IP Library Granted Patent US 8,552,154
Granted Patent B2
US 8,552,154 · App. 13/120,406 · Granted Oct 8, 2013

Anti-PD-L1 antibodies and uses therefor

Inventors: Gordon J. Freeman (Brookline, MA); Rafi Ahmed (Atlanta, GA); Timothy D. Jones (Cambridgeshire, GB); Francis J. Carr (Aberdeenshire, GB); James P. Gregson (Essex, GB)
Assignees: Emory University; Dana-Farber Cancer Institute, Inc.
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Quick Facts
Patent No.
US 8,552,154
App. No.
13/120,406
Granted
Oct 8, 2013
Kind
B2
Abstract

The present invention is based, in part, on the identification of novel human anti-PD-1, PD-L1, and PD-L2 antibodies. Accordingly, the invention relates to compositions and methods for diagnosing, prognosing, and treating conditions that would benefit from modulating PD-1, PD-L1, and/or PD-L2 activity (e.g., persistent infectious diseases, autoimmune diseases, asthma, transplant rejection, inflammatory disorders and tumors) using the novel human anti-PD-1, PD-L1, and PD-L2 antibodies described herein.

Claims (35)

1. An isolated antibody or antigen-binding fragment thereof, comprising:

a) a heavy chain variable region sequence comprising the three CDRs with the sequences of SEQ ID NOs: 13-15; and/or

b) a light chain variable region sequence comprising the three CDRs with the sequences of SEQ ID NOs:16-18,

wherein the isolated antibody, or antigen-binding fragment thereof, binds to a PD-L1 protein having the amino acid sequence of SEQ ID NO: 4, and the isolated antibody, or antigen-binding fragment thereof, is chimeric, humanized, composite, or human.

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

a) a heavy chain variable region sequence selected from the group consisting of SEQ ID NOs: 34-38, or a sequence with at least about 95% homology to a heavy chain sequence selected from the group consisting of SEQ ID NOs: 34-38; and/or

b) a light chain variable region sequence selected from the group consisting of SEQ ID NOs: 39-42, or a sequence with at least about 95% homology to a light chain sequence selected from the group consisting of SEQ ID NOs: 39-42.

3. The isolated antibody or antigen-binding fragment of claim 2 , comprising:

a) a heavy chain variable region sequence comprising SEQ ID NO: 35 or 37, or a sequence with at least about 95% homology to a heavy chain sequence comprising SEQ ID NO: 35 or 37; and

b) a light chain variable region sequence comprising SEQ ID NO: 39, 40 or 42, or a sequence with at least about 95% homology to a light chain sequence comprising SEQ ID NO: 39, 40 or 42.

4. The isolated antibody or antigen-binding fragment of claim 1 , wherein the isolated antibody or antigen-binding fragment thereof inhibits the binding of an antibody comprising a heavy chain variable region comprising the sequence of SEQ ID NO:78 and a light chain variable region comprising the sequence of SEQ ID NO:79 to Fc-PD-L1.

5. The isolated antibody or antigen-binding fragment of claim 1 , wherein the isolated antibody or antigen-binding fragment thereof inhibits a PD-L1-mediated signal.

6. A pharmaceutical composition, comprising an isolated antibody or antigen-binding fragment thereof and a pharmaceutically-acceptable carrier, wherein the antibody or antigen-binding fragment thereof comprises:

a) a heavy chain variable region sequence comprising the three CDRs with the sequences of SEQ ID NOs: 13-15; and/or

b) a light chain variable region sequence comprising the three CDRs with the sequences of SEQ ID NOs:16-18,

wherein the isolated antibody, or antigen-binding fragment thereof, binds to a PD-L1 protein having the amino acid sequence of SEQ ID NO: 4, and the isolated antibody, or antigen-binding fragment thereof, is chimeric, humanized, composite, or human.

7. A method of producing an antibody or antigen-binding fragment thereof, comprising culturing a cell that produces the antibody or antigen-binding fragment, and recovering the antibody or antigen-binding fragment produced by the cell, wherein the antibody or antigen-binding fragment thereof comprises:

a) a heavy chain variable region sequence comprising the three CDRs with the sequences of SEQ ID NOs: 13-15; and/or

b) a light chain variable region sequence comprising the three CDRs with the sequences of SEQ ID NOs:16-18,

wherein the antibody, or antigen-binding fragment thereof, binds to a PD-L1 protein having the amino acid sequence of SEQ ID NO: 4, and the antibody, or antigen-binding fragment thereof, is chimeric, humanized, composite, or human.

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

a) a heavy chain variable region sequence comprising the three CDRs with the sequences of SEQ ID NOs: 13-15; and

b) a light chain variable region sequence comprising the three CDRs with the sequences of SEQ ID NOs:16-18.

9. The isolated antibody or antigen-binding fragment of claim 8 , comprising:

a) a heavy chain variable region sequence selected from the group consisting of SEQ ID NOs: 34-38, or a sequence with at least about 95% homology to a heavy chain sequence selected from the group consisting of SEQ ID NOs: 34-38; and

b) a light chain variable region sequence selected from the group consisting of SEQ ID NOs: 39-42, or a sequence with at least about 95% homology to a light chain sequence selected from the group consisting of SEQ ID NOs: 39-42.

10. The isolated antibody or antigen-binding fragment of claim 2 , comprising:

a) a heavy chain variable region sequence selected from the group consisting of SEQ ID NOs: 34-38; and/or

b) a light chain variable region sequence selected from the group consisting of SEQ ID NOs: 39-42.

11. The isolated antibody or antigen-binding fragment of claim 10 , comprising:

a) a heavy chain variable region sequence selected from the group consisting of SEQ ID NOs: 34-38; and

b) a light chain variable region sequence selected from the group consisting of SEQ ID NOs: 39-42.

12. The isolated antibody or antigen-binding fragment of claim 11 , comprising:

a) a heavy chain variable region sequence comprising SEQ ID NO: 35 or 37; and

b) a light chain variable region sequence comprising SEQ ID NO: 39, 40 or 42.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 21, 2011
From: ANTITOPE LIMITED
To: DANA-FARBER CANCER INSTITUTE, INC.
Reel/Frame 026161/0661 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 21, 2011
From: FREEMAN, GORDON J.
To: DANA-FARBER CANCER INSTITUTE, INC.
Reel/Frame 026161/0725 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 21, 2011
From: AHMED, RAFI
To: EMORY UNIVERSITY
Reel/Frame 026161/0731 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 21, 2011
From: JONES, TIMOTHY D.; CARR, FRANCIS J.; GREGSON, JAMES P.
To: ANTITOPE LIMITED
Reel/Frame 026161/0752 →
Continuity (2)
Provisional Application 61100534 · Sep 26, 2008
Related Publication 20110271358A1 · Nov 3, 2011