IP-10 antibodies and their uses
View Patent ↗The present invention provides isolated monoclonal antibodies, particularly human antibodies, that bind to IP-10 with high affinity, inhibit the binding of IP-10 to its receptor, inhibit IP-10-induced calcium flux and inhibit IP-10-induced cell migration. Nucleic acid molecules encoding the antibodies of the invention, expression vectors, host cells and methods for expressing the antibodies of the invention are also provided. Immunoconjugates, bispecific molecules and pharmaceutical compositions comprising the antibodies of the invention are also provided. The invention also provides methods for inhibiting IP-10 activity using the antibodies of the invention, including methods for treating various inflammatory and autoimmune diseases.
1. A method of inhibiting an inflammatory or autoimmune response mediated by activated T cells or NK cells, comprising contacting the T cells or NK cells with an antibody, or antigen-binding portion thereof, which specifically binds IP-10 (SEQ ID NO: 121), such that the inflammatory or autoimmune response is inhibited, wherein the antibody or antigen-binding portion thereof:
(a) comprises heavy chain variable region CDR1, CDR2, and CDR3 sequences as set forth in SEQ ID NOs: 5, 17, and 28, respectively, and light chain variable region CDR1, CDR2, and CDR3 sequences as set forth in SEQ ID NOs: 55, 66, and 77, respectively;
(b) comprises heavy and light chain variable region sequences comprising SEQ ID NOs: 39 and 88, respectively; or
(c) binds an epitope on human IP-10 (SEQ ID NO: 121) recognized by a reference antibody, wherein the reference antibody comprises heavy and light chain variable region sequences as set forth in SEQ ID NOs: 39 and 88, respectively.
2. A method of treating an inflammatory or autoimmune disease in a subject, comprising administering to the subject an antibody, or antigen-binding portion thereof, which specifically binds IP-10 (SEQ ID NO: 121), wherein the antibody or antigen-binding portion thereof:
(a) comprises heavy chain variable region CDR1, CDR2, and CDR3 sequences as set forth in SEQ ID NOs: 5, 17, and 28, respectively, and light chain variable region CDR1, CDR2, and CDR3 sequences as set forth in SEQ ID NOs: 55, 66, and 77, respectively;
(b) comprises heavy and light chain variable region sequences comprising SEQ ID NOs: 39 and 88, respectively; or
(c) binds an epitope on human IP-10 (SEQ ID NO: 121) recognized by a reference antibody, wherein the reference antibody comprises heavy and light chain variable region sequences as set forth in SEQ ID NOs: 39 and 88, respectively.
3. The method of claim 1 or 2 , wherein the antibody, or antigen-binding portion thereof, comprises:
(a) a heavy chain variable region CDR1 comprising SEQ ID NO: 5;
(b) a heavy chain variable region CDR2 comprising SEQ ID NO: 17;
(c) a heavy chain variable region CDR3 comprising SEQ ID NO: 28;
(d) a light chain variable region CDR1 comprising SEQ ID NO: 55;
(e) a light chain variable region CDR2 comprising SEQ ID NO: 66; and
(f) a light chain variable region CDR3 comprising SEQ ID NO: 77.
4. The method of claim 1 or 2 , wherein the antibody, or antigen-binding portion thereof, comprises:
(a) a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 39; and
(b) a light chain variable region comprising the amino acid sequence of SEQ ID NO: 88.
5. The method of claim 1 or 2 , wherein the antibody, or antigen-binding portion thereof, binds an epitope on human IP-10 (SEQ ID NO: 121) recognized by a reference antibody, wherein the reference antibody comprises a heavy chain variable region comprising SEQ ID NO: 39 and a light chain variable region comprising SEQ ID NO: 88.
6. The method of claim 1 or 2 , wherein the antibody is selected from a human antibody, a chimeric antibody, or a humanized antibody.
7. The method of claim 1 or 2 , wherein the antigen binding portion is selected from a Fab antibody fragment or a single chain antibody (scFv).
8. The method of claim 1 or 2 , wherein the antibody, or antigen-binding portion thereof, is linked to a therapeutic agent.
9. The method of claim 1 or 2 , wherein the antibody, or antigen binding portion thereof is bispecific.
10. The method of claim 2 , wherein the disease is selected from the group consisting of multiple sclerosis, rheumatoid arthritis, inflammatory bowel disease, systemic lupus erythematosus, Type I diabetes, inflammatory skin disorders, autoimmune thyroid disease, Sjogren's syndrome, pulmonary inflammation, transplant rejection, spinal cord injury, brain injury (e.g., stroke), neurodegenerative diseases, gingivitis, gene therapy-induced inflammation, diseases of angiogenesis, inflammatory kidney disease, and atherosclerosis.
11. The method of claim 10 , wherein the disease is inflammatory bowel disease.
12. The method of claim 11 , wherein the disease is ulcerative colitis.
13. The method of claim 11 , wherein the disease is Crohn's disease.
14. The method of claim 2 , wherein the subject is human.
15. The method of claim 2 , wherein the antibody, or antigen-binding portion thereof, is administered by a route selected from the group consisting of subcutaneously, intramuscularly, intradermally, intraperitoneally, and intravenously.
16. The method of claim 15 , wherein the antibody, or antigen-binding portion thereof, is administered intravenously.
17. The method of claim 15 , wherein the antibody, or antigen-binding portion thereof, is administered subcutaneously.
18. The method of claim 6 , wherein the antibody is a human antibody.
19. The method of claim 1 or 2 , wherein the antibody is a full-length IgG1 antibody.
20. The method of claim 1 or 2 , wherein the antibody is a full-length IgG4 antibody.
21. The method of claim 2 , wherein the antibody, or antigen-binding portion thereof, is formulated with a pharmaceutically acceptable carrier.