IP Library Granted Patent US 11,084,880
Granted Patent B2
US 11,084,880 · App. 16/197,565 · Granted Aug 10, 2021

Anti-BCMA chimeric antigen receptor

Inventors: Jennifer Brogdon (Sudbury, MA); Eugene Choi (Cambridge, MA); Hilmar Erhard Ebersbach (Basel, CH); David Jonathan Glass (Cambridge, MA); Heather Huet (Arlington, MA); Carl H. June (Merion Station, PA); Joan Mannick (Cambridge, MA); Michael C. Milone (Cherry Hill, NJ); Leon Murphy (Cambridge, MA); Gabriela Plesa (Blue Bell, PA); Celeste Richardson (Cambridge, MA); Marco Ruella (Ardmore, PA); Reshma Singh (Cambridge, MA); Yongqiang Wang (Shanghai, CN); Qilong Wu (Shanghai, CN)
Assignees: Novartis AG; The Trustees of the University of Pennsylvania
C07K16/2878C07K14/7051C07K16/28C07K19/00A61K35/12A61K38/177A61K39/395A61K39/3955A61K39/39558A61P35/00C07H21/04C07K14/705C07K14/7151C07K2317/24C07K2317/565C07K2317/622C07K2317/92C07K2319/00C07K2319/03C07K2319/30C07K2319/33C07K2319/70C12N5/00C12N15/63
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Quick Facts
Patent No.
US 11,084,880
App. No.
16/197,565
Granted
Aug 10, 2021
Kind
B2
Abstract

The invention provides compositions and methods for treating diseases associated with expression of BCMA. The invention also relates to chimeric antigen receptor (CAR) specific to BCMA vectors encoding the same, and recombinant T cells comprising the BCMA CAR. The invention also includes methods of administering a genetically modified T cell expressing a CAR that comprises a BCMA binding domain.

Claims (64)

1. An isolated chimeric antigen receptor (CAR) polypeptide, wherein the CAR polypeptide comprises an antibody or antibody fragment which comprises an anti-B-cell maturation antigen (BCMA) binding domain, a transmembrane domain, and an intracellular signaling domain, wherein said anti-BCMA binding domain comprises:

(i) a heavy chain complementary determining region 1 (HC CDR1) comprising the amino acid sequence of SEQ ID NO: 394, a heavy chain complementary determining region 2 (HC CDR2) comprising the amino acid sequence of SEQ ID NO: 434, a heavy chain complementary determining region 3 (HC CDR3) comprising the amino acid sequence of SEQ ID NO: 474, a light chain complementary determining region 1 (LC CDR1) comprising the amino acid sequence of SEQ ID NO: 514, a light chain complementary determining region 2 (LC CDR2) comprising the amino acid sequence of SEQ ID NO: 554, and a light chain complementary determining region 3 (LC CDR3) comprising the amino acid sequence of SEQ ID NO: 594;

(ii) a HC CDR1 comprising the amino acid sequence of SEQ ID NO: 634, a HC CDR2 comprising the amino acid sequence of SEQ ID NO: 674, a HC CDR3 comprising the amino acid sequence of SEQ ID NO: 714, a LC CDR1 comprising the amino acid sequence of SEQ ID NO: 754, a LC CDR2 comprising the amino acid sequence of SEQ ID NO: 794, and a LC CDR3 comprising the amino acid sequence of SEQ ID NO: 834; or

(iii) a HC CDR1 comprising the amino acid sequence of SEQ ID NO: 874, a HC CDR2 comprising the amino acid sequence of SEQ ID NO: 914, a HC CDR3 comprising the amino acid sequence of SEQ ID NO: 954, a LC CDR1 comprising the amino acid sequence of SEQ ID NO: 994, a LC CDR2 comprising the amino acid sequence of SEQ ID NO: 1034, and a LC CDR3 comprising the amino acid sequence of SEQ ID NO: 1074; and

wherein the intracellular signaling domain comprises a primary signaling domain comprising a functional signaling domain of CD3 zeta or an amino acid sequence with 95-99% identity thereof.

2. The isolated CAR polypeptide of claim 1 , comprising:

(i) the amino acid sequence of a light chain variable region comprising the amino acid sequence of SEQ ID NO: 94;

(ii) an amino acid sequence having at least one, two or three modifications but not more than 30, 20, or 10 modifications of the amino acid sequence of a light chain variable region comprising the amino acid sequence of SEQ ID NO: 94; or

(iii) an amino acid sequence with at least 95% identity to the amino acid sequence of a light chain variable region comprising the amino acid sequence of SEQ ID NO: 94.

3. The isolated CAR polypeptide of claim 1 , comprising:

(i) the amino acid sequence of a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 79;

(ii) an amino acid sequence having at least one, two or three modifications but not more than 30, 20, or 10 modifications of the amino acid sequence of a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 79; or

(iii) an amino acid sequence with at least 95% identity to the amino acid sequence of a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 79.

4. The isolated CAR polypeptide of claim 1 , comprising the amino acid sequence of a light chain variable region comprising the amino acid sequence of SEQ ID NO: 94, and the amino acid sequence of a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 79.

5. The isolated CAR polypeptide of claim 1 , comprising:

(i) the amino acid sequence of SEQ ID NO: 49;

(ii) an amino acid sequence having at least one, two or three modifications but not more than 30, 20, or 10 modifications to SEQ ID NO: 49; or

(iii) an amino acid sequence with at least 95% identity to SEQ ID NO: 49.

6. The isolated CAR polypeptide of claim 1 , wherein the transmembrane domain comprises a transmembrane domain from a protein selected from the group consisting of the alpha, beta or zeta chain of the T-cell receptor, CD28, CD3 epsilon, CD45, CD4, CD5, CD8, CD9, CD16, CD22, CD33, CD37, CD64, CD80, CD86, CD134, CD137, and CD154.

7. The isolated CAR polypeptide of claim 1 , wherein the transmembrane domain comprises:

(i) the amino acid sequence of SEQ ID NO: 6;

(ii) an amino acid sequence having at least one, two or three modifications but not more than 20, 10, or 5 modifications of the amino acid sequence of SEQ ID NO: 6; or

(iii) a sequence with at least 95% identity to the amino acid sequence of SEQ ID NO: 6.

8. The isolated CAR polypeptide of claim 1 , wherein the anti-BCMA binding domain is connected to the transmembrane domain by a hinge region.

9. The isolated CAR polypeptide of claim 8 , wherein the hinge region comprises the amino acid sequence of SEQ ID NO: 2 or SEQ ID NO: 36, or a sequence with at least 95% identity thereto.

10. The isolated CAR polypeptide of claim 1 , wherein the intracellular signaling domain comprises a costimulatory domain, wherein the costimulatory domain comprises a functional signaling domain derived from a protein selected from the group consisting of MHC class I molecule, TNF receptor proteins, Immunoglobulin-like proteins, cytokine receptors, integrins, signaling lymphocytic activation molecules (SLAM proteins), activating NK cell receptors, BTLA, a Toll ligand receptor, OX40, CD2, CD7, CD27, CD28, CD30, CD40, CDS, ICAM-1, 4-1BB (CD137), B7-H3, ICOS (CD278), GITR, BAFFR, LIGHT, HVEM (LIGHTR), KIRDS2, SLAMF7, NKp80 (KLRF1), NKp44, NKp30, NKp46, CD19, CD4, CD8alpha, CD8beta, IL2R beta, IL2R gamma, IL7R alpha, ITGA4, VLA1, CD49a, ITGA4, IA4, CD49D, ITGA6, VLA-6, CD49f, ITGAD, CD11d, ITGAE, CD103, ITGAL, CD11a, LFA-1, ITGAM, CD11b, ITGAX, CD11c, ITGB1, CD29, ITGB2, CD18, ITGB7, NKG2D, NKG2C, TNFR2, TRANCE/RANKL, DNAM1 (CD226), SLAMF4 (CD244, 2B4), CD84, CD96 (Tactile), CEACAM1, CRTAM, Ly9 (CD229), CD160 (BY55), PSGL1, CD100 (SEMA4D), CD69, SLAMF6 (NTB-A, Ly108), SLAM (SLAMF1, CD150, IPO-3), BLAME (SLAMF8), SELPLG (CD162), LTBR, LAT, GADS, SLP-76, PAG/Cbp, CD19a, and a ligand that specifically binds with CD83.

11. The isolated CAR polypeptide of claim 1 , wherein the intracellular signaling domain comprises a costimulatory domain, wherein the costimulatory domain comprises the amino acid sequence of SEQ ID NO: 7, or a sequence with at least 95% identity to the amino acid sequence of SEQ ID NO: 7.

12. The isolated CAR polypeptide of claim 1 , wherein the intracellular signaling domain comprises a functional signaling domain of 4-1BB and/or a functional signaling domain of CD3 zeta.

13. The isolated CAR polypeptide of claim 1 , wherein the intracellular signaling domain comprises the amino acid sequence of SEQ ID NO: 7 and/or the amino acid sequence of SEQ ID NO: 9 or SEQ ID NO: 10, or a sequence with 95-99% identity to the amino acid sequence of SEQ ID NO: 7 and/or the amino acid sequence of SEQ ID NO: 9 or SEQ ID NO: 10.

14. The isolated CAR polypeptide of claim 1 , wherein the intracellular signaling domain comprises the amino acid sequence of SEQ ID NO: 7 and the amino acid sequence of SEQ ID NO: 9 or SEQ ID NO: 10, wherein the sequences comprising the intracellular signaling domain are expressed in the same frame and as a single polypeptide chain.

15. The isolated CAR polypeptide of claim 1 , further comprising a leader sequence which comprises the amino acid sequence of SEQ ID NO: 1.

16. The isolated CAR polypeptide of claim 1 , comprising:

(i) the amino acid sequence of SEQ ID NO: 109;

(ii) an amino acid sequence having at least one, two, or three modifications but not more than 30, 20, or 10 modifications to SEQ ID NO: 109; or

(iii) an amino acid sequence with at least 95% identity to SEQ ID NO: 109,

with or without a leader sequence comprising the amino acid sequence of SEQ ID NO: 1.

17. The isolated CAR polypeptide of claim 1 , wherein the intracellular signaling domain comprises a primary signaling domain, wherein the primary signaling domain comprises the amino acid sequence of SEQ ID NO: 9 or SEQ ID NO: 10, or a sequence with at least 95%-99% identity to the amino acid sequence of SEQ ID NO: 9 or SEQ ID NO: 10.

18. An isolated chimeric antigen receptor (CAR) polypeptide, wherein the CAR polypeptide comprises, from N-terminus to C-terminus:

an anti-B-cell maturation antigen (BCMA) binding domain comprising the amino acid sequence of SEQ ID NO: 49,

a transmembrane domain comprising the amino acid sequence of SEQ ID NO: 6,

a costimulatory domain comprising the amino acid sequence of SEQ ID NO: 7, and

a primary signaling domain comprising the amino acid sequence of SEQ ID NO: 9.

19. An isolated chimeric antigen receptor (CAR) polypeptide, wherein the CAR polypeptide comprises an anti-B-cell maturation antigen (BCMA) binding domain, a transmembrane domain, and an intracellular signaling domain, wherein the CAR polypeptide comprises the amino acid sequence of SEQ ID NO: 109 without a leader sequence comprising the amino acid sequence of SEQ ID NO: 1.

20. An anti-B-cell maturation antigen (BCMA) binding domain comprising:

(i) a heavy chain complementary determining region 1 (HC CDR1) comprising the amino acid sequence of SEQ ID NO: 394, a heavy chain complementary determining region 2 (HC CDR2) comprising the amino acid sequence of SEQ ID NO: 434, a heavy chain complementary determining region 3 (HC CDR3) comprising the amino acid sequence of SEQ ID NO: 474, a light chain complementary determining region 1 (LC CDR1) comprising the amino acid sequence of SEQ ID NO: 514, a light chain complementary determining region 2 (LC CDR2) comprising the amino acid sequence of SEQ ID NO: 554, and a light chain complementary determining region 3 (LC CDR3) comprising the amino acid sequence of SEQ ID NO: 594;

(ii) a HC CDR1 comprising the amino acid sequence of SEQ ID NO: 634, a HC CDR2 comprising the amino acid sequence of SEQ ID NO: 674, a HC CDR3 comprising the amino acid sequence of SEQ ID NO: 714, a LC CDR1 comprising the amino acid sequence of SEQ ID NO: 754, a LC CDR2 comprising the amino acid sequence of SEQ ID NO: 794, and a LC CDR3 comprising the amino acid sequence of SEQ ID NO: 834; or

(iii) a HC CDR1 comprising the amino acid sequence of SEQ ID NO: 874, a HC CDR2 comprising the amino acid sequence of SEQ ID NO: 914, a HC CDR3 comprising the amino acid sequence of SEQ ID NO: 954, a LC CDR1 comprising the amino acid sequence of SEQ ID NO: 994, a LC CDR2 comprising the amino acid sequence of SEQ ID NO: 1034, and a LC CDR3 comprising the amino acid sequence of SEQ ID NO: 1074.

21. The anti-BCMA binding domain of claim 20 , comprising:

(i) the amino acid sequence of a light chain variable region comprising the amino acid sequence of SEQ ID NO: 94;

(ii) an amino acid sequence having at least one, two or three modifications but not more than 30, 20 or 10 modifications of the amino acid sequence of a light chain variable region comprising the amino acid sequence of SEQ ID NO: 94;

(iii) an amino acid sequence with at least 95% identity to the amino acid sequence of a light chain variable region comprising the amino acid sequence of SEQ ID NO: 94;

(iv) the amino acid sequence of a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 79;

(v) an amino acid sequence having at least one, two or three modifications but not more than 30, 20 or 10 modifications of the amino acid sequence of a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 79; or

(vi) an amino acid sequence with at least 95% identity to the amino acid sequence of a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 79.

22. The anti-BCMA binding domain of claim 20 , comprising the amino acid sequence of a light chain variable region comprising the amino acid sequence of SEQ ID NO: 94, and the amino acid sequence of a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 79.

23. The anti-BCMA binding domain of claim 20 , comprising:

(i) the amino acid sequence of SEQ ID NO: 49;

(ii) an amino acid sequence having at least one, two or three modifications but not more than 30, 20, or 10 modifications to SEQ ID NO: 49; or

(iii) an amino acid sequence with at least 95% identity to SEQ ID NO: 49.

24. An isolated chimeric antigen receptor (CAR) polypeptide, wherein the CAR polypeptide comprises, from N-terminus to C-terminus:

an anti-B-cell maturation antigen (BCMA) binding domain comprising the amino acid sequence of SEQ ID NO: 49,

a transmembrane domain comprising the amino acid sequence of SEQ ID NO: 6,

a costimulatory domain comprising the amino acid sequence of SEQ ID NO: 7, and

a primary signaling domain comprising the amino acid sequence of SEQ ID NO: 10.

Assignments (10)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2019
From: WU, QILONG
To: CHINA NOVARTIS INSTITUTES FOR BIOMEDICAL RESEARCH
Reel/Frame 049911/0904 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2019
From: WANG, YONGQIANG
To: CHINA NOVARTIS INSTITUTES FOR BIOMEDICAL RESEARCH
Reel/Frame 049911/0940 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2019
From: EBERSBACH, HILMAR
To: NOVARTIS PHARMA AG
Reel/Frame 049912/0030 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2019
From: PLESA, GABRIELA
To: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA
Reel/Frame 049912/0034 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2019
From: JUNE, CARL H.; MILONE, MICHAEL C.; RUELLA, MARCO
To: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA
Reel/Frame 049912/0074 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2019
From: CHINA NOVARTIS INSTITUTES FOR BIOMEDICAL RESEARCH
To: NOVARTIS AG
Reel/Frame 049912/0094 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2019
From: NOVARTIS INSTITUTES FOR BIOMEDICAL RESEARCH, INC.
To: NOVARTIS AG
Reel/Frame 049912/0108 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2019
From: NOVARTIS PHARMA AG
To: NOVARTIS AG
Reel/Frame 049912/0128 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2019
From: THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA
To: NOVARTIS AG; THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA
Reel/Frame 049912/0167 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 31, 2019
From: BROGDON, JENNIFER; CHOI, EUGENE; GLASS, DAVID; HUET, HEATHER; MANNICK, JOAN; MURPHY, LEON; RICHARDSON, CELESTE; SINGH, RESHMA
To: NOVARTIS INSTITUTES FOR BIOMEDICAL RESEARCH, INC.
Reel/Frame 049914/0623 →
Priority Claims (2)
WO PCT/CN2014/082586 · Jul 21, 2014 · international
WO PCT/CN2014/090501 · Nov 6, 2014 · international
Continuity (2)
Division 14805193 · Jul 21, 2015
Related Publication 20190153061A1 · May 23, 2019
Cited By (7)
US 12,264,200 US 12,275,791 US 12,377,144 US 12,378,318 US 12,384,847 US 12,384,851 US 12,606,636