Single-Cell Transcriptomics Reveals Killing Mechanisms of Antitumor Cytotoxic CD4+ TCR-T Cells

Abstract

T cell receptor-engineered T cells (TCR-Ts) have emerged as potent cancer immunotherapies. While most research focused on classical cytotoxic CD8⁺ T cells, the application of CD4⁺ T cells in adoptive T cell therapy has gained much interest recently. However, the cytotoxic mechanisms of CD4⁺ TCR-Ts have not been fully revealed. In this study, we obtained an MHC class I-restricted MART-1_27-35-specific TCR sequence based on the single-cell V(D)J sequencing technology, and constructed MART-1_27-35-specific CD4⁺ TCR-Ts and CD8⁺ TCR-Ts. The antitumor effects of CD4⁺ TCR-Ts were comparable to those of CD8⁺ TCR-Ts <i>in vitro</i> and <i>in vivo</i>. To delineate the killing mechanisms of cytotoxic CD4⁺ TCR-Ts, we performed single-cell RNA sequencing and found that classical granule-dependent and independent cytolytic pathways were commonly used in CD4⁺ and CD8⁺ TCR-Ts, while high expression of <i>LTA</i> and various costimulatory receptors were unique features for cytotoxic CD4⁺ TCR-Ts. Further signaling pathway analysis revealed that transcription factors Runx3 and Blimp1/Tbx21 were crucial for the development and killing function of cytotoxic CD4⁺ T cells. Taken together, we report the antitumor effects and multifaceted killing mechanisms of CD4⁺ TCR-Ts, and also indicate that MHC class I-restricted CD4⁺ TCR-Ts could serve as potential adoptive T cell therapies.