Department of Rheumatology and Clinical Immunology, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Rheumatol Int. 2018 Aug;38(8):1511-1519. doi: 10.1007/s00296-018-4071-8. Epub 2018 May 30.
The aim of the study is to investigate the levels of serum interleukin-35 (IL-35) before and after treatment and its relationship with clinical parameters as well as the frequency of different subsets of CD4 T cells in patients with systemic sclerosis (SSc) to explore the role of IL-35 in the pathogenesis of SSc. The levels of serum IL-35, interferon-γ (IFN-γ), IL-4, IL-17A, and IL-10 in 49 patients with SSc and 50 age- and gender-matched healthy subjects were measured by enzyme-linked immunosorbent assay (ELISA). The percentages of peripheral blood Th1, Th2, Th17 cells and Tregs in 49 SSc patients and 20 healthy controls were characterized by flow cytometry. The relationship between the levels of serum IL-35 and the percentages of different subsets of CD4+ T cells, disease duration, the values of forced vital capacity (FVC), modified Rodnan skin scores (MRSS) or high-resolution computed tomography (HRCT) scores was analyzed in patients with SSc. The levels of serum IL-35 in SSc patients were significantly higher than that of healthy controls (P < 0.001), but significantly reduced after treatment for 3 months (P = 0.001). The levels of serum IL-35 were positively correlated with the HRCT scores in SSc patients (P = 0.014) and with disease duration in patients with diffuse cutaneous SSc (P = 0.03), but negatively correlated with the FVC values in SSc patients (P = 0.034). In comparison with that in the healthy controls, significantly decreased percentages of Th1, but increased Th2 and Th17 cells were detected in patients, leading to reduced ratios of Th1/Th2 and increased ratios of Th17/Tregs (P < 0.001). The levels of serum IL-35 were positively correlated with IL-4 (P = 0.036) and tended to be positively associated with the frequency of Tregs in SSc patients (P = 0.054). Higher levels of serum IL-35 may be associated with the development of SSc and severity of pulmonary fibrosis in SSc patients.
本研究旨在探讨系统性硬化症(SSc)患者治疗前后血清白细胞介素-35(IL-35)的水平及其与临床参数以及 CD4+T 细胞不同亚群频率的关系,以探讨 IL-35 在 SSc 发病机制中的作用。采用酶联免疫吸附试验(ELISA)检测 49 例 SSc 患者和 50 名年龄和性别匹配的健康对照者血清 IL-35、干扰素-γ(IFN-γ)、IL-4、IL-17A 和 IL-10 的水平。采用流式细胞术检测 49 例 SSc 患者和 20 名健康对照者外周血 Th1、Th2、Th17 细胞和 Tregs 的百分比。分析 SSc 患者血清 IL-35 水平与 CD4+T 细胞不同亚群百分比、疾病持续时间、用力肺活量(FVC)、改良 Rodnan 皮肤评分(MRSS)或高分辨率计算机断层扫描(HRCT)评分的关系。SSc 患者血清 IL-35 水平明显高于健康对照组(P<0.001),但治疗 3 个月后明显降低(P=0.001)。SSc 患者血清 IL-35 水平与 HRCT 评分呈正相关(P=0.014),与弥漫性皮肤 SSc 患者的疾病持续时间呈正相关(P=0.03),与 SSc 患者的 FVC 值呈负相关(P=0.034)。与健康对照组相比,患者 Th1 细胞比例明显降低,Th2 和 Th17 细胞比例明显升高,导致 Th1/Th2 比值降低,Th17/Tregs 比值升高(P<0.001)。血清 IL-35 水平与 IL-4 呈正相关(P=0.036),与 SSc 患者 Tregs 频率呈正相关趋势(P=0.054)。较高的血清 IL-35 水平可能与 SSc 的发生和 SSc 患者肺纤维化的严重程度有关。