Humanized FcγRIIB-specific antibodies and methods of use thereof
The present invention relates to humanized FcγRIIB antibodies, fragments, and variants thereof that bind human FcγRIIB with a greater affinity than said antibody binds FcγRIIA. The invention encompasses the use of the humanized antibodies of the invention for the treatment of any disease related to loss of balance of Fc receptor mediated signaling, such as cancer, autoimmune and inflammatory disease. The invention provides methods of enhancing the therapeutic effect of therapeutic antibodies by administering the humanized antibodies of the invention to enhance the effector function of the therapeutic antibodies. The invention also provides methods of enhancing the efficacy of a vaccine composition by administering the humanized antibodies of the invention. The invention encompasses methods for treating an autoimmune disease and methods for elimination of cancer cells that express FcγRIIB.
1. A humanized antibody that comprises a human Fc domain and an antigen-binding domain, wherein said antibody specifically binds the extracellular domain of human FcγRIIB via said antigen-binding domain; wherein said antigen-binding domain comprises a heavy chain variable domain comprising the amino acid sequence of SEQ ID NO:68 and a light chain variable domain comprising the amino acid sequence of SEQ ID NO: 62 or a fragment of said antibody that comprises said antigen-binding domain and specifically binds said extracellular domain of human FcγRIIB via said antigen-binding domain.
2. The fragment of the humanized antibody of claim 1 , wherein said fragment specifically binds said extracellular domain of human FcγRIIB via said antigen-binding domain.
3. The humanized antibody of claim 1 , wherein the Fc domain comprises at least one amino acid modification in the Fc domain.
4. The humanized antibody of claim 3 , wherein the Fc domain comprises a leucine at position 243, a proline at position 292, a leucine at position 300, an isoleucine at position 305, and a leucine at position 396 and wherein said positions are according to Kabat.
5. A pharmaceutical composition comprising (i) a therapeutically effective amount of the humanized antibody of claim 1 ; (ii) a cytotoxic antibody that specifically binds a cancer antigen; and (iii) a pharmaceutically acceptable carrier.