MOG-脑炎是儿童最常见的自身免疫性脑炎。

IF 1.2 4区 医学 Q4 CLINICAL NEUROLOGY
Neuropediatrics Pub Date : 2025-08-01 Epub Date: 2025-04-10 DOI:10.1055/a-2579-6247
Ruth Helena Fellmeth, Lampros Kousoulos, George Christoph Korenke, Hans-Jürgen Christen, Masyar Monazahian, Justine Dargvainiene, Klaus-Peter Wandinger, Frank Leypoldt, Kevin Rostásy
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引用次数: 0

摘要

儿童脑炎是一种由传染性或自身免疫介导过程引起的严重炎症性脑疾病。自身免疫变异在儿科人群中的频率尚不完全清楚。目的:研究下萨克森州(MERIN)脑膜炎/脑炎登记的儿童髓鞘少突胶质细胞糖蛋白(MOG)抗体(ab)介导的自身免疫性脑炎(AE)的发病率。方法:回顾两家大型儿童医院2011 - 2020年参与脑炎前瞻性研究(ME-RIN)的1341例患儿的病历。最终纳入符合可能AE诊断标准的儿童,如果有血清样本和知情再次同意。患有病原体介导性脑炎的儿童也被纳入对照组。采用基于细胞和组织的测定法(TBA)检测所有可用血清样本的MOG和抗n -甲基- d -天冬氨酸受体(NMDAR)抗体(abs)。结果:我们纳入55名儿童,其中16名患有病原体相关的脑膜脑炎。39/55例患儿为可能AE, 3/39例患儿符合MOG抗体相关疾病(MOGAD)标准。没有患者血清中含有NMDAR抗体。然而,5/39例患者符合可能的自身抗体阴性AE标准。结论:与最近的研究一致,我们的研究表明,抗体介导的AE和可能的抗体阴性AE在儿童中很少见。现有的标准似乎适合于识别AE患者,但应包括血清MOG抗体的检测。进一步未知的抗体可能在AE患儿中发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MOG-Encephalitis is the Most Prevalent Autoimmune Encephalitis in Children: MERIN Study Data on Encephalitis.

Encephalitis in children is a serious inflammatory brain disease caused by infectious or autoimmune-mediated processes. The frequency of autoimmune variants in pediatric populations is not entirely clear.To study the frequency of myelin oligodendrocyte glycoprotein (MOG) antibody (ab)-mediated autoimmune encephalitis (AE) in children included in the Meningitis/Encephalitis register of Lower Saxony (MERIN).Medical records of 1,341 children treated between 2011 and 2020 in two large children's hospitals participating in a prospective study on encephalitis (MERIN) were reviewed. Children meeting diagnostic criteria for possible AE were finally included if serum samples and informed re-consent were available. Children with pathogen-mediated encephalitis were also included as controls. All available serum samples were tested for MOG- and anti-N-methyl-D-aspartate receptor (NMDAR) antibodies (abs) using cell- and tissue-based assay (TBA).We included 55 children of whom 16 had pathogen-associated meningoencephalitis. Thirty-nine out of fifty-five children were classified as possible AE and 3/39 fulfilled the criteria for MOG ab-associated disease (MOGAD). No patients' sera harbored NMDAR abs. However, 5/39 patients fulfilled the criteria for probable, auto-ab-negative AE.In line with recent research our study suggests that ab-mediated AE and probable ab-negative AE are rare in children. The existing criteria seem suitable for identifying patients with AE but should include the testing of serum MOG abs. Further yet unknown abs may play a role in children with AE.

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来源期刊
Neuropediatrics
Neuropediatrics 医学-临床神经学
CiteScore
2.80
自引率
0.00%
发文量
94
审稿时长
>12 weeks
期刊介绍: For key insights into today''s practice of pediatric neurology, Neuropediatrics is the worldwide journal of choice. Original articles, case reports and panel discussions are the distinctive features of a journal that always keeps abreast of current developments and trends - the reason it has developed into an internationally recognized forum for specialists throughout the world. Pediatricians, neurologists, neurosurgeons, and neurobiologists will find it essential reading.
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