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Divergent ontogeny of Tissue Resident Memory and Tissue Resident Exhausted CD8<sup>+</sup> T cells underlies distinct functional potential.


ABSTRACT: Persistent antigen stimulation promotes differentiation of exhausted CD8+ T (TEX) cells. TEX cells are distinct from circulating memory T (TCIRCM) cells but share many features with tissue-resident memory (TRM) cells established following infection resolution. CD8+ T cells co-expressing residency- and exhaustion-associated molecules in chronic diseases often correlate with clinical outcomes. However, the relationship between these cells and conventional TRM or TEX cells remains unclear. Here, we show that chronic antigen stimulation drives development of tissue-resident TEX (TR-TEX) cells that are ontologically and functionally distinct from TRM cells generated after ant

SUBMITTER: Park SL 

PROVIDER: S-EPMC12363886 | biostudies-literature | 2025 Aug

REPOSITORIES: biostudies-literature