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Similar results, including elevated ROS, Fe 2+ and GPX4 levels, were observed in IMR90 cells undergoing etoposide-induced senescence (Extended Data Fig

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Breaking down the analysis to infer metabolically diverging subsets proved that our immunometabolic profiling strategy segregated naive, central memory, effector memory, terminally differentiated effector memory (T EMRA ), and CD38-expressing T cells (Supplementary Fig

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