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Assessing the expression of immunosuppressive cytokines in the newly diagnosed systemic lupus Erythematosus patients: a focus on B cells

机译:评估新诊断的全身狼疮红斑狼疮患者免疫抑制细胞因子的表达:对B细胞的关注

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The immunosuppressive effects of regulatory B-cells (Bregs) and their immunosuppressive cytokines on immune responses in autoimmune disorders, mainly systemic lupus erythematosus (SLE), have been recently established. Therefore, the purpose of this article has been the exploration of the expressions of cytokines produced by B cells in newly diagnosed SLE patients. The findings demonstrated that the gene expression of IL-10, TGF-β, IL-35, PD-L1, and FasL was significantly up-regulated in SLE patients compared to healthy subjects (P??0.05). Additionally, the results revealed that serum levels of IL-10, TGF-β, IL-35, PD-L1 were remarkably increased in patients with SLE compared to healthy subjects (P??0.0001). However, serum levels of IL-10 and TGF-β decreased significantly with increasing SLEDAI score in studied patients (P??0.05). It was concluded that the release of anti-inflammatory cytokines, particularly IL-10 and TGF-β, might inhibit immune responses and autoreactive immune cells in a compensatory manner in SLE patients with mild to moderate disease activity.
机译:最近建立了最近建立了监管B细胞(Bregs)及其免疫抑制细胞因子对自身免疫性障碍的免疫反应的影响,主要是全身性红斑狼疮(SLE)。因此,本文的目的是探讨了B细胞在新诊断的SLE患者中产生的细胞因子表达。结果表明,与健康受试者相比,在SLE患者中,IL-10,TGF-β,IL-35,PD-L1和FASL的基因表达显着上调(P?<?0.05)。另外,结果表明,与健康受试者相比,SLE与SLE的患者血清IL-10,TGF-β,IL-35,PD-L1的血清水平显着增加(P?<?0.0001)。然而,随着研究患者的增加评分增加了IL-10和TGF-β的血清IL-10和TGF-β(P?<?0.05)。结论是,抗炎细胞因子,特别是IL-10和TGF-β的释放可能在SLE患者中抑制免疫应答和自身反应性免疫细胞,以患有轻度至中等疾病活动的SLE患者。

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