通过 HLA-A*02:01 限制性抗 KRAS TCR 模拟 CAR 与双特异性 T 细胞衔接器靶向突变 KRAS

Mutations in the KRAS proto-oncogene, particularly at codon 12, are among the most frequent genetic alterations in various cancers, and KRAS G12V accounts for about 25% of all KRAS mutations observed in lung, pancreatic, and colorectal adenocarcinomas. Despite improved treatment regimes using targeted therapy and checkpoint inhibitors, cellular immunotherapy options for KRAS-mutated cancers remain elusive.

We therefore developed two TCR-mimic (TCRm) anti-KRAS G12V /HLA-A*02:01 chimeric antigen receptors (CARs) containing different hinge regions and, alternatively, a TCRm anti-KRAS G12V /HLA-A*02:01 bispecific T cell engager (BiTE) to explore immunotherapy to the highly prevalent KRAS G12V neoantigen. CAR-redirected or BiTE-exposed JNL-reporter cells demonstrated potent signaling capacity upon recognition of KRAS G12V .

Moreover, human CAR T and NK cells elicited IFN- release and cellular cytotoxicity upon encountering target cells pulsed with KRAS G12V peptide, and the anti-KRAS G12V Strep-tagII hinge CAR showed superior reactivity compared to a human IgG1-Fc hinge CAR. Similarly, a novel TCRm BiTE induced strong T cell immunity to KRAS G12V . In contrast, we observed only very low CAR or BITE-mediated responses to naturally presented KRAS G12V /HLA-A*02:01 complexes.

In summary, this study demonstrates that the mutation-derived KRAS G12V 5-14 peptide can be effectively targeted by TCRm CAR and BiTE-redirected T cells, suggesting that TCRm anti-KRAS G12V CAR or BiTE represent promising formats to advance immunotherapy to mutated KRAS neoepitopes. KEY MESSAGES: Successful development of TCRm CAR and BiTE targeting mutated KRAS/HLA-A*02:01. Anti-KRAS G12V TCRm CAR and BiTE induce potent immunity to KRAS G12V neoepitope. Anti-KRAS/HLA-I TCRm CARs and BiTEs are novel therapeutics for cancer immunotherapy.