Interferon alpha antibodies and their uses
View Patent ↗The present invention provides isolated anti-interferon alpha monoclonal antibodies, particularly human monoclonal antibodies, that inhibit the biological activity of multiple interferon (IFN) alpha subtypes but do not substantially inhibit the biological activity of IFN alpha 21 or the biological activity of either IFN beta or IFN omega. Immunoconjugates, bispecific molecules and pharmaceutical compositions comprising the antibodies of the invention are also provided. The invention also provides methods for inhibiting the biological activity of IFN alpha using the antibodies of the invention, as well as methods of treating disease or disorders mediated by IFN alpha, such as autoimmune diseases, transplant rejection and graft versus host disease, by administering the antibodies of the invention.
1. A method of treating systemic lupus erythematosus in a subject in need of treatment comprising administering to the subject an effective amount of an isolated anti-interferon alpha monoclonal antibody, or an antigen binding portion thereof, which binds an epitope on a human interferon alpha polypeptide recognized by an antibody comprising a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 19 and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 22, such that systemic lupus erythematosus in the subject is treated.
2. A method of treating systemic lupus erythematosus in a subject in need of treatment comprising administering to the subject an effective amount of an isolated anti-interferon alpha monoclonal antibody, or antigen binding portion thereof, comprising: (a) a heavy chain variable region comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 19, 34, 35, 36 and 37, and (b) a light chain variable region comprising the amino acid sequence of SEQ ID NO: 22, such that systemic lupus erythematosus in the subject is treated.
3. A method of treating systemic lupus erythematosus in a subject in need of treatment comprising administering to the subject an effective amount of an isolated anti-interferon alpha monoclonal antibody, or antigen binding portion thereof, which comprises: (a) a heavy chain variable region CDR1 comprising SEQ ID NO: 1; (b) a heavy chain variable region CDR2 comprising SEQ ID NO: 4; (c) a heavy chain variable region CDR3 comprising SEQ ID NO: 7; (d) a light chain variable region CDR1 comprising SEQ ID NO: 10; (e) a light chain variable region CDR2 comprising SEQ ID NO: 13; and (f) a light chain variable region CDR3 comprising SEQ ID NO: 16, such that systemic lupus erythematosus in the subject is treated.
4. The method of any one of claim 2 or 3 , wherein the antibody, or antigen binding portion thereof, comprises: (a) a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 19, and (b) a light chain variable region comprising the amino acid sequence of SEQ ID NO: 22.
5. The method of any one of claims 1 , 2 , and 3 , wherein anti-interferon alpha monoclonal antibody, or antigen binding portion thereof, is administered subcutaneously, intramuscularly, intraarterially, intradermally, or intravenously.
6. The method of any one of claims 1 , 2 , and 3 , wherein the anti-interferon alpha monoclonal antibody, or antigen binding portion thereof, further comprises a pharmaceutically acceptable carrier.
7. The method of any one of claims 1 , 2 , and 3 , wherein the antibody, or antigen binding portion thereof, inhibits IFN-induced surface expression of CD38 or MHC Class I on peripheral blood mononuclear cells.
8. The method of any one of claims 1 , 2 , and 3 , wherein the antibody, or antigen binding portion thereof, inhibits IFN-induced expression of IP-10 by peripheral blood mononuclear cells.
9. The method of any one of claims 1 , 2 , and 3 , wherein the antibody, or antigen binding portion thereof, inhibits dendritic cell development mediated by systemic lupus erythematosus (SLE) plasma.
10. The method of any one of claims 1 , 2 , and 3 , wherein the antibody is a human antibody.
11. The method of any one of claims 1 , 2 , and 3 , wherein the antibody is a chimeric antibody.
12. The method of any one of claims 1 , 2 , and 3 , wherein the antibody is a humanized antibody.
13. The method of any one of claims 1 , 2 , and 3 , wherein the antigen binding portion is a Fab antibody fragment.
14. The method of any one of claims 1 , 2 , and 3 , wherein the antigen binding portion is a single chain antibody (scFv).
15. The method of any one of claims 1 , 2 , and 3 , wherein the subject is human.