Takahashi Ryo, Yuki Nobuhiro
Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
1] Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore [2] Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Sci Rep. 2015 Jul 21;5:10809. doi: 10.1038/srep10809.
Plasma exchange and intravenous immunoglobulin are effective in treating Guillain-Barré syndrome (GBS) probably because the former removes IgG autoantibodies and complement and the latter inhibits complement activation subsequent to the autoantibody binding to peripheral nerve antigens. IgG degrading enzyme of Streptococcus pyogenes (IdeS) can cleave the pathogenic autoantibodies into F(ab')2 and Fc. The purpose of this study is to show whether IdeS has novel therapeutic potential for GBS. Sera with anti-ganglioside IgG antibodies from 15 patients with GBS or Miller Fisher syndrome were used. We tested whether IdeS cleaved the anti-ganglioside IgG antibodies and inhibited deposition of activated complement component on ELISA plates. IdeS efficiently cleaved IgG and blocked complement activation mediated by anti-GM1, anti-GD1a and anti-GQ1b IgG antibodies. IdeS has therapeutic potential for GBS and related conditions.
血浆置换和静脉注射免疫球蛋白对治疗吉兰-巴雷综合征(GBS)有效,可能是因为前者可清除IgG自身抗体和补体,而后者可抑制自身抗体与周围神经抗原结合后补体的激活。化脓性链球菌的IgG降解酶(IdeS)可将致病性自身抗体裂解为F(ab')2和Fc。本研究的目的是证明IdeS对GBS是否具有新的治疗潜力。使用了15例GBS或米勒费雪综合征患者含有抗神经节苷脂IgG抗体的血清。我们测试了IdeS是否能裂解抗神经节苷脂IgG抗体,并抑制活化补体成分在酶联免疫吸附测定板上的沉积。IdeS能有效裂解IgG,并阻断由抗GM1、抗GD1a和抗GQ1b IgG抗体介导的补体激活。IdeS对GBS及相关病症具有治疗潜力。