N-methyl-D-aspartate receptor dysfunction by unmutated human antibodies against the NR1 subunit

未突变的人类抗体对 NR1 亚基造成 N-甲基-D-天冬氨酸受体功能障碍

阅读:7
作者:Nina Kerstin Wenke, Jakob Kreye, Ewa Andrzejak, Adriana van Casteren, Jonas Leubner, Manuela S Murgueitio, S Momsen Reincke, Christopher Secker, Lars Schmidl, Christian Geis, Frauke Ackermann, Marc Nikolaus, Craig C Garner, Hedda Wardemann, Gerhard Wolber, Harald Prüss

Abstract

Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is the most common autoimmune encephalitis related to autoantibody-mediated synaptic dysfunction. Cerebrospinal fluid-derived human monoclonal NR1 autoantibodies showed low numbers of somatic hypermutations or were unmutated. These unexpected germline-configured antibodies showed weaker binding to the NMDAR than matured antibodies from the same patient. In primary hippocampal neurons, germline NR1 autoantibodies strongly and specifically reduced total and synaptic NMDAR currents in a dose- and time-dependent manner. The findings suggest that functional NMDAR antibodies are part of the human naïve B cell repertoire. Given their effects on synaptic function, they might contribute to a broad spectrum of neuropsychiatric symptoms. Ann Neurol 2019;85:771-776.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。