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Literature review uncovers potential CD8+ tissue-resident memory cell modulation of peripheral nerve function, highlighting mechanisms driving neuroinflammation across diverse disease contexts.
CD8 + TRM cells are indispensable for continuous surveillance of tissues and direct elimination of invading pathogens through a diverse range of effector mechanisms. They balance adhesion, metabolic adaptation, and commensal tolerance against the capacity for swift, targeted attack, using local tissue signals and immunological memory as a finely calibrated control mechanism that prevents both chronic inflammation and persistent infection. Given their strategic co-localization with the peripheral nervous system (PNS) across multiple tissues, this raises a compelling question: do CD8 + TRM cells actively regulate peripheral nerve function? In light of recent evidence on how chronic HIV infection influences mucosal CD8 + TRM cells and tissue inflammation, this article critically evaluates the existing literature to assess the evidence and potential mechanisms underlying the involvement of CD8 + TRM cells in peripheral nerve inflammation across diverse tissue and disease contexts.
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Pushpa Pandiyan (2026) studied this question.
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