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- W2022057304 endingPage "35" @default.
- W2022057304 startingPage "26" @default.
- W2022057304 abstract "T cells are required for an effective adaptive immune response. The principal function of T cells is to promote efficient removal of foreign material by identifying and mounting a specific response to nonself. A decline in T cell function in aging is thought to contribute to reduced response to infection and vaccination and an increase in autoimmunity. This may in part be due to the age-related decrease in naïve CD4(+) T cells and increase in antigen-experienced CD4(+) T cells, loss of redox homeostasis, and impaired metabolic switching. Switching between subsets is triggered by the integration of extracellular signals sensed through surface receptors and the activation of discrete intracellular metabolic pathways. This article explores how metabolic programming and loss of redox homeostasis during aging may contribute to age-associated changes in T cell phenotype and function." @default.
- W2022057304 created "2016-06-24" @default.
- W2022057304 creator A5021134199 @default.
- W2022057304 creator A5039575124 @default.
- W2022057304 creator A5042533860 @default.
- W2022057304 creator A5090155063 @default.
- W2022057304 date "2014-06-01" @default.
- W2022057304 modified "2023-09-26" @default.
- W2022057304 title "Does metabolic reprogramming underpin age-associated changes in T cell phenotype and function?" @default.
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