格林-巴利综合征
分子模拟
自身抗体
发病机制
抗体
效应器
急性无力肢体麻痹
免疫系统
急性运动性轴索神经病
医学
麻痹
免疫学
病毒
精神科
脊髓灰质炎病毒
作者
Alina Sprenger‐Svačina,Martin K. R. Svačina,Tong Gao,Gang Zhang,Kazim A. Sheikh
标识
DOI:10.1080/13543784.2024.2377323
摘要
Guillain-Barré syndrome (GBS) is a monophasic immune neuropathic disorder characterized by acute paralysis. A significant portion of patients are left with residual deficits, which presents a considerable global healthcare challenge. The precise mechanisms underlying GBS pathogenesis are not fully elucidated. Recent studies have focused on postinfectious molecular mimicry and identified involvement of IgG autoantibodies and innate immune effectors in GBS. Intravenous immunoglobulins (IVIg) and plasma exchange (PE) are two established evidence-based immunomodulatory treatments for GBS, but a significant proportion of GBS patients fails to respond adequately to either therapy. This emphasizes an urgent need for novel and more potent treatments.
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