Antibody therapeutics that bind CTLA4
View Patent ↗There is disclosed compositions and methods relating to or derived from anti-CTLA4 antibodies. More specifically, there is disclosed fully human antibodies that bind CTLA4, CTLA4-antibody binding fragments and derivatives of such antibodies, and CTLA4-binding polypeptides comprising such fragments. Further still, there is disclosed nucleic acids encoding such antibodies, antibody fragments and derivatives and polypeptides, cells comprising such polynucleotides, methods of making such antibodies, antibody fragments and derivatives and polypeptides, and methods of using such antibodies, antibody fragments and derivatives and polypeptides, including methods of treating a disease requiring either stimulation of immune responses or suppression. Stimulation is achieved using antibodies that block binding of human CTLA4 to human B7 and diseases amenable to treatment by stimulation and augmentation of prolonging of immune responses include cancers of the prostate, kidney, colon, lung or breast; pathogenic infections; diseases associated with the CNS e.g. amyloidogenic diseases including Alzheimer's disease; and diseases with inflammatory or allergic components. Diseases amenable to treatment include graft versus host disease, host versus graft disease, allergy, autoimmune diseases and other inflammatory diseases.
1. An isolated fully human anti-CTLA4 antibody of an IgG class comprising a heavy chain/light chain variable domain sequence of SEQ ID NO. 25/SEQ ID NO. 26 or SEQ ID NO: 43/SEQ ID NO: 44.
2. The fully human antibody of claim 1 , wherein the antibody has a K D of at least 1×10 −6 M.
3. An anti-CTLA4 fully human antibody fragment comprising a heavy chain/light chain variable domain sequence of SEQ ID NO. 25/SEQ ID NO. 26 or SEQ ID NO: 43/SEQ ID NO: 44, wherein the fragment is a Fab fragment or a single chain antibody comprising a heavy chain variable domain and a light chain variable domain which are connected by a peptide linker.
4. The fully human antibody fragment of claim 3 , wherein the antibody fragment has a K D of at least 1×10 −6 M.
5. A method of treating cancer in a subject in need thereof, the method comprising administering an effective amount of the antibody of claim 1 , such that the cancer is treated.
6. The method of claim 5 , wherein the cancer is selected from the group consisting of bladder cancer, blood cancer, brain cancer, breast cancer, colon cancer, fibrosarcoma, lung cancer, ovarian cancer, prostate cancer, melanoma, lymphoma, mesothelioma, and plasmacytoma.
7. A method for treating a disease requiring stimulation of an immune response, comprising administering an effective amount of the antibody of claim 1 , such that the disease is treated.
8. A method for treating a disease requiring stimulation of immune responses, comprising administering an effective amount of the antibody fragment of claim 3 , such that the disease is treated.
9. The method of claim 7 , wherein the disease is selected from the group consisting of cancers of the prostate, kidney, colon, lung or breast.
10. The method of claim 8 , wherein the disease is selected from the group consisting of cancers of the prostate, kidney, colon, lung or breast.
11. An isolated anti-CTLA4 antibody, or antigen-binding fragment thereof, comprising complementarity determining regions (CDRs) as set forth in a heavy chain/light chain variable domain sequence of SEQ ID NO. 25/SEQ ID NO. 26, or SEQ ID NO: 43/SEQ ID NO: 44.
12. The antibody, or antigen-binding fragment thereof, of claim 11 , which has a K D of at least 1×10 −6 M.
13. A pharmaceutical composition comprising the anti-CTLA4 antibody, or antigen-binding fragment thereof, of claim 11 , and a pharmaceutically acceptable carrier.
14. A method of treating cancer in a human subject in need thereof, comprising administering an effective amount of the anti-CTLA4 antibody, or antigen-binding fragment thereof, of claim 11 to the subject, such that cancer is treated.
15. The method of claim 14 , wherein the cancer is selected from the group consisting of bladder cancer, blood cancer, brain cancer, breast cancer, colon cancer, fibrosarcoma, lung cancer, ovarian cancer, prostate cancer, melanoma, lymphoma, mesothelioma, and plasmacytoma.