Compositions and methods for targeting γδ T cells with chimeric antigen receptors
The invention includes compositions comprising a chimeric antigen receptor (CAR) specific for an GD T Cell receptor (anti-GD TCR CAR), vectors comprising the same, compositions comprising anti-GD TCR CAR vectors packaged in viral particles, and recombinant T cells or other effector cells comprising the anti-GD TCR CAR of the invention. The invention also includes methods of making a genetically modified T cell expressing an anti-GD TCR CAR wherein the expressed CAR comprises an extracellular domain that binds to GD T cells or to cells expressing a GD TCR.
1. An isolated nucleic acid comprising a nucleic acid sequence encoding an anti-GD TCR CAR comprising the amino acid sequence of SEQ ID NO: 1.
2. The isolated nucleic acid of claim 1 , wherein the nucleic acid sequence encoding the anti-GD TCR CAR comprises SEQ ID NO: 9.
3. The isolated nucleic acid of claim 1 , wherein the light chain is encoded by the nucleic acid sequence of SEQ ID NO: 11 or the heavy chain is encoded by the nucleic acid sequence of SEQ ID NO: 13.
4. The isolated nucleic acid of claim 1 , wherein the VH3-23 signal peptide is encoded by the nucleic acid sequence of SEQ ID NO: 10.
5. The isolated nucleic acid of claim 1 , wherein the CD8 alpha chain hinge and transmembrane domain are encoded by a nucleic acid sequence comprising the sequence of SEQ ID NO: 14.
6. The isolated nucleic acid of claim 1 , wherein the nucleic acid sequence encoding the peptide linker comprises SEQ ID NO: 12.
7. The isolated nucleic acid of claim 1 , wherein the nucleic acid sequence encoding the CD137 intracellular domain comprises SEQ ID NO: 15.
8. The isolated nucleic acid of claim 1 , wherein the nucleic acid sequence encoding the CD3 zeta signaling domain comprises SEQ ID NO: 16.
9. A vector comprising the isolated nucleic acid of claim 1 .
10. The vector of claim 9 , wherein the vector is a lentiviral vector.
11. The vector of claim 10 , wherein the vector is a RNA vector.
12. An isolated anti-GD TCR CAR encoded by the nucleic acid of claim 1 .
13. A genetically modified cell comprising the isolated nucleic acid of claim 1 .
14. The cell of claim 13 , wherein the cell expresses the anti-GD TCR CAR and has high affinity for GD T cells.
15. The cell of claim 13 , wherein the cell expresses the anti-GD TCR CAR and induces killing of GD T cells or cells expressing GD TCR.
16. The cell of claim 13 , wherein the cell is selected from the group consisting of a helper T cell, a cytotoxic T cell, a memory T cell, regulatory T cell, a natural killer cell, a cytokine induced killer cell, a cell line thereof, a T memory stem cell and other effector cell.
17. The cell of claim 13 , wherein an endogenous CD3 and an endogenous MHCI of the cell has been knocked out using a CRISPR/CAS system.
18. A method for treating a GD T cell related disease in a subject, the method comprising: administering to the subject an effective amount of the genetically modified T cell of claim 13 .
19. The method of claim 18 , wherein the GD T cell related disease is an inflammatory or autoimmune selected from the group consisting of juvenile idiopathic arthritis, Behcet's disease, alopecia areata, systemic sclerosis, atherosclerosis, psoriasis, myositis, rheumatoid arthritis, inflammatory bowel disease, multiple sclerosis, type I diabetes, ankylosing spondylitis, autoimmune uveitis, Sjogren's syndrome, systemic lupus, and chronic cutaneous lupus.
20. The method of claim 18 , wherein the GD T cell related disease is a GD T cell lymphoma (GDTCL).
21. The method of claim 18 , wherein the subject is a human.
22. The method of claim 18 , wherein the modified T cell targets a GD T cell or a cell expressing GD TCR.