重症肌无力
乙酰胆碱受体
神经肌肉接头
抗体
自身免疫性疾病
免疫学
医学
弱点
乙酰胆碱
自身抗体
受体
化学
内分泌学
内科学
生物
神经科学
解剖
作者
Yukiko Ozawa,Akiyuki Uzawa,Tetsuya Kanai,Fumiko Oda,Naoki Kawaguchi,Keiko Hojo,Satoshi Kuwabara
标识
DOI:10.1016/j.jns.2017.08.2327
摘要
Background: Myasthenia gravis (MG) is an antibody-mediated autoimmune disease of the neuromuscular junction (NMJ). Anti-acetylcholine receptor (AChR) antibody, which is confirmed in 85-90% of MG patients, activates complements and induces the formation of membrane attack complex (MAC) which ultimately leads to NMJ destruction and muscle weakness.
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