More T cell receptors to the RAScue in cancer?

Publication Title

The Journal of clinical investigation

Document Type

Article

Publication Date

11-1-2024

Keywords

oregon; chiles; Humans; Receptors, Antigen, T-Cell; Proto-Oncogene Proteins p21(ras); Pancreatic Neoplasms; T-Lymphocytes; Antigens, Neoplasm; Neoplasms; Mutation, Missense; Mutation; HLA-A Antigens; Cancer Vaccines

Abstract

Treatment with T cells genetically engineered to express tumor-reactive T cell receptors (TCRs), known as TCR-gene therapy (TCR-T), is a promising immunotherapeutic approach for patients with cancer. The identification of optimal TCRs to use and tumor antigens to target are key considerations for TCR-T. In this issue of the JCI, Bear and colleagues report on their use of in vitro assays to characterize four HLA-A*03:01- or HLA-A*11:01-restricted TCRs targeting the oncogenic KRAS G12V mutation. The TCRs were derived from healthy donors or patients with pancreatic cancer who had received a vaccine against mutant KRAS. The most promising TCRs warrant testing in patients with KRAS G12V-positive cancers.

Area of Special Interest

Cancer

Specialty/Research Institute

Oncology

DOI

10.1172/JCI184782

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