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髓鞘少突胶质细胞糖蛋白抗体相关性视神经炎——综述。

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Optic Neuritis-A Review.

机构信息

Neuro-Ophthalmology, Department of Ophthalmology, Queen Elizabeth Hospital, University Hospitals Birmingham, Birmingham, United Kingdom .

出版信息

J Neuroophthalmol. 2021 Dec 1;41(4):e786-e795. doi: 10.1097/WNO.0000000000001234.

Abstract

Our understanding of demyelinating optic neuritis has substantially evolved over the past 2 decades. With advancements in serological testing, antibodies against myelin oligodendrocyte glycoprotein (MOG) have been recently discovered in a distinct subset of demyelinating neuroinflammatory disease. Although MOG-immunoglobulin G (IgG)-associated disorder (MOGAD) has previously been seen as a component of neuromyelitis optica spectrum disorder (NMOSD), evidence increasingly suggests that it should be distinguished as a separate condition. The distinction of MOGAD from aquaporin-4 IgG NMOSD is imperative as treatment plans need to be tailored to its unique disease course and prognosis. The purpose of this review is to explore the nature and outcomes of MOGAD optic neuritis to help guide acute and long-term immunosuppressive treatment decisions.

摘要

过去 20 年来,我们对脱髓鞘性视神经炎的认识有了很大的发展。随着血清学检测的进步,最近在一组不同的脱髓鞘神经炎症性疾病中发现了针对髓鞘少突胶质细胞糖蛋白(MOG)的抗体。虽然 MOG 免疫球蛋白 G(IgG)相关疾病(MOGAD)以前被认为是视神经脊髓炎谱系障碍(NMOSD)的一个组成部分,但越来越多的证据表明,它应该被区分开来作为一种单独的疾病。将 MOGAD 与水通道蛋白 4 IgG NMOSD 区分开来至关重要,因为需要根据其独特的疾病过程和预后制定治疗计划。本文旨在探讨 MOGAD 视神经炎的性质和结果,以帮助指导急性和长期免疫抑制治疗决策。

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