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10.1038/s41467-018-03493-5

http://scihub22266oqcxt.onion/10.1038/s41467-018-03493-5
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C5854619!5854619!29545616
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suck abstract from ncbi


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pmid29545616      Nat+Commun 2018 ; 9 (ä): ä
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  • Apolipoprotein AI prevents regulatory to follicular helper T cell switching during atherosclerosis #MMPMID29545616
  • Gaddis DE; Padgett LE; Wu R; McSkimming C; Romines V; Taylor AM; McNamara CA; Kronenberg M; Crotty S; Thomas MJ; Sorci-Thomas MG; Hedrick CC
  • Nat Commun 2018[]; 9 (ä): ä PMID29545616show ga
  • Regulatory T (Treg) cells contribute to the anti-inflammatory response during atherogenesis. Here we show that during atherogenesis Treg cells lose Foxp3 expression and their immunosuppressive function, leading to the conversion of a fraction of these cells into T follicular helper (Tfh) cells. We show that Tfh cells are pro-atherogenic and that their depletion reduces atherosclerosis. Mechanistically, the conversion of Treg cells to Tfh cells correlates with reduced expression of IL-2R? and pSTAT5 levels and increased expression of IL-6R?. In vitro, incubation of naive T cells with oxLDL prevents their differentiation into Treg cells. Furthermore, injection of lipid-free Apolipoprotein AI (ApoAI) into ApoE?/? mice reduces intracellular cholesterol levels in Treg cells and prevents their conversion into Tfh cells. Together our results suggest that ApoAI, the main protein in high-density lipoprotein particles, modulates the cellular fate of Treg cells and thus influences the immune response during atherosclerosis.
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