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首页> 外文期刊>European neurology >Expression of Th1/Th2-Related Chemokine Receptors on Peripheral T Cells and Correlation with Clinical Disease Activity in Patients with Multiple Sclerosis.
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Expression of Th1/Th2-Related Chemokine Receptors on Peripheral T Cells and Correlation with Clinical Disease Activity in Patients with Multiple Sclerosis.

机译:多发性硬化症患者外周T细胞中Th1 / Th2相关趋化因子受体的表达及其与临床疾病活动的关系。

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Th1 cells play an important role in the pathogenesis of multiple sclerosis (MS), a disease likely linked to an autoimmune process. We measured the levels of chemokines in serum or cerebrospinal fluid (CSF) samples by ELISA, and also studied the expression of Th1-related CXCR3/CCR5 chemokine receptors and Th2-related CCR4/CCR3 chemokine receptors on blood cells from MS patients using three-color flow cytometry. The Bonferroni correction was used for the statistical analysis. The levels of CXCL10, CCL3, and CCL5 in the CSF samples for the MS groups were significantly higher than those for the control group. However, the levels of CCL2 in both the CSF and serum samples for the remission group were significantly higher than those for the active group. The percentage of CXCR3-expressing CD4+ T cells in patients with MS was significantly elevated compared with the healthy controls. Moreover, MS patients in an active phase showed a more increased CD4+CXCR3+/CD4+CCR4+ ratio than patients in a remission phase. The increased percentage of CD4+CXCR3+ cells in the blood was associated with relapses in MS. This study suggested that the CD4+CXCR3+/CD4+CCR4+ ratio could be a sensitive maker of immune dysfunction in MS. Copyright (c) 2004 S. Karger AG, Basel.
机译:Th1细胞在多发性硬化症(MS)的发病机理中起着重要作用,多发性硬化症可能与自身免疫过程有关。我们使用ELISA方法测定了MS患者血细胞中血清或脑脊液(CSF)样品中趋化因子的水平,并研究了Th1相关CXCR3 / CCR5趋化因子受体和Th2相关CCR4 / CCR3趋化因子受体在MS患者血细胞中的表达。彩色流式细胞仪。 Bonferroni校正用于统计分析。 MS组CSF样品中CXCL10,CCL3和CCL5的水平显着高于对照组。然而,缓解组的脑脊液和血清样品中的CCL2水平均显着高于活性组。与健康对照组相比,MS患者中表达CXCR3的CD4 + T细胞的百分比显着升高。而且,处于活动期的MS患者比处于缓解期的患者显示出更多的CD4 + CXCR3 + / CD4 + CCR4 +比率。血液中CD4 + CXCR3 +细胞百分比的增加与MS复发有关。这项研究表明,CD4 + CXCR3 + / CD4 + CCR4 +可能是MS免疫功能异常的敏感原因。版权所有(c)2004 S.Karger AG,巴塞尔。

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