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Human skin harbors two major T cell compartments of equal size that are distinguished by expression of the chemokine receptor CCR8. In vitro studies have demonstrated that CCR8 expression is regulated by TCR engagement and the skin tissue microenvironment. To extend these observations, we examined the relationship between CCR8 + and CCR8 - skin T cells in vivo. Phenotypic, functional, and transcriptomic analyses revealed that CCR8 + skin T cells bear all the hallmarks of resident memory T cells, including homeostatic proliferation in response to IL-7 and IL-15, surface expression of tissue localization (CD103) and retention (CD69) markers, low levels of inhibitory receptors (programmed cell death protein 1, Tim-3, LAG-3), and a lack of senescence markers (CD57, killer cell lectin-like receptor subfamily G member 1). In contrast, CCR8 - skin T cells are heterogeneous and comprise variable numbers of exhausted (programmed cell death protein 1 + ), senescent (CD57 + , killer cell lectin-like receptor subfamily G member 1 + ), and effector (T-bet hi , Eomes hi ) T cells. Importantly, conventional and high-throughput sequencing of expressed TCR β-chain ( TRB ) gene rearrangements showed that these CCR8-defined populations are clonotypically distinct, suggesting unique ontogenies in response to separate antigenic challenges and/or stimulatory conditions. Moreover, CCR8 + and CCR8 - skin T cells were phenotypically stable in vitro and displayed similar levels of telomere erosion, further supporting the likelihood of a nonlinear differentiation pathway. On the basis of these results, we propose that long-lived memory T cells in human skin can be defined by the expression of CCR8.

CCR8 Expression Defines Tissue-Resident Memory T Cells in Human Skin