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首页> 外文期刊>Scandinavian journal of rheumatology >The effect of methotrexate (MTX) on expression of signalling lymphocytic activation molecule (SLAM) in patients with rheumatoid arthritis (RA) and its role in the regulation of cytokine production.
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The effect of methotrexate (MTX) on expression of signalling lymphocytic activation molecule (SLAM) in patients with rheumatoid arthritis (RA) and its role in the regulation of cytokine production.

机译:甲氨蝶呤(MTX)对类风湿关节炎(RA)患者信号转导淋巴细胞活化分子(SLAM)表达的影响及其在调节细胞因子产生中的作用。

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摘要

OBJECTIVE: To investigate the effect of methotrexate (MTX) on cytokine production by activated CD4+ T-cells in patients with rheumatoid arthritis (RA). METHODS: The effect of MTX on intracellular expression of interferon-gamma (IFN-gamma) and interleukin-4 (IL-4), and cell surface expression of signalling lymphocytic activation molecule (SLAM) from freshly isolated peripheral blood mononuclear cells (PBMCs), and after in vitro culture with or without MTX, was analysed with flow cytometry in 18 patients with RA and 20 healthy controls. RESULTS: Intracellular expression of IFN-gamma and IL-4 on freshly isolated CD4+ T-cells was significantly higher in patients with RA than in the controls (p<0.05). Intracellular expression of both IFN-gamma and IL-4 after culture with MTX was significantly lower than those after culture without MTX in patients with RA. Although no significant difference was observed in SLAM expression on freshly isolated CD4+ T-cells between patients with RA and the controls, MTX significantly decreased SLAM expression on both activated IFN-gamma+ and IL-4+CD4+ T-cells in patients with RA. CONCLUSION: In vitro modulation of the cytokine network by MTX, IFN-gamma, and IL-4 is one of the major targets for MTX, and production of IFN-gamma and IL-4 by PBMCs may be suppressed by SLAM on activated CD4+ T-cell in patients with RA.
机译:目的:探讨甲氨蝶呤(MTX)对类风湿关节炎(RA)患者活化的CD4 + T细胞产生细胞因子的影响。方法:MTX对新鲜分离的外周血单个核细胞(PBMC)中干扰素-γ(IFN-γ)和白介素-4(IL-4)的细胞内表达以及信号淋巴细胞活化分子(SLAM)的细胞表面表达的影响,在有或没有MTX的体外培养后,用流式细胞仪分析了18例RA患者和20例健康对照者。结果:RA患者新鲜分离的CD4 + T细胞中IFN-γ和IL-4的细胞内表达明显高于对照组(p <0.05)。在RA患者中,MTX培养后IFN-γ和IL-4的细胞内表达均显着低于无MTX培养后的细胞内表达。尽管RA患者与对照组之间新鲜分离的CD4 + T细胞上SLAM表达没有观察到显着差异,但MTX显着降低了RA患者活化IFN-γ+和IL-4 + CD4 + T细胞上SLAM表达。结论:MTX,IFN-γ和IL-4对细胞因子网络的体外调控是MTX的主要靶标之一,SLAM可通过活化的CD4 + T抑制PBMC产生IFN-γ和IL-4。类风湿关节炎患者的红细胞。

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