Miao Jinlin, Geng Jiejie, Zhang Kui, Li Xueyi, Li Qiang, Li Cuicui, Zhu Ping
Department of Clinical Immunology, Branch of Immune Cell Biology, State Key Discipline of Cell Biology, Xijing Hospital, Fourth Military Medical University , Shaanxi , People's Republic of China.
Mod Rheumatol. 2014 Mar;24(2):265-570. doi: 10.3109/14397595.2013.854070.
Rheumatoid arthritis (RA) is a common autoimmune disease that is primarily driven by effector T cells, particularly Th17 cells, which are mainly contained within CD4+CD161+ T cells. Thus, we aimed to explore whether the frequencies of circulating IL-17-producing CD4+CD161+ T cells and CD4+CD161+ T cells were correlated with RA disease activity.
The surface phenotype and cytokine production of blood were analyzed by flow cytometry in 52 RA patients and 17 healthy controls. The disease activity was evaluated by the 28-joint disease activity score.
The frequencies of circulating IL-17-producing CD4+CD161+ T cells and CD4+CD161+ T cells were increased in RA patients, and they were elevated in patients with active disease status compared to patients with low disease status. Furthermore, their frequencies were positively correlated with disease activity parameters. Receiver operating characteristic curve analysis revealed that IL-17-producing CD4+CD161+ T cell levels were able to distinguish disease activity with 60.7 % sensitivity and 87.5 % specificity, while CD4+CD161+ T cell levels showed 92.9 % sensitivity and 66.7 % specificity.
These results support the hypothesis that Th17 cells are involved in the pathogenesis of RA and suggest that circulating CD4+CD161+ T cells are a potential biomarker of RA disease activity.
类风湿关节炎(RA)是一种常见的自身免疫性疾病,主要由效应T细胞驱动,特别是Th17细胞,其主要存在于CD4+CD161+ T细胞中。因此,我们旨在探讨循环中产生IL-17的CD4+CD161+ T细胞和CD4+CD161+ T细胞的频率是否与RA疾病活动相关。
采用流式细胞术分析52例RA患者和17例健康对照者血液的表面表型和细胞因子产生情况。通过28个关节疾病活动评分评估疾病活动度。
RA患者循环中产生IL-17的CD4+CD161+ T细胞和CD4+CD161+ T细胞频率增加,与疾病活动度低的患者相比,疾病活动状态活跃的患者中这些细胞频率升高。此外,它们的频率与疾病活动参数呈正相关。受试者工作特征曲线分析显示,产生IL-17的CD4+CD161+ T细胞水平能够以60.7%的敏感性和87.5%的特异性区分疾病活动度,而CD4+CD161+ T细胞水平显示出92.9%的敏感性和66.7%的特异性。
这些结果支持Th17细胞参与RA发病机制的假说,并表明循环CD4+CD161+ T细胞是RA疾病活动的潜在生物标志物。