作者
Noriyuki Yamaguchi,Sonoko Misawa,Yasunori Sato,Kengo Nagashima,K. Katayama,Yukari Sekiguchi,Yuta Iwai,Hiroshi Amino,Tomoki Suichi,Takanori Yokota,Yoichiro Nishida,Nobuo Kohara,Koichi Hirata,Kazutoshi Nishiyama,Ichiro Yabe,Kenichi Kaida,Norihiro Suzuki,Hiroyuki Nodera,Shoji Tsuji,Haruki Koike,Jun‐ichi Kira,Hideki Hanaoka,Susumu Kusunoki,Satoshi Kuwabara
摘要
Background: Guillain-Barré syndrome (GBS) is an immune-mediated neuropathy that causes acute flaccid paralysis. Immunoglobulin and plasma exchange are established treatments for GBS; however, a substantial number of patients, particularly those with severe disease, have poor recovery and residual deficits. Recent studies suggest that complement activation plays a pivotal role in GBS-associated axonal degeneration, and eculizumab is a humanized monoclonal antibody that specifically binds to complement component 5 and potently inhibits complement activation.