T cell receptors and peptides derived by mutations for the treatment of cancer
The present invention relates to a method for providing a neopeptide-specific T cell, wherein the neopeptide-specific T cell forms a complex having a half-life (T½) of at least 50 s with a neopeptide-MHC monomer. The present invention further relates to a T cell obtainable by the method as well as a pharmaceutical composition comprising such T cells.
1. A method for providing a neopeptide-specific T cell, wherein the neopeptide-specific T cell forms a complex having a half-life (T 1/2 ) of at least 50 s with a neopeptide-MHC monomer, wherein said neopeptide is derived from a frameshift product of a tumor suppressor gene, the method comprising:
a) contacting a population of T cells obtained from a human subject with a detectably labeled neopeptide-MHC complex;
b) isolating a T-cell from the population of step (a) which comprises a T cell receptor (TCR) that specifically binds to the neopeptide-MHC complex or wherein the T cell is activated via binding to the neopeptide-MHC complex to obtain neopeptide-specific T cells;
c) determining the T 1/2 of the neopeptide-MHC complex formed by the neopeptide-specific T cells by measuring the signal of the detectable label comprised in the MHC monomer over a period of time; and
d) selecting neopeptide-specific T cells in which the T 1/2 is at least 50 s.
2. The method of claim 1 , wherein the neopeptide-MHC complex is a neopeptide-MHC monomer or a neopeptide-MHC multimer.
3. The method of claim 1 , wherein step b) further comprises
b.1) isolating the neopeptide-specific TCR;
b.2) determining the TCR a chain and b chain sequences;
b.3) recombinantly expressing the neopeptide-specific TCR in a T cell.
4. The method of claim 1 , wherein the neopeptide-MHC monomer further comprises a streptavidin binding peptide.
5. The method of claim 4 , wherein the neopeptide-MHC monomer reversibly binds to a streptavidin mutein.
6. The method of claim 4 , wherein step c) further comprises contacting the neopeptide-MHC monomer with a streptavidin mutein.
7. The method of claim 1 , wherein the neopeptide is expressed by a tumor suppressor gene comprising a point mutation or a frameshift mutation.
8. The method of claim 1 , wherein the neopeptide is immunogenic.
9. The method of claim 1 , wherein the neopeptide is a non-self epitope.
10. The method of claim 1 , wherein the neopeptide is selected from the group consisting of SEQ ID NO: 1-SEQ ID NO: 45 and SEQ ID NO: 58-SEQ ID NO: 62.
11. The method of claim 1 , wherein the neopeptide is HLA class I restricted.
12. The method of claim 1 , wherein the neopeptide is MHC class I presentable.
13. The method of claim 1 , wherein the T cell is a cytotoxic T cell, a regulatory T cell, a T helper cell or a NK T cell.
14. The method of claim 1 , wherein the tumor suppressor gene comprises a high frameshift mutation rate.
15. The method of claim 1 , wherein the tumor suppressor gene is one of RNF43, APC, WT1, ARID1A, GATA3, NOTCH1, NPM1, ACVR2A, PTEN, SMAD4, CDKN2A, SLC16A4, CDC27, MYO6, MLL3, TAF1, MAP2K4, TGFBR2, ACVR1B, PREX2, ARID1B, PBRM1, SMARCA2, SMARCA4, MLL2, KDM6A, SF3B1, PALB2, RPA1, ATM, STK11, MLH1, MSH2, ROBO1, ROBO2, SLIT2, MYC, GATA6, CDK6, NOV, MET, SOX9, ERBB2, PIK3CA, PIK3R3 or FGFR2, preferably RNF43 or APC.
16. The method of claim 1 , wherein the subject is a healthy donor or a non-healthy donor.
17. The method of claim 16 , wherein the non-healthy donor is a cancer patient.
18. A T cell capable of binding a neopeptide that is expressed by a tumor suppressor gene, wherein said neopeptide is derived from a frameshift product of a tumor suppressor gene and wherein the T-cell binds to the neopeptide-MHC complex with a half-life (T 1/2 ) of at least 50 s, wherein the T cell is obtained by the method as defined in claim 1 .