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Metabolic control of regulatory T cell development and function

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TRENDS IN IMMUNOLOGY
卷 36, 期 1, 页码 3-12

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ELSEVIER SCI LTD
DOI: 10.1016/j.it.2014.08.003

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资金

  1. NATIONAL CANCER INSTITUTE [R01CA176624] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI105887, R01AI101407, R37AI105887] Funding Source: NIH RePORTER
  3. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS064599] Funding Source: NIH RePORTER
  4. NCI NIH HHS [CA176624, R01 CA176624] Funding Source: Medline
  5. NIAID NIH HHS [R01 AI105887, AI101407, AI105887, R37 AI105887, R01 AI101407] Funding Source: Medline
  6. NINDS NIH HHS [R01 NS064599, NS064599] Funding Source: Medline

向作者/读者索取更多资源

Foxp3(+) regulatory T cells (Tregs) maintain immune tolerance and play an important role in immunological diseases and cancers. Recent studies have revealed an intricate relationship between Treg biology and host and microbial metabolism. Various metabolites or nutrients produced by host and commensal microbes, such as vitamins and short-chain fatty acids (SCFAs), regulate Treg generation, trafficking, and function. Furthermore, cell intrinsic metabolic programs, orchestrated by mTOR and other metabolic sensors, modulate Foxp3 induction and Treg suppressive activity. Conversely, Tregs are crucial in regulating obesity-associated inflammation and host metabolic balance, and in shaping homeostasis of gut microbiota. We review here the interplay between Tregs and metabolism, with a particular focus on how host, commensal, and cellular metabolism impinge upon Treg homeostasis and function.

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