%0 Journal Article
%A Muñoz Ruiz, Miguel
%A García Cassani, Bethania
%A Hayday, Adrian C
%T IFN-γ–dependent interactions between tissue-intrinsic γδ T cells and tissue-infiltrating CD8 T cells limit allergic contact dermatitis
%D 2023
%@ 0091-6749
%U https://hdl.handle.net/20.500.14352/116487
%X Elicitation of allergic contact dermatitis (ACD), an inflammatory type 4 hypersensitivity disease, induces skin infiltration by polyclonal effector CD8 ab T cells and precursors of tissue-resident memory T (TRM) cells. BecauseTRM have long-term potential to contribute to body-surface immunoprotection and immunopathology, their local regulation needs a fuller understanding. Objective: We sought to investigate how TRM-cell maturation mightbeinfluenced byinnate-likeT cells pre-existing withinmany epithelia. This study examined CD81 TRM-cell maturation following hapten-induced ACD in wild-type mice and in strains harboring altered compartments of dendritic intraepidermal gd T cells (DETCs), a prototypic tissue-intrinsic, innate-like T-cell compartment that reportedly regulates ACD, but by no elucidated mechanism.In addition to eliciting CD8 TRM, ACD induced DETC activation and an intimate coregulatory association of the 2 cell types. This depended on DETC sensing IFN-g produced by CD8 cells and involved programmed death-ligand 1 (PD-L1). Thus, in mice lacking DETC or lacking IFN-g receptor solely on gd cells, ACD-elicited CD8 T cells showed enhanced proliferative and effector potentials and reduced motility, collectively associated with exaggerated ACD pathology.Comparable dysregulation was elicited by PD-L1 blockade in vitro, and IFN-g–regulated PD-L1 expression was a trait of human skin-homing and intraepithelial gd T cells. The size and quality of the tissue-infiltrating CD8 T-cell response during ACD can be profoundly regulated by local innate-like T cells responding to IFN-g and involving PDL1. Thus, interindividual and tissue-specific variations in tissueintrinsic lymphocytes may influence responses to allergens and other challenges and may underpin inflammatory pathologies such as those repeatedly observed in gd T-cell–deficient settings.
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