State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou 510060, China.
Department of Endocrinology and Diabetes Center, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, China.
J Clin Endocrinol Metab. 2021 Jul 13;106(8):e3125-e3142. doi: 10.1210/clinem/dgab154.
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.
甲状腺相关性眼病(TAO)是一种与 Graves 病密切相关的器官特异性自身免疫性疾病。白细胞介素-38(IL-38)是白细胞介素-1 超家族中的一种新型细胞因子,据报道其参与了多种自身免疫性疾病的发病机制。
我们旨在评估 IL-38 与 TAO 疾病活动的关系及其在 TAO 炎症和纤维化中的作用。
收集 TAO 患者和对照者的血液样本和眼眶结缔组织。从 TAO 患者中分离眼眶成纤维细胞。采用酶联免疫吸附试验、免疫组织化学、流式细胞术、免疫荧光、实时定量 PCR 和 Western blot 分析进行检测。
在此,我们证明与对照组相比,TAO 患者的循环和眼眶结缔组织中的 IL-38 水平降低,且水平与临床活动评分呈负相关。体外,IL-38 表现出强大的抗炎和抗纤维化作用。此外,我们揭示 IL-38 可以抵消多个经典途径中星分子的磷酸化。
IL-38 在 TAO 中发挥保护作用,并与 TAO 的发病机制相关。我们的数据表明,IL-38 可能是 TAO 疾病活动的一个有前途的标志物,也是 TAO 治疗的一个潜在靶点。