IL-38 Exerts Anti-Inflammatory and Antifibrotic Effects in Thyroid-Associated Ophthalmopathy

发病机制 医学 纤维化 结缔组织 炎症 细胞因子 免疫组织化学 格雷夫斯病 甲状腺 免疫印迹 内科学 流式细胞术 免疫荧光 病理 免疫学 生物 抗体 生物化学 基因
作者
Lu Shi,Huijing Ye,Jun Huang,Yanbing Li,Xing Wang,Zhihui Xu,Jingqiao Chen,Wei Xiao,Rongxin Chen,Huasheng Yang
出处
期刊:The Journal of Clinical Endocrinology and Metabolism [Oxford University Press]
卷期号:106 (8): e3125-e3142 被引量:24
标识
DOI:10.1210/clinem/dgab154
摘要

Thyroid-associated ophthalmopathy (TAO) is an organ-specific autoimmune disease closely associated with Graves' disease. IL-38, a novel cytokine in the IL-1 superfamily, has been reported to be involved in the pathogenesis of various autoimmune diseases.We aimed to evaluate the relationship between IL-38 and TAO disease activity and its role in inflammation and fibrosis in TAO.Blood samples and orbital connective tissues were collected from TAO patients and controls. Orbital fibroblasts were isolated from patients with TAO. Enzyme-linked immunosorbent assay, immunohistochemistry, flow cytometry, immunofluorescence, quantitative real-time PCR and Western blot analysis were performed.Here, we demonstrated that IL-38 levels decreased in the circulation and orbital connective tissues of patients with TAO compared with the controls, and levels were negatively correlated with the clinical activity score. In vitro, potent anti-inflammatory and antifibrotic effects of IL-38 were observed. Furthermore, we revealed that IL-38 can counteract the phosphorylation of star molecules in multiple classical pathways.IL-38 plays a protective role in TAO and is associated with its pathogenesis. Our data suggest that IL-38 may be a promising marker of TAO disease activity and a potential target for TAO therapy.
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