Antigen reactivity defines tissue-resident memory and exhausted T cells in tumors.
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ABSTRACT: CD8+ T cells are an important weapon in the therapeutic armamentarium against cancer. While CD8+CD103+ T cells with a tissue-resident memory T (TRM) cell phenotype are associated with favorable prognoses, the tumor microenvironment also contains dysfunctional exhausted T (TEX) cells that exhibit a variety of TRM-like features. Here we deconvolute TRM and TEX cells across human cancers, ascribing markers and gene signatures that distinguish these populations and enable their functional distinction. Although TRM cells have superior functionality and are associated with long-term survival post-tumor resection, they are not associated with responsiveness to immune checkpoint blockade. Tumor-assoc
SUBMITTER: Burn TN
PROVIDER: S-EPMC12764432 | biostudies-literature | 2026 Jan
REPOSITORIES: biostudies-literature
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