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Extensive evidence has confirmed that specific ferroptosis-related metabolic signals or byproducts were involved in the function, viability, and differentiation of multiple T-cell subgroups, impacting their reactivity to inflammation, infection and tumor immunity ( As was reported recently in tumor immunity, the ferroptotic interaction between CD8+ T cell-secreted IFN- and tumor cells is known to induce the elicitation of tumor ferroptosis and reinforcement of anti-tumor activity ( Besides, regulatory T (Treg) cells with a deletion of PDK1 have been implicated in the generation of excessive ROS, which consequently leads to amplified ferroptosis of themselves (53)

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Independent component analysis: algorithms and applications

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