Identification and engineering of antibodies with variant Fc regions and methods of using same
The present invention relates to molecules, particularly polypeptides, more particularly immunoglobulins (e.g., antibodies), comprising a variant Fc region, wherein said variant Fc region comprises at least one amino acid modification relative to a wild-type Fc region, which variant Fc region binds FcγRIIIA and/or FcγRIIA with a greater affinity, relative to a comparable molecule comprising the wild-type Fc region. The molecules of the invention are particularly useful in preventing, treating, or ameliorating one or more symptoms associated with a disease, disorder, or infection. The molecules of the invention are particularly useful for the treatment or prevention of a disease or disorder where an enhanced efficacy of effector cell function (e.g., ADCC) mediated by FcγR is desired, e.g., cancer, infectious disease, and in enhancing the therapeutic efficacy of therapeutic antibodies the effect of which is mediated by ADCC.
1. A method of increasing antibody-dependent cell mediated cytotoxicity (ADCC) activity by administering to a subject an amount of an IgG antibody comprising an antigen binding region and a variant Fc region, wherein said variant Fc region:
(A) differs from a wild-type Fc region by comprising an amino acid modification at position 396, according to the EU index as in Kabat, relative to said wild-type Fc region; and
(B) binds an FcγR with an increased affinity relative to a said wild-type Fc region.
2. The method of claim 1 further comprising the administration of one or more additional cancer therapies.
3. The method of claim 2 , wherein said additional cancer therapy is selected from the group consisting of chemotherapy, radiation therapy, or surgery.
4. The method of claim 1 , wherein said patient is human.
5. The method of claim 1 , wherein said modification at position 396 is a substitution with histidine or a substitution with leucine.
6. The method of claim 5 , wherein said variant Fc region additionally comprises one or more substitutions at position 235, 243, 292, 300 and 305.
7. The method of claim 6 , wherein said modification at position 396 is a substitution with leucine, and wherein said variant Fc region additionally comprises a substitution at position 292 or 305.
8. The method of claim 6 , wherein said cancer antigen is Her2/neu.
9. The method of claim 7 , wherein said cancer antigen is Her2/neu.
10. The method of claim 1 , wherein said method additionally comprises chemotherapy, radiation therapy, or surgery.
11. The method of claim 6 , wherein said method additionally comprises chemotherapy, radiation therapy, or surgery.
12. The method of claim 7 , wherein said method additionally comprises chemotherapy, radiation therapy, or surgery.