IP Library Granted Patent US 7,662,928
Granted Patent B2
US 7,662,928 · App. 11/634,676 · Granted Feb 16, 2010

Anti-FcRn antibodies for treatment of auto/allo immune conditions

Assignee: The Research Foundation of State University of New York
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Quick Facts
Patent No.
US 7,662,928
App. No.
11/634,676
Granted
Feb 16, 2010
Kind
B2
Abstract

Antibodies to heavy chain of human FcRn are provided which function as non-competitive inhibitors of IgG binding to FcRn. The antibodies may be polyclonal, monoclonal, chimeric or humanized, or antigen binding fragments thereof. These antibodies are useful for reducing the concentration of pathogenic IgGs in individuals and therefore used as a therapeutic tool in autoimmune and alloimmune conditions.

Claims (15)

1. An isolated antibody or a fragment thereof which binds to human FcRn, is generated against heavy chain of human FcRn or a fragment thereof, functions as a non-competitive inhibitor of IgG binding to human FcRn and does not bind beta-2-microglobulin, and wherein the antibody or the fragment thereof binds with specificity to a peptide consisting of the sequence GEEFMNFDLKQGT (SEQ ID NO:1).

2. The antibody of claim 1 , wherein the antibody is a murine antibody.

3. The antibody of claim 1 , wherein the antibody is selected from the group consisting of polyclonal and monoclonal.

4. The antibody of claim 1 , wherein the antibody is chimeric or humanized.

5. The antibody fragment of claim 1 , wherein the fragment is selected from the group consisting of Fab, F(ab)′ 2 , Fv and ScFv.

6. The antibody of claim 1 , wherein binding to FcRn is independent of the pH over a pH range of 6.0 to 8.0.

7. The antibody of claim 3 , wherein the antibody is a monoclonal antibody.

8. A method for reducing binding of IgG to FcRn in an individual comprising the steps of

providing an isolated antibody or a fragment thereof which binds to human FcRn, is generated against heavy chain of human FcRn or a fragment thereof, is a non-competitive inhibitor of IgG binding to human FcRn and does not bind beta-2-microglobulin, and wherein the antibody or the fragment thereof binds with specificity to a peptide consisting of the sequence GEEFMNFDLKQGT (SEQ ID NO:1; and

administering the antibody or the fragment thereof to an individual in an amount sufficient to inhibit the binding of IgG to FcRn in the individual.

9. The method of claim 8 , wherein the individual has an autoimmune or alloimmune disease.

10. The method of claim 9 , wherein the autoimmune disease is immune thrombocytopenia.

11. The method of claim 10 , wherein the individual is a human.

12. The method of claim 8 , wherein the antibody is administered at a dosage of 1 mg/kg to 2 g/kg.

13. The method of claim 12 , wherein the antibody is administered at a dosage of 1 mg/kg to 200 mg/kg.

Assignments (3)
CONFIRMATORY LICENSE Recorded Sep 26, 2014
From: STATE UNIVERSITY OF NEW YORK AT BUFFALO
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 033831/0863 →
CONFIRMATORY LICENSE Recorded Aug 17, 2010
From: STATE UNIVERSITY OF NEW YORK AT BUFFALO
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 024845/0683 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 30, 2009
From: BALTHASAR, JOSEPH P.; HANSEN, RYAN J.; JIN, FENG
To: THE RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK
Reel/Frame 022622/0909 →
Continuity (3)
Continuation In Part 1091440300 · Aug 9, 2004
Provisional Application 6076215100 · Jan 25, 2006
Related Publication 20070092507A1 · Apr 26, 2007