Potential contribution of interleukin-33 to the development of interstitial lung disease in patients with primary Sjogren's Syndrome

被引:33
作者
Zhao, Lin [1 ,2 ]
Yao, Lutian [3 ]
Yuan, Lin [1 ]
Xia, Liping [1 ]
Shen, Hui [1 ]
Lu, Jing [1 ]
机构
[1] China Med Univ, Affiliated Hosp 1, Dept Rheumatol, Shenyang 110001, Peoples R China
[2] Dalian Med Univ, Affiliated Hosp 2, Dept Rheumatol, Dalian 116021, Peoples R China
[3] China Med Univ, Shenyang 110001, Peoples R China
关键词
Primary Sjogren's Syndrome; Interleukin-33; sST2; Interstitial lung disease; RHEUMATOID-ARTHRITIS; SOLUBLE ST2; IL-33; CELLS; PROTEIN; SIGNALS;
D O I
10.1016/j.cyto.2013.07.006
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
Objective: To determine whether interleukin (IL)-33 and soluble ST2 (sST2) are associated with primary Sjogren's Syndrome (pSS). Methods: Serum levels of IL-33 and sST2 in 110 pSS patients and 78 healthy controls were measured by enzyme-linked immunosorbent assay (ELISA). Immunoglobulins, rheumatoid factors (RF), antinuclear antibody (ANA), anti-SSA/RO-52 antibody, anti-SSB antibody and erythrocyte sedimentation rate (ESR) were measured by standard laboratory techniques. Interstitial lung disease (ILD) was identified on high-resolution computed tomography (HRCT). Disease activity in pSS was scored with the European League Against Rheumatism Sjogren's Syndrome Disease Activity Index (ESSDAI). Results: Serum levels of IL-33 and sST2 were significantly elevated in pSS patients, especially in patients with ILD. There was significant positive correlation between IL-33 and RF, anti-SSB antibody. Conclusion: IL-33/sST2 may be involved in the pathogenesis of pSS and partly contribute to the ILD in pSS patients. (c) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:22 / 24
页数:3
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