Recent Advances in Neuromyelitis Optica Spectrum Disorder: Pathogenesis, Mechanisms and Potential Treatments

Author:

Du Yi1ORCID,Li Kaijun1ORCID,Liu Wei1ORCID,Song Ruitong1ORCID,Luo Meifeng1ORCID,He Jianfeng1ORCID,Xu Xiaoyu2ORCID,Qu Xiaosheng3ORCID

Affiliation:

1. Department of Ophthalmology, the First Affiliated Hospital of Guangxi Medical University, 530021, Nanning,China

2. Doheny Eye Institute, Department of Ophthalmology, University of California, Los Angeles, CA 90033,United States

3. National Engineering Laboratory of Southwest Endangered Medicinal Resources Development, Guangxi Botanical Garden of Medicinal Plants, 530023, Nanning,China

Abstract

: Neuromyelitis optica spectrum disorder (NMOSD) is an acute or subacute demyelinating disease that affects mainly the optic nerve and spinal cord. A major proportion of NMOSD cases have a relationship with autoimmunity to aquaporin 4 (AQP4) found on the central nervous system. NMOSD can occur repeatedly, causing symptoms such as decreased vision and weakness of limbs. The main goal of current therapy is to relieve acute symptoms and prevent recurrence of the disease. Without timely and appropriate treatment, the recurrence and disability rates are high. In the present work, we review recent advances in the diagnosis and treatment of patients with NMOSD, as well as the pathogenesis and mechanisms of AQP4-IgG-seropositive NMOSD.

Publisher

Bentham Science Publishers Ltd.

Subject

Drug Discovery,Pharmacology

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