IP Library Granted Patent US 8,779,108
Granted Patent B2
US 8,779,108 · App. 13/511,538 · Granted Jul 15, 2014

Targeted binding agents against B7-H1

Inventors: Christophe Queva (Bainbridge Island, WA); Michelle Morrow (Cambridge, GB); Scott Hammond (Gaithersburg, MD); Marat Alimzhanov (Wellesley, MA); John Babcook (Vancouver, CA); Ian Nevin Foltz (Burnaby, CA); Jaspal Singh Kang (Surrey, CA); Laura Sekirov (Burnaby, CA); Melanie Boyle (Cambridge, GB); Matthieu Chodorge (Cambridge, GB); Ross A. Stewart (Cambridge, GB); Kathleen Ann Mulgrew (Gaithersburg, MD)
Assignee: MedImmune, Limited
C07K16/2827C07K2317/70C07K2317/56C07K2317/21C07K2317/76A61K2039/505C07K2317/92C07K2317/33C07K2317/34
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Quick Facts
Patent No.
US 8,779,108
App. No.
13/511,538
Granted
Jul 15, 2014
Kind
B2
Abstract

Human monoclonal antibodies directed against B7-H1 and uses of these antibodies in diagnostics and for the treatment of diseases associated with the activity and/or expression of B7-H1 are disclosed. Additionally, hybridomas or other cell lines expressing such antibodies are disclosed.

Claims (67)

1. An antibody or fragment thereof wherein the antibody binds to the same epitope on the extracellular domain of human B7-H1 as any one of an antibody comprising:

(a) a heavy chain variable domain amino acid sequence encoded by a polynucleotide in a plasmid designated 2.7A4_G which was deposited at the National Collections of Industrial and Marine Bacteria (NCIMB) under deposit number 41598 and a light chain variable domain amino acid sequence encoded by the polynucleotide in a plasmid designated 2.7A4_G which was deposited at the NCIMB under deposit number 41598; or

(b) a heavy chain variable domain amino acid sequence encoded by a polynucleotide in a plasmid designated 2.14H9_G which was deposited at the NCIMB under deposit number 41597 and a light chain variable domain amino acid sequence encoded by the polynucleotide in a plasmid designated 2.14H9_G which was deposited at the NCIMB under deposit number 41597; or

(c) a heavy chain variable domain amino acid sequence encoded by a polynucleotide in a plasmid designated 2.9D10_NG which was deposited at the NCIMB under deposit number 41599 and a light chain variable domain amino acid sequence encoded by the polynucleotide in a plasmid designated 2.9D10_NG which was deposited at the NCIMB under deposit number 41599.

2. The antibody or fragment thereof of claim 1 , wherein the antibody binds an epitope on the extracellular domain of human B7-H1 comprising at least two of the following three amino acid residues of Asp at position 122, Arg at position 125 or Arg at position 113.

3. The antibody or fragment thereof of claim 2 , wherein the antibody exhibits no binding to an epitope comprising Ile at position 54, Ser at position 117, and Ala at position 121 on human B7-H1, as determined by a competition assay.

4. The antibody or fragment thereof of claim 2 , wherein the antibody loses its ability to bind to human B7-H1 if the Arg at position 113 on said human B7-H1 is mutated to an Ala, or to a Tyr, or to a Leu, as determined by a competition assay as compared to binding to wild-type B7-H1.

5. The antibody or fragment thereof of claim 2 , wherein said antibody loses its ability to bind to human B7-H1 if the Arg at position 125 on said human B7-H1 is mutated to an Ala, or to a Gln, or to a Ser, as determined by a competition assay as compared to binding to wild-type B7-H1.

6. The antibody or fragment thereof of claim 2 , wherein said antibody retains its ability to bind to human B7-H1 if the Arg at position 123 on said human B7-H1 is mutated to an Ala, or to a Phe, or to a Thr, as determined by a competition assay as compared to binding to wild-type B7-H1.

7. The antibody or fragment thereof of claim 1 , wherein the antibody binds at least two of the following three amino acid residues of Phe at position 19, Thr at position 20 or Asp at position 122 on human B7-H1.

8. The antibody or fragment thereof of claim 7 , wherein the antibody exhibits no binding to an epitope comprising Ile at position 54, Met at position 115, Ser at position 117, and Ala at position 121 on human B7-H1, as determined by a competition assay as compared to binding to wild-type B7-H1.

9. The antibody or fragment thereof of claim 7 , wherein said antibody loses its ability to bind to human B7-H1 if the Phe at position 19 on said human B7-H1 is mutated to an Ala, or to a Gly, or to a Ser, as determined by a competition assay as compared to binding to wild-type B7-H1.

10. The antibody or fragment thereof claim 7 , wherein said antibody loses its ability to bind to human B7-H1 if the Thr at position 20 on said human B7-H1 is mutated to an Ala, or to a Val, or to a Asp, as determined by a competition assay as compared to binding to wild-type B7-H1.

11. The antibody or fragment thereof claim 7 , wherein said antibody loses its ability to bind to human B7-H1 if the Asp at position 122 on said human B7-H1 is mutated to an Asn, or to a Glu, as determined by a competition assay as compared to binding to wild-type B7-H1.

12. The antibody or fragment thereof of claim 7 , wherein said antibody retains its ability to bind to human B7-H1 if the Arg at position 123 on said human B7-H1 is mutated to an Ala, or to a Phe, or to a Thr, as determined by a competition assay as compared to binding to wild-type B7-H1.

13. The antibody or fragment thereof of claim 1 , wherein said antibody binds human B7-H1 with a Kd of less than 1.0 nM, as determined by BIAcore.

14. The antibody or fragment thereof of claim 13 , wherein said antibody binds human B7-H1 with a Kd of less than 200 pM, as determined by BIAcore.

15. The antibody or fragment thereof of claim 1 , wherein said antibody is a monoclonal antibody.

16. The antibody or fragment thereof of claim 15 , wherein said antibody is a fully human monoclonal antibody.

17. The antibody of claim 1 , wherein said antibody is a binding fragment selected from the group consisting of a Fab, Fab′, F(ab′) 2 , Fv and dAb fragment.

18. An antibody or fragment thereof having an amino acid sequence comprising:

a heavy chain variable domain amino acid sequence encoded by a polynucleotide in a plasmid designated 2.7A4_G which was deposited at the National Collections of Industrial and Marine Bacteria (NCIMB) under deposit number 41598 and a light chain variable domain amino acid sequence encoded by the polynucleotide in a plasmid designated 2.7A4_G which was deposited at the NCIMB under deposit number 41598; or

a heavy chain variable domain amino acid sequence encoded by a polynucleotide in a plasmid designated 2.14H9_G which was deposited at the NCIMB under deposit number 41597 and a light chain variable domain amino acid sequence encoded by the polynucleotide in a plasmid designated 2.14H9_G which was deposited at the NCIMB under deposit number 41597; or

a heavy chain variable domain amino acid sequence encoded by a polynucleotide in a plasmid designated 2.9D10_NG which was deposited at the NCIMB under deposit number 41599 and a light chain variable domain amino acid sequence encoded by the polynucleotide in a plasmid designated 2.9D10_NG which was deposited at the NCIMB under deposit number 41599.

19. The antibody or fragment thereof of claim 1 having an amino acid sequence comprising:

a VH CDR1 having the amino acid sequence of SEQ ID NO: 3; and

a VH CDR2 having the amino acid sequence of SEQ ID NO: 4; and

a VH CDR3 having the amino acid sequence of SEQ ID NO: 5; and

a VL CDR1 having the amino acid sequence of SEQ ID NO: 8; and

a VL CDR2 having the amino acid sequence of SEQ ID NO: 9; and

a VL CDR3 having the amino acid sequence of SEQ ID NO: 10; or

a VH CDR1 having the amino acid sequence of SEQ ID NO: 23; and

a VH CDR2 having the amino acid sequence of SEQ ID NO: 24; and

a VH CDR3 having the amino acid sequence of SEQ ID NO: 25; and

a VL CDR1 having the amino acid sequence of SEQ ID NO: 28; and

a VL CDR2 having the amino acid sequence of SEQ ID NO: 29; and

a VL CDR3 having the amino acid sequence of SEQ ID NO: 30; or

a VH CDR1 having the amino acid sequence of SEQ ID NO: 13; and

a VH CDR2 having the amino acid sequence of SEQ ID NO: 14; and

a VH CDR3 having the amino acid sequence of SEQ ID NO: 15; and

a VL CDR1 having the amino acid sequence of SEQ ID NO: 18; and

a VL CDR2 having the amino acid sequence of SEQ ID NO: 19; and

a VL CDR3 having the amino acid sequence of SEQ ID NO: 20; or

a VH CDR1 having the amino acid sequence of SEQ ID NO: 63; and

a VH CDR2 having the amino acid sequence of SEQ ID NO: 64; and

a VH CDR3 having the amino acid sequence of SEQ ID NO: 65; and

a VL CDR1 having the amino acid sequence of SEQ ID NO: 68; and

a VL CDR2 having the amino acid sequence of SEQ ID NO: 69; and

a VL CDR3 having the amino acid sequence of SEQ ID NO: 70; or

a VH CDR1 having the amino acid sequence of SEQ ID NO: 73; and

a VH CDR2 having the amino acid sequence of SEQ ID NO: 74; and

a VH CDR3 having the amino acid sequence of SEQ ID NO: 75; and

a VL CDR1 having the amino acid sequence of SEQ ID NO: 78; and

a VL CDR2 having the amino acid sequence of SEQ ID NO: 79; and

a VL CDR3 having the amino acid sequence of SEQ ID NO: 80.

20. The antibody or fragment thereof of claim 18 , wherein said antibody further comprises an Fc variant, wherein the Fc region comprises at least one amino acid selected from the group consisting of 234F, 235F, and 331S, as numbered by the EU index as set forth in Kabat.

21. A nucleic acid molecule encoding the antibody of claim 20 .

22. A cultured host cell transfected with a vector comprising the nucleic acid molecule of claim 21 .

23. An antibody produced by a method comprising, culturing said host cell of claim 22 , wherein said host cell expresses the antibody.

24. A composition comprising the antibody of claim 1 .

25. A pharmaceutical composition comprising the antibody of claim 1 and a pharmaceutically acceptable carrier.

26. A method of repressing B7-H1-mediated T cell inhibition in an animal comprising, administering to an animal in need thereof an effective amount of the composition of claim 24 .

27. The method of claim 26 , wherein said animal is human.

28. A purified antibody or antibody fragment, wherein the antibody or the fragment immunospecifically binds B7-H1 and comprises a heavy chain variable domain having at least 90% identity to the amino acid of SEQ ID NO:72 and comprises a light chain variable domain having at least 90% identity to the amino acid sequence of SEQ ID NO:77, wherein said antibody has the activity of binding to B7-H1.

29. A composition comprising the antibody of claim 28 .

30. A pharmaceutical composition comprising the antibody of claim 28 and a pharmaceutically acceptable carrier.

31. A method of repressing B7-H1-mediated T cell inhibition in an animal comprising, administering to an animal in need thereof an effective amount of the composition of claim 29 .

Assignments (7)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 4, 2012
From: AMGEN BRITISH COLUMBIA
To: MEDIMMUNE LIMITED
Reel/Frame 029075/0460 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 4, 2012
From: MEDIMMUNE LLC
To: MEDIMMUNE LIMITED
Reel/Frame 029075/0499 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 4, 2012
From: ASTRAZENECA AB
To: MEDIMMUNE LIMITED
Reel/Frame 029075/0521 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 30, 2012
From: MORROW, MICHELLE; BOYLE, MELANIE; CHODORGE, MATTHIEU; STEWART, ROSS A.
To: MEDIMMUNE LIMITED
Reel/Frame 028874/0777 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 30, 2012
From: QUEVA, CHRISTOPHE; BABCOOK, JOHN; FOLTZ, IAN; SEKIROV, LAURA; KANG, JASPAL SINGH
To: AMGEN BRITISH COLUMBIA
Reel/Frame 028876/0194 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 30, 2012
From: HAMMOND, SCOTT; MULGREW, KATHLEEN ANN
To: MEDIMMUNE, LLC
Reel/Frame 028874/0919 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 30, 2012
From: ALIMZHANOV, MARAT
To: ASTRAZENECA AB
Reel/Frame 028875/0103 →
Continuity (2)
Provisional Application 61264061 · Nov 24, 2009
Related Publication 20130034559A1 · Feb 7, 2013