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Ductal epithelial expression of Ro52 correlates with inflammation in salivary glands of patients with primary Sjögrens syndrome

机译:Ro52的导管上皮表达与原发性干燥综合征患者唾液腺中的炎症相关

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摘要

Ro52 is an E3 ubiquitin ligase with a prominent regulatory role in inflammation. The protein is a common target of circulating autoantibodies in rheumatic autoimmune diseases, particularly Sjögren's syndrome (SS). In this study we aimed to investigate the expression of the SS target autoantigen Ro52 in salivary glands of patients with primary Sjögren's syndrome (pSS). Ro52 expression was assessed by immunohistochemical staining of paraffin-embedded and frozen salivary gland biopsies from 28 pSS patients and 19 non-pSS controls from Swedish and Norwegian registries, using anti-human Ro52 monoclonal antibodies. The degree and pattern of staining and inflammation was then evaluated. Furthermore, secreted Ro52 protein was measured in saliva and serum samples from the same individuals through a catch-enzyme-linked immunosorbent assay (ELISA). Ro52 was highly expressed in all the focal infiltrates in pSS patients. Interestingly, a significantly higher degree of Ro52 expression in ductal epithelium was observed in the patients compared to the non-pSS controls (P < 0·03). Moreover, the degree of ductal epithelial expression of Ro52 correlated with the level of inflammation (Spearman's r = 0·48, P < 0·0120). However, no secreted Ro52 protein could be detected in serum and saliva samples of these subjects. Ro52 expression in ductal epithelium coincides with degree of inflammation and is up-regulated in pSS patients. High expression of Ro52 might result in the breakage of tolerance and generation of Ro52 autoantibodies in genetically susceptible individuals. We conclude that the up-regulation of Ro52 in ductal epithelium might be a triggering factor for disease progression in SS.
机译:Ro52是一种E3泛素连接酶,在炎症中具有重要的调节作用。该蛋白是风湿性自身免疫性疾病,特别是干燥综合征(SS)中循环自身抗体的常见靶标。在这项研究中,我们旨在研究SS靶标自身抗原Ro52在原发性干燥综合征(pSS)患者唾液腺中的表达。通过使用抗人Ro52单克隆抗体,对来自28位pSS患者和来自瑞典和挪威注册表的19位非pSS对照的石蜡包埋和冷冻唾液活检组织进行免疫组织化学染色,评估Ro52的表达。然后评估染色和炎症的程度和模式。此外,通过捕获酶联免疫吸附测定(ELISA)在同一个人的唾液和血清样品中测量了分泌的Ro52蛋白。 Ro52在pSS患者的所有病灶浸润中高表达。有趣的是,与非pSS对照相比,在患者的导管上皮中观察到Ro52表达的明显升高(P <0·03)。此外,Ro52的导管上皮表达程度与炎症水平相关(Spearman r = 0·48,P <0·0120)。然而,在这些受试者的血清和唾液样品中未检测到分泌的Ro52蛋白。在pSS患者中,导管上皮中的Ro52表达与炎症程度相吻合并且上调。 Ro52的高表达可能会导致遗传易感个体中的耐受性破坏并产生Ro52自身抗体。我们得出的结论是,导管上皮中Ro52的上调可能是SS疾病进展的触发因素。

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