Anti-complement C1s antibodies
The present disclosure provides antibodies that bind complement C1s protein; and nucleic acid molecules that encode such antibodies. In some embodiments, such anti-complement C1s antibodies inhibit proteolytic activity of C1s. The present disclosure also provides compositions comprising such antibodies, and methods to produce and use such antibodies, nucleic acid molecules, and compositions.
1. A humanized antibody that binds complement C1s protein and comprises:
a light chain variable region that comprises a CDR-L1 amino acid sequence set forth in SEQ ID NO: 9, a CDR-L2 amino acid sequence set forth in SEQ ID NO: 10, and a CDR-L3 amino acid sequence set forth in SEQ ID NO: 11;
a heavy chain variable region that comprises a CDR-H1 amino acid sequence set forth in SEQ ID NO: 12, a CDR-H2 amino acid sequence set forth in SEQ ID NO: 13, and a CDR-H3amino acid sequence set forth in SEQ ID NO: 14; and
a human Fc region.
2. The humanized antibody of claim 1 , wherein the human Fc region is a human IgG Fc region.
3. The humanized antibody of claim 2 , wherein the human IgG Fc region is a human IgG4 Fc region.
4. A pharmaceutical composition comprising the humanized antibody of claim 1 .
5. The pharmaceutical composition of claim 4 further comprising a pharmaceutically-acceptable carrier, diluent, or excipient.
6. A humanized antibody that binds complement C1s protein and comprises:
a CDR-L1 sequence, a CDR-L2sequence, and a CDR-L3 sequence of an antibody light chain variable region that comprises the amino acid sequence set forth in SEQ ID NO: 15;
a CDR-H1 sequence, a CDR-H2 sequence, and a CDR-H3 sequence of an antibody heavy chain variable region that comprises the amino acid sequence set forth in SEQ ID NO: 16; and
a human Fc region.
7. The humanized antibody of claim 6 , wherein the human Fc region is a human IgG Fc region.
8. The humanized antibody of claim 7 , wherein the human IgG Fc region is a human IgG4 Fc region.
9. A pharmaceutical composition comprising the humanized antibody of claim 6 .
10. The pharmaceutical composition of claim 9 further comprising a pharmaceutically-acceptable carrier, diluent, or excipient.