Department of Neurology, Xichang Road No.295, Kunming 650000, China.
Department of Neurology, Xichang Road No.295, Kunming 650000, China.
Mult Scler Relat Disord. 2019 Jan;27:412-418. doi: 10.1016/j.msard.2018.12.002. Epub 2018 Dec 3.
Neuromyelitis optica (NMO) and NMO spectrum disorder (NMOSD) are inflammatory CNS syndromes mainly involving the optic nerve and/or spinal cord and characterized by the presence of serum aquaporin-4 immunoglobulin G antibodies (AQP4-IgG). The pathology of NMOSD is complicated, while therapies for NMOSD are limited and only partially effective in most cases. This review article focuses on the main pathology of NMOSD involving AQP4-IgG and lymphocyte function. We also review the existing therapeutic methods and potential new treatments. Experimental NMO animal models are crucial for further research into NMO pathology and treatment. However, no AQP4-IgG-immunized animals have been reported. The establishment of NMO models is therefore difficult and primarily depends on the generation of transgenic mice or transcranial manipulation using human or monoclonal mouse anti-AQP4 antibodies. Advantages and disadvantages of each model are discussed.
视神经脊髓炎(NMO)和 NMO 谱系疾病(NMOSD)是主要累及视神经和/或脊髓的中枢神经系统炎症综合征,其特征是存在血清水通道蛋白 4 免疫球蛋白 G 抗体(AQP4-IgG)。NMOSD 的病理学较为复杂,而 NMOSD 的治疗方法有限,且在大多数情况下仅部分有效。本文主要聚焦于涉及 AQP4-IgG 和淋巴细胞功能的 NMOSD 的主要病理学,同时还对现有的治疗方法和潜在的新疗法进行综述。实验性 NMO 动物模型对于深入研究 NMO 病理学和治疗方法至关重要,但目前尚未有报道使用 AQP4-IgG 免疫动物。因此,NMO 模型的建立较为困难,主要依赖于转基因小鼠的产生或使用人源或单克隆鼠抗 AQP4 抗体进行经颅操作。本文对每种模型的优缺点进行了讨论。