Shenzhen Research Institute of Shandong University, Shenzhen, Guangdong, China (mainland).
Department of Rheumatology, Qilu Hospital of Shandong University, Ji'nan, Shandong, China (mainland).
Med Sci Monit. 2018 Aug 14;24:5660-5667. doi: 10.12659/MSM.909254.
BACKGROUND Anti-inflammatory mediators such as mucin-domain containing-3 (TIM-3) and IL-37 play an important role in the regulation of Th1-mediated immunity. This study was designed to investigate the proportions of various T cell subsets and monocytes in the peripheral blood of rheumatoid arthritis (RA) patients, as well as the level of TIM-3 on these cells and serum cytokine levels. MATERIAL AND METHODS We enrolled 59 RA patients and 46 age- and sex-matched healthy controls in this study. The proportion of T cells and TIM-3 expression on these T cells were determined by flow cytometry. Cytokine levels in serum were determined by ELISA. RESULTS Compared with the healthy controls, the proportions of CD3+CD4+ T cells and CD3+CD4+CD25+CD127low T cells in the peripheral blood were significantly higher in RA patients. However, RA patients had significantly lower proportions of CD3+CD8+ T cells and CD3+CD4-CD8- T cells. TIM-3 was highly expressed on CD3+CD4+, CD3+CD8+, CD3+CD4+CD25+CD127low, and CD3+CD4-CD8- T cells, as well as CD14+ monocytes, in RA patients. Nevertheless, no correlation between TIM-3 level and an RA disease activity score of 28 was found. The elevated serum levels of IL-6 and IL-37 were positively correlated with tumor necrosis factor-α (TNF-α). CONCLUSIONS Both pro-inflammatory cytokines (TNF-α and IL-6) and anti-inflammatory mediators (TIM-3 and IL-37) simultaneously contribute to the pathogenesis of RA. TIM-3 and IL-37 may be used as potential biomarkers of active RA.
黏蛋白结构域包含 3(TIM-3)和白细胞介素 37(IL-37)等抗炎介质在调节 Th1 介导的免疫中发挥重要作用。本研究旨在探讨类风湿关节炎(RA)患者外周血中各种 T 细胞亚群和单核细胞的比例,以及这些细胞上 TIM-3 的表达水平和血清细胞因子水平。
我们纳入了 59 例 RA 患者和 46 名年龄和性别匹配的健康对照者进行本研究。通过流式细胞术测定 T 细胞比例和这些 T 细胞上 TIM-3 的表达。通过 ELISA 测定血清细胞因子水平。
与健康对照组相比,RA 患者外周血中 CD3+CD4+T 细胞和 CD3+CD4+CD25+CD127low T 细胞的比例明显升高。然而,RA 患者 CD3+CD8+T 细胞和 CD3+CD4-CD8-T 细胞的比例明显降低。TIM-3 在 RA 患者的 CD3+CD4+、CD3+CD8+、CD3+CD4+CD25+CD127low 和 CD3+CD4-CD8-T 细胞以及 CD14+单核细胞上高表达。然而,并未发现 TIM-3 水平与 RA 疾病活动评分 28 之间存在相关性。升高的血清 IL-6 和 IL-37 水平与肿瘤坏死因子-α(TNF-α)呈正相关。
促炎细胞因子(TNF-α和 IL-6)和抗炎介质(TIM-3 和 IL-37)均共同参与 RA 的发病机制。TIM-3 和 IL-37 可能作为 RA 活动的潜在生物标志物。