Compositions and methods for treating cancer
Disclosed are compositions and methods for targeted treatment of cancer. The present disclosure provides chimeric antigen receptors and cells expressing such chimeric antigen receptors. In certain embodiments, engineered cells expressing the chimeric antigen receptors are specific for a low density cancer antigen or peptide in groove antigen.
1. A CAR polypeptide comprising an amino acid sequence set forth in SEQ ID NOs: 7, 9, 11, 13, 30, or 34.
2. The CAR polypeptide of claim 1 , wherein the CAR polypeptide comprises SEQ ID NO: 7.
3. The CAR polypeptide of claim 1 , wherein the CAR polypeptide comprises SEQ ID NO: 9.
4. The CAR polypeptide of claim 1 , wherein the CAR polypeptide comprises SEQ ID NO: 11.
5. The CAR polypeptide of claim 1 , wherein the CAR polypeptide comprises SEQ ID NO: 13.
6. The CAR polypeptide of claim 1 , wherein the CAR polypeptide comprises SEQ ID NO: 30.
7. The CAR polypeptide of claim 1 , wherein the CAR polypeptide comprises SEQ ID NO: 34.
8. An immune cell expressing the CAR polypeptide of claim 1 .
9. A composition comprising immune cells expressing the CAR of claim 1 .
10. A nucleic acid encoding the CAR polypeptide of claim 1 .
11. An immune cell comprising the nucleic acid of claim 10 .
12. The immune cell of claim 11 , wherein the immune cell is a leukocyte, a lymphocyte, a monocyte, a macrophage, a dendritic cell, a mast cell, a neutrophil, a basophil, an eosinophil, an αβT cell, γδT cell, a Natural Killer (NK) cell, a Natural Killer T (NKT) cell, an innate lymphoid cell (ILC), a cytokine induced killer (CIK) cell, a cytotoxic T lymphocyte (CTL), a lymphokine activated killer (LAK) cell, or a regulatory T cell.
13. A method of treating a tumor in a subject, the method comprising administering a composition comprising cells expressing a CAR polypeptide of claim 1 .
14. The method of claim 13 , wherein the method further comprises conjointly administering to the subject a second CAR polypeptide comprising:
a) a 4-1BB domain in the costimulatory region of the CAR polypeptide,
b) at least one intracytoplasmic signaling region comprising a cluster of differentiation 3 zeta (CD3/ζ domain, and
c) an extracellular domain specific for a peptide in groove cancer antigen.
15. The method of claim 14 , wherein the second CAR polypeptide comprises a cluster of differentiation 8 alpha (CD8/α) peptide in the hinge/transmembrane region.
16. A cell bank comprising cells for adoptive immunotherapy, wherein the cells express the CAR of claim 1 .
17. A nucleic acid encoding a CAR polypeptide, wherein the nucleic acid has a sequence set forth in SEQ ID NOs: 14, 15, 35 or 36.
18. The nucleic acid encoding the CAR polypeptide of claim 17 , wherein the nucleic acid comprises SEQ ID NO: 14.
19. The nucleic acid encoding the CAR polypeptide of claim 17 , wherein the nucleic acid comprises SEQ ID NO: 15.
20. The nucleic acid encoding the CAR polypeptide of claim 17 , wherein the nucleic acid comprises SEQ ID NO: 35.
21. The nucleic acid encoding the CAR polypeptide of claim 17 , wherein the nucleic acid comprises SEQ ID NO: 36.