353, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:355 and a variable light chain comprising the amino acid sequence of SEQ ID NO:357, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:359 and a variable light chain comprising the amino acid sequence of SEQ ID NO:361, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:363 and a variable light chain comprising the amino acid sequence of SEQ ID NO:365, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:367 and a variable light chain comprising the amino acid sequence of SEQ ID NO:369, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:371 and a variable light chain comprising the amino acid sequence of SEQ ID NO:373, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:375 and a variable light chain comprising the amino acid sequence of SEQ ID NO:377, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:379 and a variable light chain comprising the amino acid sequence of SEQ ID NO:381, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:383 and a variable light chain comprising the amino acid sequence of SEQ ID NO:385, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:387 and a variable light chain comprising the amino acid sequence of SEQ ID NO:389, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:391 and a variable light chain comprising the amino acid sequence of SEQ ID NO:393, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:395 and a variable light chain comprising the amino acid sequence of SEQ ID NO:397, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:399 and a variable light chain comprising the amino acid sequence of SEQ ID NO:401, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:403 and a variable light chain comprising the amino acid sequence of SEQ ID NO:405, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:407 and a variable light chain comprising the amino acid sequence of SEQ ID NO:409, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:411 and a variable light chain comprising the amino acid sequence of SEQ ID NO:413, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:415 and a variable light chain comprising the amino acid sequence of SEQ ID NO:417, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:419 and a variable light chain comprising the amino acid sequence of SEQ ID NO:421, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:423 and a variable light chain comprising the amino acid sequence of SEQ ID NO:425, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:427 and a variable light chain comprising the amino acid sequence of SEQ ID NO:429, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:431 and a variable light chain comprising the amino acid sequence of SEQ ID NO:433, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:435 and a variable light chain comprising the amino acid sequence of SEQ ID NO:437, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:439 and a variable light chain comprising the amino acid sequence of SEQ ID NO:441, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:443 and a variable light chain comprising the amino acid sequence of SEQ ID NO:445, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:447 and a variable light chain comprising the amino acid sequence of SEQ ID NO:449, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:451 and a variable light chain comprising the amino acid sequence of SEQ ID NO:453, a variable heavy chain comprising the amino acid sequence of SEQ ID NO:455 and a variable light chain comprising the amino acid sequence of SEQ ID NO:457, or a variable heavy chain comprising the amino acid sequence of SEQ ID NO:459 and a variable light chain comprising the amino acid sequence of SEQ ID NO:461.
In one embodiment, the binding molecules having SARS-CoV neutralizing activity are the binding molecules comprising at least a CDR3 region, preferably a heavy chain CDR3 region, comprising the amino acid sequence selected from the group consisting of SEQ ID NO:11 and SEQ ID NO:12. In a further embodiment, the binding molecules having SARS-CoV neutralizing activity are the binding molecules comprising a variable heavy chain comprising an amino acid sequence selected from the group consisting of SEQ ID NO:35 and SEQ ID NO:37. In yet a further embodiment, the binding molecules having SARS-CoV neutralizing activity are the binding molecules comprising a variable heavy chain comprising the amino acid sequence of SEQ ID NO:35 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41 or a variable heavy chain comprising the amino acid sequence of SEQ ID NO:37 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41. In a preferred embodiment the binding molecules having SARS-CoV neutralizing activity of the invention are administered in IgG1 or IgA (for instance for mucosal administration) format.
Another aspect of the invention includes functional variants of binding molecules as defined herein. A molecule is considered to be a functional variant of a binding molecule described herein, if the molecule is capable of competing for specifically binding to SARS-CoV or a fragment thereof with the parent binding molecules. In other words, when the functional variant is still capable of binding to SARS-CoV or a fragment thereof. Functional variants include, but are not limited to, derivatives that are substantially similar in primary structural sequence, but which contain e.g., in vitro or in vivo modifications, chemical and/or biochemical, that are not found in the parent binding molecule. Such modifications include, inter alia, acetylation, acylation, ADP-ribosylation, amidation, covalent attachment of flavin, covalent attachment of a heme moiety, covalent attachment of a nucleotide or nucleotide derivative, covalent attachment of a lipid or lipid derivative, covalent attachment of phosphotidylinositol, cross-linking, cyclization, disulfide bond formation, demethylation, formation of covalent cross-links, formation of cysteine, formation of pyroglutamate, formylation, gamma-carboxylation, glycosylation, GPI-anchor formation, hydroxylation, iodination, methylation, myristoylation, oxidation, pegylation, proteolytic processing, phosphorylation, prenylation, racemization, selenoylation, sulfation, transfer-RNA mediated addition of amino acids to proteins such as arginylation, ubiquitination, and the like.
Alternatively, functional variants can be binding molecules as defined in the invention comprising an amino acid sequence containing substitutions, insertions, deletions or combinations thereof of one or more amino acids compared to the amino acid sequences of the parent binding molecules. Furthermore, functional variants can comprise truncations of the amino acid sequence at either or both the amino or carboxy termini. Functional variants described herein may have the same or different, either higher or lower, binding affinities compared to the parent binding molecule but are still capable of binding to SARS-CoV or a fragment thereof. For instance, functional variants described herein may have increased or decreased binding affinities for SARS-CoV or a fragment thereof compared to the parent binding molecules. Preferably, the amino acid sequences of the variable regions, including, but not limited to, framework regions, hypervariable regions, in particular the CDR3 regions, are modified. Generally, the light chain and the heavy chain variable regions comprise three hypervariable regions, comprising three CDRs, and more conserved regions, the so-called framework regions (FRs). The hypervariable regions comprise amino acid residues from CDRs and amino acid residues from hypervariable loops. Functional variants intended to fall within the scope of the invention have at least about 50% to about 99%, preferably at least about 60% to about 99%, more preferably at least about 70% to about 99%, even more preferably at least about 80% to about 99%, most preferably at least about 90% to about 99%, in particular at least about 95% to about 99%, and in particular at least about 97% to about 99% amino acid sequence homology with the parent binding molecules as defined herein. Computer algorithms such as, inter alia, Gap or Bestfit known to a person skilled in the art can be used to optimally align amino acid sequences to be compared and to define similar or identical amino acid residues. Functional variants can be obtained by altering the parent binding molecules or parts thereof by general molecular biology methods known in the art including, but not limited to, error-prone PCR, oligonucleotide-directed mutagenesis and site-directed mutagenesis. Preferably, the functional variants of the invention have SARS-CoV neutralizing activity. This neutralizing activity may either be higher or be lower compared to the parent binding molecules. Furthermore, the functional variants may inhibit or down-regulate SARS-CoV replication, are complement fixing binding molecules capable of assisting in the lysis of enveloped SARS-CoV and/or act as opsonins and augment phagocytosis of SARS-CoV either by promoting its uptake via Fc or C3b receptors or by agglutinating SARS-CoV to make it more easily phagocytosed.
In yet a further aspect, the invention includes immunoconjugates, i.e., molecules comprising at least one binding molecule or functional variant thereof as defined herein and further comprising at least one tag, such as, inter alia, a detectable moiety/agent. Also contemplated in the invention are mixtures of immunoconjugates described herein or mixtures of at least one immunoconjugates described herein and another molecule, such as a therapeutic agent or another binding molecule or immunoconjugate. In a further embodiment, the immunoconjugates of the invention may comprise more than one tag. These tags can be the same or distinct from each other and can be joined/conjugated non-covalently to the binding molecules. The tag(s) can also be joined/conjugated directly to the binding molecules through covalent bonding, including, but not limited to, disulfide bonding, hydrogen bonding, electrostatic bonding, recombinant fusion and conformational bonding. Alternatively, the tag(s) can be joined/conjugated to the binding molecules by means of one or more linking compounds. Techniques for conjugating tags to binding molecules are well known to the skilled artisan.
The tags of the immunoconjugates of the invention may be therapeutic agents, but preferably they are detectable moieties/agents. Immunoconjugates comprising a detectable agent can be used diagnostically to, for example, assess if a subject has been infected with SARS-CoV or monitor the development or progression of a SARS-CoV infection as part of a clinical testing procedure to, e.g., determine the efficacy of a given treatment regimen. However, they may also be used for other detection and/or analytical and/or diagnostic purposes. Detectable moieties/agents include, but are not limited to, enzymes, prosthetic groups, fluorescent materials, luminescent materials, bioluminescent materials, radioactive materials, positron emitting metals, and nonradioactive paramagnetic metal ions.
The tags used to label the binding molecules for detection and/or analytical and/or diagnostic purposes depend on the specific detection/analysis/diagnosis techniques and/or methods used such as, inter alia, immunohistochemical staining of (tissue) samples, flow cytometric detection, scanning laser cytometric detection, fluorescent immunoassays, enzyme-linked immunosorbent assays (ELISAs), radioimmunoassays (RIAs), bioassays (e.g., neutralization assays), Western blotting applications, etc. For immunohistochemical staining of tissue samples preferred labels are enzymes that catalyze production and local deposition of a detectable product. Enzymes typically conjugated to binding molecules to permit their immunohistochemical visualization are well-known and include, but are not limited to, acetylcholinesterase, alkaline phosphatase, beta-galactosidase, glucose oxidase, horseradish peroxidase, and urease. Typical substrates for production and deposition of visually detectable products include, but are not limited to, o-nitrophenyl-beta-D-galactopyranoside (ONPG), o-phenylenediamine dihydrochloride (OPD), p-nitrophenyl phosphate (PNPP), p-nitrophenyl-beta-D-galactopryanoside (PNPG), 3′, 3′-diaminobenzidine (DAB), 3-amino-9-ethylcarbazole (AEC), 4-chloro-1-naphthol (CN), 5-bromo-4-chloro-3-indolyl-phosphate (BCIP), ABTS, BluoGal, iodonitrotetrazolium (INT), nitroblue tetrazolium chloride (NBT), phenazine methosulfate (PMS), phenolphthalein monophosphate (PMP), tetramethyl benzidine (TMB), tetranitroblue tetrazolium (TNBT), X-Gal, X-Gluc, and X-glucoside. Other substrates that can be used to produce products for local deposition are luminescent substrates. For example, in the presence of hydrogen peroxide, horseradish peroxidase can catalyze the oxidation of cyclic diacylhydrazides such as luminol. Next to that, binding molecules of the immunoconjugate of the invention can also be labeled using colloidal gold or they can be labeled with radioisotopes, such as 33P, 32P, 35S, 3H, and 125I. Binding molecules of the invention can be attached to radionuclides directly or indirectly via a chelating agent by methods well known in the art.
When the binding molecules described herein are used for flow cytometric detections, scanning laser cytometric detections, or fluorescent immunoassays, they can usefully be labeled with fluorophores. A wide variety of fluorophores useful for fluorescently labeling the binding molecules described herein include, but are not limited to, Alexa Fluor and Alexa Fluor&commat dyes, BODIPY dyes, Cascade Blue, Cascade Yellow, Dansyl, lissamine rhodamine B, Marina Blue, Oregon Green 488, Oregon Green 514, Pacific Blue, rhodamine 6G, rhodamine green, rhodamine red, tetramethylrhodamine, Cy2, Cy3, Cy3.5, Cy5, Cy5.5, Cy7, fluorescein isothiocyanate (FITC), allophycocyanin (APC), R-phycoerythrin (PE), peridinin chlorophyll protein (PerCP), Texas Red, fluorescence resonance energy tandem fluorophores such as PerCP-Cy5.5, PE-Cy5, PE-Cy5.5, PE-Cy7, PE-Texas Red, and APC-Cy7. When the binding molecules described herein are used for secondary detection using labeled avidin, streptavidin, captavidin or neutravidin, the binding molecules may be labeled with biotin to form suitable prosthetic group complexes.
When the immunoconjugates of the invention are used for in vivo diagnostic use, the binding molecules can also be made detectable by conjugation to e.g., magnetic resonance imaging (MRI) contrast agents, such as gadolinium diethylenetriaminepentaacetic acid, to ultrasound contrast agents or to X-ray contrast agents, or by radioisotopic labeling.
A suitable luminescent material includes, but is not limited to luminol and suitable bioluminescent materials include, but are not limited to, luciferase, luciferin, and aequorin.
Furthermore, the binding molecules, functional variants or immunoconjugates of the invention can also be attached to solid supports, which are particularly useful for in vitro immunoassays or purification of SARS-CoV or a fragment thereof. Such solid supports might be porous or nonporous, planar or nonplanar and include, but are not limited to, glass, cellulose, polyacrylamide, nylon, polystyrene, polyvinyl chloride or polypropylene supports. The binding molecules can also, for example, usefully be conjugated to filtration media, such as NHS-activated Sepharose or CNBr-activated Sepharose for purposes of immunoaffinity chromatography. They can also usefully be attached to paramagnetic microspheres, typically by biotin-streptavidin interaction. The microspheres can be used for isolation of SARS-CoV or a fragment thereof from a sample containing SARS-CoV or a fragment thereof. As another example, the binding molecules described herein can usefully be attached to the surface of a microtiter plate for ELISA.
The binding molecules described herein or functional fragments thereof can be fused to marker sequences, such as a peptide to facilitate purification. Examples include, but are not limited to, the hexa-histidine tag, the hemagglutinin (HA) tag, the myc tag or the flag tag.
Alternatively, an antibody can be conjugated to a second antibody to form an antibody heteroconjugate. In another aspect, the binding molecules described herein may be conjugated/attached to one or more antigens. Preferably, these antigens are antigens which are recognized by the immune system of a subject to which the binding molecule-antigen conjugate is administered. The antigens may be identical but may also differ from each other. Conjugation methods for attaching the antigens and binding molecules are well known in the art and include, but are not limited to, the use of cross-linking agents. The binding molecules will bind to SARS-CoV and the antigens attached to the binding molecules will initiate a powerful T-cell attack on the conjugate which will eventually lead to the destruction of the SARS-CoV.
Next to producing immunoconjugates chemically by conjugating, directly or indirectly via for instance a linker, the immunoconjugates can be produced as fusion proteins comprising the binding molecules described herein and a suitable tag. Fusion proteins can be produced by methods known in the art such as, e.g., recombinantly by constructing nucleic acid molecules comprising nucleotide sequences encoding the binding molecules in frame with nucleotide sequences encoding the suitable tag(s) and then expressing the nucleic acid molecules.
Another aspect of the invention is to provide a nucleic acid molecule encoding at least a binding molecule or functional fragment thereof described herein. Such nucleic acid molecules can be used as intermediates for cloning purposes, e.g., in the process of affinity maturation described above. In a preferred embodiment, the nucleic acid molecules are isolated or purified.
The skilled person will appreciate that functional variants of these nucleic acid molecules are also intended to be a part of the invention. Functional variants are nucleic acid sequences that can be directly translated, using the standard genetic code, to provide an amino acid sequence identical to that translated from the parent nucleic acid molecules.
Preferably, the nucleic acid molecules encode binding molecules comprising a CDR3 region, preferably a heavy chain CDR3 region, comprising an amino acid sequence selected from the group consisting of SEQ ID NO:1, SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, SEQ ID NO:7, SEQ ID NO:8, SEQ ID NO:9, SEQ ID NO:10, SEQ ID NO:11, SEQ ID NO:12, SEQ ID NO:13, SEQ ID NO:75, SEQ ID NO:76, SEQ ID NO:77, SEQ ID NO:78, SEQ ID NO:291, SEQ ID NO:292, SEQ ID NO:293, SEQ ID NO:294, SEQ ID NO:295, SEQ ID NO:296, SEQ ID NO:297, SEQ ID NO:298, SEQ ID NO:299, SEQ ID NO:300 and SEQ ID NO:301.
Even more preferably, the nucleic acid molecules encode binding molecules comprising a variable heavy chain comprising an amino acid sequence selected from the group consisting of SEQ ID NO:15, SEQ ID NO:17, SEQ ID NO:19, SEQ ID NO:21, SEQ ID NO:23, SEQ ID NO:25, SEQ ID NO:27, SEQ ID NO:29, SEQ ID NO:31, SEQ ID NO:33, SEQ ID NO:35, SEQ ID NO:37, SEQ ID NO:39, SEQ ID NO:80, SEQ ID NO:82, SEQ ID NO:84, SEQ ID NO:86, SEQ ID NO:303, SEQ ID NO:307, SEQ ID NO:311, SEQ ID NO:315, SEQ ID NO:319, SEQ ID NO:323, SEQ ID NO:327, SEQ ID NO:331, SEQ ID NO:335, SEQ ID NO:339, SEQ ID NO:343, SEQ ID NO:347, SEQ ID NO:351, SEQ ID NO:355, SEQ ID NO:359, SEQ ID NO:363, SEQ ID NO:367, SEQ ID NO:371, SEQ ID NO:375, SEQ ID NO:379, SEQ ID NO:383, SEQ ID NO:387, SEQ ID NO:391, SEQ ID NO:395, SEQ ID NO:399, SEQ ID NO:403, SEQ ID NO:407, SEQ ID NO:411, SEQ ID NO:415, SEQ ID NO:419, SEQ ID NO:423, SEQ ID NO:427, SEQ ID NO:431, SEQ ID NO:435, SEQ ID NO:439, SEQ ID NO:443, SEQ ID NO:447, SEQ ID NO:451, SEQ ID NO:455 and SEQ ID NO:459.
In yet another embodiment, the nucleic acid molecules encode binding molecules comprising a variable heavy chain comprising the amino acid sequence of SEQ ID NO:15 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:17 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:19 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:21 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:23 and a variable light chain comprising the amino acid sequence of SEQ ID NO:43, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:25 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:27 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:29 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:31 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:33 and a variable light chain comprising the amino acid sequence of SEQ ID NO:45, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:35 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:37 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:39 and a variable light chain comprising the amino acid sequence of SEQ ID NO:45, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:80 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:82 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:84 and a variable light chain comprising the amino acid sequence of SEQ ID NO:88, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:86 and a variable light chain comprising the amino acid sequence of SEQ ID NO:41, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:303 and a variable light chain comprising the amino acid sequence of SEQ ID NO:305, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:307 and a variable light chain comprising the amino acid sequence of SEQ ID NO:309, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:311 and a variable light chain comprising the amino acid sequence of SEQ ID NO:313, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:315 and a variable light chain comprising the amino acid sequence of SEQ ID NO:317, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:319 and a variable light chain comprising the amino acid sequence of SEQ ID NO:321, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:323 and a variable light chain comprising the amino acid sequence of SEQ ID NO:325, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:327 and a variable light chain comprising the amino acid sequence of SEQ ID NO:329, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:331 and a variable light chain comprising the amino acid sequence of SEQ ID NO:333, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:335 and a variable light chain comprising the amino acid sequence of SEQ ID NO:337, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:339 and a variable light chain comprising the amino acid sequence of SEQ ID NO:341, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:343 and a variable light chain comprising the amino acid sequence of SEQ ID NO:345, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:347 and a variable light chain comprising the amino acid sequence of SEQ ID NO:349, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:351 and a variable light chain comprising the amino acid sequence of SEQ ID NO:353, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:355 and a variable light chain comprising the amino acid sequence of SEQ ID NO:357, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:359 and a variable light chain comprising the amino acid sequence of SEQ ID NO:361, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:363 and a variable light chain comprising the amino acid sequence of SEQ ID NO:365, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:367 and a variable light chain comprising the amino acid sequence of SEQ ID NO:369, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:371 and a variable light chain comprising the amino acid sequence of SEQ ID NO:373, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:375 and a variable light chain comprising the amino acid sequence of SEQ ID NO:377, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:379 and a variable light chain comprising the amino acid sequence of SEQ ID NO:381, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:383 and a variable light chain comprising the amino acid sequence of SEQ ID NO:385, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:387 and a variable light chain comprising the amino acid sequence of SEQ ID NO:389, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:391 and a variable light chain comprising the amino acid sequence of SEQ ID NO:393, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:395 and a variable light chain comprising the amino acid sequence of SEQ ID NO:397, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:399 and a variable light chain comprising the amino acid sequence of SEQ ID NO:401, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:403 and a variable light chain comprising the amino acid sequence of SEQ ID NO:405, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:407 and a variable light chain comprising the amino acid sequence of SEQ ID NO:409, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:411 and a variable light chain comprising the amino acid sequence of SEQ ID NO:413, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:415 and a variable light chain comprising the amino acid sequence of SEQ ID NO:417, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:419 and a variable light chain comprising the amino acid sequence of SEQ ID NO:421, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:423 and a variable light chain comprising the amino acid sequence of SEQ ID NO:425, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:427 and a variable light chain comprising the amino acid sequence of SEQ ID NO:429, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:431 and a variable light chain comprising the amino acid sequence of SEQ ID NO:433, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:435 and a variable light chain comprising the amino acid sequence of SEQ ID NO:437, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:439 and a variable light chain comprising the amino acid sequence of SEQ ID NO:441, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:443 and a variable light chain comprising the amino acid sequence of SEQ ID NO:445, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:447 and a variable light chain comprising the amino acid sequence of SEQ ID NO:449, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:451 and a variable light chain comprising the amino acid sequence of SEQ ID NO:453, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:455 and a variable light chain comprising the amino acid sequence of SEQ ID NO:457, or they encode a variable heavy chain comprising the amino acid sequence of SEQ ID NO:459 and a variable light chain comprising the amino acid sequence of SEQ ID NO:461.
In a specific embodiment of the invention, the nucleic acid molecules encoding the variable heavy chain of the binding molecules described herein comprise a nucleotide sequence selected from the group consisting of SEQ ID NO:14, SEQ ID NO:16, SEQ ID NO:18, SEQ ID NO:20, SEQ ID NO:22, SEQ ID NO:24, SEQ ID NO:26, SEQ ID NO:28, SEQ ID NO:30, SEQ ID NO:32, SEQ ID NO:34, SEQ ID NO:36, SEQ ID NO:38, SEQ ID NO:79, SEQ ID NO:81, SEQ ID NO:83, SEQ ID NO:85, SEQ ID NO:302, SEQ ID NO:306, SEQ ID NO:310, SEQ ID NO:314, SEQ ID NO:318, SEQ ID NO:322, SEQ ID NO:326, SEQ ID NO:330, SEQ ID NO:334, SEQ ID NO:338, SEQ ID NO:342, SEQ ID NO:346, SEQ ID NO:350, SEQ ID NO:354, SEQ ID NO:358, SEQ ID NO:362, SEQ ID NO:366, SEQ ID NO:370, SEQ ID NO:374, SEQ ID NO:378, SEQ ID NO:382, SEQ ID NO:386, SEQ ID NO:390, SEQ ID NO:394, SEQ ID NO:398, SEQ ID NO:402, SEQ ID NO:406, SEQ ID NO:410, SEQ ID NO:414, SEQ ID NO:418, SEQ ID NO:422, SEQ ID NO:426, SEQ ID NO:430, SEQ ID NO:434, SEQ ID NO:438, SEQ ID NO:442, SEQ ID NO:446, SEQ ID NO:450, SEQ ID NO:454, and SEQ ID NO:458.
In yet another specific embodiment of the invention, the nucleic acid molecules encoding the variable light chain of the binding molecules described herein comprise a nucleotide sequence selected of the group consisting of SEQ ID NO:40, SEQ ID NO:42, SEQ ID NO:44, SEQ ID NO:87, SEQ ID NO:304, SEQ ID NO:308, SEQ ID NO:312, SEQ ID NO:316, SEQ ID NO:320, SEQ ID NO:324, SEQ ID NO:328, SEQ ID NO:332, SEQ ID NO:336, SEQ ID NO:340, SEQ ID NO:344, SEQ ID NO:348, SEQ ID NO:352, SEQ ID NO:356, SEQ ID NO:360, SEQ ID NO:364, SEQ ID NO:368, SEQ ID NO:372, SEQ ID NO:376, SEQ ID NO:380, SEQ ID NO:384, SEQ ID NO:388, SEQ ID NO:392, SEQ ID NO:396, SEQ ID NO:400, SEQ ID NO:404, SEQ ID NO:408, SEQ ID NO:412, SEQ ID NO:416, SEQ ID NO:420, SEQ ID NO:424, SEQ ID NO:428, SEQ ID NO:432, SEQ ID NO:436, SEQ ID NO:440, SEQ ID NO:444, SEQ ID NO:448, SEQ ID NO:452, SEQ ID NO:456 and SEQ ID NO:460.
It is another aspect of the invention to provide vectors, i.e., nucleic acid constructs, comprising one or more nucleic acid molecules described herein. Vectors can be derived from plasmids such as, inter alia, F, R1, RP1, Col, pBR322, TOL, Ti, etc; cosmids; phages such as lambda, lambdoid, M13, Mu, P1, P22, Qβ, T-even, T-odd, T2, T4, T7, etc; plant viruses such as, inter alia, alfalfa mosaic virus, bromovirus, capillovirus, carlavirus, carmovirus, caulivirus, clostervirus, comovirus, cryptovirus, cucumovirus, dianthovirus, fabavirus, fijivirus, furovirus, geminivirus, hordeivirus, ilarvirus, luteovirus, machlovirus, marafivirus, necrovirus, nepovirus, phytorepvirus, plant rhabdovirus, potexvirus, potyvirus, sobemovirus, tenuivirus, tobamovirus, tobravirus, tomato spotted wilt virus, tombusvirus, tymovirus, etc.; or animal viruses such as, inter alia, adenovirus, arenaviridae, baculoviridae, Birnaviridae, bunyaviridae, calciviridae, cardioviruses, coronaviridae, corticoviridae, cystoviridae, Epstein-Barr virus, enteroviruses, filoviridae, flaviviridae, Foot-and-Mouth disease virus, hepadnaviridae, hepatitis viruses, herpesviridae, immunodeficiency viruses, influenza virus, inoviridae, iridoviridae, orthomyxoviridae, papovaviruses, paramyxoviridae, parvoviridae, picornaviridae, poliovirus, polydnaviridae, poxyiridae, reoviridae, retroviruses, rhabdoviridae, rhinoviruses, Semliki Forest virus, tetraviridae, togaviridae, toroviridae, vaccinia virus, vescular stomatitis virus, etc. Vectors can be used for cloning and/or for expression of the binding molecules described herein and might even be used for gene therapy purposes. Vectors comprising one or more nucleic acid molecules described herein operably linked to one or more expression-regulating nucleic acid molecules are also covered by the invention. The choice of the vector is dependent on the recombinant procedures followed and the host used. Introduction of vectors in host cells can be effected by, inter alia, calcium phosphate transfection, virus infection, DEAE-dextran mediated transfection, lipofectamin transfection or electroporation. Vectors may be autonomously replicating or may replicate together with the chromosome into which they have been integrated. Preferably, the vectors contain one or more selection markers. The choice of the markers may depend on the host cells of choice, although this is not critical to the invention as is well known to persons skilled in the art. They include, but are not limited to, kanamycin, neomycin, puromycin, hygromycin, Zeocin®, thymidine kinase gene from Herpes simplex virus (HSV-TK), dihydrofolate reductase gene from mouse (dhfr). Vectors comprising one or more nucleic acid molecules encoding the binding molecules as described above operably linked to one or more nucleic acid molecules encoding proteins or peptides that can be used to isolate the binding molecules are also covered by the invention. These proteins or peptides include, but are not limited to, glutathione-S-transferase, maltose binding protein, metal-binding polyhistidine, green fluorescent protein, luciferase and beta-galactosidase.
Hosts containing one or more copies of the vectors mentioned above are an additional subject of the invention. Preferably, the hosts are host cells. Host cells include, but are not limited to, cells of mammalian, plant, insect, fungal or bacterial origin. Bacterial cells include, but are not limited to, cells from Gram positive bacteria such as several species of the genera Bacillus, Streptomyces and Staphylococcus or cells of Gram negative bacteria such as several species of the genera Escherichia, such as E. coli, and Pseudomonas. In the group of fungal cells preferably yeast cells are used. Expression in yeast can be achieved by using yeast strains such as, inter alia, Pichia pastoris, Saccharomyces cerevisiae and Hansenula polymorpha. Furthermore, insect cells such as cells from Drosophila and Sf9 can be used as host cells. Besides that, the host cells can be plant cells such as, inter alia, cells from crop plants such as forestry plants, or cells from plants providing food and raw materials such as cereal plants, or medicinal plants, or cells from ornamentals, or cells from flower bulb crops. Transformed (transgenic) plants or plant cells are produced by known methods, for example, Agrobacterium-mediated gene transfer, transformation of leaf discs, protoplast transformation by polyethylene glycol-induced DNA transfer, electroporation, sonication, microinjection or bolistic gene transfer. Additionally, a suitable expression system can be a baculovirus system. Expression systems using mammalian cells such as Chinese Hamster Ovary (CHO) cells, COS cells, BHK cells or Bowes melanoma cells are preferred in the invention. Mammalian cells provide expressed proteins with posttranslational modifications that are most similar to natural molecules of mammalian origin. Since the invention deals with molecules that may have to be administered to humans, a completely human expression system would be particularly preferred. Therefore, even more preferably, the host cells are human cells. Examples of human cells are, inter alia, HeLa, 911, AT1080, A549, 293 and HEK293T cells. Preferred mammalian cells are human retina cells such as 911 cells or the cell line deposited at the European Collection of Cell Cultures (ECACC), CAMR, Salisbury, Wiltshire SP4 OJG, Great Britain on 29 Feb. 1996 under number 96022940 and marketed under the trademark PER.C6® (PER.C6 is a registered trademark of Crucell Holland B.V.). For the purposes of this application “PER.C6” refers to cells deposited under number 96022940 or ancestors, passages up-stream or downstream as well as descendants from ancestors of deposited cells, as well as derivatives of any of the foregoing.
In preferred embodiments, the human producer cells comprise at least a functional part of a nucleic acid sequence encoding an adenovirus E1 region in expressible format. In even more preferred embodiments, the host cells are derived from a human retina and immortalized with nucleic acids comprising adenoviral E1 sequences, such as the cell line deposited at the European Collection of Cell Cultures (ECACC), CAMR, Salisbury, Wiltshire SP4 OJG, Great Britain on 29 Feb. 1996 under number 96022940 and marketed under the trademark PER.C6™, and derivatives thereof. Production of recombinant proteins in host cells can be performed according to methods well known in the art. The use of the cells marketed under the trademark PER.C6™ as a production platform for proteins of interest has been described in PCT International Publication WO 00/63403 the disclosure of which is incorporated herein by reference in its entirety.
A method of producing a binding molecule or a functional variant described herein is an additional part of the invention. The method comprises the steps of a) culturing a host described herein under conditions conducive to the expression of the binding molecule or functional variant, and b) optionally, recovering the expressed binding molecule or functional variant. The expressed binding molecules or functional variants thereof can be recovered from the cell free extract, but preferably they are recovered from the culture medium. Methods to recover proteins, such as binding molecules, from cell free extracts or culture medium are well known to the man skilled in the art. Binding molecules or functional variants thereof as obtainable by the above-described method are also a part of the invention.
Alternatively, next to the expression in hosts, such as host cells, the binding molecules or functional variants thereof of the invention can be produced synthetically by conventional peptide synthesizers or in cell-free translation systems using RNA nucleic acid derived from DNA molecules described herein. Binding molecule or functional variants thereof as obtainable by the above-described synthetic production methods or cell-free translation systems are also a part of the invention.
In yet another embodiment, human binding molecules of the invention can also be produced in transgenic, non-human, mammals such as, inter alia, rabbits, goats or cows, and secreted into for instance the milk thereof.
In yet another alternative embodiment, binding molecules described herein, preferably human binding molecules specifically binding to SARS-CoV or a fragment thereof, may be generated by transgenic non-human mammals, such as for instance transgenic mice or rabbits that express human immunoglobulin genes. Preferably, the transgenic non-human mammals have a genome comprising a human heavy chain transgene and a human light chain transgene encoding all or a portion of the human binding molecules as described above. The transgenic non-human mammals can be immunized with a purified or enriched preparation of SARS-CoV or a fragment thereof. Protocols for immunizing non-human mammals are well established in the art. See, Using Antibodies: A Laboratory Manual, supra and Current Protocols in Immunology, Edited by: J. E. Coligan, A. M. Kruisbeek, D. H. Margulies, E. M. Shevach, W. Strober (2001), John Wiley & Sons Inc., New York, the disclosures of which are incorporated herein by reference. Immunization protocols often include multiple immunizations, either with or without adjuvants such as Freund's complete adjuvant and Freund's incomplete adjuvant, but may also include naked DNA immunizations. In another embodiment, the human binding molecules are produced by B cells or plasma cells derived from the transgenic animals. In yet another embodiment, the human binding molecules are produced by hybridomas which are prepared by fusion of B cells obtained from the above-described transgenic non-human mammals to immortalized cells. B cells, plasma cells and hybridomas as obtainable from the above-described transgenic non-human mammals and human binding molecules as obtainable from the above-described transgenic non-human mammals, B cells, plasma cells and hybridomas are also a part of the invention.
In a further aspect, provided is a method of identifying binding molecules, preferably human binding molecules such as human monoclonal antibodies or fragments thereof, described herein, or nucleic acid molecules described herein, and comprises the steps of a) contacting a phage library of binding molecules, preferably human binding molecules, with SARS-CoV or a fragment thereof, b) selecting at least once for a phage binding to the SARS-CoV or the fragment thereof, and c) separating and recovering the phage binding to the SARS-CoV or the fragment thereof. The selection step described herein is preferably performed in the presence of SARS-CoV which is inactivated. The SARS-CoV may be isolated or non-isolated, e.g., present in serum and/or blood of an infected individual. Alternatively, the selection step may be performed in the presence of a fragment of SARS-CoV such as an extracellular part of the SARS-CoV, one or more proteins or (poly)peptides derived from SARS-CoV, fusion proteins comprising these proteins or (poly)peptides, and the like. Phage display methods for identifying and obtaining binding molecules, e.g., antibodies, are by now well-established methods known by the person skilled in the art. They are e.g., described in U.S. Pat. No. 5,696,108; Burton and Barbas, 1994; de Kruif et al., 1995b; and Phage Display: A Laboratory Manual. Edited by: C. F. Barbas, D. R. Burton, J. K. Scott and G. J. Silverman (2001), Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. All these references are herewith incorporated herein in their entirety. For the construction of phage display libraries, collections of human monoclonal antibody heavy and light chain variable region genes are expressed on the surface of bacteriophage, preferably filamentous bacteriophage, particles, in, for example, single-chain Fv (scFv) or in Fab format (see, de Kruif et al., 1995b). Large libraries of antibody fragment-expressing phages typically contain more than 1.0*109 antibody specificities and may be assembled from the immunoglobulin V regions expressed in the B lymphocytes of immunized- or non-immunized individuals. In a specific embodiment of the invention, the phage library of binding molecules, preferably scFv phage library, is prepared from RNA isolated from cells obtained from a subject that has been vaccinated or exposed to a SARS-CoV. RNA can be isolated from, inter alia, bone marrow or peripheral blood, preferably peripheral blood lymphocytes. The subject can be an animal vaccinated or exposed to SARS-CoV, but is preferably a human subject which has been vaccinated or has been exposed to SARS-CoV. Preferably, the human subject has recovered from SARS-CoV.
Alternatively, phage display libraries may be constructed from immunoglobulin variable regions that have been partially assembled in vitro to introduce additional antibody diversity in the library (semi-synthetic libraries). For example, in vitro assembled variable regions contain stretches of synthetically produced, randomized or partially randomized DNA in those regions of the molecules that are important for antibody specificity, e.g., CDR regions. SARS-CoV specific phage antibodies can be selected from the library by immobilizing target antigens such as antigens from SARS-CoV on a solid phase and subsequently exposing the target antigens to a phage library to allow binding of phages expressing antibody fragments specific for the solid phase-bound antigen(s). Non-bound phages are removed by washing and bound phages eluted from the solid phase for infection of Escherichia coli (E. coli) bacteria and subsequent propagation. Multiple rounds of selection and propagation are usually required to sufficiently enrich for phages binding specifically to the target antigen(s). If desired, before exposing the phage library to target antigens the phage library can first be subtracted by exposing the phage library to non-target antigens bound to a solid phase. Phages may also be selected for binding to complex antigens such as complex mixtures of SARS-CoV proteins or (poly)peptides, host cells expressing one or more proteins or (poly)peptides of SARS-CoV, or SARS-CoV itself. Antigen specific phage antibodies can be selected from the library by incubating a solid phase with bound thereon a preparation of inactivated SARS-CoV with the phage antibody library to let, for example, the scFv or Fab part of the phage bind to the proteins/polypeptides of the SARS-CoV preparation. After incubation and several washes to remove unbound and loosely attached phages, the phages that have bound with their scFv or Fab part to the preparation are eluted and used to infect Escherichia coli to allow amplification of the new specificity. Generally, one or more selection rounds are required to separate the phages of interest from the large excess of non-binding phages. Alternatively, known proteins or (poly)peptides of the SARS-CoV can be expressed in host cells and these cells can be used for selection of phage antibodies specific for the proteins or (poly)peptides. A phage display method using these host cells can be extended and improved by subtracting non-relevant binders during screening by addition of an excess of host cells comprising no target molecules or non-target molecules that are similar, but not identical, to the target, and thereby strongly enhance the chance of finding relevant binding molecules. This process is referred to as the MABSTRACT™ process. See, also, U.S. Pat. No. 6,265,150, which is incorporated herein by reference.
In yet a further aspect, provided is a method of obtaining a binding molecule, preferably a human binding molecule or a nucleic acid molecule described herein, wherein the method comprises the steps of a) performing the above-described method of identifying binding molecules, preferably human binding molecules such as human monoclonal antibodies or fragments thereof described herein, or nucleic acid molecules described herein, and b) isolating from the recovered phage the human binding molecule and/or the nucleic acid encoding the human binding molecule. Once a new monoclonal phage antibody has been established or identified with the above mentioned method of identifying binding molecules or nucleic acid molecules encoding the binding molecules, the DNA encoding the scFv or Fab can be isolated from the bacteria or phages and combined with standard molecular biological techniques to make constructs encoding bivalent scFvs or complete human immunoglobulins of a desired specificity (e.g., IgG, IgA or IgM). These constructs can be transfected into suitable cell lines and complete human monoclonal antibodies can be produced (see, Huls et al., 1999; Boel et al., 2000).
In a further aspect, the invention is directed to a phage library of binding molecules, preferably a scFv phage display library which is prepared from RNA isolated from cells obtained from a subject that has been vaccinated or exposed to a SARS-CoV. RNA can be isolated from, inter alia, bone marrow or peripheral blood, preferably peripheral blood lymphocytes. The subject can be an animal vaccinated or exposed to SARS-CoV, but is preferably a human subject which has been vaccinated or has been exposed to SARS-CoV. Preferably the human subject has recovered from SARS-CoV.
In yet a further aspect, provided is compositions comprising at least one binding molecule, at least one functional variant or fragment thereof, at least one immunoconjugate described herein or a combination thereof. In addition to that, the compositions may comprise, inter alia, stabilizing molecules, such as albumin or polyethylene glycol, or salts. Preferably, the salts used are salts that retain the desired biological activity of the binding molecules and do not impart any undesired toxicological effects. Examples of such salts include, but are not limited to, acid addition salts and base addition salts. Acid addition salts include, but are not limited to, those derived from nontoxic inorganic acids, such as hydrochloric, nitric, phosphoric, sulfuric, hydrobromic, hydroiodic, phosphorous and the like, as well as from nontoxic organic acids such as aliphatic mono- and dicarboxylic acids, phenyl-substituted alkanoic acids, hydroxy alkanoic acids, aromatic acids, aliphatic and aromatic sulfonic acids and the like. Base addition salts include, but are not limited to, those derived from alkaline earth metals, such as sodium, potassium, magnesium, calcium and the like, as well as from nontoxic organic amines, such as N,N′-dibenzylethylenediamine, N-methylglucamine, chloroprocaine, choline, diethanolamine, ethylenediamine, procaine and the like. If necessary, the binding molecules described herein may be coated in or on a material to protect them from the action of acids or other natural or non-natural conditions that may inactivate the binding molecules.
In yet a further aspect, provided do compositions comprise at least one nucleic acid molecule as defined in the invention. The compositions may comprise aqueous solutions such as aqueous solutions containing salts (e.g., NaCl or salts as described above), detergents (e.g., SDS) and/or other suitable components.
Furthermore, the invention pertains to pharmaceutical compositions comprising at least one binding molecule described herein, at least one functional variant or fragment thereof, at least one immunoconjugate described herein, at least one composition described herein, or combinations thereof. The pharmaceutical composition of the invention further comprises at least one pharmaceutically acceptable excipient.
A pharmaceutical composition described herein can further comprise at least one other therapeutic, prophylactic and/or diagnostic agent. Preferably, the pharmaceutical composition comprises at least one other prophylactic and/or therapeutic agent. Preferably, the further therapeutic and/or prophylactic agents are agents capable of preventing and/or treating an infection and/or a condition resulting from SARS-CoV. Therapeutic and/or prophylactic agents include, but are not limited to, anti-viral agents. Such agents can be binding molecules, small molecules, organic or inorganic compounds, enzymes, polynucleotide sequences etc.
Examples of anti-viral agents include, but are not limited to, abacavir, acyclovir, adefovir, afovirsen, amantadine, amprenavir, AZT, camptothecins, castanospermine, cidofovir, D4T, ddC, ddI, d4T, delavirdine, didanosine, efavirenz, famciclovir, fialuridine, foscarnet, FTC, ganciclovir, GG167, idoxuridine, indinavir, interferon alpha, lamivudine, lobucavir, loviride, nelfinavir, nevirapine, oseltamivir, penciclovir, pirodavir, ribavirin, rimantadine, ritonavir, saquinavir, sICAM-1, sorivudine, stavudine, trifluridine, 3TC, valacyclovir, vidarabine, zalcitabine, zanamivir, zidovudine, and pharmaceutically acceptable salts, acids or derivatives of any of the above. Other agents that are currently used to treat patients infected with SARS-CoV are interferon-alpha, steroids and potential replicase inhibitors. Furthermore, patients infected with SARS-CoV are currently treated by transfusion of serum produced from blood donated by recovering/recovered SARS patients who have produced antibodies after being exposed to the virus. Agents capable of preventing and/or treating an infection with SARS-CoV and/or a condition resulting from SARS-CoV that are in the experimental phase might also be used as other therapeutic and/or prophylactic agents useful in the invention.
The binding molecules or pharmaceutical compositions described herein can be tested in suitable animal model systems prior to use in humans. Such animal model systems include, but are not limited to, mice, rats, chicken, cows, monkeys, pigs, dogs, rabbits, etc. Any animal system well-known in the art may be used.
Typically, pharmaceutical compositions must be sterile and stable under the conditions of manufacture and storage. The binding molecules, variant or fragments thereof, immunoconjugates, nucleic acid molecules or compositions of the invention can be in powder form for reconstitution in the appropriate pharmaceutically acceptable excipient before or at the time of delivery. In the case of sterile powders for the preparation of sterile injectable solutions, the preferred methods of preparation are vacuum drying and freeze-drying (lyophilization) that yield a powder of the active ingredient plus any additional desired ingredient from a previously sterile-filtered solution thereof.
Alternatively, the binding molecules, variant or fragments thereof, immunoconjugates, nucleic acid molecules or compositions of the invention can be in solution and the appropriate pharmaceutically acceptable excipient can be added and/or mixed before or at the time of delivery to provide a unit dosage injectable form. Preferably, the pharmaceutically acceptable excipient used in the invention is suitable to high drug concentration, can maintain proper fluidity, and, if necessary, can delay absorption.
The choice of the optimal route of administration of the pharmaceutical compositions will be influenced by several factors including the physico-chemical properties of the active molecules within the compositions, the urgency of the clinical situation and the relationship of the plasma concentrations of the active molecules to the desired therapeutic effect. For instance, if necessary, the binding molecules described herein can be prepared with carriers that will protect them against rapid release, such as a controlled release formulation, including implants, transdermal patches, and microencapsulated delivery systems. Biodegradable, biocompatible polymers can, inter alia, be used, such as ethylene vinyl acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoesters, and polylactic acid. Furthermore, it may be necessary to coat the binding molecules with, or co-administer the binding molecules with, a material or compound that prevents the inactivation of the binding molecules. For example, the binding molecules may be administered to a subject in an appropriate carrier, for example, liposomes, or a diluent.
The routes of administration can be divided into two main categories, oral and parenteral administration. These two categories include, but are not limited to, bolus, buccal, epidermal, epidural, inhalation, intra-abdominal, intra-arterial, intra-articular, intrabronchial, intracapsular, intracardiac, intracartilaginous, intracavitary, intracelial, intracelebellar, intracerebronventricular, intracolic, intracervical, intradermal, intragastric, intrahepatic, intramedullary, intramuscular, intramyocardial, intranasal, intra-ocular intra-orbital, intra-osteal, intrapelvic, intrapericardiac, intraperitoneal, intraplaque, intrapleural, intraprostatic, intrapulmonary, intrarectal, intrarenal, intraretinal, intraspinal, intrasternal, intrasynovial, intrathecal, intrathoracic, intratumoral, intra-uterine, intravenous, intraventricular, intravesical, rectal, spinal, subarachnoid, subcapsular, subcutaneous, subcuticular, sublingual, topical, transdermal, transmucosal, transtracheal, and vaginal administration. The preferred administration route is intravenous, particularly preferred is intramuscular.
Oral dosage forms can be formulated, inter alia, as tablets, troches, lozenges, aqueous or oily suspensions, dispersible powders or granules, emulsions, hard capsules, soft gelatin capsules, syrups or elixirs, pills, dragees, liquids, gels, or slurries. These formulations can contain pharmaceutically excipients including, but not limited to, inert diluents such as calcium carbonate, sodium carbonate, lactose, calcium phosphate or sodium phosphate; granulating and disintegrating agents such as corn starch or alginic acid; binding agents such as starch, gelatin or acacia; lubricating agents such as calcium stearate, glyceryl behenate, hydrogenated vegetable oils, magnesium stearate, mineral oil, polyethylene glycol, sodium stearyl, fumarate, stearic acid, talc, zinc stearate; preservatives such as n-propyl-p-hydroxybenzoate; coloring, flavoring or sweetening agents such as sucrose, saccharine, glycerol, propylene glycol or sorbitol; vegetable oils such as arachis oil, olive oil, sesame, oil or coconut oil; mineral oils such as liquid paraffin; wetting agents such as benzalkonium chloride, docusate sodium, lecithin, poloxamer, sodium lauryl sulfate, sorbitan esters; and thickening agents such as agar, alginic acid, beeswax, carboxymethyl cellulose calcium, carageenan, dextrin or gelatin.
The pharmaceutical compositions of the invention can also be formulated for parenteral administration. Formulations for parenteral administration can be, inter alia, in the form of aqueous or non-aqueous isotonic sterile non-toxic injection or infusion solutions or suspensions. Preferred parenteral administration routes include intravenous, intraperitoneal, epidural, intramuscular and intratumoral injection or infusion. The solutions or suspensions may comprise agents that are non-toxic to recipients at the dosages and concentrations employed such as 1,3-butanediol, Ringer's solution, Hank's solution, isotonic sodium chloride solution, oils such as synthetic mono- or diglycerides or fatty acids such as oleic acid, local anesthetic agents, preservatives, buffers, viscosity or solubility increasing agents, water-soluble antioxidants such as ascorbic acid, cysteine hydrochloride, sodium bisulfate, sodium metabisulfite, sodium sulfite and the like, oil-soluble antioxidants such as ascorbyl palmitate, butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), lecithin, propyl gallate, alpha-tocopherol, and the like, and metal chelating agents, such as citric acid, ethylenediamine tetraacetic acid (EDTA), sorbitol, tartaric acid, phosphoric acid, and the like.
In a further aspect, the binding molecules, functional variants, immunoconjugates, compositions, or pharmaceutical compositions of the invention can be used as a medicament. So, a method of treatment and/or prevention of a SARS-CoV infection using the binding molecules, functional variants, immunoconjugates, compositions, or pharmaceutical compositions of the invention is another part of the invention. The above-mentioned molecules can, inter alia, be used in the diagnosis, prophylaxis, treatment, or combination thereof, of one or more conditions resulting from SARS-CoV. They are suitable for treatment of yet untreated patients suffering from a condition resulting from SARS-CoV and patients who have been or are treated from a condition resulting from SARS-CoV. They protect against further infection by SARS-CoV and/or will retard the onset or progress of the symptoms associated with SARS. They may even be used in the prophylaxis of SARS in for instance people exposed to the SARS-CoV such as hospital personnel taking care of suspected SARS patients.
The above-mentioned molecules or compositions may be employed in conjunction with other molecules useful in diagnosis, prophylaxis and/or treatment. They can be used in vitro, ex vivo or in vivo. For instance, the binding molecules, functional variants, immunoconjugates or pharmaceutical compositions of the invention can be co-administered with a vaccine against SARS-CoV. Alternatively, the vaccine may also be administered before or after administration of the molecules of the invention. Administration of the molecules of the invention with a vaccine might be suitable for post-exposure prophylaxis and might also decrease possible side effects of a live-attenuated vaccine in immunocompromised recipients.
The molecules are typically formulated in the compositions and pharmaceutical compositions of the invention in a therapeutically or diagnostically effective amount. Dosage regimens can be adjusted to provide the optimum desired response (e.g., a therapeutic response). A suitable dosage range may for instance be 0.1-100 mg/kg body weight, preferably 0.5-15 mg/kg body weight. Furthermore, for example, a single bolus may be administered, several divided doses may be administered over time or the dose may be proportionally reduced or increased as indicated by the exigencies of the therapeutic situation. The molecules and compositions described herein are preferably sterile. Methods to render these molecules and compositions sterile are well known in the art. The other molecules useful in diagnosis, prophylaxis and/or treatment can be administered in a similar dosage regimen as proposed for the binding molecules described herein. If the other molecules are administered separately, they may be administered to a patient prior to (e.g., 2 minutes, 5 minutes, 10 minutes, 15 minutes, 30 minutes, 45 minutes, 60 minutes, 2 hours, 4 hours, 6 hours, 8 hours, 10 hours, 12 hours, 14 hours, 16 hours, 18 hours, 20 hours, 22 hours, 24 hours, 2 days, 3 days, 4 days, 5 days, 7 days, 2 weeks, 4 weeks or 6 weeks before), concomitantly with, or subsequent to (e.g., 2 minutes, 5 minutes, 10 minutes, 15 minutes, 30 minutes, 45 minutes, 60 minutes, 2 hours, 4 hours, 6 hours, 8 hours, 10 hours, 12 hours, 14 hours, 16 hours, 18 hours, 20 hours, 22 hours, 24 hours, 2 days, 3 days, 4 days, 5 days, 7 days, 2 weeks, 4 weeks or 6 weeks after) the administration of one or more of the binding molecules or pharmaceutical compositions of the invention. The exact dosing regimen is usually sorted out during clinical trials in human patients.
Human binding molecules and pharmaceutical compositions comprising the human binding molecules are particularly useful, and often preferred, when to be administered to human beings as in vivo therapeutic agents, since recipient immune response to the administered antibody will often be substantially less than that occasioned by administration of a monoclonal murine, chimeric or humanized binding molecule.
In another aspect, the invention concerns the use of binding molecules, preferably human binding molecules, functional variants thereof, immunoconjugates described herein, nucleic acid molecules described herein, compositions or pharmaceutical compositions described herein in the preparation of a medicament for the diagnosis, prophylaxis, treatment, or combination thereof, of a condition resulting from SARS-CoV.
Next to that, kits comprising at least one binding molecule, preferably human binding molecule, described herein, at least one functional variant thereof described herein, at least one immunoconjugate described herein, at least one nucleic acid molecule described herein, at least one composition described herein, at least one pharmaceutical composition described herein, at least one vector described herein, at least one host described herein or a combination thereof are also a part of the invention. Optionally, the above-described components of the kits of the invention are packed in suitable containers and labeled for diagnosis, prophylaxis and/or treatment of the indicated conditions. The above-mentioned components may be stored in unit or multi-dose containers, for example, sealed ampules, vials, bottles, syringes, and test tubes, as an aqueous, preferably sterile, solution or as a lyophilized, preferably sterile, formulation for reconstitution. The containers may be formed from a variety of materials such as glass or plastic and may have a sterile access port (for example, the container may be an intravenous solution bag or a vial having a stopper pierceable by a hypodermic injection needle). The kit may further comprise more containers comprising a pharmaceutically acceptable buffer, such as phosphate-buffered saline, Ringer's solution and dextrose solution. It may further include other materials desirable from a commercial and user standpoint, including other buffers, diluents, filters, needles, syringes, culture medium for one or more of the suitable hosts. Associated with the kits can be instructions customarily included in commercial packages of therapeutic, prophylactic or diagnostic products, that contain information about, for example, the indications, usage, dosage, manufacture, administration, contraindications and/or warnings concerning the use of such therapeutic, prophylactic or diagnostic products.
The invention further pertains to a method of detecting a SARS-CoV in a sample, wherein the method comprises the steps of a) contacting a sample with a diagnostically effective amount of a binding molecule, a functional variant or an immunoconjugate described herein, and b) determining whether the binding molecule, functional variant, or immunoconjugate specifically binds to a molecule of the sample. The sample may be a biological sample including, but not limited to blood, serum, urine, tissue or other biological material from (potentially) infected subjects, or a nonbiological sample such as water, drink, etc. The (potentially) infected subjects may be human subjects, but also animals that are suspected as carriers of SARS-CoV might be tested for the presence of SARS-CoV using the binding molecules, functional variants or immunoconjugates of the invention. The sample may first be manipulated to make it more suitable for the method of detection. Manipulation mean, inter alia, treating the sample suspected to contain and/or containing SARS-CoV in such a way that the SARS-CoV will disintegrate into antigenic components such as proteins, (poly)peptides or other antigenic fragments. Preferably, the binding molecules, functional variants or immunoconjugates of the invention are contacted with the sample under conditions which allow the formation of an immunological complex between the binding molecules and SARS-CoV or antigenic components thereof that may be present in the sample. The formation of an immunological complex, if any, indicating the presence of SARS-CoV in the sample, is then detected and measured by suitable means. Such methods include, inter alia, homogeneous and heterogeneous binding immunoassays, such as radioimmunoassays (RIA), ELISA, immunofluorescence, immunohistochemistry, FACS, BIACORE and Western blot analyses.
Preferred assay techniques, especially for large-scale clinical screening of patient sera and blood and blood-derived products are ELISA and Western blot techniques. ELISA tests are particularly preferred. For use as reagents in these assays, the binding molecules, functional variants or immunoconjugates of the invention are conveniently bonded to the inside surface of microtiter wells. The binding molecules, functional variants or immunoconjugates of the invention may be directly bonded to the microtiter well. However, maximum binding of the binding molecules, functional variants or immunoconjugates of the invention to the wells might be accomplished by pretreating the wells with polylysine prior to the addition of the binding molecules, functional variants or immunoconjugates of the invention. Furthermore, the novel the binding molecules, functional variants or immunoconjugates of the invention may be covalently attached by known means to the wells. Generally, the binding molecules, functional variants or immunoconjugates of the invention are used in a concentration of between 0.01 to 100 μg/ml for coating, although higher as well as lower amounts may also be used. Samples are then added to the wells coated with the binding molecules, functional variants or immunoconjugates of the invention.
Furthermore, the binding molecules or functional variants of the invention can be used to identify epitopes of SARS-CoV. The epitopes can be linear, but also structural and/or conformational. In one embodiment, binding of binding molecules or functional variants of the invention to a series of overlapping peptides, such as 15-mer peptides, of a protein from SARS-CoV can be analyzed by means of PEPSCAN analysis (see, inter alia, WO 84/03564, WO 93/09872, Slootstra et al. 1996). The binding of binding molecules to each peptide can be tested in a PEPSCAN-based enzyme-linked immuno assay (ELISA). In another embodiment, a random peptide library comprising peptides from SARS-CoV can be screened for peptides capable of binding to the binding molecules or functional variants of the invention. In the above assays the use of neutralizing binding molecules may identify one or more neutralizing epitopes. The peptides/epitopes found can be used as vaccines and for the diagnosis of SARS. In yet a further embodiment, the binding of (neutralizing) binding molecules of the invention to domains of a surface protein of SARS-CoV, such as the spike glycoprotein, may be analyzed. Alternatively, the binding molecules described herein may identify one or more epitopes of another protein of SARS-CoV including, but not limited to, the membrane protein (M protein), the small envelope protein (E protein) and the nucleocapsid protein (N protein). In a preferred embodiment binding molecule 018 recognized epitopes on the N protein. These epitopes might be useful in the treatment but also in the detection of SARS-CoV.
In a further aspect, provided is a method of screening a binding molecule or a functional variant of a binding molecule for specific binding to the same epitope of a SARS-CoV as the epitope bound by a binding molecule or functional variant of the invention, wherein the method comprises the steps of a) contacting a binding molecule or a functional variant to be screened, a binding molecule or functional variant of the invention and a SARS-CoV or fragment thereof, b) measure if the binding molecule or functional variant to be screened is capable of competing for specifically binding to the SARS-CoV or fragment thereof with the binding molecule or functional variant of the invention. In a further step it may be determined if the screened binding molecules that are capable of competing for specifically binding to the SARS-CoV or fragment thereof have neutralizing activity. A binding molecule or functional variant that is capable of competing for specifically binding to the SARS-CoV or fragment thereof with the binding molecule or functional variant of the invention is another part of the invention. In the above-described screening method, “specifically binding to the same epitope” also contemplates specific binding to substantially or essentially the same epitope as the epitope bound by the binding molecules described herein. The capacity to block, or compete with, the binding of the binding molecules described herein to SARS-CoV typically indicates that a binding molecule to be screened binds to an epitope or binding site on SARS-CoV that structurally overlaps with the binding site on SARS-CoV that is immunospecifically recognized by the binding molecules described herein. Alternatively, this can indicate that a binding molecule to be screened binds to an epitope or binding site which is sufficiently proximal to the binding site immunospecifically recognized by the binding molecules described herein to sterically or otherwise inhibit binding of the binding molecules described herein to SARS-CoV.
In general, competitive inhibition is measured by means of an assay, wherein an antigen composition, i.e., a composition comprising SARS-CoV or fragments thereof, is admixed with reference binding molecules, i.e., the binding molecules described herein, and binding molecules to be screened. Usually, the binding molecules to be screened are present in excess. Protocols based upon ELISAs and Western blotting are suitable for use in such simple competition studies. In certain embodiments, one may pre-mix the reference binding molecules with varying amounts of the binding molecules to be screened (e.g., 1:10, 1:20, 1:30, 1:40, 1:50, 1:60, 1:70, 1:80, 1:90 or 1:100) for a period of time prior to applying to the antigen composition. In other embodiments, the reference binding molecules and varying amounts of binding molecules to be screened can simply be admixed during exposure to the antigen composition. In any event, by using species or isotype secondary antibodies one will be able to detect only the bound reference binding molecules, the binding of which will be reduced by the presence of a binding molecule to be screened that recognizes substantially the same epitope. In conducting a binding molecule competition study between a reference binding molecule and any binding molecule to be screened (irrespective of species or isotype), one may first label the reference binding molecule with a detectable label, such as, e.g., biotin, an enzymatic, a radioactive or other label to enable subsequent identification. In these cases, one would pre-mix or incubate the labeled reference binding molecules with the binding molecules to be screened at various ratios (e.g., 1:10, 1:20, 1:30, 1:40, 1:50, 1:60, 1:70, 1:80, 1:90 or 1:100) and (optionally after a suitable period of time) then assay the reactivity of the labeled reference binding molecules and compare this with a control value in which no potentially competing binding molecule was included in the incubation. The assay may again be any one of a range of immunological assays based upon antibody hybridization, and the reference binding molecules would be detected by means of detecting their label, e.g., using streptavidin in the case of biotinylated reference binding molecules or by using a chromogenic substrate in connection with an enzymatic label (such as 3,3′5,5′-tetramethylbenzidine (TMB) substrate with peroxidase enzyme) or by simply detecting a radioactive label. A binding molecule to be screened that binds to the same epitope as the reference binding molecule will be able to effectively compete for binding and thus will significantly reduce reference binding molecule binding, as evidenced by a reduction in bound label. The reactivity of the (labeled) reference binding molecule in the absence of a completely irrelevant binding molecule would be the control high value. The control low value would be obtained by incubating the labeled reference binding molecule with unlabelled reference binding molecules of exactly the same type, when competition would occur and reduce binding of the labeled reference binding molecule. In a test assay, a significant reduction in labeled reference binding molecule reactivity in the presence of a binding molecule to be screened is indicative of a binding molecule that recognizes the same epitope, i.e., one that “cross-reacts” with the labeled reference binding molecule.
Binding molecules identified by these competition assays (“competitive binding molecules” or “cross-reactive binding molecules”) include, but are not limited to, antibodies, antibody fragments, and other binding agents that bind to an epitope or binding site bound by the reference binding molecule, i.e., a binding molecule of the invention, as well as antibodies, antibody fragments and other binding agents that bind to an epitope or binding site sufficiently proximal to an epitope bound by the reference binding molecule for competitive binding between the binding molecules to be screened and the reference binding molecule to occur. Preferably, the competitive binding molecules will, when present in excess, inhibit specific binding of a reference binding molecule to a selected target species by at least 10%, preferably by at least 25%, more preferably by at least 50%, and most preferably by at least 75%-90% or even greater. The identification of one or more competitive binding molecules that bind to about, substantially, essentially or at the same epitope as the binding molecules described herein is a straightforward technical matter. As the identification of competitive binding molecules is determined in comparison to a reference binding molecule, i.e., a binding molecule of the invention, it will be understood that actually determining the epitope to which the reference binding molecule and the competitive binding molecule bind is not in any way required in order to identify a competitive binding molecule that binds to the same or substantially the same epitope as the reference binding molecule.
In yet a further aspect, the invention relates to a method of identifying a binding molecule, preferably a human binding molecule, potentially having neutralizing activity against SARS-CoV, wherein the method comprises the steps of (a) contacting a collection of binding molecules on the surface of replicable genetic packages with the SARS-CoV under conditions conducive to binding, (b) separating and recovering binding molecules that bind to the SARS-CoV from binding molecules that do not bind, (c) isolating at least one recovered binding molecule, (d) verifying if the binding molecule isolated has neutralizing activity against the SARS-CoV, characterized in that the SARS-CoV in step a is inactivated. The inactivated SARS-CoV may be purified before being inactivated. Purification may be performed by means of purification methods suitable for viruses such as for instance centrifugation through a glycerol cushion. The inactivated SARS-CoV in step (a) may be immobilized to a suitable material before use.
A replicable genetic package as used herein can be prokaryotic or eukaryotic and includes cells, spores, bacteria, viruses, phage, bacteriophage, and polysomes. A preferred replicable genetic package is a phage. The binding molecules, such as, e.g., single chain Fvs, are displayed on the replicable genetic package, i.e., they are attached to a group or molecule located at an exterior surface of the replicable genetic package. The replicable genetic package is a screenable unit comprising a binding molecule to be screened linked to a nucleic acid molecule encoding the binding molecule. The nucleic acid molecule should be replicable either in vivo (e.g., as a vector) or in vitro (e.g., by PCR, transcription and translation). In vivo replication can be autonomous (as for a cell), with the assistance of host factors (as for a virus) or with the assistance of both host and helper virus (as for a phagemid). Replicable genetic packages displaying a collection of binding molecules is formed by introducing nucleic acid molecules encoding exogenous binding molecules to be displayed into the genomes of the replicable genetic packages to form fusion proteins with endogenous proteins that are normally expressed from the outer surface of the replicable genetic packages. Expression of the fusion proteins, transport to the outer surface and assembly results in display of exogenous binding molecules from the outer surface of the replicable genetic packages.
The inactivation of the SARS-CoV may be performed by viral inactivation methods well known to the skilled artisan such as, inter alia, pasteurization (wet heat), i.e., heat treatment while still in aqueous solution, at 60° C. for ten hours; dry heat treatment, i.e., heat treatment in the lyophilized state, at 80° C. for 72 hours; vapor heat treatment at 60° C. for ten hours and then 80° C. for one hour; treatment with low pH, i.e., pH 4 for six hours to 21 days; treatment with organic solvent/detergent, i.e., addition of organic solvents and detergents (Triton X-100 or Tween-80®) to the virus; treatment by means of cold ethanol fractionation; column chromatography; nanofiltration; UV/light irradiation; gamma-irradiation; and addition of iodine. Preferably, the inactivation is performed by gamma- or UV-irradiation. Methods to test if a virus is still infective or partly or completely inactivated are well known to the person skilled in the art.
In a further aspect, the invention pertains to a binding molecule having neutralizing activity against the SARS-CoV and being obtainable by the identification method as described above. A pharmaceutical composition comprising the binding molecule, the pharmaceutical composition further comprising at least one pharmaceutically acceptable excipient is also an aspect of the invention. Pharmaceutically acceptable excipients are described above. The pharmaceutical composition described herein may further comprise at least one other therapeutic agent. Suitable agents have been described above.
The invention further relates to the binding molecule or a pharmaceutical composition described herein for use as a medicament. They can be used in the diagnosis, prophylaxis, treatment, or combination thereof of a condition resulting from SARS-CoV.
To illustrate the invention, the following examples are provided. The examples are not intended to limit the scope of the invention in any way.
Antibody fragments were selected using antibody phage display libraries and technology, essentially as described in U.S. Pat. No. 6,265,150 and in WO 98/15833, both of which are incorporated herein in their entirety. All procedures were performed at room temperature unless stated otherwise. An inactivated SARS-CoV preparation (Frankfurt 1 strain) was prepared as follows. Medium from Vero cells which were infected with SARS-CoV strain Frankfurt 1 was harvested as soon as cyotopathic effect (CPE) was observed. Cell debris was removed by centrifugation of the harvested medium for 15 minutes at 3000 rpm. The obtained supernatant was collected, spun again for 15 minutes at 3000 rpm and transferred to a clean tube. Subsequently, ultracentrifuge tubes were filled with 10 ml sterile 25% glycerol in PBS. Twenty ml of the cleared supernatant was gently applied on the glycerol cushion and the tubes were spun for two hours at 20,000 rpm at 4° C. The supernatant was discarded and the virus pellets were resuspended in 1 ml TNE buffer (10 mM Tris-HCl pH 7.4, 1 mM EDTA, 200 mM NaCl) and stored at ±80° C. Next, the resuspended virus pellets were gamma-irradiated at 45 kGy on dry ice. Subsequently, they were tested for the absence of infectivity in cell culture. If absence of infectivity was established, the thus obtained inactivated SARS-CoV preparation was used for selection of single-chain phage antibodies specifically binding to SARS-CoV.
The inactivated virus preparation and heat-inactivated fetal bovine serum (FBS) were coated overnight at 4° C. onto the surface of separate MAXISORP™ plastic tubes (Nunc). The tubes were blocked for two hours in 3 ml PBS containing 2% FBS and 2% fat free milk powder (2% PBS-FM). After two hours, the FBS-coated tube was emptied and washed three times with PBS. To this tube, 500 μl (approximately 1013 cfu) of a phage display library expressing single-chain Fv fragments (scFvs) essentially prepared as described by De Kruif et al. (1995a) and references therein (which are incorporated herein in their entirety), 500 μl 4% PBS-FM and 2 ml 2% PBS-FM were added. The tube was sealed and rotated slowly at room temperature for two hours. Subsequently, the obtained blocked phage library (3 ml) was transferred to a SARS-CoV preparation-coated tube that had been washed three times with PBS. Tween-20 was added to a final concentration of 0.05% and binding was allowed to proceed for two hours on a slowly rotating wheel at room temperature or at 37° C. The tube was emptied and washed ten times with PBS containing 0.05% Tween-20, followed by washing ten times with PBS. One ml glycine-HCL (0.05 M, pH 2.2) was added to elute bound phages, and the tube was rotated slowly for ten minutes. For neutralization purposes, the eluted phages were added to 500 μl 1 M Tris-HCl pH 7.4. To this mixture, 5 ml of exponentially growing XL-1 blue bacterial culture was added. The obtained culture was incubated for thirty minutes at 37° C. without shaking. Then, the bacteria were plated on TYE agar plates containing ampicillin, tetracycline and glucose. After overnight incubation of the plates at 37° C., the colonies were scraped from the plates and used to prepare an enriched phage library, essentially as described by De Kruif et al. (1995a) and WO 02/103012 (both are incorporated by reference herein). Briefly, scraped bacteria were used to inoculate 2TY medium containing ampicillin, tetracycline and glucose and grown at a temperature of 37° C. to an OD 600 nm of ˜0.3. CT or VCSM13 helper phages were added and allowed to infect the bacteria after which the medium was changed to 2TY containing ampicillin, tetracycline and kanamycin. Incubation was continued overnight at 30° C. The next day, the bacteria were removed from the 2TY medium by centrifugation after which the phages in the obtained supernatant were precipitated using polyethylene glycol 6000/NaCl. Finally, the phages were dissolved in a small volume of PBS containing 1% BSA, filter-sterilized and used for a next round of selection. The selection/re-infection procedure was performed two or three times. After each round of selection, individual E. coli colonies were used to prepare monoclonal phage antibodies. Essentially, individual colonies were grown to log-phase and infected with VCSM13 helper phages after which phage antibody production was allowed to proceed overnight. Phage antibody containing supernatants were tested in ELISA for binding activity to the SARS-CoV preparation which was coated to 96-well plates. In the above-described selection, the phage antibodies called SC03-001, SC03-002, SC03-003, SC03-004, SC03-005, SC03-006, SC03-007, SC03-008, SC03-009, SC03-0010, SC03-012, SC03-013, SC03-014, and SC03-015 were obtained.
To overcome selection of previously identified phage antibodies, alternative selections in the presence of scFvs corresponding to the previous selected phage antibodies were performed as follows. ScFvs of the phage antibodies SC03-001, SC03-002, SC03-003, SC03-004, SC03-005, SC03-006, SC03-007, SC03-008, SC03-009, SC03-0010, SC03-012, SC03-013, SC03-014 and SC03-015 were produced as described before in De Kruif et al. (1995b). The buffer of the scFvs was adjusted to 1×PBS. Then the scFvs were mixed with 500 μl (approximately 1013 cfu) of a phage display library expressing single-chain Fv fragments essentially prepared as described by De Kruif et al. (1995a) and references therein (which are incorporated herein in their entirety). Next, the obtained mixture was blocked in an FBS-coated tube as described above and subsequently selection was carried out with the obtained blocked mixture essentially as described above for the blocked phage library. In this alternative selection, the phage antibodies called SC03-016, SC03-017 and SC03-018 were obtained.
Selected single-chain phage antibodies that were obtained in the screens described above, were validated in ELISA for specificity, i.e., binding to the SARS-CoV preparation prepared as described supra. Additionally, the single-chain phage antibodies were also tested for binding to 10% FBS. For this purpose, the SARS-CoV preparation or 10% FBS preparation was coated to MAXISORP™ ELISA plates. After coating, the plates were blocked in 2% PBS-FM. The selected single-chain phage antibodies were incubated in an equal volume of 4% PBS-FM to obtain blocked phage antibodies. The plates were emptied, washed three times with PBS, after which the blocked phage antibodies were added. Incubation was allowed to proceed for one hour, the plates were washed in PBS containing 0.05% Tween-20® and bound phage antibodies were detected (using OD 492 nm measurement) using an anti-M13 antibody conjugated to peroxidase. As a control, the procedure was performed simultaneously using no single-chain phage antibody or control single-chain phage antibody directed against thyroglobulin (SC02-006) (see, De Kruif et al. 1995a and 1995b) or control single-chain phage antibody directed against CD46 (SC02-300). Both controls served as a negative control. As shown in Table 1 and
As shown in Table 2 and
From the selected specific single chain phage antibody (scFv) clones plasmid DNA was obtained and nucleotide sequences were determined according to standard techniques. The nucleotide sequences of the scFvs (including restriction sites for cloning) called SC03-001, SC03-002, SC03-003, SC03-004, SC03-005, SC03-006, SC03-007, SC03-008, SC03-009, SC03-0010, SC03-012, SC03-013, SC03-014 and SC03-015 are shown in SEQ ID NO:46, SEQ ID NO:48, SEQ ID NO:50, SEQ ID NO:89, SEQ ID NO:52, SEQ ID NO:54, SEQ ID NO:56, SEQ ID NO:58, SEQ ID NO:60, SEQ ID NO:62, SEQ ID NO:64, SEQ ID NO:66, SEQ ID NO:68 and SEQ ID NO:70, respectively. The amino acid sequences of the scFvs called SC03-001, SC03-002, SC03-003, SC03-004, SC03-005, SC03-006, SC03-007, SC03-008, SC03-009, SC03-0010, SC03-012, SC03-013, SC03-014 and SC03-015 are shown in SEQ ID NO:47, SEQ ID NO:49, SEQ ID NO:51, SEQ ID NO:90, SEQ ID NO:53, SEQ ID NO:55, SEQ ID NO:57, SEQ ID NO:59, SEQ ID NO:61, SEQ ID NO:63, SEQ ID NO:65, SEQ ID NO:67, SEQ ID NO:69 and SEQ ID NO:71, respectively. Furthermore, the nucleotide sequences of the scFvs (including restriction sites for cloning) called SC03-016, SC03-017 and SC03-018 are shown in SEQ ID NO:91, SEQ ID NO:93 and SEQ ID NO:95, respectively. The amino acid sequences of the scFvs called SC03-016, SC03-017 and SC03-018 are shown in SEQ ID NO:92, SEQ ID NO:94 and SEQ ID NO:96, respectively.
The VH and VL gene identity (see, I. M. Tomlinson, S. C. Williams, O. Ignatovitch, S. J. Corbett., G. Winter, V-BASE Sequence Directory, Cambridge United Kingdom: MRC Centre for Protein Engineering (1997)) and heavy chain CDR3 compositions of the scFvs specifically binding the SARS-CoV preparation are depicted in Table 3.
Methods for the cloning and expression of bivalent scFv fragments in the Pichia pastoris system were based on protocols provided by the supplier (Invitrogen) in “A Manual of Methods for Expression of Recombinant Proteins Using pPICZ and pPICZα in Pichia pastoris (Version F).” The bivalent scFv expression vector pPicZbiFVH (see,
1. A restriction site (NcoI) was introduced by PCR-generated point mutation directly after the KEK2 cleavage site of the signal peptide to facilitate cloning into the vector.
2. A second NcoI restriction site was removed by PCR generated point mutation inside the coding region of the sh ble gene.
3. A synthetic fragment comprising the hinge region of murine IgG3 and a linker fragment was introduced between the restriction sites NotI and XbaI.
All modifications were confirmed by sequencing. ScFvs were cloned into pPicZbiFVH from the phage display expression vector by directional cloning using the restriction sites NcoI and NotI. The Pichia pastoris strain SMD1168 kek1:suc1 (ATCC #204414) was transformed with 5-10 μg of linearized construct cDNA by electroporation according to the manufacturer's protocols (supra). The transformed cells were plated on YPDS agar containing 250 μg/ml Zeocin® and incubated at 30° C. for three to four days. High producing clones were selected by colony lift immunoblot screening, as follows. Pre-wet nitrocellulose membranes were layered over the transformation plates and a fraction of each colony was lifted onto the membrane. The membrane was then placed colony side up on YPD agar containing 0.5% methanol and incubated overnight at 30° C. The membranes were then washed repeatedly with Tris buffered saline containing 0.5% Tween-20 (TBST) to remove colonies, then blocked for 30 minutes with TBST and 4% non-fat milk powder. The membranes were then placed in TBST containing 4% non-fat milk powder and horseradish peroxidase conjugated anti-c-myc antibody (Roche) for one hour. Finally, the membranes were washed extensively in TBST followed by a PBS washing step and scFv-secreting colonies were revealed by a chemofluorescence detection system (Apbiochem). Selected high producers were purified by streaking on YPD plates and were subsequently used for bivalent scFv expression. Small-scale expression cultures were carried out in shaker flasks essentially as described by the manufacturer's protocols (supra). BMGY medium was used for the cell expansion phase, while BMMY medium was used during the bivalent scFv expression phase. After 48 hours of induction, supernatants were clarified by repeated centrifugation. The supernatant was conditioned for purification by the addition of 1 M Na2HPO4 pH 8 to a concentration of 20 mM, 0.5 M Imidazole to a concentration of 10 mM, 5 M NaCl to a concentration of 500 mM. Hereafter, the samples were purified by immobilized metal affinity chromatography followed by anion exchange chromatography on an AKTAprime FPLC-system (Pharmacia). A 5 ml HiTrap chelating column (Pharmacia) was charged with NiSO4 and equilibrated according to the manufacturer's instructions. Conditioned supernatant was loaded directly onto the column and washed extensively in equilibration buffer (20 mM Na2PO4 pH 8, 10 mM imidazole). Bivalent scFv were eluted directly off the column on to a 1 ml sepharose Q HP column (Pharmacia) in the presence of 250 mM imidazole pH 8.5. The column was then washed in 20 mM Tris-HCl pH 8, then briefly in 20 mM Na2PO4 pH 7.3, and bivalent scFvs were eluted off the column over a gradient of 0-0.5 M NaCl in 7 column volumes. Fractions were then measured for protein content and were analyzed for activity and purity. The bivalent scFvs of the selected scFvs called SC03-001, SC03-002, SC03-003, SC03-005, SC03-006, SC03-007, SC03-008, SC03-009, SC03-0010, SC03-012, SC03-013, SC03-014 and SC03-015 were called pyBi03-001C02, pyBi03-002C02, pyBi03-003C02, pyBi03-005C02, pyBi03-006C02, pyBi03-007C02, pyBi03-008C02, pyBi03-009C02, pyBi03-010C02, pyBi03-012C02, pyBi03-013C02, pyBi03-014C02, pyBi03-015C02, respectively.
Heavy and light chain variable regions of the scFvs called SC03-001, SC03-002, SC03-009, SC03-013, SC03-014 and SC03-018 were PCR-amplified using oligonucleotides to append restriction sites and/or sequences for expression in the IgG expression vectors pSyn-C03-HCγ1 (see, SEQ ID NO:110) and pSyn-C05-Cκ (see, SEQ ID NO:111), respectively. The VL gene shared between scFvs was amplified using oligonucleotides 5K-I (SEQ ID NO:112) and sy3K-C (SEQ ID NO:113) (see, below) and the PCR products cloned into vector pSyn-C05-Cκ. Nucleotide sequences for all constructs were verified according to standard techniques known to the skilled artisan. VH genes were amplified using the following oligonucleotide set: 5H-B (SEQ ID NO:114) and sy3H-A (SEQ ID NO:115). Thereafter, the PCR products were cloned into vector pSyn-C03-HCγ1 and nucleotide sequences were verified according to standard techniques known to the skilled person in the art.
5H-Bacctgtcttgaattctccatggccgaggtgcagctggtggagtctg (SEQ ID NO:114)
sy3H-A gcccttggtgctagcgctggagacggtcaccagggtgccctggcccc (SEQ ID NO:115)
5K-I acctgtctcgagttttccatggctgacatccagatgacccagtctccatcctcc (SEQ ID NO:112)
sy3K-C gggaccaaggtggagatcaaacggaccgtggccgcccccagc (SEQ ID NO:113)
The resulting expression constructs pgG103-001C03, pgG103-002C03, pgG103-009C03, pgG103-013C03, pgG103-014C03 and pgG103-018C03 encoding the anti-SARS-CoV human IgG1 heavy chains were transiently expressed in combination with the pSyn-C05-VkI construct encoding the common light chain in 293T cells and supernatants containing IgG1 antibodies were obtained. The nucleotide sequences of the heavy chains of the antibodies called 03-001, 03-002, 03-009, 03-013, 03-014, and 03-018 are shown in SEQ ID NOS:116, 118, 120, 122, 124, and 126, respectively. The amino acid sequences of the heavy chains of the antibodies called 03-001, 03-002, 03-009, 03-013, 03-014, and 03-018 are shown in SEQ ID NOS:117, 119, 121, 123, 125, and 127, respectively.
The nucleotide sequences of the light chain of antibodies 003-001, 03-002, 03-009, 03-013, 03-014, and 03-018 is shown in SEQ ID NO:128. The amino acid sequences of the light chain of antibodies 03-001, 03-002, 03-009, 03-013, 03-014 and 03-018 is shown in SEQ ID NO:129. Essentially as described above, the antibodies called 03-006 and 03-015 were generated. The nucleotide sequences of the heavy chains of the antibodies called 03-006 and 03-015 are shown in SEQ ID NO:471 and SEQ ID NO:473, respectively. The amino acid sequences of the heavy chains of the antibodies called 03-006 and 03-015 are shown in SEQ ID NO:472 and SEQ ID NO:474, respectively. The nucleotide sequences of the light chain of antibodies 03-006 and 03-015 are shown in SEQ ID NO:475 and SEQ ID NO:477, respectively. The amino acid sequences of the light chain of antibodies 03-006 and 03-015 are shown in SEQ ID NO:476 and SEQ ID NO:478, respectively. Subsequently, the recombinant human monoclonal antibodies were purified over protein-A columns and size-exclusion columns using standard purification methods used generally for immunoglobulins (see, e.g., WO 00/63403 which is incorporated by reference herein).
To determine whether the above selected single-chain phage antibodies bind to similar or overlapping epitopes which are recognized by the recombinant human monoclonal anti-SARS-CoV antibodies of the invention a competition ELISA was performed. Briefly, a gamma-irradiated SARS-CoV preparation was immobilized as described supra. The immobilized SARS-CoV preparation and the selected single-chain phage antibodies were blocked in an equal volume of 4% ELK in PBS. Subsequently, the blocked immobilized SARS-CoV preparation was incubated with a blocked single-chain phage antibody in the presence or absence of 1 μg/ml of an anti-SARS-CoV IgG for one hour at room temperature. Binding of the single-chain phage antibody was monitored as described supra. A reduction of binding of the single-chain phage antibody to the SARS-CoV preparation in the presence of anti-SARS-CoV IgG compared to binding of single-chain phage antibody alone indicated that similar or overlapping epitopes were recognized by the single-chain phage antibody and the anti-SARS-CoV IgG. As shown in
The SARS-CoV neutralization assay was performed on Vero cells (ATCC CCL 81). The SARS-CoV strains used in the neutralization assay were the Frankfurt 1 strain (for the complete genome of this strain see EMBL-database accession #AY291315) and the Frankfurt 2 strain, derived from a patient who acquired the infection from the Frankfurt 1—index case (Rickerts et al. 2003). This latter SARS-isolate has not yet been sequenced. Virus stocks of the strains were used in a titer of 4×103 TCID50/ml (50% tissue culture infective dose per ml), with the titer calculated according to the well known method of Spearman and Kaerber. Recombinant human anti-SARS-CoV bivalent scFvs and recombinant human anti-SARS-CoV antibodies produced as described above were prescreened by serially two-fold dilution of the undiluted material in PBS starting from 1:10 (dilution range 1:10-1:320). A neutralization titer of ≧1:10 was regarded as specific evidence of reactivity of the bivalent scFvs or the antibodies against SARS-CoV in the prescreening assay. To determine the antibody-concentration-dependent neutralizing activity the bivalent scFvs or the antibodies against SARS-CoV were then adjusted to a protein concentration of 10 μg/ml and serially two-fold diluted in PBS (dilution range 1:2 to 1:512). In general, the neutralization assay worked as follows. 25 μl of the respective bivalent scFv or antibody dilutions were mixed with 25 μl of virus suspension (=approx. 100 TCID50/25 μl) and incubated for one hour at 37° C. The suspension was then pipetted two times in triplicate into 96-well plates. Next, 50 μl of a freshly trypsinized and homogenized suspension of Vero cells (1:3 split of the confluent cell monolayer of a T75-flask), resuspended in DMEM containing 10% w/v fetal calf serum and antibiotics, were added. The inoculated cells were cultured for three to four days at 37° C. and observed daily for the development of cytopathic effect (CPE). CPE was compared to the positive control (virus inoculated cells) and negative controls (mock-inoculated cells or cells incubated with bivalent scFv or antibody only). The complete absence of CPE in an individual cell culture was defined as protection (=100% titer reduction). The serum dilution giving protection in 66% percent of wells was defined as the neutralizing antibody titer. Serum from one of the two well characterized SARS-patients was used as a positive control for the neutralization assay; the clinical history of these two patients has been published (see, Rickerts et al. 2003).
As shown in Table 4, the bivalent scFvs called pyBi03-001C02, pyBi03-002C02, pyBi03-003C02, pyBi03-005C02, pyBi03-006C02, pyBi03-007C02, pyBi03-008C02, pyBi03-009C02, pyBi03-010C02, pyBi03-012C02, pyBi03-013C02, pyBi03-014C02, pyBi03-015C02 were tested for SARS-CoV neutralizing activity. Furthermore, two negative controls, i.e., pyBi02-148C02 (bivalent scFv binding to antigen L6) and pyBi02-006C02 (bivalent scFv binding to thyroglobulin) and one positive control, i.e., serum from a SARS-patient, were tested for neutralizing activity. It is clear from Table 4 that the bivalent scFvs pyBi03-013C02 and pyBi03-014C02 displayed significant neutralizing activity. The bivalents neutralize the Frankfurt 1 or Frankfurt 2 strain at a dilution factor of 80 or 160 in the above-described prescreening assay. In the light of the OD values and the neutralization titer, the neutralizing antibodies are useful in the prophylaxis and/or treatment of a condition resulting from SARS infection. Neutralization data obtained with human monoclonal anti-SARS-CoV antibodies indicated that the antibodies called 03-013 and 03-014 displayed neutralizing activity (data not shown). This confirmed the above results for the bivalent single chain Fvs.
In an alternative embodiment the SARS-CoV neutralization assay is performed on Vero cells (ATCC CCL 81). The SARS-CoV strain used in the assay is the Frankfurt 1 strain (for the complete genome of this strain see EMBL-database accession #AY291315). The strain is used in a titer of 1.6×106 TCID50/ml (50% tissue culture infective dose per ml). Recombinant antibodies (in phage antibody, scFv, bivalent or IgG1 format) are adjusted to a concentration of 10 μg/ml and then serially ten-fold or two-fold diluted in PBS to determine optimal inhibitory concentrations. 25 μl of the recombinant antibody are mixed with 25 μl of virus suspension (=150 TCID50/25 μl) and incubated for one hour at 37° C. The suspension is then inoculated in triplicate onto sub-confluent Vero cells (approximately 80% density) grown in 96-well cell-culture plates. The inoculated cells are cultured for three to four days at 37° C. and observed daily for the development of cytopathic effect (CPE). CPE is compared to the positive control (virus inoculated cells) and negative controls (mock-inoculated cells or cells incubated with recombinant antibody only).
In yet another embodiment, the SARS-CoV neutralization assay was performed on Vero cells (ATCC CCL 81) as follows. The SARS-CoV strain SCV-P4(5688) used in this assay was obtained from patient 5688 (who died from SARS) and then passaged four times on Vero cells (see, Fouchier et al. (2003), Kuiken et al. (2003); strain is also called HK-39849 (GenBank accession number AY278491)). The virus strain was used in a titer of 2×103 TCID50/ml (50% tissue culture infective dose per ml), with the titer calculated according to the method of Spearman and Kaerber which is well known to the average skilled person. Recombinant expressed human anti-SARS-CoV antibodies were screened by serially two-fold dilution in PBS starting at a concentration of 50 μg/ml (dilution range 50-0.025 μg/ml). 50 μl of virus suspension (10, 30 or 100 TCID50/50 μl) was mixed with 50 μl of the respective recombinant human anti-SARS-CoV antibody dilution and incubated for one hour at 37° C. The suspension was then pipetted two times in triplicate into 96-well plates containing an 80% confluent monolayer of Vero cells (seeded 16 to 20 hours in advance at a density of 1×104 cells per well in DMEM containing 5% FBS). The Vero cells were cultured for four days at 37° C. and observed daily for the development of cytopathic effect (CPE). CPE was compared to the positive control (virus inoculated cells) and negative controls (mock-inoculated cells or cells incubated with recombinant antibody only). The complete absence of CPE in an individual cell culture was defined as protection (=100% titer reduction). The dilution giving protection in 66% percent of wells was defined as the neutralizing antibody titer. The results are shown in Table 7. On the upper row the concentration of the antibody in μg/ml is shown. In the left column of Table 7 the TCID50 and name of the antibody used are shown. From Table 7 it can be clearly deduced that the human anti-SARS-CoV antibodies called 03-013 and 03-014 have SARS-CoV neutralizing activity. Complete protection from infectivity of 100TCID50 was reached at 170 nM for 03-013 and 42 nM for 03-014. In comparison, the control antibody 02-027, a human monoclonal anti-EpCAM antibody, contained no neutralizing activity at all. The antibody called 03-006 did not show neutralizing capacity at the normal IgG dilution range, however subsequent neutralization assays revealed that 03-006 was capable of neutralizing SARS-CoV, but only at concentrations in the μM range (data not shown).
Vero cells (ATCC CCL 81), which were grown to sub-confluency, were inoculated with a multiplicity of infection (moi) of 0.1 with the Frankfurt-1 strain of SARS-CoV. The cells were observed daily for any cyotopathic effect (CPE), which usually became first visible on day two. As soon as CPE appeared, cells were gently harvested using a cell scraper, washed once in PBS and spread in a thin layer onto microscopic slides coated with Teflon grids. The cell suspensions were allowed to dry for 30 minutes and the slides were then fixed in ice-cold acetone for 15 minutes and stored at −80° C. until further use. Recombinant human antibodies against SARS-CoV were brought to a concentration of 10 μg/ml and were then further diluted two-fold in PBS. The microscopic slides were brought to room temperature and 20 μl of the recombinant antibody suspension were spotted per field (the microscopic slides contain ten or twelve fields). Sera from patients which have been infected with SARS-CoV were used as positive controls and serum of uninfected subjects as negative controls (see, Rickerts et al. 2003). Slides were incubated in a humid chamber at 37° C. for one hour and washed two times in PBS at room temperature. Working solutions of fluorescein-isothiocyanate-labeled secondary antibodies, i.e., anti-huIgG-FITC, were prepared as is known in the art. Twenty μl of the secondary antibody was applied to each spot on the slides. After a further incubation of 30 minutes at 37° C., slides were washed again twice and coverslips were mounted on the slides. Slides were read using a fluorescent microscope, comparing the specific fluorescence (number of fluorescent cells and morphology) of the slides contacted with the recombinant antibodies with the slides contacted with the positive and negative controls. In Table 5, the data of the IIF assay are presented. The recombinant human monoclonal anti-SARS-CoV antibodies called 03-014 and 03-018 showed clear cytoplasmic staining of the cells infected with SARS-CoV. Clear staining was also observed with the recombinant human monoclonal anti-SARS-CoV antibody called 03-009 (data not shown).
All procedures were performed at room temperature unless stated otherwise. An inactivated SARS-CoV preparation (Frankfurt 1 strain) was prepared as follows. Medium from Vero cells which were infected with O.I. moi SARS-CoV strain Frankfurt 1 was harvested as soon as cyotopathic effect (CPE) was observed. Cells were once frozen at −20° C. and thawed. Cell debris was removed by centrifugation of the harvested medium for 15 minutes at 3000 rpm. The obtained supernatant was collected, spun again for 15 minutes at 3000 rpm and transferred to a clean tube. Subsequently, ultracentrifuge tubes were filled with 10 ml sterile 25% v/v glycerol in PBS. 20 ml of the cleared supernatant was gently applied on the glycerol cushion and the tubes were spun for two hours at 20,000 rpm at 4° C. in a Beckman SW28 rotor. The supernatant was discarded and the virus pellets were resuspended in 1 ml TNE buffer (10 mM Tris-HCl pH 7.4, 1 mM EDTA, 200 mM NaCl) and stored at −80° C. Next, the resuspended virus pellets were either gamma-irradiated with a dose at 45 kGy on dry ice, or UV-irradiated at 4° C. for 15 minutes (UV-B radiation 280-350 nm; λmax 306 nm). Subsequently, they were tested for the absence of infectivity in cell culture. If absence of infectivity was established, the thus obtained inactivated SARS-CoV preparations were used for further experiments. To determine whether the isolated anti-SARS-CoV human IgG antibodies were capable of binding SARS preparations that were inactivated as described supra ELISA experiments were performed. The SARS-CoV preparations were diluted 1:250 in coating buffer (50 mM carbonate buffer, pH 9.6) and immobilized over night at 4° C. on MAXISORP™ ELISA plates. The ELISA plates were washed three times with PBS and incubated with human anti-SARS-CoV and control IgG (called 02-027) at concentrations of 1 and 5 μg/ml in PBS containing 1% BSA for one hour at room temperature. Subsequently, the plates were washed two times with PBS containing 0.05% Tween-20 and IgG bound was detected using an anti-human-IgG-HRP-conjugate (Pharmingen) at 492 nm.
As shown in
To determine if upon denaturation of a SARS-CoV preparation, more antigen becomes accessible for the isolated recombinant human monoclonal anti-SARS-CoV antibodies and to determine which antigens are detected by the human monoclonal anti-SARS-CoV antibodies, the following sandwich ELISA was performed. For the detection of bound antigens, different anti-SARS-CoV rabbit antisera were used. The sandwich ELISA was performed as follows. Human anti-SARS-CoV antibodies or the control antibody called 02-300 (an antibody against CD46) were immobilized over night at 4° C. to MAXISORP™ ELISA plates at a concentration of 5 μg/ml in coating buffer (50 mM carbonate buffer, pH 9.6). The plates were washed three times with PBS and blocked with PBS containing 1% BSA. Next, a gamma-irradiated SARS-CoV preparation prepared as described herein was denatured by diluting the preparation 1:10 in RIPA buffer (150 mM NaCl, 1% Nonidet P-40, 0.5% deoxycholate, 0.1% sodium dodecyl sulphate, 50 mM Tris, pH 8.0) followed by an incubation of one hour at room temperature. Subsequently, the denatured virus preparation was diluted 1:10 in PBS containing 1% BSA and the immobilized human IgGs were incubated with the denatured virus preparation for one hour at room temperature. To recognize which proteins of the SARS-CoV were detected by the immobilized recombinant human monoclonal anti-SARS-CoV antibodies polyclonal rabbit antibodies recognizing the complete SARS-CoV, the spike protein of SARS-CoV (Imgenex IMG-542 or IMG-557) or the nucleocapsid protein of SARS-CoV (Imgenex IMG-543). Finally, bound rabbit IgG was detected (using OD 492 nm measurement) using an anti-rabbit-IgG-HRP-conjugate (Dako).
As shown in
Fifteen-mer linear and looped/cyclic peptides were synthesized from proteins of SARS-CoV and screened using credit-card format mini-PEPSCAN cards (455 peptide formats/card) as described previously (see, inter alia, WO 84/03564, WO 93/09872, Slootstra et al. 1996). All peptides were acetylated at the amino terminus. In short, series of overlapping peptides, which were either in linear form or in looped/cyclic form, of all the (potential) proteins of SARS-CoV Urbani, these proteins being called spike protein (the protein-id of the surface spike glycoprotein in the EMBL-database is AAP13441), protein X1 (the protein-id of protein X1 is AAP13446), protein X2 (the protein-id of protein X1 is AAP13447), E protein (the protein-id of the small envelope protein, E protein, is AAP13443), M protein (the protein-id of the membrane protein, M protein, is AAP13444), protein X3 (the protein-id of protein X3 is AAP13448), protein X4 (the protein-id of protein X4 is AAP13449), protein X5 (the protein-id of protein X5 is AAP13450), and N protein (the protein-id of the nucleocapsid protein, N protein, is AAP13445), were produced and tested for binding to the recombinant human anti-SARS-CoV antibodies of the invention by means of PEPSCAN analysis.
Because the Urbani proteins indicated above are also found in identical or highly homologous form in other SARS-CoV strains, the antigenic peptides found in the analysis method may not only be used for detection of the SARS-CoV strain Urbani and the prevention and/or treatment of a condition resulting from the SARS-CoV strain Urbani, but may also be useful in detecting SARS-CoV in general and preventing and/or treating a condition resulting from SARS-CoV in general. The protein-id of the surface spike glycoprotein of for instance the SARS-CoV strains TOR2, Frankfurt 1 and HSR 1 in the EMBL-database is AAP41037, AAP33697 and AAP72986. The accession number in the EMBL-database of the complete genome of the strains TOR2, Frankfurt 1 and HSR 1 is AY274119, AY291315 and AY323977, respectively. Under these accession numbers the amino acid sequence of the other (potential) proteins of these strains can be found.
As indicated above, several proteins of SARS-CoV, such as, inter alia, the spike protein and the N protein, are shared by all SARS-CoV strains. However, the strains TOR2, Frankfurt 1 and HSR 1 contain open reading frames encoding (potential) proteins that are not present in the SARS-CoV strain Urbani. In the SARS-CoV strain called TOR2 these (potential) proteins are called Orf9, Orf10, Orf13 and Orf14. The first three of these (potential) proteins are also found in the SARS-CoV strains called Frankfurt 1 and HSR 1. In these strains the (potential) proteins are called Orf7b, Orf8a and Orf9b, respectively. The coding sequence (CDS) of the (potential) proteins of SARS-CoV TOR2 is shown under EMBL-database accession number AY274119, the coding sequence (CDS) of the (potential) proteins of SARS-CoV HSR 1 can be found under accession number AY323977, the coding sequence (CDS) of the (potential) proteins of SARS-CoV Frankfurt 1 can be found under accession number AY291315. Series of overlapping peptides, which were either in linear form or in looped/cyclic form, of all the (potential) proteins of SARS-CoV TOR2 were also produced and tested for binding to the recombinant human anti-SARS-CoV antibodies of the invention by means of PEPSCAN analysis. Because the TOR2 proteins indicated above are also found in identical or highly homologous form in several other SARS-CoV strains, such as for instance the strains called Frankfurt 1 and HSR 1, the peptides found in the analysis method may not only be used for detection of the SARS-CoV strain TOR2 and the prevention and/or treatment of a condition resulting from the SARS-CoV strain TOR2, but may also be useful in detecting SARS-CoV strains which express these (potential) proteins and preventing and/or treating a condition resulting from SARS-CoV which express these (potential) proteins.
In all looped peptides position-2 and position-14 were replaced by a cysteine (acetyl-XCXXXXXXXXXXXCX-minicard). If other cysteines besides the cysteines at position-2 and position-14 were present in a prepared peptide, the other cysteines were replaced by an alanine. The looped peptides were synthesized using standard Fmoc-chemistry and deprotected using trifluoric acid with scavengers. Subsequently, the deprotected peptides were reacted on the cards with a 0.5 mM solution of 1,3-bis(bromomethyl)benzene in ammonium bicarbonate (20 mM, pH 7.9/acetonitril (1:1 (v/v)). The cards were gently shaken in the solution for 30 to 60 minutes, while completely covered in the solution. Finally, the cards were washed extensively with excess of H2O and sonicated in disrupt-buffer containing 1% SDS/0.1% beta-mercaptoethanol in PBS (pH 7.2) at 70° C. for 30 minutes, followed by sonication in H2O for another 45 minutes.
Recombinant human anti-SARS-CoV antibodies were tested for binding to each linear and looped peptide in a PEPSCAN-based enzyme-linked immuno assay (ELISA). The 455-well creditcard-format polypropylene cards, containing the covalently linked peptides, were incubated with the antibodies (1 μg/ml; diluted in blocking solution which contains 5% horse-serum (v/v) and 5% ovalbumin (w/v)) (4° C., overnight). After washing, the peptides were incubated with anti-human antibody peroxidase (dilution 1/1000) (one hour, 25° C.), and subsequently, after washing, the peroxidase substrate 2,2′-azino-di-3-ethylbenzthiazoline sulfonate (ABTS) and 2 μl/ml 3% H2O2 were added. Controls (for linear and looped) were incubated with anti-human antibody peroxidase only. After one hour, the color development was measured. The color development of the ELISA was quantified with a CCD-camera and an image processing system. The setup consisted of a CCD-camera and a 55 mm lens (Sony CCD Video Camera XC-77RR, Nikon micro-nikkor 55 mm f/2.8 lens), a camera adaptor (Sony Camera adaptor DC-77RR) and the Image Processing Software package Optimas, version 6.5 (Media Cybernetics, Silver Spring, Md. 20910, U.S.A.). Optimas runs on a pentium II computer system.
The recombinant human anti-SARS-CoV-antibodies were tested for binding to the 15-mer linear and looped/cyclic peptides synthesized as described supra. Relevant binding of a peptide to a recombinant human anti-SARS-CoV antibody was calculated as follows. The average OD-value for each antibody was calculated for the respective proteins (sum of OD-values of all peptides/total number of peptides). Next, the standard deviation of this average was calculated. The standard deviation was multiplied by two and the obtained value was added to the average value to obtain the correction factor. The OD-value of each peptide was then divided by this correction factor. If a value of 0.9 or higher was found, then relevant binding was considered to be present between the specific peptide and the respective antibody. Particularly interesting appear to be domains comprising several relevant peptides. These domains are indicated (colored grey) in Table 6. The recombinant human anti-SARS-CoV antibody called 03-018 reacted with peptides of the nucleocapsid (N) protein. The peptides recognized include NGPQSNQRSAPRITF (SEQ ID NO:97), GPQSNQRSAPRITFG (SEQ ID NO:98), PQSNQRSAPRITFGG (SEQ ID NO:99), QSNQRSAPRITFGGP (SEQ ID NO:100), SNQRSAPRITFGGPT (SEQ ID NO:101), NQRSAPRITFGGPTD (SEQ ID NO:102), QRSAPRITFGGPTDS (SEQ ID NO:103), RSAPRITFGGPTDST (SEQ ID NO:104), SAPRITFGGPTDSTD (SEQ ID NO:105), APRITFGGPTDSTDN (SEQ ID NO:106), PRITFGGPTDSTDNN (SEQ ID NO:107), RITFGGPTDSTDNNQ (SEQ ID NO:108) and ITFGGPTDSTDNNQN (SEQ ID NO:109). The highest binding of the recombinant human anti-SARS-CoV antibody called 03-018 was with a continuous series of linear and looped peptides starting with the sequence GPQSNQRSAPRITFG (SEQ ID NO:98) and ending with the sequence RSAPRITFGGPTDST (SEQ ID NO:104), thereby mapping the minimal binding site of 03-018 to the sequence RSAPRITFG (SEQ ID NO:468), which corresponds with residues 11-19 of the N protein. Strikingly, this linear epitope is conserved in the N protein sequence of all published human SARS-CoV and animal SARS-CoV-like isolates, but is absent in other members of the family of Coronaviridae. The PEPSCAN analysis further revealed that the recombinant human N protein specific anti-SARS-CoV antibody called 03-009 did not recognize a stretch of linear or looped amino acids on the N protein suggesting that this antibody recognizes a non-linear/conformational epitope of the N protein. All of the above peptides or parts thereof are useful in the detection of SARS-CoV in general.
In another assay, the single chain phage antibodies are analyzed for their ability to bind HEK293T cells that recombinantly express proteins of the SARS-CoV. To this purpose HEK293T cells are transfected with a plasmid carrying a cDNA sequence encoding the envelope (E) protein, membrane (M) protein or spike (S) protein from SARS-CoV strain Frankfurt 1 or with the empty vector. Stable transfectants are selected using standard techniques known to a person skilled in the art (see, J. E. Coligan, B. M. Dunn, H. L. Ploegh, D. W. Speicher and P. T. Wingfield (eds.) (2001) Current protocols in protein science, volume I, John Wiley & Sons, Inc., New York). For flow cytometry analysis, single-chain phage antibodies are first blocked in an equal volume of 4% PBS-M for 15 minutes at 4° C. prior to the staining of the transfected HEK293T cells. The blocked phage antibodies are added to control transfected HEK293T cells and HEK293T cells transfected with the SARS-CoV proteins mentioned above. The binding of the single chain phage antibodies to the cells is visualized using a biotinylated anti-M13 antibody (Santa Cruz Biotechnology) followed by streptavidin-phycoerythrin (Caltag).
In yet another assay, scFv antibodies were analyzed for their ability to bind to portions of the spike (S) protein and the complete nucleocapsid (N) protein of SARS-CoV. The cDNA encoding the S protein of the SARS-CoV strain Frankfurt 1 was adapted to the codon-bias of Homo sapiens genes and gene-optimized for optimal expression by Geneart (Regensburg, Germany). The codon-optimized nucleotide sequence of the S protein is shown in SEQ ID NO:462. The amino acid sequence encoded by this codon-optimized nucleotide sequence is shown in SEQ ID NO:463.
DNA encoding for the N-terminal 565 amino acids (portion called 5565, cf., SEQ ID NO:462) was cloned as a KpnI-BamHI fragment in pAdapt (Havenga et al., 2001) that was modified by insertion of the polylinker of the vector called pcDNA3.1/myc-His C (Invitrogen) (vector called pAdapt/myc-His C).
DNA encoding for the N-terminal 826 amino acids (portion called 5826) was cloned as KpnI-EcoRV fragment in pAdapt that was modified by insertion of the polylinker of the vector called pcDNA3.1/myc-His B (Invitrogen) (vector called pAdapt/myc-His B).
DNA encoding for the N-terminal 1195 amino acids (portion called S1195) is constructed as follows. A DNA fragment is amplified from codon-optimized S protein cDNA using the oligonucleotide primers: XhoISpikeRevCOG 5′-gttcctcgaggggccacttgatgtactgc-3′ (SEQ ID NO:464) and SpikeCOG seq 1 5′-ccaggtgaagcagatgta-3′ (SEQ ID NO:465). The resulting fragment is cloned as BstEII-XhoI fragment together with a KpnI-BstEII fragment derived from the codon-optimized S protein cDNA (alternatively, a restriction site other than BstEII, which is unique in the amplified fragment can be used) in pAdapt that is modified by insertion of the polylinker of the vector called pcDNA3.1/myc-His A (Invitrogen) (vector called pAdapt/myc-His A).
A fragment corresponding to amino acid residues 318-510 of the S protein (portion called S318-510) was amplified on S gene cDNA using the oligonucleotide primers: EcoRIspikeFor318 5′-cctggaattctccatggccaacatcaccaacc-3′ (SEQ ID NO:469) and XbaIspikeRev510 5′-gaagggccctctagacacggtggcagg-3′ (SEQ ID NO:470). The resulting fragment was digested with EcoRI-XbaI and cloned into pHAVT20/myc His A to yield pHAVT20/myc-His A S318-510. In this vector expression of fragment S318-510 fused to the HAVT20 leader sequence was under control of the human, full-length, immediate-early CMV promoter.
DNA encoding for the nucleocapsid protein was amplified from total random hexamer cDNA from the SARS-CoV strain Frankfurt 1 using the oligonucleotide primers KpnINCFor 5′-cttggtaccgccaccatgtctgataatggacc-3′ (SEQ ID NO:466) and XbaINCRev 5′-gttctctagatgcctgagttgaatcagc-3′ (SEQ ID NO:467) and cloned as KpnI-XbaI fragment in pAdapt/myc-His A. DNA transfections were performed in HEK293T cells for transient expression using standard techniques. The S protein derived fragments and nucleocapsid (N) protein were used directly from culture supernatant or cell lysates. Alternatively, the fragments and nucleocapsid (N) protein were purified from culture supernatant using Ni-NTA (QIAGEN®).
The ELISA for the detection of scFv antibodies to the S protein derived fragments or the nucleocapsid (N) protein was performed as follows. Wells of ELISA plates were coated overnight with 5 μg/ml anti-myc antibody in 50 mM bicarbonate buffer pH 9.6. In case of the UV-inactivated SARS-CoV preparation, the wells were coated with the preparation as described above. The wells of the plates were washed three times with PBS containing 0.05% Tween and blocked for two hours at 37° C. with PBS containing 1% BSA. The wells coated with anti-myc antibody were incubated with culture supernatant or cell lysate containing the myc-tagged fragment S565 or nucleocapsid (N) protein diluted in PBS containing 1% BSA for one hour at room temperature. The wells were washed three times with PBS containing 0.05% Tween. Next, the scFvs SC03-014 and SC03-009 were diluted in PBS containing 0.05% Tween and were incubated for one hour at room temperature. The wells were washed three times with PBS containing 0.05% Tween and incubated for 1 hour at room temperature using an anti-VSV-HRP conjugate (for scFv). As shown in
To further investigate binding to the SARS coronavirus fragments and proteins, the following experiments were performed with the monoclonal antibodies 03-001, 03-002, 03-006, 03-009, 03-013, 03-014, 03-015 and 03-018. Full length N protein from transfected HEK293T cell lysates was captured on an ELISA plate by means of an anti-myc antibody as described above and incubated with the above mentioned IgG molecules.
In order to rank the affinities of the monoclonal antibodies binding the N protein, a titration of IgG concentration (by diluting the antibodies in PBS containing 1% ELK) followed by ELISA as described above was performed. Titration of the monoclonal antibodies showed that 03-009 bound better to the N protein than 03-018 (see,
To further explore the antibody binding sites within the N protein, a competition ELISA on immobilized N protein was performed. Captured N protein was incubated with 1 μg/ml (non-saturating) biotinylated antibody 03-009 without competing antibody or in the presence of a 25- or 50-fold excess of competing antibody (antibody 03-009 or 03-018). Bound biotinylated antibody 03-009 was detected with streptavidin-conjugated-HRP (BD Pharmingen) and developed as described above. Results (see,
Subsequently, the interaction of the above antibodies with the S protein was evaluated. Binding of the antibodies to the full length S protein expressed on HEK293T cells was first investigated by flow cytometry. The transfected cells were incubated with human IgGs at a concentration of 10 μg/ml for one hour on ice. Cells were washed three times, incubated for 45 minutes with biotinylated goat anti-human IgG followed by a ten minute incubation with streptavidin-conjugated phycoerythin. The analysis showed that the monoclonal antibodies 03-006, 03-013, 03-014 and 03-015 specifically bound S protein transfected HEK293T cells (see,
To further localize the binding site of these antibodies within the S protein, binding to a recombinant soluble fragment encompassing S protein residues 1-565 (S565) was tested by means of ELISA as described above. Within the antibody panel binding the full length S protein on the HEK293T cells, all antibodies except 03-015 bound to fragment S565 (see,
To further narrow the binding site of the antibodies, binding to a recombinant fragment comprising residues 318-510 of the S protein (S318-510) was evaluated.
As shown in a titration experiment performed similarly as the titration experiment described above, antibody 03-014 appeared to bind S565 with a higher affinity than the antibodies 03-006 and 03-013 (see,
Using a similar set-up as described above, a competition ELISA was performed. Captured S565 was incubated with 1 μg/ml (nonsaturating) biotinylated antibody 03-014 without competing antibody or in the presence of a 25- or 50-fold excess of competing IgG (antibody 03-006 or 03-014). Bound biotinylated antibody 03-014 was detected with streptavidin-conjugated-HRP (BD Pharmingen) and developed as described above. The competition ELISA revealed that binding of antibody 03-014 was unaffected in the presence of a 25- or 50-fold excess of unlabeled 03-006 and it was concluded that their binding sites do not overlap (see,
Flow cytometry analysis was used to assay binding of the fragments of the S protein to angiotensin-converting enzyme 2 (ACE2), the natural receptor for SARS-CoV infectivity (Li et al., 2003). Vero cells expressing ACE2 (measured by means of a polyclonal anti-ACE2 antibody (R&D systems)) were incubated for one hour at 4° C. with saturating concentrations of the myc-tagged 5565 fragment. As a control, the Vero cells were incubated with a myc-tagged bivalent scFv 02-006. Alternatively, the S565 fragment was incubated with the IgG antibodies 03-014 (anti-SARS-CoV S protein antibody), 03-018 (anti-SARS-CoV N protein antibody) or 02-027 (anti-EPCAM control antibody) prior to incubation with the Vero cells. After three washes, bound fragment and the control protein were detected by flow cytometry analysis by using biotinylated anti-myc antibody (Santa Cruz Biotechnology Inc.) and streptavidin-conjugated phycoerythrin (Caltag). All incubations and washes were performed at 4° C. in PBS, supplemented with 0.5% bovine serum albumin (BSA). As shown in
Lymphocytes were obtained from a patient recovered from SARS-CoV (see, Rickerts et al. 2003) and frozen in liquid nitrogen. The lymphocytes were quickly thawed in a 37° C. water bath and transferred to wet-ice. The lymphocytes were diluted with cold DMEM culture medium to a final volume of 50 ml in a 50 ml tube and centrifuged for 5 minutes at 350×g. The obtained cell pellet was suspended in 5 ml DMEM and cell density was determined microscopically using trypan-blue exclusion to visualize dead cells. All cells (˜5×106) were spun again for 5 minutes at 350×g, decanted and suspended in residual fluid (DMEM). Total RNA was prepared from these cells using organic phase separation (TRIZOL™) and subsequent ethanol precipitation. The obtained RNA was dissolved in DEPC treated ultrapure water and the concentration was determined by OD 260 nm measurement. Thereafter, the RNA was diluted to a concentration of 100 ng/μl. Next, 1 μg of RNA was converted into cDNA as follows: To 10 μl total RNA, 13 μl DEPC treated ultrapure water and 1 μl random hexamers (500 ng/μl) were added and the obtained mixture was heated at 65° C. for five minutes and quickly cooled on wet-ice. Then, 8 μl 5× First-Strand buffer, 2 μl dNTP (10 mM each), 2 μl DTT (0.1 M), 2 μl Rnase-inhibitor (40 U/μl) and 2 μl SUPERSCRIPT™III MMLV reverse transcriptase (200 U/μl) were added to the mixture, incubated at room temperature for five minutes and incubated for one hour at 50° C. The reaction was terminated by heat inactivation, i.e., by incubating the mixture for 15 minutes at 75° C.
The obtained cDNA products were diluted to a final volume of 200 μl with DEPC treated ultrapure water. The OD260 nm of a 50 times diluted solution (in 10 mM Tris buffer) of the dilution of the obtained cDNA products gave a value of 0.1.
Five to 10 μl of the diluted cDNA products were used as template for PCR amplification of the immunoglobulin gamma heavy chain family and kappa or lambda light chain sequences using specific oligonucleotide primers (see, Tables 8-15). PCR reaction mixtures contained, besides the diluted cDNA products, 25 pmol sense primer and 25 pmol anti-sense primer in a final volume of 50 μl of 20 mM Tris-HCl (pH 8.4), 50 mM KCl, 2.5 mM MgCl2, 250 μM dNTPs and 1.25 units Taq polymerase. In a heated-lid thermal cycler having a temperature of 96° C., the mixtures obtained were quickly melted for two minutes, followed by 30 amplification cycles of: 30 seconds at 96° C., 30 seconds at 60° C. and 60 seconds at 72° C. In a first round amplification, each of nine sense directed primers (see, Table 8; covering all families of heavy chain variable regions) was combined with an IgG specific constant region anti-sense primer called HuCIgG 5′-GTC CAC CTT GGT GTT GCT GGG CTT-3′ (SEQ ID NO:131) yielding nine products of about 650 basepairs. These products were purified on a 2% agarose gel and isolated from the gel using QIAGEN® gel extraction columns. One-tenth of each of the isolated products was used in an identical PCR reaction as described above using the same nine sense primers (covering all families of heavy chain variable regions), whereby each sense primer was combined with one of the four J-region specific anti-sense primers (see, Table 9). This resulted in 36 products of approximately 350 basepairs. The products obtained were purified on a 2% agarose gel and isolated from the gel using QIAGEN® gel extraction columns. In a third round, 1/10 of each of the isolated products was subjected to re-amplification with the same set of primers as in the second round with the proviso that the primers used were extended with restriction sites (see, Table 10) to enable directed cloning in the phage display vector pDV-C05 (see,
The light chain immunoglobulin sequences were amplified from the same cDNA preparation in a similar three round PCR procedure and identical reaction parameters as described above for the heavy chain regions with the proviso that the primers depicted in Tables 11 to 15 were used. The first amplification was performed using a set of seventeen light chain variable region sense primers (eleven for the lambda light chain (see, Table 11) and six for the kappa light chain (see, Table 12)) each combined with an anti-sense primer recognizing the C-kappa called HuCk 5′-ACACTCTCCCCTGTTGAAGCT CTT-3′ (see, SEQ ID NO:158) or C-lambda constant region HuCλ2 5′-TGAACATTCTGTAGGGGCCACTG-3′ (see, SEQ ID NO:159) or HuCλ7 5′-AGAGCATTCTGCAGGGGCCACTG-3′ (see, SEQ ID NO:160) (the HuCλ2 and HuCλ7 anti-sense primers were mixed to equimolarity before use), yielding 17 products of about 600 basepairs. These products were purified on a 2% agarose gel and isolated from the gel using QIAGEN® gel extraction columns. One-tenth of each of the isolated products was used in an identical PCR reaction as described above using the same seventeen sense primers, whereby each lambda light chain sense primer was combined with one of the three Jlambda-region specific anti-sense primers (see, Table 13) and each kappa light chain sense primer was combined with one of the five Jkappa-region specific anti-sense primers (see, Table 14). This resulted in 63 products of approximately 350 basepairs. The products obtained were purified on a 2% agarose gel and isolated from the gel using QIAGEN® gel extraction columns. In a third round, 1/10 of each of the isolated products was subjected to re-amplification with the same set of primers as in the second round with the proviso that the primers used were extended with restriction sites (see, Table 15) to enable directed cloning in the heavy chain library or sublibrary vector. This resulted again in 63 products. These products were pooled to a total of ten fractions. This number of fractions was chosen to maintain the natural distribution of the different light chain families within the library and to over or under represent certain families. The number of alleles within a family was used to determine the percentage of representation within a library (see, Table 16). Next, the fractions were digested with SalI and NotI and ligated in the heavy chain library or sublibrary vector, which was cut with the same restriction enzymes, using the same ligation procedure and volumes as described above for the heavy chain library or sublibrary. Ligation purification and subsequent transformation of the resulting definitive library was also performed as described above for the heavy chain library or sublibrary. The transformants were grown in 30 dishes (three dishes per pooled fraction; dimension of dish: 240 mm×240 mm) containing 2TY agar supplemented with 50 μg/ml ampicillin and 4.5% glucose. All bacteria were harvested in 2TY culture medium containing 50 μg/ml ampicillin and 4.5% glucose, mixed with glycerol to 15% (v/v) and frozen in 1.5 ml aliquots at −80° C. Rescue and selection of the library were performed as described supra for the non-immune libraries.
Additionally, a naïve phage display library of scFvs was prepared. For that purpose, healthy donor peripheral blood lymphocytes were used as source of immuno globulin transcripts. Using the protocols described above, immunoglobulin gamma VH regions were amplified and cloned into a PDV-C05 vector already containing a VkIII light chain fragment. This resulted in a non-immunized, naïve library expressing scFv with a fixed VkIII light chain variable region and having a size of approximately 10×106.
Antibody fragments were selected essentially as described previously (see, Example 1). For the selections described below an UV-inactivated SARS-CoV preparation was used (for preparation thereof see Example 9). In contrast to the selections described in Example 1, no pre-subtraction using heat-inactivated fetal bovine serum coated MAXISORP™ tubes (Nunc) was performed. To the SARS-CoV coated tubes, 500 μl (approximately 1013 cfu) of a naïve or an immune phage display library expressing single chain Fv fragments (scFvs) (see, Example 13 for the construction of these libraries), one volume of 4% PBS-FM and Tween-20 to a final concentration of 0.05% was added.
For the naïve phage display library selections, binding was allowed to proceed for 1 hour on a slowly rotating wheel at 37° C. followed by an incubation of 30 minutes without agitation. The tubes were emptied and washed as follows: first round, ten times with PBS containing 0.05% Tween-20 (PBST) and ten times with PBS; second round, 15 times with PBST and ten times with PBS; third round 15 times with PBST and 15 times with PBS.
For the immune phage display library selections which consisted of a single round only, binding was allowed to proceed at 37° C. or room temperature as described above. The following selections and washes were performed: incubation at 37° C., washing five times with PBST and five times with PBS; incubation at 37° C., washing ten times with PBST and ten times with PBS; incubation at room temperature, washing ten times with PBST and ten times with PBS. Bound phages were eluted and processed as described in Example 1. Phages derived from individual colonies were tested in ELISA for binding activity to SARS-CoV coated to 96-well plates.
In the selections from the naïve phage display library the phage antibodies called SC03-019 and SC03-059 were obtained. In the selections from the immune phage display library the phage antibodies called SC03-020, SC03-021, SC03-022, SC03-023, SC03-024, SC03-025, SC03-026, SC03-027, SC03-029, SC03-030, SC03-031, SC03-032, SC03-033, SC03-034, SC03-035, SC03-036, SC03-037, SC03-038, SC03-039, SC03-040, SC03-041, SC03-042, SC03-043, SC03-044, SC03-045, SC03-046, SC03-047, SC03-048, SC03-049, SC03-050, SC03-051, SC03-052, SC03-053, SC03-054, SC03-055, SC03-056, SC03-057 and SC03-058 were obtained.
Selected single-chain phage antibodies that were obtained in the screens described in Example 14 were validated in ELISA for specificity, i.e., binding to the SARS-CoV preparation mentioned in Example 14, essentially as described in Example 2. In contrast to Example 2, the single-chain phage antibodies were not tested for binding to 10% FBS.
As shown in Table 17, the selected phage antibodies called SC03-019, SC03-020, SC03-021, SC03-022, SC03-023, SC03-024, SC03-025, SC03-026, SC03-027, SC03-029, SC03-030, SC03-031, SC03-032, SC03-033, SC03-034, SC03-035, SC03-036, SC03-037, SC03-038, SC03-039, SC03-040, SC03-041, SC03-042, SC03-043, SC03-044, SC03-045, SC03-046, SC03-047, SC03-048, SC03-049, SC03-050, SC03-051, SC03-052, SC03-053, SC03-054, SC03-055, SC03-056, SC03-057, SC03-058 and SC03-059 displayed significant binding to the immobilized SARS-CoV preparation. As a control, the procedure was performed simultaneously using no single-chain phage antibody.
From the selected specific single chain phage antibody (scFv) clones (see, Example 14) plasmid DNA was obtained and nucleotide sequences were determined according to standard techniques. The nucleotide sequences of the scFvs (including restriction sites for cloning) called SC03-019, SC03-020, SC03-021, SC03-022, SC03-023, SC03-024, SC03-025, SC03-026, SC03-027, SC03-029, SC03-030, SC03-031, SC03-032, SC03-033, SC03-034, SC03-035, SC03-036, SC03-037, SC03-038, SC03-039, SC03-040, SC03-041, SC03-042, SC03-043, SC03-044, SC03-045, SC03-046, SC03-047, SC03-048, SC03-049, SC03-050, SC03-051, SC03-052, SC03-053, SC03-054, SC03-055, SC03-056, SC03-057, SC03-058 and SC03-059 are shown in SEQ ID NO:211, SEQ ID NO:213, SEQ ID NO:215, SEQ ID NO:217, SEQ ID NO:219, SEQ ID NO:221, SEQ ID NO:223, SEQ ID NO:225, SEQ ID NO:227, SEQ ID NO:229, SEQ ID NO:231, SEQ ID NO:233, SEQ ID NO:235, SEQ ID NO:237, SEQ ID NO:239, SEQ ID NO:241, SEQ ID NO:243, SEQ ID NO:245, SEQ ID NO:247, SEQ ID NO:249, SEQ ID NO:251, SEQ ID NO:253, SEQ ID NO:255, SEQ ID NO:257, SEQ ID NO:259, SEQ ID NO:261, SEQ ID NO:263, SEQ ID NO:265, SEQ ID NO:267, SEQ ID NO:269, SEQ ID NO:271, SEQ ID NO:273, SEQ ID NO:275, SEQ ID NO:277, SEQ ID NO:279, SEQ ID NO:281, SEQ ID NO:283, SEQ ID NO:285, SEQ ID NO:287 and SEQ ID NO:289, respectively.
The amino acid sequences of the scFvs called SC03-019, SC03-020, SC03-021, SC03-022, SC03-023, SC03-024, SC03-025, SC03-026, SC03-027, SC03-029, SC03-030, SC03-031, SC03-032, SC03-033, SC03-034, SC03-035, SC03-036, SC03-037, SC03-038, SC03-039, SC03-040, SC03-041, SC03-042, SC03-043, SC03-044, SC03-045, SC03-046, SC03-047, SC03-048, SC03-049, SC03-050, SC03-051, SC03-052, SC03-053, SC03-054, SC03-055, SC03-056, SC03-057, SC03-058 and SC03-059 are shown in SEQ ID NO:212, SEQ ID NO:214, SEQ ID NO:216, SEQ ID NO:218, SEQ ID NO:220, SEQ ID NO:222, SEQ ID NO:224, SEQ ID NO:226, SEQ ID NO:228, SEQ ID NO:230, SEQ ID NO:232, SEQ ID NO:234, SEQ ID NO:236, SEQ ID NO:238, SEQ ID NO:240, SEQ ID NO:242, SEQ ID NO:244, SEQ ID NO:246, SEQ ID NO:248, SEQ ID NO:250, SEQ ID NO:252, SEQ ID NO:254, SEQ ID NO:256, SEQ ID NO:258, SEQ ID NO:260, SEQ ID NO:262, SEQ ID NO:264, SEQ ID NO:266, SEQ ID NO:268, SEQ ID NO:270, SEQ ID NO:272, SEQ ID NO:274, SEQ ID NO:276, SEQ ID NO:278, SEQ ID NO:280, SEQ ID NO:282, SEQ ID NO:284, SEQ ID NO:286, SEQ ID NO:288 and SEQ ID NO:290, respectively.
The VH and VL gene identity (see, I. M. Tomlinson, S. C. Williams, O. Ignatovitch, S. J. Corbett, G. Winter, V-BASE Sequence Directory, Cambridge United Kingdom: MRC Centre for Protein Engineering (1997)) and heavy chain CDR3 compositions of the scFvs specifically binding the SARS-CoV preparation are depicted in Table 18.
The experiment was performed to investigate the neutralizing capacity of the anti-SARS-CoV monoclonal antibodies of the invention in vivo essentially as described by Emini et al. (1990). Briefly, the human monoclonal anti-SARS-CoV antibody 03-014 and the control anti-Epcam antibody 02-027 were pre-incubated in vitro with two different titers (103 and 104 TCID50) of the SARS-CoV strain SCV-P4 (5688) (obtained from patient 5688, see above). Antibody concentrations used were extrapolated from the concentration of antibody needed to neutralize 100TCID50 of virus in a volume of 100 μl (i.e., 6.25 μg/ml; see in vitro neutralization data in Example 7) and multiplied by twenty (i.e., 0.13 mg/ml for 1000TCID50, 1.3 mg/ml for 10,000TCID50). The virus/antibody mixtures obtained were used to infect ferrets via the intratracheal route (Fouchier et al. 2003). Cell cultures of Vero 118 cells were inoculated in parallel to verify the in vitro neutralizing activity of the monoclonal antibody 03-014 and the expected infectivity of the virus in case of pre-incubation with the control antibody. Ferrets were monitored for signs of disease and shedding of virus (RT-PCR) and ultimately sacrificed and examined by histopathology.
High dose and low dose solutions of the monoclonal antibody 03-014 and the control antibody were prepared as follows. The working solution of the monoclonal antibody 03-014 had a concentration of 1.44 mg/ml. 4.87 ml of this working solution was brought into a 15 ml tube (high dose solution, 1.44 mg/ml final concentration). To obtain the low dose solution, 541 μl of the working solution was added to 2.46 ml PBS (low dose solution, 0.26 mg/ml final concentration) and mixed well. 2.7 ml of this low dose solution was brought into a 15 ml tube.
The starting solution of the control antibody had a concentration of 3.90 mg/ml. 2.10 ml of this starting solution was added to 3.58 ml PBS to obtain a working solution with a final concentration of 1.44 mg/ml. 4.87 ml of this working solution was brought into a 15 ml tube (high dose solution, 1.44 mg/ml final concentration). To obtain the low dose solution, 541 μl of the working solution was added to 2.46 ml PBS (low dose solution, 0.26 mg/ml final concentration) and mixed well. 2.7 ml of this low dose solution was brought into a 15 ml tube.
After preparation of the high dose and low dose solutions of the monoclonal antibodies, the high dose and low dose solution of the SARS-CoV were prepared. The starting solution of the SARS-CoV had a concentration of 107 TCID50/ml. The starting solution was thawed at 37° C. and 100 μl of this solution was added to 900 μl PBS and mixed well. The working solution thus obtained had a concentration of 106 TCID50/ml.
To obtain a high dose SARS-CoV solution 200 μl working solution was added to 1.8 ml PBS and mixed well (high dose SARS-CoV solution, 100,000 TCID50/ml). To obtain a low dose SARS-CoV solution 200 μl high dose solution was added to 1.8 ml PBS and mixed well. After that, the thus obtained diluted high dose solution was further diluted by adding 1.2 ml of this diluted high dose solution to 4.8 ml PBS and mixing (low dose SARS-CoV solution, 2,000 TCID50/ml).
Next, the high dose and low dose solutions of the monoclonal antibodies were mixed with the high and low dose SARS-CoV solutions at 37° C. for one hour. The following groups were prepared.
Group 1: 2.7 ml low dose SARS-CoV solution was added to 2.7 ml low dose solution of the monoclonal antibody 03-014 and mixed well (final concentration of SARS-CoV was 1,000 TCID50/ml; final concentration of monoclonal antibody 03-014 0.13 mg/ml; total volume 5.4 ml).
Group 2: 0.54 ml high dose SARS-CoV solution was added to 4.87 ml high dose solution of the monoclonal antibody 03-014 and mixed well (final concentration of SARS-CoV was 10,000 TCID50/ml; final concentration of monoclonal antibody 03-014 1.3 mg/ml; total volume 5.4 ml).
Group 3: 2.7 ml low dose SARS-CoV solution was added to 2.7 ml low dose solution of the monoclonal control antibody and mixed well (final concentration of SARS-CoV was 1,000 TCID50/ml; final concentration of monoclonal control antibody 0.13 mg/ml; total volume 5.4 ml).
Group 4: 0.54 ml high dose SARS-CoV solution was added to 4.87 ml high dose solution of the monoclonal control antibody and mixed well (final concentration of SARS-CoV was 10,000 TCID50/ml; final concentration of monoclonal control antibody 1.3 mg/ml; total volume 5.4 ml).
1.1 ml of the solution of each of the four groups was removed for inoculation of Vero 118 cell cultures. One ml of the solution of each of the four groups was added to a separate well of substrate plates (each plate containing six wells). Each well contained an 80% monolayer of Vero 118 cells. The monolayers were prepared by trypsinizing Vero 118 cells, diluting them in DMEM with 5% FBS, seeding 2*106 Vero 118 cells per separate well and incubating the cells for 16 to 20 hours at 37° C. with 2 ml DMEM containing sodium bicarbonate 0.75%, L-glutamine 2 mM and penicillin/streptomycin (10 U/ml). The plates with the above solutions were incubated overnight at 37° C. The medium was replaced by fresh medium and the plates were incubated for a further three to five days at 37° C. and monitored for CPE.
To each of the remaining amounts (4.3 ml) of each of the four groups 8.6 ml PBS was added. Prior to any handling or sampling, the animals were anesthetized by means of light ketamine (2.5 mg/kg) and domitor (0.1 ml/kg), followed by antisedan (0.05 ml/kg). Before inoculation, from each ferret a nasal swab was taken (day 0). Each ferret was intratracheally inoculated with 3 ml of the respective solutions as indicated in the scheme shown in Table 19. Nasal swabs alone were taken from each ferret as indicated in the scheme shown in Table 19 (day 2). Animals were checked every day for clinical symptoms such as respiratory problems, erythema and lethargy. Animals were weighed every other day. From each ferret nasal and pharyngeal swabs were taken as indicated in the scheme shown in Table 19 (day 4 or 7). Swabs were preserved in standard virus transport medium and stored at −80° C. Ferrets were euthanized by means of total exsanguination under full anesthesia by means of ketamine (5 mg/kg) and domitor (0.1 ml/kg) as indicated in the scheme shown in Table 19 (day 4 or 7). Next, the samples were analyzed by RT-PCR with primers and probes specific for the nucleoprotein (NP) gene of SARS-CoV to quantify SARS-CoV in lung tissues as described in Kuiken et al. 2003.
As shown in
SARS-CoV titers in the lung were obtained using an in vitro virus titration assay. Lung samples were collected and weighed and transferred to a 5 ml tubes containing 1 ml RPMI1640 medium. The samples were transferred to ice, homogenized and cellular debris was pelleted by centrifugation. From the supernatant ten-fold serial dilutions were prepared starting with a dilution of 1:10. 100 μl of the homogenate dilutions were added to 80% confluent monolayers of Vero 118 cells in a 96-well plate. The cells were incubated for five days and the occurrence cytopathogenic effect (CPE) was scored. SARS-CoV lung titers were expressed as TCID50/ml and were calculated according to the Reed and Muench method.
As shown in
The analysis of the pathology in the ferret lungs was performed according to the following procedure. Necropsies were done according to a standard protocol; one lung of each ferret was inflated with 10% neutral-buffered formalin by intrabronchial intubation and suspended in 10% neutral-buffered formalin overnight. Samples were collected in a standard manner (one from the cranial part of the lung, one from the medial and two from the caudal part), embedded in paraffin, cut at 5 μm and stained with hematoxylin and eosin (HE). For semi-quantitative assessment of SARS-CoV-infection-associated inflammation in the lung, each HE-stained section was examined for inflammatory foci by light microscopy using a 2.5× objective. If any suspect lesions were seen, they were examined at higher power to determine whether typical characteristics are present (intra-alveolar oedema, neutrophils and macrophages in alveolar lumina, type 2 pneumocyte hyperplasia). Lung sections were scored as followed: −, no SARS lesions; +, mild SARS lesions; ++, moderate SARS lesions; +++, marked SARS lesions. The final score for each animal is the cumulative score of two lung sections. Sections were examined in a blinded manner.
As shown in
To address whether the human anti-SARS-CoV monoclonal antibodies can be efficacious in a prophylactic setting a SARS-CoV challenge experiment has been performed in ferrets. One day prior to the SARS-CoV challenge ferrets were administered 10 mg/kg of monoclonal 03-014 IgG1 antibody intraperitoneally (i.p.). Prior to all experimental procedures the animals were anesthetized as described supra. Two groups of four animals were treated with either a human monoclonal control IgG1 antibody (02-027, anti-Epcam antibody) or with the monoclonal anti-SARS-CoV 03-014 IgG1 antibody. The anti-SARS-CoV 03-014 antibody (concentration 1.23 mg/ml) was used undiluted for i.p. administration. The 02-027 control IgG1 antibody (concentration 3.9 mg/ml) was diluted 1:2 in PBS to achieve a final concentration of 1.3 mg/ml. The volume needed for the injection of the 10 mg/kg dose was based on the weight of the individual ferrets and varied between 6.5 and 8 ml. The antibodies were injected at ambient temperature. Prior to the antibody transfer and prior to the SARS-CoV challenge, serum samples were obtained from each animal to assess the SARS-CoV neutralization titer as described before. All animals were challenged with 104 TCID50 of the SARS-CoV strain SCV-P4 (5688). To this purpose the 5866 SARS-CoV virus stock (concentration: 107 TCID50/ml) was thawed and 100 μl of the virus stock was added to 900 μl PBS (at room temperature) to obtain a working virus stock of 106 TCID50/ml. To obtain the final solution containing the challenge dose of 104 TCID50 per 3 ml challenge dose, 100 μl virus working stock was added to 30 ml PBS (at room temperature). Each ferret was inoculated intratracheally with 3 ml of virus mixture as described supra. Serum, pharyngeal swab and tissue samples were obtained according to Table 20. SARS-CoV excretion in pharyngeal swabs, SARS-CoV titers in lung tissue and lung pathology were analyzed as described supra.
In the control group, shedding of SARS-CoV in the throat was apparent two and four days after challenge. By contrast, pharyngeal excretion was completely abolished in three of the 03-014-treated animals (see,
Importantly, the differences in both pharyngeal and pulmonary viral titers between the control group and the 03-014 group were accompanied by a complete protection from macroscopic lung pathology in the group treated with 03-014 compared to the control group, who all showed multifocal lesions (p=0.029). Upon microscopic analysis, these lesions showed alveolar changes resembling diffuse alveolar damage as well as peribronchial, peribrochiolar, and perivascular lymphocytic cuffing.
Taken together, these results demonstrate that passive transfer of the 03-014 anti-SARS-CoV antibody was able to abolish SARS-CoV induced pulmonary lesions as well as SARS-CoV excretion in animals that had obtained sufficient 03-014 IgG serum titers (see, Ter Meulen et al. 2004).
Supernatants of SARS-CoV producing Vero cells were harvested 24 hours p.i. and used directly for indirect, two-step immuno-gold-labeling. SARS-CoV was adsorbed to carbon- and Pioloform-coated copper grids. After two washing steps with blocking buffer (PBS comprising 0.1% bovine serum albumin), the grids were incubated with the human monoclonal control IgG1 antibody (02-027, anti-Epcam antibody) or with the monoclonal anti-SARS-CoV 03-014 IgG1 antibody by floating on respective droplets for 30 minutes at room temperature. Next, surplus antibody was removed using a strip of filter paper and two washing steps on blocking buffer. Bound monoclonal antibodies were detected by incubation on droplets of anti-hu-IgG-gold-5 nm conjugates (British Biocell Corp). The grids were negative contrasted with 1% uranyl acetate and evaluated at a ZEISS EM 10 A transmission electron microscope.
Incubation with the monoclonal anti-SARS-CoV 03-014 IgG1 antibody lead to a dense gold-label of the outer peplomer region of the SARS-CoV (see,
In a similar way, ultra-thin sections of Vero cells infected with SARS-CoV were analyzed by electron microscopy. In
The diversity within the region 318-510 of the S protein was determined as follows. A list containing more than 146 genomes or genes encoding complete human SARS-CoV or fragments thereof was compiled. In 114 cases, an open reading frame encoding for full-length spike (S) protein was identified. Alignment of the spike amino acid residues 318-510 revealed 30 spike proteins, in which the region 318-510 was not identical to that of the spike protein of strain Frankfurt 1 (see, GenBank accession number AY291315), which was used herein. The mutations, strains and Genbank numbers are depicted in Table 21. To investigate if 03-014 bound the S protein of all currently known human SARS-CoV isolates, eight recombinant spike fragments harboring the different amino acid substitutions as shown in Table 21 were generated. To this end, the above substitutions were introduced in the pHAVT20/myc-His A S318-510 vector using the Stratagene's QuikChange II site-directed mutagenesis kit according to the manufacturer's instructions. In case a sequence contained multiple amino acid substitutions, the process of mutagenesis, sequence analysis and confirmation was repeated for every single substitution. To rule out the introduction of additional mutations in the plasmid outside the gene of interest, the mutated (592 by EcoRI-XbaI) fragment was recloned in EcoRI-XbaI cut pHAVT20/myc-His A. The resulting plasmids were transfected into 293T cells, and binding of 03-014 was evaluated by means of ELISA as described in Example 12. In addition, binding of HRP-conjugated monoclonal anti-His6 antibody (Roche) to each mutant was evaluated essentially as described above. Binding of anti-His6 and 03-014 to the wild-type S318-510 fragment derived from the Frankfurt 1 strain was set at 100%. Binding of the monoclonal anti-His6 antibody and 03-014 to the mutated S318-510 fragments was expressed as percentage of binding compared to the wild-type S318-510 fragment.
As shown in
Different SARS-CoV strains were used to evaluate the potency and breadth of protection of the anti-SARS-CoV antibodies. The SARS-CoV strains HKU-36, HKU-39849, HKU-66, and HKU-61567 were passaged on FRhK-4 cells for two or three times before testing (see, Table 22). Strain HKU-61644 was passaged on Vero cells and tested after passage 1 and 15. The SARS-CoV neutralization assay was performed on FRhK-4 cells as follows. A 500 μl 100 μg/ml stock solution of antibody was prepared in maintenance medium (MM, MEM supplemented with 1% fetal calf serum). From this stock solution, two-fold serial dilutions were prepared. 220 μl 100 μg/ml stock solution was added in duplo in a 96-well plate from which 110 μl was taken and mixed with 110 μl MM in each of the nine subsequent wells. 110 μl of the tenth well was discarded, which resulted in ten wells containing 110 μl 0.2-100 μg/ml antibody. 110 μl of the antibody dilution was mixed with 110 μl of the different SARS-CoV isolates at a concentration of 2000 TCID50/ml with the titer calculated according to the method of Reed and Muench. At this stage, in a 220 μl volume, antibody concentrations varied from 0.1 to 50 μg/ml in the presence of 1000 TCID50/ml SARS-CoV. The 96-well plate containing the antibody virus mixtures was preincubated for one to two hours at 37° C. 100 μl of the virus-antibody mixtures were added in quadruplicate to wells from a second 96-well tissue culture plate containing confluent FRhK-4 cells in 100 μl MM and incubated at 37° C. During this final incubation step, 100 TCID50 of SARS-CoV was present in the presence of antibody concentrations varying from 0.05 to 25 μg/ml. The cells were cultured at 37° C. and observed for the development of CPE at 72 and 96 hours. CPE is compared to a positive control (SARS-CoV inoculated cells) and a negative control (cells incubated with MM only). The antibody neutralization titer was determined as the concentration of antibody which gives 100% protection of the quadruplicate cell cultures. The monoclonal anti-SARS-CoV antibody 03-014 completely neutralized 100 TCID50 of all tested SARS-CoV isolates at a concentration of 12.5 μg/ml (see, Table 22). This indicates that antibody 03-014 is able to neutralize a variety of SARS-CoV isolates.
apremix of challenge dose and optimal concentration antibody
bsplit based on sacrification
cS means swabs; LT means lung tissue after sacrification
| Number | Date | Country | Kind |
|---|---|---|---|
| PCT/EP03/50328 | Jul 2003 | EP | regional |
| PCT/EP03/50391 | Sep 2003 | EP | regional |
| PCT/EP03/50723 | Oct 2003 | EP | regional |
| PCT/EP03/50883 | Nov 2003 | EP | regional |
| PCT/EP03/50943 | Dec 2003 | EP | regional |
| PCT/EP04/50067 | Feb 2004 | EP | regional |
| PCT/EP04/50127 | Feb 2004 | EP | regional |
| PCT/EP04/50334 | Mar 2004 | EP | regional |
| PCT/EP04/50464 | Apr 2004 | EP | regional |
| PCT/EP04/50516 | Apr 2004 | EP | regional |
| PCT/EP04/50643 | Apr 2004 | EP | regional |
This application is a continuation of co-pending U.S. Ser. No. 11/337,300, filed Jan. 20, 2006, now U.S. patent Ser. No. ______, which is a continuation of PCT International Patent Application No. PCT/EP2004/051568, filed on Jul. 21, 2004, designating the United States of America, and published, in English, as PCT International Publication No. WO 2005/012360 A2 on Feb. 10, 2005, which application claims priority to International Patent Application No. PCT/EP04/050643 filed Apr. 29, 2004, and claims priority to International Patent Application No. PCT/EP04/050516 filed Apr. 14, 2004, which claims priority to International Patent Application No. PCT/EP04/050464 filed Apr. 7, 2004, which claims priority to International Patent Application No. PCT/EP04/050334 filed Mar. 19, 2004, which claims priority to International Patent Application No. PCT/EP04/050127 filed Feb. 13, 2004, which claims priority to International Patent Application No. PCT/EP04/050067 filed Feb. 2, 2004, which claims priority to International Patent Application No. PCT/EP03/50943 filed Dec. 4, 2003, which claims priority to International Patent Application No. PCT/EP03/50883 filed Nov. 24, 2003, which claims priority to International Patent Application No. PCT/EP03/50723 filed Oct. 16, 2003, which claims priority to International Patent Application No. PCT/EP03/50391 filed Sep. 1, 2003, which, in turn, claims priority to International Patent Application No. PCT/EP03/50328 filed Jul. 22, 2003, the contents of the entirety of each of which are incorporated by this reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 11337300 | Jan 2006 | US |
| Child | 12590973 | US | |
| Parent | PCT/EP04/51568 | Jul 2004 | US |
| Child | 11337300 | US |
