视神经脊髓炎
发病机制
补体系统
替代补体途径
免疫学
补体依赖性细胞毒性
经典补体途径
医学
水通道蛋白4
补语(音乐)
神经科学
抗体
病理
生物
单克隆抗体
遗传学
表型
基因
互补
抗体依赖性细胞介导的细胞毒性
出处
期刊:Chinese Journal of Ocular Fundus Diseases
[Chinese Medical Association]
日期:2019-05-25
卷期号:35 (3): 291-295
标识
DOI:10.3760/cma.j.issn.1005-1015.2019.03.019
摘要
Neuromyelitis optica (NMO) is a kind of demyelinating disorder that preferentially affects the optic nerves and spinal cord and results in permanent vision loss. NMO pathogenesis is thought to involve binding of anti-aquaporin-4 (AQP4) auto-antibodies to astrocytes, which causes complement-dependent cytotoxicity (CDC) and downstream inflammation leading to oligodendrocyte and neuronal injury. Vasculocentric deposition of activated complement is a prominent feature of NMO pathology. In recent years, a number of groups have found complements play an important role in the pathogenesis of NMO, and basic researches in NMO therapy due to its specificity and uniformity. Its inhibition would protect against proteins in the classical complement pathway so that cure the disease. This review will expound the the role of complement signaling pathway in the pathogenesis of NMO, and provide reference for a more in-depth understanding and clinical treatments of NMO.
Key words:
Neuromyelitis optica; Complement C1; Complement C3; Complement C5; Review
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