BCMA chimeric antigen receptors and uses thereof
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.
1. An isolated chimeric antigen receptor (CAR) comprising an anti-BCMA binding domain, a transmembrane domain, and an intracellular signaling domain comprising a primary signaling domain and a costimulatory signaling domain, wherein the anti-BCMA binding domain comprises a heavy chain variable region (VH) comprising a heavy chain complementarity determining region 1 (HC CDR1) of SEQ ID NO: 86, a heavy chain complementarity determining region 2 (HC CDR2) of SEQ ID NO: 87, and a heavy chain complementarity determining region 3 (HC CDR3) of SEQ ID NO: 88, a light chain complementarity determining region 1 (LC CDR1) of SEQ ID NO: 95, a light chain complementarity determining region 2 (LC CDR2) of SEQ ID NO: 96, and a light chain complementarity determining region 3 (LC CDR3) of SEQ ID NO: 97, wherein:
(a) the primary signaling domain:
(i) comprises a functional signaling domain of CD3 zeta or FcR gamma; or
(ii) comprises the amino acid sequence of SEQ ID NO: 9 or 10, or an amino acid sequence having at least about 85%, 90%, 95%, or 99% sequence identity thereto; and
(b) the costimulatory signaling domain:
(i) comprises a functional signaling domain of 4-1BB (CD137), OX40, CD2, CD27, CD28, ICAM-1, LFA-1, or ICOS (CD278); or
(ii) comprises the amino acid sequence of SEQ ID NO: 7, or an amino acid sequence having at least about 85%, 90%, 95%, or 99% sequence identity thereto.
2. The CAR of claim 1 , wherein the VH comprises the amino acid sequence of SEQ ID NO: 93, or an amino acid sequence having at least about 85%, 90%, 95%, or 99% sequence identity thereto.
3. The CAR of claim 1 , wherein the VL comprises the amino acid sequence of SEQ ID NO: 102, or an amino acid sequence having at least about 85%, 90%, 95%, or 99% sequence identity thereto.
4. The CAR of claim 1 , wherein the VH and VL comprise the amino acid sequences of SEQ ID NOs: 93 and 102, respectively.
5. The CAR of claim 1 , wherein the anti-BCMA binding domain comprises a single-chain fragment variable (scFv) comprising the amino acid sequence of SEQ ID NO: 105, or an amino acid sequence having at least about 85%, 90%, 95%, or 99% sequence identity thereto.
6. The CAR of claim 1 , wherein the CAR comprises the amino acid sequence of SEQ ID NO: 107, or an amino acid sequence having at least about 85%, 90%, 95%, or 99% sequence identity thereto.
7. The CAR of claim 1 , wherein the VH and VL are connected by a linker comprising the amino acid sequence of SEQ ID NO: 63 or 104.
8. The CAR of claim 1 , wherein:
(i) the transmembrane domain comprises a transmembrane domain of a protein chosen from the alpha, beta, or zeta chain of T-cell receptor, CD28, CD3 epsilon, CD45, CD4, CD5, CD8, CD9, CD16, CD22, CD33, CD37, CD64, CD80, CD86, CD134, CD137, or CD154; or
(ii) the transmembrane domain comprises the amino acid sequence of SEQ ID NO: 6, or an amino acid sequence having at least about 85%, 90%, 95%, or 99% sequence identity thereto.
9. The CAR of claim 1 , wherein the anti-BCMA binding domain is connected to the transmembrane domain by a hinge region, wherein the hinge region comprises the amino acid sequence of SEQ ID NO: 2, 3, or 4, or an amino acid sequence having at least about 85%, 90%, 95%, or 99% sequence identity thereto.
10. The CAR of claim 1 , wherein the intracellular signaling domain comprises a costimulatory signaling domain comprising a functional signaling domain of 4-1BB and a primary signaling domain comprising a functional signaling domain of CD3 zeta.
11. The CAR of claim 1 , wherein the CAR further comprises a leader sequence comprising the amino acid sequence of SEQ ID NO: 1.
12. The CAR of claim 1 , wherein the CAR comprises one or more of the following properties:
(i) the CAR, when expressed in a cell, activates NFAT signaling in the cell in the presence of BCMA-expressing cells;
(ii) the CAR, when expressed in a cell, induces cytotoxicity of BCMA-expressing cells; and
(iii) the CAR, when expressed in a cell, induces expression of a cytokine in the cell in the presence of BCMA-expressing cells.
13. An anti-BCMA binding domain comprising a heavy chain variable region (VH) comprising a heavy chain complementarity determining region 1 (HC CDR1) of SEQ ID NO: 86, a heavy chain complementarity determining region 2 (HC CDR2) of SEQ ID NO: 87, and a heavy chain complementarity determining region 3 (HC CDR3) of SEQ ID NO: 88, and a light chain variable region (VL) comprising a light chain complementarity determining region 1 (LC CDR1) of SEQ ID NO: 95, a light chain complementarity determining region 2 (LC CDR2) of SEQ ID NO: 96, and a light chain complementarity determining region 3 (LC CDR3) of SEQ ID NO: 97.
14. The anti-BCMA binding domain of claim 13 , wherein the VH and VL comprise the amino acid sequences of SEQ ID NOs: 93 and 102, respectively.
15. A chimeric antigen receptor (CAR) that binds to BCMA, comprising, from N-terminus to C-terminus:
(i) leader sequence of SEQ ID NO: 1;
(ii) a HC CDR1 of SEQ ID NO: 86;
(iii) a HC CDR2 of SEQ ID NO: 87;
(iv) a HC CDR3 of SEQ ID NO: 88;
(v) a LC CDR1 of SEQ ID NO: 95;
(vi) a LC CDR2 of SEQ ID NO: 96;
(vii) a LC CDR3 of SEQ ID NO: 97;
(viii) a CD8 transmembrane domain and hinge of SEQ ID NO: 202;
(ix) a functional signaling domain of 4-1BB of SEQ ID NO: 7; and
(x) a functional signaling domain of CD3 zeta of SEQ ID NO: 10.
16. The CAR of claim 15 , which comprises: (i) a VH region of SEQ ID NO: 93 and a VL region of SEQ ID NO: 102; or (b) a scFv of SEQ ID NO: 105.
17. The CAR of claim 15 , which comprises an amino acid sequence of SEQ ID NO: 257 or SEQ ID NO: 107.