High levels of cerebrospinal fluid soluble triggering receptor expressed on myeloid cells 2 might be a biomarker of activity in pediatric patients with MOG-AD

Myelin oligodendrocyte glycoprotein antibody disease (MOG-AD) is characterized by its monophasic or relapsing course and inflammatory demyelinating condition which is unable to be classified in typical multiple sclerosis (MS) or other known neuroinflammatory conditions. In the condition of neuroinfl...

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Published in:Frontiers in pediatrics Vol. 10; p. 908527
Main Authors: Zhou, Anna, Zhang, Weihua, Ren, Changhong, Zhou, Ji, Chang, Haoxiao, Ren, Xiaotun
Format: Journal Article
Language:English
Published: Frontiers Media S.A 13-10-2022
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Summary:Myelin oligodendrocyte glycoprotein antibody disease (MOG-AD) is characterized by its monophasic or relapsing course and inflammatory demyelinating condition which is unable to be classified in typical multiple sclerosis (MS) or other known neuroinflammatory conditions. In the condition of neuroinflammatory, activated microglia are essential for demyelination. The secreted ectodomain of soluble triggering receptor expressed on myeloid cells 2 (sTREM2), expressed by microglial cells, is associated with abnormal biological pathways. It is known that the cerebrospinal fluid (CSF) sTREM2 concentration is much higher in neuroinflammatory and neurodegeneration diseases. However, the role of activated microglia has not been reported in MOG-AD pediatric patients. For the first time, the increased CSF and serum sTREM2 concentration in pediatric patients with MOG-AD is investigated in this work, showing evidence of microglia activation in MOG-AD. CSF sTREM2 levels significantly correlated with clinical inflammatory indexes and adapted modified Rankin Scale score, indicating the potential value of sTREM2 as a severity biomarker.
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Reviewed by: Matthew Adams, Wayne State University, United States; Philippe Horellou, INSERM U1184 Centre de Recherche en Immunologie des Infections Virales et des Maladies Auto-Immunes, France; Susanna Felsenstein, University of Liverpool, United Kingdom
This article was submitted to Pediatric Immunology, a section of the journal Frontiers in Pediatrics
Edited by: Trevor Owens, University of Southern Denmark, Denmark
ISSN:2296-2360
2296-2360
DOI:10.3389/fped.2022.908527