Huang Yusen, Wang Tianwei, Wang Fangruyue, Wu Yujing, Ai Jia, Zhang Ying, Shao Meiyan, Fang Le
Department of Neurology, China-Japan Union Hospital of Jilin University, Changchun, China.
Department of Radiology, China-Japan Union Hospital of Jilin University, Changchun, China.
Front Immunol. 2024 Nov 19;15:1423107. doi: 10.3389/fimmu.2024.1423107. eCollection 2024.
Neuromyelitis optica spectrum disorders (NMOSD) is a rare autoimmune disorder that causes severe inflammation in the central nervous system (CNS), primarily affecting the optic nerves, spinal cord, and brainstem. Aquaporin-4 immunoglobulin G antibodies (AQP4-IgG) are a diagnostic marker of the disease and play a significant role in its pathogenesis, though the exact mechanism is not yet fully understood. To develop rodent models that best simulate the pathological and physiological processes of NMOSD, researchers have been continuously exploring how to establish the ideal model. In this process, two key issues arise: 1) how the AQP4 antibody crosses the blood-brain barrier, and 2) the source of the AQP4 antibody. These two factors are critical for the successful development of rodent models of NMOSD. This paper reviews the current state of research on these two aspects.
视神经脊髓炎谱系障碍(NMOSD)是一种罕见的自身免疫性疾病,可导致中枢神经系统(CNS)严重炎症,主要影响视神经、脊髓和脑干。水通道蛋白4免疫球蛋白G抗体(AQP4-IgG)是该疾病的诊断标志物,在其发病机制中起重要作用,尽管确切机制尚未完全明确。为了建立最能模拟NMOSD病理和生理过程的啮齿动物模型,研究人员一直在不断探索如何建立理想模型。在此过程中,出现了两个关键问题:1)AQP4抗体如何穿过血脑屏障,以及2)AQP4抗体的来源。这两个因素对于成功建立NMOSD啮齿动物模型至关重要。本文综述了这两个方面的研究现状。