Antibodies to human complement C2B
Provided are antibodies and antigen-binding fragments thereof that bind specifically to human complement factor C2 and are capable of inhibiting activation of the classical and lectin pathways of the complement system. The antibodies and antigen-binding fragment exhibit improved manufacturability, pharmacokinetics, and antigen sweeping. Also provided are pharmaceutical compositions comprising the antibodies and antigen-binding fragments, nucleic acids and vectors encoding the antibodies and antigen-binding fragments, host cells comprising the nucleic acids or vectors, and methods of making and using the antibodies and antigen-binding fragments. The antibodies and antigen-binding fragments can be used to inhibit the classical pathway of complement activation in a subject, e.g., a human. The antibodies and antigen-binding fragments can also be used to inhibit the lectin pathway of complement activation in a subject, e.g., a human.
1. A method of inhibiting classical pathway of complement activation in a subject, comprising administering to a subject in need thereof an effective amount of a monoclonal antibody or antigen-binding fragment thereof that specifically binds to human complement factor C2, wherein said monoclonal antibody or fragment thereof comprises:
a VH domain comprising the amino acid sequence set forth in SEQ ID NO: 3; and
a VL domain comprising the amino acid sequence set forth in SEQ ID NO: 2.
2. The method of claim 1 , wherein the monoclonal antibody or antigen-binding fragment thereof comprises a full-length monoclonal antibody.
3. The method of claim 1 , wherein the monoclonal antibody comprises a human IgG heavy chain constant domain.
4. The method of claim 3 , wherein the heavy chain constant domain comprises a human IgG1 heavy chain constant domain.
5. The method of claim 4 , wherein the human IgG1 heavy chain constant domain comprises the amino acid sequence set forth in SEQ ID NO: 4.
6. The method of claim 3 , wherein the heavy chain constant domain comprises a human IgG4 heavy chain constant domain.
7. The method of claim 6 , wherein the human IgG4 heavy chain constant domain comprises the amino acid sequence set forth in SEQ ID NO: 5.
8. The method of claim 3 , wherein the monoclonal antibody comprises a heavy chain comprising the amino acid sequence set forth as SEQ ID NO: 6 and a light chain comprising the amino acid sequence set forth as SEQ ID NO: 7.
9. The method of claim 3 , wherein the monoclonal antibody comprises a heavy chain comprising the amino acid sequence set forth as SEQ ID NO: 8 and a light chain comprising the amino acid sequence set forth as SEQ ID NO: 7.
10. A method of inhibiting lectin pathway of complement activation in a subject, comprising administering to a subject in need thereof an effective amount of a monoclonal antibody or antigen-binding fragment thereof, that specifically binds to human complement factor C2, wherein said monoclonal antibody or fragment thereof comprises:
a VH domain comprising the amino acid sequence set forth in SEQ ID NO: 3; and
a VL domain comprising the amino acid sequence set forth in SEQ ID NO: 2.
11. The method of claim 10 , wherein the subject is a human.
12. The method of claim 1 , wherein the subject is a human.
13. The method of claim 1 , wherein the subject suffers from an autoimmune disease.
14. The method of claim 13 , wherein the autoimmune disease is selected from the group consisting of allergic neuritis; type II collagen-induced arthritis; myasthenia gravis; hemolytic anemia; glomerulonephritis; idiopathic membranous nephropathy; rheumatoid arthritis; systemic lupus erythematosus; immune complex-induced vasculitis; adult respiratory distress syndrome; stroke; xenotransplantation; allotransplantation; multiple sclerosis; burn injuries; extracorporeal dialysis and blood oxygenation; inflammatory disorders, including sepsis and septic shock; toxicity induced by in vivo administration of cytokines or monoclonal antibodies; antibody-mediated rejection of allografts such as kidney allografts; multiple trauma; ischemia-reperfusion injuries; and myocardial infarction.
15. The method of claim 1 , wherein the administering is by injection or infusion.
16. The method of claim 15 , wherein the administering is intravenous, subcutaneous, or local.
17. The method of claim 16 , wherein the administration is one or more bolus injections or divided into several doses over time.
18. The method of claim 10 , wherein the subject suffers from an autoimmune disease.
19. The method of claim 10 , wherein the administering is by injection or infusion.
20. The method of claim 19 , wherein the administering is intravenous, subcutaneous, or local.