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Inducible costimulator is essential for collagen-induced arthritis.

机译:诱导共刺激剂对于胶原诱导的关节炎至关重要。

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摘要

CD4(+) helper Th cells play a major role in the pathogenesis of rheumatoid arthritis. Th cell activation, differentiation, and immune function are regulated by costimulatory molecules. Inducible costimulator (ICOS) is a novel costimulatory receptor expressed on activated T cells. We, as well as others, recently demonstrated its importance in Th2 cytokine expression and Ab class switching by B cells. In this study, we examined the role of ICOS in rheumatoid arthritis using a collagen-induced arthritis model. We found that ICOS knockout mice on the DBA/1 background were completely resistant to collagen-induced arthritis and exhibited absence of joint tissue inflammation. These mice, when immunized with collagen, exhibited reduced anti-collagen IgM Ab's in the initial stage and IgG2a Ab's at the effector phase of collagen-induced arthritis. Furthermore, ICOS regulates the in vitro and in vivo expression of IL-17, a proinflammatory cytokine implicated in rheumatoid arthritis. These data indicate that ICOS is essential for collagen-induced arthritis and may suggest novel means for treating patients with rheumatoid arthritis.
机译:CD4(+)辅助Th细胞在类风湿关节炎的发病机制中起主要作用。细胞活化、分化和免疫功能受共刺激分子的调节。诱导共刺激因子 (ICOS) 是一种在活化的 T 细胞上表达的新型共刺激受体。我们和其他人最近证明了它在 Th2 细胞因子表达和 B 细胞抗体类转换中的重要性。在这项研究中,我们使用胶原诱导的关节炎模型检查了ICOS在类风湿性关节炎中的作用。我们发现DBA/1背景的ICOS敲除小鼠对胶原诱导的关节炎完全抵抗,并且没有关节组织炎症。当用胶原蛋白免疫时,这些小鼠在胶原诱导的关节炎的初始阶段表现出抗胶原IgM抗体的减少,在效应期表现出IgG2a抗体的减少。此外,ICOS 调节 IL-17 的体外和体内表达,IL-17 是一种与类风湿性关节炎有关的促炎细胞因子。这些数据表明,ICOS对胶原诱导的关节炎至关重要,并可能为治疗类风湿性关节炎患者提供新的方法。

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