IP Library Granted Patent US 8,734,791
Granted Patent B2
US 8,734,791 · App. 13/406,347 · Granted May 27, 2014

Optimized fc variants and methods for their generation

Inventors: Gregory Alan Lazar (Alhambra, CA); Arthur J. Chirino (Camarillo, CA); Wei Dang (Pasadena, CA); John R. Desjarlais (Pasadena, CA); Stephen K. Doberstein (San Francisco, CA); Robert J. Hayes (Radnor, PA); Sher Bahadur Karki (Pasadena, CA); Omid Vafa (Monrovia, CA)
Assignee: Xencor, Inc.
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Quick Facts
Patent No.
US 8,734,791
App. No.
13/406,347
Granted
May 27, 2014
Kind
B2
Abstract

The present invention relates to optimized Fc variants, methods for their generation, and antibodies and Fc fusions comprising optimized Fc variants.

Claims (11)

1. A method of decreasing antibody-dependent cell-mediated cytotoxicity (ADCC) in a human comprising administering to a human a composition comprising a variant antibody of a human parent antibody which variant mediates antibody-dependent cell-mediated cytotoxicity (ADCC) in the presence of human peripheral blood mononuclear cells less effectively than the parent antibody, wherein said variant antibody comprises an amino acid substitution at position 328 in the Fc region, wherein numbering is according to the EU index.

2. The method of claim 1 , wherein said amino acid substitution is selected from the group consisting of 328A, 328E, 328F, 328H, 328M, 328N, and 328Q.

3. The method of claim 1 , wherein said amino acid substitution is 328F.

4. The method of claim 1 , wherein said variant antibody is a variant IgG antibody.

5. The method of claim 4 , wherein said variant IgG antibody is a variant IgG1 antibody.

6. The method of claim 1 , wherein said variant antibody is selected from the group consisting of a human antibody, a humanized antibody, and a monoclonal antibody.

7. The method of claim 6 , wherein said variant antibody is a humanized antibody.

8. The method of claim 1 , wherein said variant antibody comprises an engineered glycoform.

9. The method of claim 1 , wherein said variant antibody has specificity for a target antigen selected from the group consisting of CD19, CD20, CD22, CD30, CD33, CD40, CD40L, CD52, Her2/neu, EGFR, EpCAM, MUC1, GD3, CEA, CA 125, IgE, HLA-DR, TNF-alpha, MUC18, prostate specific membrane antigen (PMSA), VEGF, CTLA-4, IL-6, IL-6R, CD3, C5, FGFR-3, and IgE.

10. The method of claim 9 , wherein said variant antibody has specificity for the target antigen CD 19.

11. A method of decreasing antibody-dependent cell-mediated cytotoxicity (ADCC) in a human comprising administering to a human a composition comprising a variant antibody of a human parent antibody which variant mediates antibody-dependent cell-mediated cytotoxicity (ADCC) in the presence of human peripheral blood mononuclear cells less effectively than the parent antibody, wherein said variant antibody comprises an amino acid substitution 328F in the Fc region, wherein numbering is according to the EU index.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 14, 2014
From: LAZAR, GREGORY ALAN; DESJARLAIS, JOHN RUDOLF; MARSHALL, SHANNON ALICIA; DAHIYAT, BASSIL I.
To: XENCOR, INC.
Reel/Frame 032669/0963 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 29, 2014
From: LAZAR, GREGORY ALAN; CHIRINO, ARTHUR J.; DANG, WEI; DESJARLAIS, JOHN R.; DOBERSTEIN, STEPHEN KOHL; HAYES, ROBERT J.; KARKI, SHER BAHADUR; VAFA, OMID
To: XENCOR, INC.
Reel/Frame 032079/0036 →
Continuity (11)
Continuation 11927444 · Oct 29, 2007
Continuation 10822231 · Mar 26, 2004
Continuation In Part 10672280 · Sep 26, 2003
Continuation In Part 10379392 · Mar 3, 2003
Provisional Application 60477839 · Jun 12, 2003
Provisional Application 60467606 · May 2, 2003
Provisional Application 60442301 · Jan 23, 2003
Provisional Application 60414433 · Sep 27, 2002
Provisional Application 60384197 · May 29, 2002
Provisional Application 60360843 · Mar 1, 2002
Related Publication 20130058919A1 · Mar 7, 2013