IP Library › Granted Patent US 8,981,065
Granted Patent B2
US 8,981,065 · App. 13/936,486 · Granted Mar 17, 2015

Human anti-KIR antibodies

Inventors: Alessandro Moretta (Genoa, IT); Mariella Della Chiesa (Genoa, IT); Pascale Andre (Marseille, FR); Laurent Gauthier (Marseille, FR); Francois Romagne (La Ciotat, FR); Peter Andreas Nicolai Reumert Wagtmann (Rungsted Kyst, DK); Ivan Svendsen (Smorum, DK); Stefan Zahn (Bagsvaerd, DK); Anders Svensson (Malmo, SE); Matthias Thorolfsson (Charlottenland, DK); Soren Berg Padkaer (Vaerlose, DK); Kristian Kjaergaard (Bagsvaerd, DK); Pieter Johannes Louis Spee (Allerod, DK); Michael Wilken (Hundested, DK)
Assignees: Novo Nordisk A/S—Novo Alle; Innate Pharma S.A.S.; University of Genoa
C07K16/28C07K16/2803C07K2299/00C07K2317/21C07K2317/55C07K2317/56C07K2317/92C07K2317/34
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Quick Facts
Patent No.
US 8,981,065
App. No.
13/936,486
Granted
Mar 17, 2015
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 (37)

1. An isolated human, humanized, or chimeric antibody, or antigen-binding fragment thereof, that binds to each one of human KIR2DL1, human KIR2DL2, and human KIR2DL3, but which does not bind human KIR2DS4, said antibody comprising:

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

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

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

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

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

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

(b) a VL region having the amino acid sequence set forth in SEQ ID NO: 15 and a VH region having the amino acid sequence set forth in SEQ ID NO: 17.

2. The isolated antibody or antigen-binding fragment of claim 1 , which further does not bind to human KIR2DS3.

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

4. The isolated antibody or antigen-binding fragment of claim 1 , which antibody or antigen-binding fragment 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 antibody or antigen-binding fragment of claim 1 , which antibody or antigen-binding fragment 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 antibody or antigen-binding fragment of claim 1 , which antibody or antigen-binding fragment potentiates the lytic activity of an NK cell against a human target cell that expresses a human HLA-C class I molecule.

7. The isolated antibody or antigen-binding fragment of claim 1 , said antibody or antigen-binding fragment comprising:

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

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

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

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

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

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

8. The isolated antibody or antigen-binding fragment of claim 7 , which antibody or antigen-binding fragment is an IgG4 antibody.

9. The isolated antibody or antigen-binding fragment of claim 1 , which antibody or antigen-binding fragment has a dissociation constant (Kd) for human KIR2DL1 of no more than about 0.45 nM.

10. The isolated antibody or antigen-binding fragment of claim 1 , which antibody or antigen-binding fragment has a Kd for human KIR2DL3 of no more than about 0.025 nM.

11. The isolated antibody or antigen-binding fragment of claim 1 , which antibody or antigen-binding fragment is a monoclonal antibody.

12. The isolated antibody or antigen-binding fragment of claim 11 , which antibody or antigen-binding fragment is an IgG1, IgG2, IgG3, or IgG4 antibody.

13. The isolated antibody or antigen-binding fragment of claim 11 , which antibody or antigen-binding fragment is an IgG4 antibody.

14. The isolated antibody or antigen-binding fragment of claim 1 , which antibody or antigen-binding fragment is an IgG4 antibody.

15. A pharmaceutical composition comprising an antibody or antigen-binding fragment of claim 1 in an amount effective to detectably potentiate NK cell cytotoxicity in a patient and a pharmaceutically acceptable carrier or excipient.

16. The pharmaceutical composition of claim 15 , comprising Polysorbate 80, sucrose, or a combination thereof.

17. The composition of claim 15 , wherein the human or humanized antibody or antigen-binding fragment comprises:

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

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

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

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

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

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

18. The composition of claim 15 , wherein the antibody or antigen-binding fragment is an IgG4 antibody.

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 (5)
Division 13347832 · Jan 11, 2012
Division 12244170 · Oct 2, 2008
Continuation 11630176
Provisional Application 60642808 · Jan 11, 2005
Related Publication 20130287770A1 · Oct 31, 2013