IP Library › Granted Patent US 8,119,775
Granted Patent B2
US 8,119,775 · App. 12/244,170 · Granted Feb 21, 2012

Human anti-KIR antibodies

Assignees: University of Genoa; Innate Pharma S.A.S.; Novo Nordisk A/S
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Quick Facts
Patent No.
US 8,119,775
App. No.
12/244,170
Granted
Feb 21, 2012
Kind
B2
Abstract

Compositions and methods for regulating an immune response in a subject are described. More particularly, described are human antibodies that regulate the activity of NK cells and allow a potentiation of NK cell cytotoxicity in mammalian subjects, and antibodies having antigen-binding properties similar to those of human monoclonal antibody 1-7F9 or 1-4F1. Described also are also fragments and derivatives of such antibodies, as well as pharmaceutical compositions comprising the same and their uses, particularly for use in therapy, to increase NK cell activity or cytotoxicity in subjects.

Claims (39)

1. An isolated human antibody that binds to each one of human KIR2DL1, human KIR2DL2, and human KIR2DL3, but which does not bind human KIR2DS4, said human antibody comprising:

(a)(i) a heavy chain CDR1 amino acid sequence corresponding to residues 31-35 of SEQ ID NO:17;

(a)(ii) a heavy chain CDR2 amino acid sequence corresponding to residues 50-65 of SEQ ID NO:17;

(a)(iii) a heavy chain CDR3 amino acid sequence corresponding to residues 99-112 of SEQ ID NO:17;

(a)(iv) a light chain CDR1 amino acid sequence corresponding to residues 24-34 of SEQ ID NO:15;

(a)(v) a light chain CDR2 amino acid sequence corresponding to residues 50-56 of SEQ ID NO:15; and

(a)(vi) a light chain CDR3 amino acid sequence corresponding to residues 89-97 or SEQ ID NO:15; or

(b) a VL region comprising SEQ ID NO: 15 and a VH region comprising SEQ ID NO: 17.

2. The isolated human antibody of claim 1 , which further does not bind to human KIR2DS3.

3. The isolated human antibody of claim 2 , which antibody has a Kd for human KIR2DL3 of no more than about 0.025 nM.

4. The isolated human antibody of claim 1 , which antibody blocks the binding of at least one of human KIR2DL1, human KIR2DL2, and human KIR2DL3 to a human HLA-C class I molecule.

5. The isolated human antibody of claim 1 , which antibody blocks the binding of a human HLA-Cw4 molecule to human KIR2DL1 and the binding of a human HLA-Cw3 molecule to at least one of human KIR2DL2 or human KIR2DL3.

6. The isolated human antibody of claim 1 , which antibody potentiates the lytic activity of an NK cell against a human target cell a human HLA-C class I molecule.

7. The isolated human antibody of claim 1 , said antibody comprising:

(a)(i) a heavy chain CDR1 amino acid sequence corresponding to residues 31-35 of SEQ ID NO:17;

(a)(ii) a heavy chain CDR2 amino acid sequence corresponding to residues 50-65 of SEQ ID NO:17;

(a)(iii) a heavy chain CDR3 amino acid sequence corresponding to residues 99-112 of SEQ ID NO:17;

(a)(iv) a light chain CDR1 amino acid sequence corresponding to residues 24-34 of SEQ ED NO:15;

(a)(v) a light chain CDR2 amino acid sequence corresponding to residues 50-56 of SEQ ID NO:15; and

(a)(vi) a light chain CDR3 amino acid sequence corresponding to residues 89-97 of SEQ ID NO:15.

8. The isolated human antibody of claim 7 , which antibody is an IgG4 antibody.

9. The isolated human antibody of claim 1 , said antibody comprising a VL region comprising SEQ ID NO: 15 and a VH region comprising SEQ ID NO: 17.

10. The isolated human antibody of claim 1 , which antibody has a dissociation constant (Kd) for human KIR2DL1 of no more than about 0.45 nM.

11. The isolated human antibody of claim 1 , which antibody has a Kd for human KIR2DL3 of no more than about 0.025 nM.

12. The isolated human antibody of claim 1 , which antibody is a monoclonal antibody.

13. The isolated human antibody of claim 12 , which antibody is an IgG1, IgG2, IgG3, or IgG4 antibody.

14. The isolated human antibody of claim 13 , which antibody is an IgG4 antibody.

15. The isolated human antibody of claim 1 , which antibody is an IgG4 antibody.

16. A pharmaceutical composition comprising a human antibody of claim 1 in an amount effective to detectably potentiate NK cell cytotoxicity in a patient and a pharmaceutically acceptable carrier or excipient.

17. The pharmaceutical composition of claim 16 , comprising Polysorbatc 80, sucrose, or a combination thereof.

18. The composition of claim 16 , wherein the antibody comprises:

(a)(i) a heavy chain CDR1 amino acid sequence corresponding to residues 31-35 of SEQ ID NO:17;

(a)(ii) a heavy chain CDR2 amino acid sequence corresponding to residues 50-65 of SEQ ID NO:17:

(a)(ii) a heavy chain CDR3 amino acid sequence corresponding to residues 99-112 of SEQ JD NO: 17;

(a)(iv) a light chain CDR1 amino acid sequence corresponding to residues 24-34 of SEQ ID NO:15;

(a)(v) a light chain CDR2 amino acid sequence corresponding to residues 50-56 of SEQ ID NO:15; and

(a)(vi) a light chain CDR3 amino acid sequence corresponding to residues 89-97 of SEQ JD NO:15.

19. The composition of claim 16 , wherein the antibody comprises a VL region comprising SEQ ID NO: 15 and a VH region comprising SEQ ID NO: 17.

20. The composition of claim 16 , wherein the antibody is an IgG4 antibody.

Assignments (1)
SECURITY AGREEMENT Recorded Apr 4, 2012
From: INNATE PHARMA S.A.
To: BRISTOL-MYERS SQUIBB COMPANY
Reel/Frame 027991/0966 →
Priority Claims (3)
WO PCT/DK2004/000470 · Jul 1, 2004 · international
WO PCT/IB2004/002464 · Jul 1, 2004 · international
DK 2005 00025 · Jan 6, 2005 · national
Continuity (3)
Continuation 11630176
Provisional Application 60642808 · Jan 11, 2005
Related Publication 20090081240A1 · Mar 26, 2009