Hino-Fukuyo Naomi, Haginoya Kazuhiro, Nakashima Ichiro, Sato Douglas Kazutoshi, Takahashi Toshiyuki, Misu Tatsuro, Fujihara Kazuo, Hirose Mieko, Kakisaka Yosuke, Uematsu Mitsugu, Kobayashi Tomoko, Kure Shigeo
Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.
Brain Dev. 2015 Oct;37(9):849-52. doi: 10.1016/j.braindev.2015.02.006. Epub 2015 Mar 3.
Myelin-oligodendrocyte glycoprotein and aquaporin-4 have been extensively analyzed as targets for humoral immune reactions in central nervous system (CNS) demyelinating diseases, and the results indicated a possible role of these antibodies in the pathogenesis of various demyelinating diseases.
To investigate the antibody titer levels against myelin-oligodendrocyte glycoprotein and aquaporin-4 in pediatric patients with inflammatory CNS disorders, and to evaluate clinical significance to study anti-myelin-oligodendrocyte glycoprotein antibodies.
Sera at onset from patients with acute disseminated encephalomyelitis (ADEM) in 7, optic neuritis (ON) in 5, pediatric MS in 4 and neuromyelitis optica in one were tested for myelin-oligodendrocyte glycoprotein and aquaporin-4 antibodies using cell-based assays with live transfected cells. The duration of the observation periods ranged from 1 to 21 years (median, 10 years). We also described clinical course of patients with positive anti-myelin-oligodendrocyte glycoprotein antibodies.
Among 17 patients diagnosed with inflammatory CNS demyelinating diseases nine (52%) were positive to anti-myelin-oligodendrocyte glycoprotein antibodies. Of note, all cases with positive anti-myelin-oligodendrocyte glycoprotein antibodies showed seronegativity against anti-aquaporin-4 antibodies and had a favorable prognosis.
This preliminary report showed that anti-myelin-oligodendrocyte glycoprotein antibodies testing at onset could be a useful tool predicting clinical outcome of children with ADEM, ON, and MS.
髓鞘少突胶质细胞糖蛋白和水通道蛋白4作为中枢神经系统(CNS)脱髓鞘疾病体液免疫反应的靶点已得到广泛分析,结果表明这些抗体在各种脱髓鞘疾病的发病机制中可能起作用。
研究炎症性中枢神经系统疾病患儿中抗髓鞘少突胶质细胞糖蛋白和水通道蛋白4的抗体滴度水平,并评估抗髓鞘少突胶质细胞糖蛋白抗体的临床意义。
采用基于活转染细胞的细胞检测法,检测7例急性播散性脑脊髓炎(ADEM)、5例视神经炎(ON)、4例儿童多发性硬化症(MS)和1例视神经脊髓炎患者发病时血清中的髓鞘少突胶质细胞糖蛋白和水通道蛋白4抗体。观察期为1至21年(中位数为10年)。我们还描述了抗髓鞘少突胶质细胞糖蛋白抗体阳性患者的临床病程。
在17例诊断为炎症性中枢神经系统脱髓鞘疾病的患者中,9例(52%)抗髓鞘少突胶质细胞糖蛋白抗体呈阳性。值得注意的是,所有抗髓鞘少突胶质细胞糖蛋白抗体阳性的病例抗水通道蛋白4抗体均为血清阴性,且预后良好。
本初步报告表明,发病时检测抗髓鞘少突胶质细胞糖蛋白抗体可能是预测ADEM、ON和MS患儿临床结局的有用工具。