髓鞘少突胶质细胞糖蛋白
实验性自身免疫性脑脊髓炎
自身抗体
免疫学
抗体
生物
自身免疫
脑脊髓炎
效应器
多发性硬化
髓鞘
自身免疫性疾病
少突胶质细胞
体液免疫
糖蛋白
免疫球蛋白G
医学
免疫系统
作者
Reza Taghipour-Mirakmahaleh,Françoise Morin,Yu Zhang,Louis Bourhoven,Louis‐Charles Béland,Qun Zhou,Julie Jaworski,Anna Park,Juan Manuel Domínguez,Jacques Corbeil,Eoin P. Flanagan,Romain Marignier,Catherine Larochelle,Steven M. Kerfoot,Luc Vallières
标识
DOI:10.1073/pnas.2424988122
摘要
Autoantibodies contribute to many autoimmune diseases, yet there is no approved therapy to neutralize them selectively. A popular mouse model, experimental autoimmune encephalomyelitis (EAE), could serve to develop such a therapy, provided we can better understand the nature and importance of the autoantibodies involved. Here, we report the finding of autoantibody-secreting extrafollicular plasmablasts in EAE induced with specific myelin oligodendrocyte glycoprotein (MOG) antigens. Single-cell RNA sequencing reveals that these cells produce nonaffinity-matured IgG antibodies. These include pathogenic antibodies competing for shared binding space on MOG's extracellular domain. Interestingly, the synthetic anti-MOG antibody 8-18C5 can prevent the binding of pathogenic antibodies from either EAE mice or people with MOG antibody disease. Moreover, an 8-18C5 variant carrying the NNAS mutation, which inactivates its effector functions, can reduce EAE severity and promote functional recovery. In brief, this study provides not only a comprehensive characterization of the humoral response in EAE models but also a proof of concept for a therapy to antagonize pathogenic anti-MOG antibodies.
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