医学
重症肌无力
免疫抑制
促炎细胞因子
临床试验
发病机制
药理学
免疫学
补体系统
免疫系统
内科学
炎症
作者
Sanem Pınar Uysal,John A. Morren
标识
DOI:10.1080/14656566.2024.2332610
摘要
Introduction Myasthenia gravis (MG) is an autoimmune condition targeting the neuromuscular junction, which manifests with neuromuscular symptoms of varying severity and significant morbidity. The mainstay of treatment in MG is mitigation of the immune cascade with steroids and non-steroidal immunosuppressive therapies. The therapeutic strategies in MG are transitioning from broad and indiscriminate immunosuppression to novel agents targeting key steps in MG pathogenesis, including T cell activation, B cell proliferation, complement activation, maintenance of pathogenic antibody production, and proinflammatory cytokine production.
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