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10.3389/fimmu.2017.00311

http://scihub22266oqcxt.onion/10.3389/fimmu.2017.00311
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C5359241!5359241!28377767
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suck abstract from ncbi


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pmid28377767      Front+Immunol 2017 ; 8 (ä): ä
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  • Immunometabolic Regulation of Interleukin-17-Producing T Helper Cells: Uncoupling New Targets for Autoimmunity #MMPMID28377767
  • Binger KJ; Côrte-Real BF; Kleinewietfeld M
  • Front Immunol 2017[]; 8 (ä): ä PMID28377767show ga
  • Interleukin-17-producing T helper (Th17) cells are critical for the host defense of bacterial and fungal pathogens and also play a major role in driving pathogenic autoimmune responses. Recent studies have indicated that the generation of Th17?cells from naïve CD4+ T cells is coupled with massive cellular metabolic adaptations, necessary to cope with different energy and metabolite requirements associated with switching from a resting to proliferative state. Furthermore, Th17?cells have to secure these metabolic adaptations when facing nutrient-limiting environments, such as at the sites of inflammation. Accumulating data indicates that this metabolic reprogramming is significantly linked to the differentiation of T helper cells and, particularly, that the metabolic changes of Th17?cells and anti-inflammatory Forkhead box P3+ regulatory T cells are tightly and reciprocally regulated. Thus, a better understanding of these processes could offer potential new targets for therapeutic interventions for autoimmune diseases. In this mini-review, we will highlight some of the recent advances and discoveries in the field, with a particular focus on metabolic demands of Th17?cells and their implications for autoimmunity.
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