IP Library Granted Patent US 11,053,315
Granted Patent B2
US 11,053,315 · App. 15/945,779 · Granted Jul 6, 2021

Anti-ILT4 antibodies and antigen-binding fragments

Inventors: Barbara Joyce-Shaikh (San Jose, CA); Luis A. Zuniga (Palo Alto, CA); Milan Blanusa (Jena, IE); Andrea Claudia Schuster (Jena, DE); Kornelia Schultze (Jena, DE)
Assignees: Merck Sharp & Dohme Corp.; Agenus Inc.
C07K16/2803A61P35/00C07K16/2818C07K16/2896A61K2039/505C07K2317/21C07K2317/33C07K2317/56C07K2317/565C07K2317/76C07K2317/92
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Quick Facts
Patent No.
US 11,053,315
App. No.
15/945,779
Granted
Jul 6, 2021
Kind
B2
Abstract

The present invention provides antibodies and antigen-binding fragments thereof that bind to ILT4 (immunoglobulin-like transcript 4) and combinations thereof, e.g., with an anti-PD1 antibody. Also provided are methods of use thereof, for example, for treating or preventing cancer in a subject; and methods of making such antibodies and fragments.

Claims (27)

1. An antibody or antigen-binding fragment thereof that binds human ILT4, comprising: a heavy chain variable domain comprising: a CDR-H1 having an amino acid sequence of GYYWS (SEQ ID NO: 16), a CDR-H2 having an amino acid sequence of EINHSGSTNYNPSLKS (SEQ ID NO: 47) or EINHAGSTNYNPSLKS (SEQ ID NO: 48), and a CDR-H3 having an amino acid sequence of LPTRWVTTRYFDL (SEQ ID NO: 18); and a light chain variable domain comprising: a CDR-L1 having an amino acid sequence of TGSSSNIGAGYDVH (SEQ ID NO: 19), a CDR-L2 having an amino acid sequence of GNSNRPS(SEQ ID NO: 49), GQSNRPS(SEQ ID NO: 50), GESNRPS(SEQ ID NO: 51), GDSNRPS(SEQ ID NO: 52), GNANRPS(SEQ ID NO: 53), GQANRPS(SEQ ID NO: 54), GEANRPS(SEQ ID NO: 55), or GDANRPS(SEQ ID NO: 56), and a CDR-L3 having an amino acid sequence of QSFDNSLSAYV (SEQ ID NO: 21).

2. The antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody or antigen-binding fragment thereof is glycosylated with CHO N-linked glycans.

3. A pharmaceutical composition comprising the antibody or antigen-binding fragment thereof of claim 1 and a pharmaceutically acceptable carrier.

4. The pharmaceutical composition of claim 3 , further comprising a therapeutic agent.

5. The antibody or antigen-binding fragment thereof of claim 1 , comprising a light chain variable domain comprising an amino acid sequence that is at least 90% identical to the amino acid sequence set forth in SEQ ID NO:58, 70, 71, 72, 73, or 77, and a heavy chain variable domain comprising an amino acid sequence that is at least 90% identical to the amino acid sequence set forth in SEQ ID NO:57, 63, or 69.

6. The antibody or antigen-binding fragment thereof of claim 1 , comprising a light chain variable domain comprising the amino acid sequence set forth in SEQ ID NO:58, 70, 71, 72, 73, or 77, and a heavy chain variable domain comprising the amino acid sequence set forth in SEQ ID NO:57, 63, or 69.

7. The antibody or antigen-binding fragment thereof of claim 1 , comprising a light chain comprising an amino acid sequence that is at least 90% identical to the amino acid sequence set forth in SEQ ID NO:3, 4, 5, 6, 7, or 45, and a heavy chain comprising an amino acid sequence that is at least 90% identical to the amino acid sequence set forth in SEQ ID NO:1, 2, 79, 80, or 81.

8. The antibody or antigen-binding fragment thereof of claim 1 , comprising a light chain comprising the amino acid sequence set forth in SEQ ID NO:3, 4, 5, 6, 7, or 45, and a heavy chain comprising the amino acid sequence set forth in SEQ ID NO:1, 2, 79, 80, or 81.

9. The antibody or antigen-binding fragment thereof of claim 1 , wherein the antibody or antigen-binding fragment thereof is glycosylated with engineered yeast N-linked glycans.

10. The antibody or antigen-binding fragment thereof of claim 1 , comprising a light chain variable domain comprising an amino acid sequence that is at least 90% identical to the amino acid sequence set forth in SEQ ID NO:58, and a heavy chain variable domain comprising an amino acid sequence that is at least 90% identical to the amino acid sequence set forth in SEQ ID NO:57.

11. The antibody or antigen-binding fragment thereof of claim 1 , comprising a light chain comprising an amino acid sequence that is at least 90% identical to the amino acid sequence set forth in SEQ ID NO:7 and a heavy chain comprising an amino acid sequence that is at least 90% identical to the amino acid sequence set forth in SEQ ID NO:2.

12. An antibody that consists of two heavy chains and two light chains, wherein:

each light chain comprises the amino acid sequence set forth in SEQ ID NO:58 and each heavy chain comprises the amino acid sequence set forth in SEQ ID NO:57;

(ii) each light chain comprises the amino acid sequence set forth in SEQ ID NO:58 and each heavy chain comprises the amino acid sequence set forth in SEQ ID NO:57;

wherein the light chain further comprises the amino acid sequence set forth in SEQ ID NO:90 or the heavy chain further comprises the amino acid sequence set forth in SEQ ID NO:89;

(iii) each light chain comprises the amino acid sequence set forth in SEQ ID NO:7 and each heavy chain comprises the amino acid sequence set forth in SEQ ID NO:2; or

(iv) each light chain consists of the amino acid sequence set forth in SEQ ID NO:7 and each heavy chain consists of the amino acid sequence set forth in SEQ ID NO:2.

13. The antibody of claim 12 , wherein each light chain comprises the amino acid sequence set forth in SEQ ID NO:58 and each heavy chain comprises the amino acid sequence set forth in SEQ ID NO:57.

14. A pharmaceutical composition comprising the antibody of claim 13 and a pharmaceutically acceptable carrier.

15. The antibody of claim 12 , wherein each light chain comprises the amino acid sequence set forth in SEQ ID NO:7 and each heavy chain comprises the amino acid sequence set forth in SEQ ID NO:2.

16. The antibody of claim 12 , wherein each light chain consists of the amino acid sequence set forth in SEQ ID NO:7 and each heavy chain consists of the amino acid sequence set forth in SEQ ID NO:2.

17. A pharmaceutical composition comprising the antibody of claim 12 and a pharmaceutically acceptable carrier.

18. A pharmaceutical composition comprising: (i) an antibody that consists of two heavy chains and two light chains, wherein each light chain consists of the amino acid sequence set forth in SEQ ID NO:7 and each heavy chain consists of the amino acid sequence set forth in SEQ ID NO:2, and (ii) an anti-PD-1 antibody.

19. The pharmaceutical composition of claim 18 , wherein the anti-PD-1 antibody is pembrolizumab.

20. The pharmaceutical composition of claim 18 , wherein the anti-PD-1 antibody is nivolumab.

21. An antibody or antigen-binding fragment thereof that binds human ILT4, comprising a heavy chain variable domain comprising: a CDR-H1 having an amino acid sequence of GYYWS (SEQ ID NO: 16), a CDR-H2 having an amino acid sequence of EINHAGSTNYNPSLKS (SEQ ID NO: 48), and a CDR-H3 having an amino acid sequence of LPTRWVTTRYFDL (SEQ ID NO: 18); and a light chain variable domain comprising: a CDR-L1 having an amino acid sequence of TGSSSNIGAGYDVH (SEQ ID NO: 19), a CDR-L2 having an amino acid sequence of GDSNRPS (SEQ ID NO: 52), and a CDR-L3 having an amino acid sequence of QSFDNSLSAYV (SEQ ID NO: 21).

22. A pharmaceutical composition comprising the antibody or antigen-binding fragment thereof of claim 21 and a pharmaceutically acceptable carrier.

Assignments (4)
MERGER Recorded Aug 8, 2022
From: MERCK SHARP & DOHME CORP.
To: MERCK SHARP & DOHME LLC
Reel/Frame 061102/0145 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 28, 2019
From: BLANUSA, MILAN; SCHUSTER, ANDREA CLAUDIA; SCHULTZE, KORNELIA
To: AGENUS SWITZERLAND INC.
Reel/Frame 049292/0839 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 28, 2019
From: AGENUS SWITZERLAND INC.
To: AGENUS INC.
Reel/Frame 049293/0244 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 1, 2018
From: ZUNIGA, LUIS A.; JOYCE-SHAIKH, BARBARA
To: MERCK SHARP & DOHME CORP.
Reel/Frame 045683/0584 →
Continuity (2)
Provisional Application 62483019 · Apr 7, 2017
Related Publication 20180298096A1 · Oct 18, 2018
Cited By (1)
US 12,344,670