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CD8+ cytotoxic T lymphocyte activation is a critical step in the adaptive immune response, where CD8+ T cells (cytotoxic T cells) recognize antigenic peptides bound to MHC class I molecules on the surface of antigen-presenting cells or infected/malignant target cells. This triggers T cell receptor (TCR) signaling, further stabilized by the interaction of CD8 with MHC I. Full activation requires additional costimulatory signals (such as CD28 binding to CD80 or CD86) and cytokine signaling, often provided by dendritic cells and CD4+ helper T cells. Upon activation, CD8+ T cells proliferate and differentiate into effector and memory cells, using secreted cytotoxic granules (perforin, granzymes) and death-ligand signaling (FasL) to induce apoptosis in targets. This process plays essential roles in clearing infections, controlling cancer, and regulating adaptive immunity. Dysregulation of activation can result in autoimmunity, immunopathology, or failure of immune response
Promote antigen-dependent activation and clonal expansion Enhance or block costimulatory signals (e.g., CD28/CD80/86) Interfere with TCR–MHC engagement Modulate cytokine signals (e.g., IFNγ, IL-2)
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