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CD8<sup>+</sup> T cell-derived CD40L mediates noncanonical cytotoxicity in CD40-expressing cancer cells.


ABSTRACT: T cells and their effector functions, in particular the canonical cytotoxicity of CD8+ T cells involving perforin, granzymes, Fas ligand (FasL), and tumor necrosis factor related apoptosis inducing ligand (TRAIL), are crucial for tumor immunity. Here, we reveal a previously unidentified mechanism by which CD40L-expressing CD8+ T cells induce cytotoxicity in cancer cells. In murine models, up to 50% of tumor-specific CD8+ T cells expressed CD40L, and conditional CD40L ablation in CD8+ T cells alone led to tumor formation. Mechanistically, CD40L+CD8+ T cells can induce cell death in CD40-expressing cancer cells by triggering caspase-8 activation. We demonstrate that a gene signature for resistance to CD40 signaling-induced cel

SUBMITTER: Schiele P 

PROVIDER: S-EPMC12094236 | biostudies-literature | 2025 May

REPOSITORIES: biostudies-literature