Bispecific OR-gate chimeric antigen receptor responsive to CD19 and CD20
A CD19-OR-CD20 chimeric antigen receptor (CAR) protein construct is provided. Also provided are nucleic acids encoding the CD19-OR-CD20 CAR; and methods of use, e.g. in the treatment of B cell malignancies. The CD19-OR-CD20 CAR of the invention is a bispecific CAR that can trigger T-cell activation upon detection of either CD19 or CD20 (or both). It is a single molecule that confers two-input recognition capability upon human T cells engineered to stably express this CAR.
1. A method of killing tumor cells in a cancer patient comprising administering to the patient a population of T cells expressing a polypeptide comprising a CD19-O R-CD20 chimeric antigen receptor (CAR) comprising, in order: anti-CD20 scFv comprising a light chain variable region and heavy chain variable region from SEQ ID NO:3; (G45)4 linker; anti-CD19 scFv comprising a heavy chain variable region and light chain variable region from SEQ ID NO:4; spacer domain of SEQ ID NO:5; transmembrane domain of SEQ ID NO:6; 4-1BB cytoplasmic signaling domain of SEQ ID NO:8; and CD3 zeta cytoplasmic signaling domain of SEQ ID NO:9, wherein the tumor cells express CD19 or CD20.
2. The method of claim 1 , wherein the tumor cells are lymphoma cells.
3. The method of claim 1 , wherein the transmembrane domain is CD28 transmembrane domain.
4. The method of claim 1 , wherein the CAR further comprises sortable tag.
5. The method of claim 4 , wherein the sortable tag is truncated EGFR.
6. The method of claim 4 , wherein the sortable tag is a fluorescent protein.
7. The method of claim 1 , wherein the population of cells abrogates antigen loss by the tumor cells.
8. A method of treating a B-cell leukemia or lymphoma in a patient comprising administering to the patient a population of T cells expressing a polypeptide comprising a CD19-0R-CD20 chimeric antigen receptor (CAR) comprising, in order: anti-CD20 scFv comprising a light chain variable region and heavy chain variable region from SEQ ID NO:3; (G45)4 linker; anti-CD19 scFv comprising a heavy chain variable region and light chain variable region from SEQ ID NO:4; spacer domain of SEQ ID NO:5; transmembrane domain of SEQ ID NO:6; 1BB cytoplasmic signaling domain of SEQ ID NO:8; and CD3 zeta cytoplasmic signaling domain of SEQ ID NO:9, wherein the B-cell leukemia or lymphoma expresses CD19 or CD20.
9. The method of claim 8 , wherein the population of cells abrogates antigen loss by the cancer cells.
10. The method of claim 1 , wherein the patient is a human patient.
11. The method of claim 8 , wherein the patient is a human patient.