Elevation of Serum IL-35 in Patients with Primary Sjogren's Syndrome

被引:11
作者
Han, Meiling [1 ]
Li, Yuxuan [1 ]
Liu, Siyan [1 ]
Jiang, Shenyi [1 ]
Yuan, Lin [1 ]
Xia, Liping [1 ]
Shen, Hui [1 ]
Lu, Jing [1 ]
机构
[1] China Med Univ, Affiliated Hosp 1, Dept Rheumatol & Immunol, 155 Nanjing North St, Shenyang 110001, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
primary Sjogren's syndrome; interleukin-35; disease activity; disease duration; autoantibody production; COLLAGEN-INDUCED ARTHRITIS; T-CELLS; RHEUMATOID-ARTHRITIS; SYSTEMIC-SCLEROSIS; DISEASE; INTERLEUKIN-35; SUPPRESSION; CYTOKINE; GROWTH;
D O I
10.1089/jir.2018.0059
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Interleukin-35 (IL-35) is a critical anti-inflammatory cytokine in autoimmune disease. In the current study, we aimed to investigate the serum IL-35 levels and its clinical association in patients with primary Sjogren's syndrome (pSS) and to investigate whether or not IL-35 participates in the pathogenesis of pSS. One hundred seventy-six pSS patients and 60 healthy controls (HCs) were recruited. Disease activity was assessed according to EULAR SS disease activity index. Serum IL-35 levels were quantified by enzyme-linked immunosorbent assay. The correlations between the serum IL-35 levels with the clinical parameters were analyzed by a Spearman's correlation test. The serum IL-35 levels in the patients with pSS were significantly increased compared with the HCs. The serum IL-35 levels were elevated in the patients with pSS. Strikingly, the serum IL-35 levels in pSS patients with short disease duration (<1 year) were significantly lower compared with HCs. However, the serum IL-35 levels in pSS patients with medium (1-2 year) and long disease duration (>2 years) were higher compared with HCs. We also found a positive correlation between expression of IL-35 and erythrocyte sedimentation rate, disease activity, and immunoglobulin G. Furthermore, the pSS patients with RF-positive showed high serum IL-35 levels. These findings suggest that IL-35 could play a key role in pSS pathogenesis. In addition, our results highlight the potential exploitation of IL-35 as a biomarker of disease activity and may represent a novel therapeutic agent for pSS.
引用
收藏
页码:452 / 456
页数:5
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