The Antitumor Effects of Vaccine-Activated CD8 T Cells Associate with Weak TCR Signaling and Induction of Stem-Like Memory T Cells.

To understand why vaccine-activated tumor-specific T cells often fail to generate antitumor effects, we studied two α-fetoprotein-specific CD8 T cells (Tet and Tet) that had different antitumor effects. We found that Tet required high antigen doses for reactivation, but could survive persistent antigen stimulation and maintain their effector functions. In contrast, Tet had a low threshold of reactivation, but underwent exhaustion and apoptosis in the presence of persistent antigen. , Tet cells expanded more than Tet upon reencountering antigen and generated stronger antitumor effects. The different antigen responsiveness and antitumor effects of Tet and Tet cells correlated with their activation and differentiation states. Compared with Tet, the population of Tet cells was less activated and contained more stem-like memory T cells (Tscm) that could undergo expansion The TCR signaling strength on Tet was weaker than Tet, correlating with more severe Tet TCR downregulation. Weak TCR signaling may halt T-cell differentiation at the Tscm stage during immune priming and also explains why Tet reactivation requires a high antigen dose. Weak TCR signaling of Tet cells in the effector stage will also protect them from exhaustion and apoptosis when they reencounter persistent antigen in tumor lesion, which generates antitumor effects. Further investigation of TCR downregulation and manipulation of TCR signaling strength may help design cancer vaccines to elicit a mix of tumor-specific CD8 T cells, including Tscm, capable of surviving antigen restimulation to generate antitumor effects. .