Influences of metabolism and lipid homeostasis on regulatory vs. conventional T cells and implications for autoimmunity

被引:0
作者
Nguyen, Madison A. [1 ]
Lee, Sarah S. [1 ,2 ]
Walsh, Craig M. [1 ,2 ,3 ]
机构
[1] Univ Calif Irvine, Charlie Dunlop Sch Biol Sci, Mol Biol & Biochem Dept, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Sue & Bill Gross Stem Cell Res Ctr, Irvine, CA 92697 USA
[3] Univ Calif Irvine, Inst Immunol, Irvine, CA 92697 USA
关键词
regulatory T cells; lipid metabolism; metabolic reprograming; mevalonate (MVA) pathway; mTOR; autoimmune disease; PPAR-GAMMA; EFFECTOR FUNCTION; DIFFERENTIATION; TH17; ACTIVATION; SURVIVAL; GLUCOSE; MTORC1; PROLIFERATION; LYMPHOCYTES;
D O I
10.3389/fimmu.2025.1613230
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Regulatory T cells are essential for suppressing an overactive immune system, especially concerning autoimmune disease, tumor growth, and inflammatory disease. This suppressive nature of regulatory T cells is largely due to their metabolic profiles determined by metabolic reprogramming upon activation and subsequent differentiation. As regulatory T cells tend to process and cycle energy differently from other T cell subsets, we are interested in what metabolic processes support regulatory T cell function. This review will consider how regulatory T cells compare with conventional T cells in terms of their participation in distinct metabolic pathways and how the presence of regulatory T cell-specific molecules influences proliferation and suppressive function. Additionally, this review will identify possible metabolic targets of regulatory T cells that could be targeted for development of autoimmune disease therapies.
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页数:9
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