Cells for immunotherapy engineered for targeting antigen present both on immune cells and pathological cells
Methods of developing genetically engineered immune cells for immunotherapy, which can be endowed with Chimeric Antigen Receptors targeting an antigen marker that is common to both the pathological cells and said immune cells (ex: CD38, CS1 or CD70) by the fact that the genes encoding said markers are inactivated in said immune cells by a rare cutting endonuclease such as TALEN, Cas9 or argonaute.
1. A method of preparing a cytotoxic T cell for immunotherapy of a leukemia or lymphoma cell comprising:
(a) inactivating or mutating a gene encoding an antigen marker selected from CD38, CD70, and CS1 in a cytotoxic T cell, said antigen marker being present both on the surface of said cytotoxic T cell and the leukemia or lymphoma cell; and
(b) expressing in said cytotoxic T cell a transgene encoding a chimeric antigen receptor (CAR) directed against said antigen marker present at the surface of said leukemia or lymphoma cell.
2. The method according to claim 1 , wherein said antigen marker is CS1.
3. The method according to claim 1 , wherein said antigen marker is CD38.
4. The method according to claim 1 , further comprising activating and expanding the cytotoxic T cell.
5. The method according to claim 1 , further comprising purifying the resulting cytotoxic T cell by excluding the cells presenting said marker antigen at their surface.
6. The method according to claim 1 , wherein said cytotoxic T cell is obtained from a donor.
7. The method according to claim 1 , wherein said cytotoxic T cell is obtained from a leukemia or lymphoma patient.
8. The method according to claim 1 , wherein inactivating or mutating the gene is performed using a rare-cutting endonuclease.
9. The method according to claim 8 , wherein the rare-cutting endonuclease is a TAL-nuclease.
10. The method according to claim 8 , wherein said endonuclease is expressed from transfected mRNA.
11. The method according to claim 1 , further comprising inactivating a gene encoding a component of the T-cell receptor (TCR).
12. The method according to claim 11 , wherein said component of the T-cell receptor is TCRa.
13. The method according to claim 1 , wherein said CAR expressing cytotoxic T cell is expanded in-vitro.
14. The method according to claim 1 , wherein said CAR expressing cytotoxic T cell is expanded in-vivo.
15. The method according to claim 1 , wherein said leukemia or lymphoma cell is a malignant cell.
16. The method according to claim 1 , wherein said leukemia or lymphoma cell is a B-cell.
17. The method according to claim 1 , wherein the cytotoxic T cell is formulated as a medicament.
18. A method for treating a leukemia or lymphoma in a patient in need thereof, comprising administering an amount of the cytotoxic T cell prepared according to claim 1 to the patient in need thereof.
19. The method according to claim 18 , wherein the cancer is lymphoma.
20. The method according to claim 18 , wherein the cancer is leukemia.
21. An engineered cytotoxic T cell obtainable according to the method of claim 1 .
22. The engineered cytotoxic T cell according to claim 21 , wherein the cytotoxic T cell comprises a phenotype of [CAR CS38] + [CS38] − .
23. The engineered cytotoxic T cell according to claim 21 , wherein the cytotoxic T cell comprises a phenotype of [CAR CS70] + [CS70] − .
24. The engineered cytotoxic T cell according to claim 21 , wherein the cytotoxic T cell comprises a phenotype of [CAR CS1] + [CS1] − .
25. A method for treating a patient comprising:
diagnosing said patient for the presence of leukemia or lymphoma cells presenting an antigen marker selected from CD38, CD70, and CS1;
preparing a population of engineered cytotoxic T cells according to claim 1 ; and
administrating said engineered cytotoxic T cells to said patient diagnosed for said leukemia or lymphoma cells.
26. The method according to claim 1 , wherein said antigen marker is CD70.