生物
脑膜
神经科学
抗原
豁免特权
抗原呈递
多发性硬化
脑脊液
中枢神经系统
神经免疫学
免疫系统
病理
免疫学
炎症
神经炎症
T细胞
医学
作者
Justin Rustenhoven,Antoine Drieu,Tornike Mamuladze,Kalil Alves de Lima,Taitea Dykstra,Morgan Wall,Zachary Papadopoulos,Mitsuhiro Kanamori,Andrea Francesca Salvador,Wendy Baker,Mackenzie Lemieux,Sandro Dá Mesquita,Andrea Cugurra,James A. J. Fitzpatrick,Sanja Sviben,Ross G. Kossina,Peter O. Bayguinov,Reid Townsend,Qiang Zhang,Petra Erdmann-Gilmore
出处
期刊:Cell
[Cell Press]
日期:2021-01-27
卷期号:184 (4): 1000-1016.e27
被引量:483
标识
DOI:10.1016/j.cell.2020.12.040
摘要
Despite the established dogma of central nervous system (CNS) immune privilege, neuroimmune interactions play an active role in diverse neurological disorders. However, the precise mechanisms underlying CNS immune surveillance remain elusive; particularly, the anatomical sites where peripheral adaptive immunity can sample CNS-derived antigens and the cellular and molecular mediators orchestrating this surveillance. Here, we demonstrate that CNS-derived antigens in the cerebrospinal fluid (CSF) accumulate around the dural sinuses, are captured by local antigen-presenting cells, and are presented to patrolling T cells. This surveillance is enabled by endothelial and mural cells forming the sinus stromal niche. T cell recognition of CSF-derived antigens at this site promoted tissue resident phenotypes and effector functions within the dural meninges. These findings highlight the critical role of dural sinuses as a neuroimmune interface, where brain antigens are surveyed under steady-state conditions, and shed light on age-related dysfunction and neuroinflammatory attack in animal models of multiple sclerosis.
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