Update on T cells in the virally infected brain: friends and foes

被引:20
|
作者
Ai, Shenjian [1 ]
Klein, Robyn S. [1 ,2 ,3 ]
机构
[1] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA
[3] Washington Univ, Sch Med, Dept Neurosci, St Louis, MO USA
关键词
cognition; glia; neuroimmune; T cells; viral encephalitis; WEST-NILE-VIRUS; CENTRAL-NERVOUS-SYSTEM; FUNCTIONAL OUTCOMES; RESPONSES; ENCEPHALITIS; PROTECTION; CLEARANCE; PARALYSIS; BARRIER; CXCL10;
D O I
10.1097/WCO.0000000000000825
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose of review The present review will outline neuroprotective and neurotoxic effects of central nervous system (CNS) infiltrating T cells during viral infections. Evidence demonstrating differential roles for antiviral effector and resident memory T-cell subsets in virologic control and immunopathology in the CNS will be discussed. Potential therapeutic targets emanating from a growing understanding of T-cell-initiated neuropathology that impacts learning and memory will also be delineated. Recent findings The critical role for T cells in preventing and clearing CNS infections became incontrovertible during the era of acquired immunodeficiency syndrome. Recent studies have further defined differential roles of T-cell subsets, including resident memory T cells (Trm), in antiviral immunity and, unexpectedly, in postinfectious cognitive dysfunction. Mechanisms of T-cell-mediated effects include differential innate immune signaling within neural cells that are virus-specific. T-cell cytokines that are essential for cell-mediated virologic control during neurotropic viral infections have recently been identified as potential targets to prevent post-infection memory disorders. Further identification of T-cell subsets, their antigen specificity, and postinfection localization of Trm will enhance the efficacy of immunotherapies through minimization of immunopathology.
引用
收藏
页码:405 / 412
页数:8
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