We show that STAT5b is important for the in vivo accumulation of CD4+ CD25(high) T cells with regulatory cell function. A patient homozygous for a missense A630P STAT5b mutation displayed immune dysregulation and decreased numbers of CD4+ CD25(high) T cells. STAT5b(A630P/A630P) CD4+ CD25(high) T cells had low expression of forkhead box P3 and an impaired ability to suppress the proliferation of or to kill CD4+ CD25- T cells. Expression of CD25, a component of the high-affinity IL-2R, was also reduced in response to IL-2 or after in vitro propagation. The impact of the STAT5b mutation was selective in that IL-2-mediated up-regulation of the common gamma-chain cytokine receptor and perforin, and activation-induced expressions of CD154 and IFN-gamma were normal. These results indicate that STAT5b propagates an important IL-2-mediated signal for the in vivo accumulation of functional regulatory T cells.

译文

:我们表明STAT5b对于具有调节性细胞功能的CD4 CD25(high)T细胞在体内的积累很重要。一名纯合的错义A630P STAT5b突变患者表现出免疫失调和CD4 CD25(高)T细胞数量减少。 STAT5b(A630P / A630P)CD4 CD25(高)T细胞叉头盒P3的表达低,抑制CD4 CD25- T细胞增殖或杀死CD4 CD25-T细胞的能力受损。高亲和力IL-2R的组成部分CD25的表达也响应IL-2或在体外繁殖后降低。 STAT5b突变的影响是选择性的,因为IL-2介导了共同的γ链细胞因子受体和穿孔素的上调,并且激活诱导的CD154和IFN-γ的表达是正常的。这些结果表明STAT5b传播重要的IL-2介导的信号,用于体内功能性调节性T细胞的蓄积。

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