Broegelmann Research Laboratory, Department of Clinical Science, University of Bergen, Bergen, Norway.
Clin Exp Immunol. 2014 Jul;177(1):244-52. doi: 10.1111/cei.12341.
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.
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(尤其是干燥综合征,SS)中循环自身抗体的常见靶标。在这项研究中,我们旨在研究原发性干燥综合征(pSS)患者唾液腺中 SS 靶自身抗原 Ro52 的表达。使用抗人 Ro52 单克隆抗体,通过对来自瑞典和挪威登记处的 28 例 pSS 患者和 19 例非 pSS 对照者的石蜡包埋和冷冻唾液腺活检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试验(ELISA)测量来自同一个体的唾液和血清样本中的分泌型 Ro52 蛋白。Ro52 在所有 pSS 患者的局灶性浸润中均高度表达。有趣的是,与非 pSS 对照者相比,患者的导管上皮中 Ro52 的表达程度明显更高(P < 0·03)。此外,导管上皮中 Ro52 的表达程度与炎症程度相关(Spearman r = 0·48,P < 0·0120)。然而,在这些受试者的血清和唾液样本中均未检测到分泌型 Ro52 蛋白。导管上皮中的 Ro52 表达与炎症程度一致,并在 pSS 患者中上调。Ro52 的高表达可能导致在遗传易感个体中打破耐受并产生 Ro52 自身抗体。我们得出结论,Ro52 在导管上皮中的上调可能是 SS 疾病进展的触发因素。