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In contrast with adaptive memory, which lies on the gene recombination of antigen receptors and proliferation of specific lymphocyte clones, TI is triggered by the interplay between pathogen-associated molecular patterns (PAMPs) or damage-associated molecular patterns (DAMPs) and pattern recognition receptors (PRRs) on the innate immune cells, followed by long-term metabolic and epigenetic changes (99, 100) ( Figures 2 , 3 )

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