Molecules that bind to cd94/nkg2a heterodimer polypeptides
US-2024415889-A1 · Dec 19, 2024 · US
US9353187B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9353187-B2 |
| Application number | US-201313773485-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 21, 2013 |
| Priority date | Sep 27, 2002 |
| Publication date | May 31, 2016 |
| Grant date | May 31, 2016 |
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The present invention relates to optimized Fc variants, methods for their generation, and antibodies and Fc fusions comprising optimized Fc variants.
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We claim: 1. A method of mediating antibody-dependent cell-mediated cytotoxicity (ADCC) in a human comprising administering to a human a composition comprising a variant antibody of a parent antibody which variant mediates antibody-dependent cell-mediated cytotoxicity (ADCC) in the presence of human peripheral blood mononuclear cells more effectively than the parent antibody, wherein said variant comprises a 239D substitution in the Fc region, wherein numbering is according to the EU index. 2. A method of mediating antibody-dependent cell-mediated cytotoxicity (ADCC) in a human comprising administering to a human a composition comprising a variant antibody of a parent antibody which variant mediates antibody-dependent cell-mediated cytotoxicity (ADCC) in the presence of human peripheral blood mononuclear cells more effectively than the parent antibody, wherein said variant comprises a 239E substitution in the Fc region, wherein numbering is according to the EU index. 3. A method according to claim 1 or 2 wherein said variant antibody is a monoclonal antibody. 4. A method according to claim 1 or 2 wherein said variant antibody is a humanized antibody. 5. A method according to claim 1 or 2 wherein said variant antibody is a chimeric antibody. 6. A method according to claim 1 or 2 wherein said antibody binds to CD19. 7. A method according to claim 1 or 2 wherein said antibody binds to IgE. 8. A method according to claim 1 or 2 wherein said parent antibody is a human IgG1. 9. A method according to claim 1 or 2 wherein said variant antibody binds to a target antigen selected from the group consisting of CD20, CD30, CD33, CD37, CD38 and CD3.
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