| CPC C07K 16/30 (2013.01) [A61K 39/395 (2013.01); A61K 40/11 (2025.01); A61K 40/31 (2025.01); A61K 40/42 (2025.01); A61P 1/18 (2018.01); A61P 35/00 (2018.01); C07K 14/7051 (2013.01); C07K 14/70517 (2013.01); C07K 14/70521 (2013.01); C07K 16/44 (2013.01); C12N 15/62 (2013.01); G01N 33/574 (2013.01); G01N 33/57484 (2013.01); G01N 33/6893 (2013.01); A61K 2039/505 (2013.01); C07K 2317/76 (2013.01); C07K 2319/00 (2013.01); C07K 2319/03 (2013.01); C07K 2319/30 (2013.01)] | 16 Claims |
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1. A method for treating rheumatoid arthritis in an individual comprising administering to the individual an effective amount of an antibody that specifically binds to an epitope comprising N-acetylglucosamine or N-acetyl-galactosamine; wherein the antibody comprises a light chain variable region comprising an HVR-L1 sequence of SEQ ID NO: 5, an HVR-L2 sequence of FTSX1LX2S (SEQ ID NO: 25), and an HVR-L3 sequence of SEQ ID NO: 9, wherein X1 is T or S and X2 is Q or E, and wherein the antibody comprises a heavy chain variable region comprising an HVR-H1 sequence of SEQ ID NO: 1, an HVR-H2 sequence of SEQ ID NO: 2, and an HVR-H3 sequence of SEQ ID NO: 3.
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