Department of Neurology, Wroclaw Medical University, 50-556 Wroclaw, Poland.
Int J Mol Sci. 2021 Mar 10;22(6):2801. doi: 10.3390/ijms22062801.
Neuromyelitis optica (NMO) is an immune-mediated demyelinative disorder of the central nervous system affecting mainly the optical nerves and the spinal cord. The recurrent course of the disease, with exacerbations and incomplete remissions, causes accumulating disability, which has a profound impact upon patients' quality of life. The discovery of antibodies against aquaporin 4 (AQP4) and their leading role in NMO etiology and the formulation of diagnostic criteria have improved appropriate recognition of the disease. In recent years, there has been rapid progress in understanding the background of NMO, leading to an increasing range of treatment options. On the basis of a review of the relevant literature, the authors present currently available therapeutic strategies for NMO as well as ongoing research in this field, with reference to key points of immune-mediated processes involved in the background of the disease.
视神经脊髓炎(NMO)是一种免疫介导的中枢神经系统脱髓鞘疾病,主要影响视神经和脊髓。疾病的反复发作,伴有恶化和不完全缓解,导致累积残疾,对患者的生活质量产生深远影响。水通道蛋白 4(AQP4)抗体的发现及其在 NMO 病因学中的主导作用,以及诊断标准的制定,提高了对该疾病的正确认识。近年来,对 NMO 背景的理解取得了快速进展,导致治疗选择的范围不断扩大。基于对相关文献的回顾,作者提出了目前用于 NMO 的治疗策略以及该领域正在进行的研究,并参考了疾病背景下涉及的免疫介导过程的关键点。