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ABSTRACT: Background and objective
Tumor antigen-escape variants undermine immunotherapy by subverting lymphocyte effector functions and reshaping tumor-immune dynamics. It is essential to delineate functional interplay within immune networks during tumor progression. We investigated whether homeostatic crosstalk between CD8+T cells and natural killer (NK) cells preempts tumor antigen-escape.Methods
Adoptive CD8+T cell transfers were administered before (D-7, homeostatic pre-priming) or after (D+1) tumor establishment in Rag1-/- and Rag1-/-γc-/- mice. Antigen presentation, immune activation, proliferation, cytotoxicity, and memory were quantified by flow cytometry, live bioluminescence and conf
SUBMITTER: Uzhachenko RV
PROVIDER: S-EPMC12497863 | biostudies-literature | 2025
REPOSITORIES: biostudies-literature