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These findings establish developmental imprinting as an important determinant of CD8+ T cell heterogeneity and identify CXCR3+IL-18Rα+ CD8+ T cells as key effectors for antitumor immunity.
A spatially resolved multi-omic atlas of the aging mouse thymus is generated and reframe thymic involution as spatial stromal reorganization that links stromal remodeling to impaired thymopoiesis, central tolerance, and immune aging.
It is observed that aging disproportionately affects Ly6d− compared to Ly6d+ TEPCs, with implications for rejuvenation of aging thymic epithelia, and insights into the developmental pathways of TEC lineages and their maintenance are provided.
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