HMGB1
重症肌无力
发病机制
自身抗体
乙酰胆碱受体
炎症
免疫学
医学
自身免疫性疾病
内分泌学
病理
内科学
受体
抗体
作者
Bibinu Maimaitiming,Akiyuki Uzawa,Yukiko Ozawa,Manato Yasuda,Yuta Kojima,Tetsuya Kanai,Satoshi Kuwabara
出处
期刊:Neuroreport
[Lippincott Williams & Wilkins]
日期:2021-05-17
卷期号:32 (9): 803-807
被引量:3
标识
DOI:10.1097/wnr.0000000000001665
摘要
Myasthenia gravis (MG) is an autoimmune disease with autoantibodies against the mainly nicotinic acetylcholine receptor (AChR). High mobility group box1 (HMGB1) acts as a danger signal and drives the pathogenesis of autoimmune-mediated diseases. However, the role of HMGB1 in the pathogenesis of MG is not fully understood. Therefore, in this study, we analyzed serum levels of HMGB1 and immunohistochemical HMGB1 staining of muscle tissues in the passive transfer MG model to investigate the role of HMGB1 in MG. As a result, serum HMGB1 levels tended to be higher and the quantitative score of muscle pathology showed greater HMGB1 deposition (P = 0.02) along with sparser AChR staining and more severe inflammation in the passive transfer MG rats (n = 6) than those in control rats (n = 6). These findings indicate that HMGB1 is an important mediator and biomarker for inflammation in the pathogenesis of MG and can be a therapeutic target in MG.
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