Avota E, Avots A, Niewiesk S, Kane L P, Bommhardt U, ter Meulen V, Schneider-Schaulies S
Institute for Virology and Immunobiology, University of Würzburg, Würzburg, Germany.
Nat Med. 2001 Jun;7(6):725-31. doi: 10.1038/89106.
Surface-contact-mediated signaling induced by the measles virus (MV) fusion and hemagglutinin glycoproteins is necessary and sufficient to induce T-cell unresponsiveness in vitro and in vivo. To define the intracellular pathways involved, we analyzed interleukin (IL)-2R signaling in primary human T cells and in Kit-225 cells. Unlike IL-2-dependent activation of JAK/STAT pathways, activation of Akt kinase was impaired after MV contact both in vitro and in vivo. MV interference with Akt activation was important for immunosuppression, as expression of a catalytically active Akt prevented negative signaling by the MV glycoproteins. Thus, we show here that MV exploits a novel strategy to interfere with T-cell activation during immunosuppression.
麻疹病毒(MV)融合蛋白和血凝素糖蛋白诱导的表面接触介导信号传导对于在体外和体内诱导T细胞无反应性而言是必要且充分的。为了确定其中涉及的细胞内途径,我们分析了原代人T细胞和Kit-225细胞中的白细胞介素(IL)-2R信号传导。与IL-2依赖的JAK/STAT途径激活不同,MV接触后,体外和体内的Akt激酶激活均受损。MV对Akt激活的干扰对于免疫抑制很重要,因为具有催化活性的Akt的表达可阻止MV糖蛋白的负信号传导。因此,我们在此表明,MV在免疫抑制过程中采用了一种新策略来干扰T细胞激活。