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首页> 外文期刊>Clinical & developmental immunology. >Expansion of Circulating T Follicular Helper Cells in Children with Acute Henoch-Sch?nlein Purpura
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Expansion of Circulating T Follicular Helper Cells in Children with Acute Henoch-Sch?nlein Purpura

机译:急性Henoch-Schonlein Purpura循环T滤泡辅助细胞的膨胀

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摘要

Henoch-Sch?nlein purpura (HSP) is a common systemic small vessel vasculitis in children with disorder autoimmune responses. T follicular helper (TFH) cells play crucial roles in regulating immune responses. The aim of our study was to investigate the probable role of TFH cells in the pathogenesis of children with HSP. In this study, the frequency of circulating CXCR5~(+)CD4~(+)TFH cells with inducible costimulator (ICOS) expression in the children with acute HSP was significantly higher than that in healthy controls (HCs) but not CXCR5~(+)CD4~(+)TFH cells with programmed death-1 (PD-1) expression. Moreover, serum levels of IL-21 and IL-6 cytokines, IgA, and C3 in HSP children were also significantly higher than those in HCs. A positive correlation was observed between the frequencies of circulating ICOS~(+)CXCR5~(+)CD4~(+)TFH cells and the serum IL-21 or IgA levels of acute HSP children, respectively. Additionally, the mRNA expression levels of interleukin- (IL-) 21, IL-6, and transcriptional factors (B-cell lymphoma-6, Bcl-6) were also significantly increased in peripheral blood from acute HSP children compared to HCs. Taken together, these findings suggest that TFH cells and associated molecules might play critical roles in the pathogenesis of HSP, which are possible therapeutic targets in HSP children.
机译:HENOCH-SCH?NLEIN PURPURA(HSP)是患有自身免疫反应的儿童常见的全身性小血管血管炎。 T卵泡辅助杆(TFH)细胞在调节免疫反应中起关键作用。我们的研究目的是探讨TFH细胞在HSP儿童发病机制中的可能作用。在该研究中,循环CXCR5〜(+)CD4〜(+)TFH细胞的频率与急性HSP的诱导型共刺激器(ICOS)表达明显高于健康对照(HCS)但不是CXCR5〜(+ )CD4〜(+)TFH细胞,具有编程死亡-1(PD-1)表达。此外,HSP儿童中IL-21和IL-6细胞因子,IgA和C3的血清水平也显着高于HCS中的IL-21和C3。在循环ICOS〜(+)CXCR5〜(+)CD4〜(+)TFH细胞和血清IL-21或IGA水平的急性HSP儿童的频率之间观察到阳性相关性。另外,与HCS相比,来自急性HSP儿童的外周血,白细胞介素 - (IL-)21,IL-6和转录因子(B细胞淋巴瘤-6,BCL-6)的mRNA表达水平也显着增加。在一起,这些发现表明TFH细胞和相关分子可能在HSP的发病机制中发挥关键作用,其在HSP儿童中是可能的治疗靶标。

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