脑膜
淋巴细胞性脉络膜脑膜炎
生物
病毒性脑膜炎
免疫学
小胶质细胞
病毒学
脑膜炎
巨噬细胞
中枢神经系统
免疫系统
医学
脑脊液
炎症
细菌性脑膜炎
体外
CD8型
神经科学
精神科
生物化学
作者
Julie Rebejac,Elisa Eme‐Scolan,Laurie Arnaud,Sarah Kharbouche,Matei Teleman,Lionel Spinelli,Emeline Gallo,Annie Roussel‐Queval,Ana Zarubica,Amandine Sansoni,Quentin Bardin,Philippe Hoest,Marie‐Cécile Michallet,Carine Brousse,Karine Crozat,Monica Manglani,Zhaoyuan Liu,Florent Ginhoux,Dorian B. McGavern,Marc Dalod
出处
期刊:Immunity
[Cell Press]
日期:2022-11-01
卷期号:55 (11): 2103-2117.e10
被引量:52
标识
DOI:10.1016/j.immuni.2022.10.005
摘要
The surface of the central nervous system (CNS) is protected by the meninges, which contain a dense network of meningeal macrophages (MMs). Here, we examined the role of tissue-resident MM in viral infection. MHC-II− MM were abundant neonatally, whereas MHC-II+ MM appeared over time. These barrier macrophages differentially responded to in vivo peripheral challenges such as LPS, SARS-CoV-2, and lymphocytic choriomeningitis virus (LCMV). Peripheral LCMV infection, which was asymptomatic, led to a transient infection and activation of the meninges. Mice lacking macrophages but conserving brain microglia, or mice bearing macrophage-specific deletion of Stat1 or Ifnar, exhibited extensive viral spread into the CNS. Transcranial pharmacological depletion strategies targeting MM locally resulted in several areas of the meninges becoming infected and fatal meningitis. Low numbers of MHC-II+ MM, which is seen upon LPS challenge or in neonates, corelated with higher viral load upon infection. Thus, MMs protect against viral infection and may present targets for therapeutic manipulation.
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