Department of Animal Model Development, Brain Research Institute, Niigata University, 1-757 Asahimachi-dori, Chuoku, Niigata 951-8585, Japan.
Department of Multiple Sclerosis Therapeutics, School of Medicine, Fukushima Medical University, 1 Hikarigaoka, Fukushima 960-1247, Japan.
Int J Mol Sci. 2023 Aug 29;24(17):13368. doi: 10.3390/ijms241713368.
Although there is a substantial amount of data on the clinical characteristics, diagnostic criteria, and pathogenesis of myelin oligodendrocyte glycoprotein (MOG) autoantibody-associated disease (MOGAD), there is still uncertainty regarding the MOG protein function and the pathogenicity of anti-MOG autoantibodies in this disease. It is important to note that the disease characteristics, immunopathology, and treatment response of MOGAD patients differ from those of anti-aquaporin 4 antibody-positive neuromyelitis optica spectrum disorders (NMOSDs) and multiple sclerosis (MS). The clinical phenotypes of MOGAD are varied and can include acute disseminated encephalomyelitis, transverse myelitis, cerebral cortical encephalitis, brainstem or cerebellar symptoms, and optic neuritis. The frequency of optic neuritis suggests that the optic nerve is the most vulnerable lesion in MOGAD. During the acute stage, the optic nerve shows significant swelling with severe visual symptoms, and an MRI of the optic nerve and brain lesion tends to show an edematous appearance. These features can be alleviated with early extensive immune therapy, which may suggest that the initial attack of anti-MOG autoantibodies could target the structures on the blood-brain barrier or vessel membrane before reaching MOG protein on myelin or oligodendrocytes. To understand the pathogenesis of MOGAD, proper animal models are crucial. However, anti-MOG autoantibodies isolated from patients with MOGAD do not recognize mouse MOG efficiently. Several studies have identified two MOG epitopes that exhibit strong affinity with human anti-MOG autoantibodies, particularly those isolated from patients with the optic neuritis phenotype. Nonetheless, the relations between epitopes on MOG protein remain unclear and need to be identified in the future.
虽然髓鞘少突胶质细胞糖蛋白(MOG)自身抗体相关性疾病(MOGAD)的临床特征、诊断标准和发病机制有大量数据,但 MOG 蛋白功能和抗 MOG 自身抗体在该病中的致病性仍存在不确定性。需要注意的是,MOGAD 患者的疾病特征、免疫病理学和治疗反应与抗水通道蛋白 4 抗体阳性视神经脊髓炎谱系疾病(NMOSD)和多发性硬化(MS)不同。MOGAD 的临床表型多种多样,包括急性播散性脑脊髓炎、横贯性脊髓炎、大脑皮质脑炎、脑干或小脑症状和视神经炎。视神经炎的频率表明视神经是 MOGAD 中最易受损的病变。在急性期,视神经明显肿胀,伴有严重的视觉症状,视神经和脑部病变的 MRI 往往显示水肿外观。早期广泛的免疫治疗可以缓解这些特征,这可能表明抗 MOG 自身抗体的初始攻击可能在到达髓鞘或少突胶质细胞上的 MOG 蛋白之前,针对血脑屏障或血管膜上的结构。为了了解 MOGAD 的发病机制,合适的动物模型至关重要。然而,从 MOGAD 患者中分离出的抗 MOG 自身抗体不能有效地识别小鼠 MOG。几项研究已经确定了两个与人类抗 MOG 自身抗体具有强亲和力的 MOG 表位,特别是那些从视神经炎表型患者中分离出来的表位。然而,MOG 蛋白上的表位之间的关系仍不清楚,需要在未来确定。