Antibodies against
Compositions and methods for the treatment or prevention of Clostridium difficile infection in a subject are provided. The compositions comprise antibodies to Clostridium difficile toxin B. The methods provide for administering the antibodies to a subject in an amount effective to reduce or eliminate or prevent relapse from Clostridium difficile bacterial infection.
1. An isolated antibody or antigen-binding portion thereof comprising a heavy chain variable region (VH) and a light chain variable region (VL),
wherein the heavy chain variable region comprises three complementarity determining regions (CDRs), CDR1, CDR2, and CDR3, having the amino acid sequences set forth in SEQ ID NOs: 126, 127, and 128, respectively, or the amino acid sequences set forth in SEQ ID NOs: 110, 127, and 128, respectively, and
wherein the light chain variable region comprises three CDRs, CDR1, CDR2, and CDR3, having the amino acid sequences set forth in SEQ ID NOs: 118, 119, and 120, respectively; and
wherein the antibody or antigen-binding portion thereof specifically binds to Clostridium difficile ( C. difficile ) toxin B.
2. The antibody or antigen-binding portion thereof of claim 1 , wherein the heavy chain variable region comprises the amino acid sequence SEQ ID NO: 109 and wherein the light chain variable region comprises the amino acid sequence SEQ ID NO: 101.
3. The antibody or antigen-binding portion thereof of claim 1 , wherein the heavy chain variable region comprises the amino acid sequence SEQ ID NO: 125 and wherein the light chain variable region comprises the amino acid sequence SEQ ID NO: 117.
4. The antibody or antigen-binding portion thereof of claim 1 , wherein the heavy chain variable region comprises the amino acid sequence SEQ ID NO: 141 and wherein the light chain variable region comprises the amino acid sequence SEQ ID NO: 133.
5. The antibody or antigen-binding portion thereof of claim 1 , wherein the heavy chain variable region comprises the amino acid sequence set forth in SEQ ID NO: 43, and wherein the light chain variable region comprises the amino acid sequence set forth in SEQ ID NO: 35.
6. The antibody or antigen-binding portion thereof of claim 1 , wherein the dissociation constant (K D ) of the antibody or antigen-binding portion thereof binding to C. difficile toxin B is less than about 8.6×10 −9 M.
7. The antibody or antigen-binding portion thereof of claim 1 , which comprises an IgG constant region, IgE constant region, IgD constant region, IgM constant region, an IgA constant region, or any fragment thereof.
8. The antibody or antigen-binding portion thereof of claim 1 , which is functionally linked to another molecule.
9. The antibody or antigen-binding portion thereof of claim 8 , wherein the functionally linked molecule is an antibody, detectable agent, a cytotoxic agent, a pharmaceutical agent, a protein or peptide that mediates association with another molecule, an amino acid linker, a signal sequence, or an immunogenic carrier.
10. The antibody or antigen-binding portion thereof of claim 1 , which is humanized or chimeric.
11. The antibody or antigen-binding portion thereof of claim 1 , which is an scFv, a Fab fragment, an F(ab′)2, or a disulfide-linked Fv.
12. A composition comprising the antibody or antigen-binding portion thereof of claim 1 , and a pharmaceutically acceptable carrier.
13. A kit comprising the antibody or antigen-binding portion thereof of claim 1 and one or more of an antibody that binds to C. difficile toxin A, a therapeutic agent, a coupling agent, a material for preparing the antibody for administration, or a pharmaceutically acceptable carrier.
14. The kit of claim 13 , further comprising: one or more of C. difficile whole toxin B, toxoid B, toxin B fragment 4, or toxin B fragment 1.
15. A method of treating a C. difficile associated disease (CDAD), comprising administering to a subject an effective amount of the antibody or antigen-binding portion thereof of claim 1 , wherein the subject is infected, or is believed to be infected, with C. difficile.
16. The method of claim 15 , wherein the antibody or antigen-binding portion thereof is administered intravenously, subcutaneously, intramuscularly or transdermally.
17. The method of claim 15 , further comprising administering a second agent.
18. The method of claim 17 , wherein the second agent is a different antibody or antigen-binding portion thereof.
19. The method of claim 17 , wherein the second agent is an antibiotic.
20. The method of claim 19 , wherein the antibiotic is vancomycin, metronidazole, or fidaxomicin.
21. The antibody or antigen-binding portion thereof of claim 1 , wherein the antibody or antibody-binding portion thereof binds to fragment 1 of C. difficile Toxin B.
22. An isolated antibody heavy chain variable region, wherein the heavy chain variable region comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 43, 109, 125, and 141,
wherein an antibody or antigen-binding binding portion thereof comprising the heavy chain variable region and a light chain variable region comprising the amino acid sequence SEQ ID NO: 35, 101, 117, or 133, respectively, can specifically bind to C. difficile toxin B.
23. An isolated antibody light chain variable region, wherein the light chain variable region comprises an amino acid sequence selected from the group consisting of SEQ ID NO: 35, 101, 117, or 133,
wherein an antibody or antigen-binding binding portion thereof comprising the light chain variable region and a heavy chain variable region comprising the amino acid sequence SEQ ID NO: 43, 109, 125, or 141, respectively, can specifically bind to C. difficile toxin B.