Department of Biochemistry, Medical University of Warsaw, 02-097 Warsaw, Poland.
Department of Otolaryngology, Medical Centre for Postgraduate Education, 03-242 Warsaw, Poland.
Mediators Inflamm. 2021 Mar 11;2021:8891324. doi: 10.1155/2021/8891324. eCollection 2021.
Graves' ophthalmopathy (GO) is a chronic autoimmune inflammatory disorder involving orbital tissues. A receptor for advanced glycation end products (RAGE) and its ligand high mobility group box 1 (HMGB1) protein trigger inflammation and cell proliferation and are involved in the pathogenesis of various chronic inflammatory diseases. This study was aimed to evaluate RAGE and HMGB1 expression in GO to determine its potential clinical significance. To the best of our knowledge, this is the first study showing RAGE and HMGB1 expression in orbital tissue using immunohistochemistry. Sections of orbital adipose tissue obtained from patients diagnosed with GO (23 patients; 36 orbits) and normal controls (NC) (15 patients; 15 orbits) were analyzed by immunohistochemistry for RAGE and HMGB1 expression. Expression profiles were then correlated with clinical data of the study group. RAGE and HMGB1 expression were elevated in GO patients in comparison with NC ( = 0.001 and = 0.02, respectively). We observed a correlation between RAGE expression and occurrence of dysthyroid optic neuropathy (DON) ( = 0.05) and levels of TSH Receptor Antibodies (TRAb) ( = 0.01). Overexpression of RAGE and HMGB1 might be associated with GO pathogenesis. In addition, RAGE and HMGB1 proteins may be considered as promising therapeutic targets, but this requires further research.
格雷夫斯眼病(GO)是一种涉及眼眶组织的慢性自身免疫性炎症性疾病。晚期糖基化终产物(RAGE)受体及其配体高迁移率族蛋白 1(HMGB1)蛋白触发炎症和细胞增殖,并参与各种慢性炎症性疾病的发病机制。本研究旨在评估 GO 中 RAGE 和 HMGB1 的表达,以确定其潜在的临床意义。据我们所知,这是首次使用免疫组织化学法显示眼眶组织中 RAGE 和 HMGB1 表达的研究。使用免疫组织化学法分析了从诊断为 GO(23 例患者;36 只眼眶)和正常对照组(NC)(15 例患者;15 只眼眶)患者中获得的眼眶脂肪组织切片中 RAGE 和 HMGB1 的表达。然后将表达谱与研究组的临床数据相关联。与 NC 相比,GO 患者的 RAGE 和 HMGB1 表达升高(=0.001 和=0.02)。我们观察到 RAGE 表达与甲状腺功能亢进性视神经病变(DON)的发生(=0.05)和 TSH 受体抗体(TRAb)水平(=0.01)之间存在相关性。RAGE 和 HMGB1 的过表达可能与 GO 的发病机制有关。此外,RAGE 和 HMGB1 蛋白可以被认为是有前途的治疗靶点,但这需要进一步的研究。