MOG-IgG-Associated Optic Neuritis, Encephalitis, and Myelitis: Lessons Learned From Neuromyelitis Optica Spectrum Disorder.

MOG-IgG-Associated Optic Neuritis, Encephalitis, and Myelitis: Lessons Learned From Neuromyelitis Optica Spectrum Disorder.
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DOI:
10.3389/fneur.2018.00217
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发表时间:
2018
影响因子:
3.4
通讯作者:
Sato DK
Sato DK
中科院分区:
医学3区
文献类型:
--
作者:
Dos Passos GR;Oliveira LM;da Costa BK;Apostolos-Pereira SL;Callegaro D;Fujihara K;Sato DK

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在一些诊断为血清阴性视神经脊髓炎谱系障碍(NMOSD)的病例中发现了髓鞘少突胶质细胞糖蛋白(MOG-IgG)抗体。MOG-IgG允许鉴定一个亚组,其临床病程与水通道蛋白-4- igg抗体血清阳性的NMOSD患者不同。MOG-IgG与更广泛的临床表型相关,不限于NMOSD,大多数病例表现为视神经炎(ON)、脑炎伴脑脱髓鞘病变和/或脊髓炎。因此,我们提出mog - igg相关视神经炎、脑炎和脊髓炎(MONEM)这一术语。根据临床特征,这些患者目前可能被诊断为NMOSD、急性播散性脑脊髓炎、小儿多发性硬化症、横断面脊髓炎或on。通过特定的基于细胞的检测,MOG-IgG正成为中枢神经系统炎症性疾病的潜在生物标志物。我们回顾了越来越多的关于MONEM的证据,重点是它的临床方面。
Antibodies against myelin oligodendrocyte glycoprotein (MOG-IgG) have been found in some cases diagnosed as seronegative neuromyelitis optica spectrum disorder (NMOSD). MOG-IgG allowed the identification of a subgroup with a clinical course distinct from that of NMOSD patients who are seropositive for aquaporin-4-IgG antibodies. MOG-IgG is associated with a wider clinical phenotype, not limited to NMOSD, with the majority of cases presenting with optic neuritis (ON), encephalitis with brain demyelinating lesions, and/or myelitis. Therefore, we propose the term MOG-IgG-associated Optic Neuritis, Encephalitis, and Myelitis (MONEM). Depending on the clinical characteristics, these patients may currently be diagnosed with NMOSD, acute disseminated encephalomyelitis, pediatric multiple sclerosis, transverse myelitis, or ON. With specific cell-based assays, MOG-IgG is emerging as a potential biomarker of inflammatory disorders of the central nervous system. We review the growing body of evidence on MONEM, focusing on its clinical aspects.
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