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首页> 外文期刊>Rheumatology >Potential role of Th17 cells in the pathogenesis of adult-onset Still's disease.
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Potential role of Th17 cells in the pathogenesis of adult-onset Still's disease.

机译:Th17细胞在成人性Still病发病机理中的潜在作用。

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摘要

OBJECTIVE: To investigate the potential role of Th type 17 (Th17) cells and Th17-related cytokines in the pathogenesis of adult-onset Still's disease (AOSD). METHODS: The frequencies of circulating Th17 cells in 24 patients with active untreated AOSD, 16 patients with active SLE and 12 healthy volunteers were determined using intracellular cytokine staining and flow cytometry. Serum levels of Th17-related cytokines, including IL-1beta, IL-6, IL-17, IL-18, IL-21 and IL-23 were measured by ELISA. RESULTS: Significantly higher median frequencies of circulating Th17 cells were found in active untreated AOSD patients (1.01%) and active SLE patients (1.26%) than in healthy volunteers (0.12%, both P<0.001). The frequencies of circulating Th17 cells were positively correlated with activity score (r=0.527, P<0.01) and serum ferritin levels (r=0.724, P<0.001) in AOSD patients, and correlated with SLEDAI (r=0.663, P<0.01) in SLE patients. Additionally, the frequencies of circulating Th17 cells were positively and significantly correlated with serum levels of IL-1beta, IL-6, IL-17, IL-18, IL-21 and IL-23 in both AOSD and SLE patients. The frequencies of circulating Th17 cells and serum IL-17 levels significantly decreased after effective therapy in AOSD patients (both P<0.001). CONCLUSION: Elevated frequencies of circulating Th17 cells and a positive correlation with disease activity in our AOSD patients suggest that Th17 cells contribute to the pathogenesis of this disease. Dysregulation of Th17 cells may be a common pathogenic mechanism that underlies the development of both AOSD and SLE.
机译:目的:探讨Th型17(Th17)细胞和Th17相关细胞因子在成年Still病(AOSD)发病机理中的潜在作用。方法:使用细胞内细胞因子染色和流式细胞仪测定24例未经治疗的AOSD患者,16例SLE和12例健康志愿者的Th17细胞的循环频率。通过ELISA测量血清中Th17相关细胞因子的水平,包括IL-1β,IL-6,IL-17,IL-18,IL-21和IL-23。结果:活跃的未经治疗的AOSD患者(1.01%)和活跃的SLE患者(1.26%)的循环Th17细胞中位频率明显高于健康志愿者(0.12%,均P <0.001)。 AOSD患者的循环Th17细胞频率与活动评分(r = 0.527,P <0.01)和血清铁蛋白水平(r = 0.724,P <0.001)呈正相关,与SLEDAI相关(r = 0.663,P <0.01)。 )在SLE患者中。另外,在AOSD和SLE患者中,循环中的Th17细胞的频率与IL-1β,IL-6,IL-17,IL-18,IL-21和IL-23的血清水平呈正相关且显着相关。在AOSD患者中,有效治疗后循环Th17细胞的频率和血清IL-17水平显着降低(均P <0.001)。结论:在我们的AOSD患者中,循环中的Th17细胞的频率升高与疾病活动呈正相关,提示Th17细胞是该疾病的发病机制。 Th17细胞失调可能是导致AOSD和SLE共同发展的常见致病机制。

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