IP Library Granted Patent US 11,013,802
Granted Patent B2
US 11,013,802 · App. 15/834,290 · Granted May 25, 2021

Anti-CTLA-4 antibodies and methods of use thereof

Inventors: Marc van Dijk (Bosch en Duin, NL); Cornelia Anne Mundt (Lörrach, DE); Gerd Ritter (New York, NY); David Schaer (Mamaroneck, NY); Jedd David Wolchok (New York, NY); Taha Merghoub (Jersey City, NJ); Nicholas Stuart Wilson (Medford, MA); David Adam Savitsky (Boxford, MA); Mark Arthur Findeis (Belmont, MA); Dennis John Underwood (Boston, MA); Jean-Marie Cuillerot (Somerville, MA); Igor Proscurshim (Carlisle, MA); Olga Shebanova (Somerville, MA)
Assignees: AGENUS INC.; LUDWIG INSTITUTE FOR CANCER RESEARCH LTD; MEMORIAL SLOAN KETTERING CANCER CENTER
A61K39/39558A61P11/00A61P35/04C07K16/2818A61K2039/505A61K2039/507A61K2039/572C07K2317/21C07K2317/52C07K2317/55C07K2317/732C07K2317/76Y02A50/30
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Quick Facts
Patent No.
US 11,013,802
App. No.
15/834,290
Granted
May 25, 2021
Kind
B2
Abstract

The instant disclosure provides antibodies that specifically bind to CTLA-4 (e.g., human CTLA-4) and antagonize CTLA-4 function. Also provided are pharmaceutical compositions comprising these antibodies, nucleic acids encoding these antibodies, expression vectors and host cells for making these antibodies, and methods of treating a subject using these antibodies.

Claims (51)

1. An isolated polynucleotide encoding a VH, or a VH and a VL, of an antibody that specifically binds to human CTLA-4, wherein the antibody comprises:

(a) CDRH1 comprises the amino acid sequence of SYSMN (SEQ ID NO: 10);

(b) CDRH2 comprises the amino acid sequence of SISSSSSYIYYAXSVKG (SEQ ID NO: 18), wherein X is E or D;

(c) CDRH3 comprises the amino acid sequence of VGLXGPFDI (SEQ ID NO: 19), wherein X is F or M;

(d) CDRL1 comprises the amino acid sequence of RASQSVSRYLG (SEQ ID NO: 15);

(e) CDRL2 comprises the amino acid sequence of GASTRAT (SEQ ID NO: 16); and

(f) CDRL3 comprises the amino acid sequence of QQYGSSPWT (SEQ ID NO: 17), and wherein the CDRH1, CDRH2, and CDRH3 sequences of the antibody are not SEQ ID NOs: 10, 11, and 13, respectively.

2. The isolated polynucleotide of claim 1 , wherein CDRH1, CDRH2, CDRH3, CDRL1, CDRL2, and CDRL3 comprise the amino acid sequences set forth in SEQ ID NOs: 10, 12, 14, 15, 16, and 17, respectively.

3. The isolated polynucleotide of claim 1 , wherein:

(a) the VH comprises an amino acid sequence which is at least 75%, 80%, 85%, 90%, 95%, 99%, or 100% identical to an amino acid sequence selected from the group consisting of SEQ ID NOs: 2, 4, 5, 6, 7 and 8; and/or

(b) the VL comprises an amino acid sequence which is at least 75%, 80%, 85%, 90%, 95%, 99%, or 100% identical to the amino acid sequence of SEQ ID NO: 9.

4. The isolated polynucleotide of claim 1 , wherein the VH and the VL comprise the amino acid sequences set forth in SEQ ID NOs: 2 and 9; 4 and 9; 5 and 9; 6 and 9; 7 and 9; or 8 and 9, respectively.

5. The isolated polynucleotide of claim 1 , wherein the polynucleotide further encodes:

(a) a human IgG 1 heavy chain constant region, optionally wherein the human IgG1 heavy chain constant region is a variant of a wild type human IgG heavy chain constant region, wherein the variant binds to FcγRIIIA with a higher affinity than the wild type human IgG1 heavy chain constant region binds to FcγRIIIA; and/or

(b) a light chain constant region selected from the group consisting of human Igκ and Igλ.

6. The isolated polynucleotide of claim 5 , wherein the amino acid sequence of the IgG 1 heavy chain constant region comprises S239D/A330L/I332E mutations, numbered according to the EU numbering system.

7. The isolated polynucleotide of claim 1 , wherein the polynucleotide encodes:

(a) an antibody heavy chain comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 23, 24, 25, and 26; and/or

(b) an antibody light chain comprising the amino acid sequence of SEQ ID NO: 27.

8. The isolated polynucleotide of claim 1 , wherein the polynucleotide encodes an antibody heavy chain and an antibody light chain comprising the amino acid sequences of SEQ ID NOs: 23 and 27; 24 and 27; 25 and 27; or 26 and 27, respectively.

9. An isolated vector comprising the isolated polynucleotide of claim 1 .

10. A host cell comprising the isolated polynucleotide of claim 1 .

11. A method of producing an antibody that specifically binds to human CTLA-4 comprising culturing the host cell of claim 10 so that the polynucleotide is expressed and the antibody is produced.

12. A host cell comprising:

(a) a first polynucleotide encoding a VH comprising

(i) a CDRH1 comprising the amino acid sequence of SYSMN (SEQ ID NO: 10);

(ii) a CDRH2 comprising the amino acid sequence of SISSSSSYIYYAXSVKG (SEQ ID NO: 18), wherein X is E or D;

(iii) a CDRH3 comprising the amino acid sequence of VGLXGPFDI (SEQ ID NO: 19), wherein X is F or M; and

(b) a second polynucleotide encoding a VL comprising

(i) a CDRL1 comprising the amino acid sequence of RASQSVSRYLG (SEQ ID NO: 15);

(ii) a CDRL2 comprising the amino acid sequence of GASTRAT (SEQ ID NO: 16); and

(iii) a CDRL3 comprising the amino acid sequence of QQYGSSPWT (SEQ ID NO: 17),

and wherein the CDRH1, CDRH2, and CDRH3 sequences are not SEQ ID NOs: 10, 11, and 13, respectively.

13. The host cell of claim 12 , wherein:

(a) the first polynucleotide encodes a VH comprising a CDRH1, CDRH2, CDRH3 comprising the amino acid sequences set forth in SEQ ID NOs: 10, 12, and 14, respectively; and

(a) the second polynucleotide encodes a VL comprising a CDRL1, CDRL2, and CDRL3 comprising the amino acid sequences set forth in SEQ ID NOs: 15, 16, and 17, respectively.

14. The host cell of claim 12 , wherein

(a) the VH comprises an amino acid sequence which is at least 75%, 80%, 85%, 90%, 95%, 99%, or 100% identical to an amino acid sequence selected from the group consisting of SEQ ID NOs: 2, 4, 5, 6, 7 and 8; and/or

(b) the VL comprises an amino acid sequence which is at least 75%, 80%, 85%, 90%, 95%, 99%, or 100% identical to the amino acid sequence of SEQ ID NO: 9.

15. The host cell of claim 12 , wherein the VH and the VL comprise the amino acid sequences set forth in SEQ ID NOs: 2 and 9; 4 and 9; 5 and 9; 6 and 9; 7 and 9; or 8 and 9, respectively.

16. The host cell of claim 12 , wherein:

(a) the first polynucleotide encodes a human IgG 1 heavy chain constant region, optionally wherein the human IgG1 heavy chain constant region is a variant of a wild type human IgG heavy chain constant region, wherein the variant binds to FcγRIIIA with a higher affinity than the wild type human IgG1 heavy chain constant region binds to FcγRIIIA; and/or

(b) the second polynucleotide encodes a light chain constant region selected from the group consisting of human Igκ and Igλ.

17. The host cell of claim 16 , wherein the amino acid sequence of the IgG 1 heavy chain constant region comprises S239D/A330L/I332E mutations, numbered according to the EU numbering system.

18. The host cell of claim 12 , wherein:

(a) the first polynucleotide encodes an antibody heavy chain comprising an amino acid sequence selected from the group consisting of SEQ ID NOs: 23, 24, 25, and 26; and/or

(b) the second polynucleotide encodes an antibody light chain comprising the amino acid sequence of SEQ ID NO: 27.

19. The host cell of claim 12 , wherein the first and second polynucleotides encode the antibody heavy chain and an antibody light chain sequences of SEQ ID NOs: 23 and 27; 24 and 27; 25 and 27; or 26 and 27, respectively.

20. The host cell of claim 12 , wherein the first polynucleotide and the second polynucleotide are comprised within a single vector; or

wherein the first polynucleotide and the second polynucleotide are comprised within separate vectors.

21. A method of producing an antibody that specifically binds to human CTLA-4 comprising culturing the host cell of claim 12 so that the polynucleotide is expressed and the antibody is produced.

Assignments (6)
SECURITY INTEREST Recorded Mar 31, 2025
From: AGENUS, INC.
To: LIGAND PHARMACEUTICALS INCORPORATED
Reel/Frame 070680/0634 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 9, 2018
From: SCHAER, DAVID; WOLCHOK, JEDD DAVID; MERGHOUB, TAHA
To: MEMORIAL SLOAN KETTERING CANCER CENTER
Reel/Frame 046602/0273 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 8, 2018
From: RITTER, GERD
To: LUDWIG INSTITUTE FOR CANCER RESEARCH LTD
Reel/Frame 046589/0338 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 27, 2018
From: WILSON, NICHOLAS STUART; SAVITSKY, DAVID ADAM; FINDEIS, MARK ARTHUR; UNDERWOOD, DENNIS JOHN; CUILLEROT, JEAN-MARIE; PROSCURSHIM, IGOR; SHEBANOVA, OLGA
To: AGENUS INC.
Reel/Frame 046488/0706 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 27, 2018
From: VAN DIJK, MARC; MUNDT, CORNELIA ANNE
To: AGENUS SWITZERLAND INC.
Reel/Frame 046488/0720 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 27, 2018
From: AGENUS SWITZERLAND INC.
To: AGENUS INC.
Reel/Frame 046488/0743 →
Continuity (2)
Provisional Application 62431272 · Dec 7, 2016
Related Publication 20180185481A1 · Jul 5, 2018
Cited By (3)
US 12,415,857 US 12,448,451 US 12,492,257