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Myelin-oligodendrocyte glycoprotein antibody-associated disease
The Lancet Neurology ( IF 46.5 ) Pub Date : 2021-08-19 , DOI: 10.1016/s1474-4422(21)00218-0
Romain Marignier 1 , Yael Hacohen 2 , Alvaro Cobo-Calvo 3 , Anne-Katrin Pröbstel 4 , Orhan Aktas 5 , Harry Alexopoulos 6 , Maria-Pia Amato 7 , Nasrin Asgari 8 , Brenda Banwell 9 , Jeffrey Bennett 10 , Fabienne Brilot 11 , Marco Capobianco 12 , Tanuja Chitnis 13 , Olga Ciccarelli 2 , Kumaran Deiva 14 , Jérôme De Sèze 15 , Kazuo Fujihara 16 , Anu Jacob 17 , Ho Jin Kim 18 , Ingo Kleiter 19 , Hans Lassmann 20 , Maria-Isabel Leite 21 , Christopher Linington 22 , Edgar Meinl 23 , Jacqueline Palace 21 , Friedemann Paul 24 , Axel Petzold 25 , Sean Pittock 26 , Markus Reindl 27 , Douglas Kazutoshi Sato 28 , Krzysztof Selmaj 29 , Aksel Siva 30 , Bruno Stankoff 31 , Mar Tintore 3 , Anthony Traboulsee 32 , Patrick Waters 21 , Emmanuelle Waubant 33 , Brian Weinshenker 34 , Tobias Derfuss 4 , Sandra Vukusic 1 , Bernhard Hemmer 35
Affiliation  

Myelin-oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is a recently identified autoimmune disorder that presents in both adults and children as CNS demyelination. Although there are clinical phenotypic overlaps between MOGAD, multiple sclerosis, and aquaporin-4 antibody-associated neuromyelitis optica spectrum disorder (NMOSD) cumulative biological, clinical, and pathological evidence discriminates between these conditions. Patients should not be diagnosed with multiple sclerosis or NMOSD if they have anti-MOG antibodies in their serum. However, many questions related to the clinical characterisation of MOGAD and pathogenetic role of MOG antibodies are still unanswered. Furthermore, therapy is mainly based on standard protocols for aquaporin-4 antibody-associated NMOSD and multiple sclerosis, and more evidence is needed regarding how and when to treat patients with MOGAD.



中文翻译:

髓鞘少突胶质细胞糖蛋白抗体相关疾病

髓鞘少突胶质细胞糖蛋白抗体相关疾病 (MOGAD) 是一种最近发现的自身免疫性疾病,在成人和儿童中表现为中枢神经系统脱髓鞘。尽管 MOGAD、多发性硬化症和水通道蛋白 4 抗体相关的视神经脊髓炎谱系障碍 (NMOSD) 之间存在临床表型重叠,但累积的生物学、临床和病理学证据可区分这些疾病。如果患者血清中含有抗 MOG 抗体,则不应被诊断为多发性硬化症或 NMOSD。然而,与 MOGAD 的临床特征和 MOG 抗体的致病作用相关的许多问题仍未得到解答。此外,治疗主要基于水通道蛋白 4 抗体相关 NMOSD 和多发性硬化症的标准方案,

更新日期:2021-08-19
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