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中枢神经系统病毒感染中的 Toll 样受体。

Toll-like receptors in CNS viral infections.

机构信息

Department of Pathology (Neuropathology), Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA.

出版信息

Curr Top Microbiol Immunol. 2009;336:63-81. doi: 10.1007/978-3-642-00549-7_4.

DOI:10.1007/978-3-642-00549-7_4
PMID:19688328
Abstract

Protection against viral infections is critically dependent upon the early production of significant levels of type 1 interferons and the expression of interferon-stimulated genes that function as the effectors of innate antiviral immunity. Activation of Toll-like receptors on cells of the immune system is known to play an important role in this process. In this chapter we review evidence for a role of TLRs in innate immune responses against viral infections of the central nervous system. By far the most extensive literature pertains to TLR3. Data from various laboratories have shown that TLR3 is expressed in cells endogenous to the CNS, particularly in astrocytes and microglia. Triggering TLR3 by synthetic dsRNA, poly I:C effectively induces innate antiviral responses as well as boosts adaptive immune responses. Additional experiments show cooperative responses between TLRs (3, 7/8 and 9) in mounting an effective antiviral immune response in the periphery. Perhaps the most exciting data are from patient populations that document the critical role that specific TLRs play in specific CNS infections. Studies also suggest that inappropriate activation of the TLRs can result in a pathogenic outcome rather than a protective one. Since TLR ligands are being actively considered for their antiviral and potential adjuvant effects, this will be an important issue to address in the context of the CNS environment.

摘要

针对病毒感染的保护作用极大地依赖于 1 型干扰素的早期大量产生和干扰素刺激基因的表达,这些基因作为先天抗病毒免疫的效应物发挥作用。免疫系统细胞上 Toll 样受体的激活被认为在这个过程中起着重要作用。在本章中,我们回顾了 TLR 在针对中枢神经系统病毒感染的先天免疫反应中的作用的证据。到目前为止,最广泛的文献涉及 TLR3。来自不同实验室的数据表明,TLR3 在内源表达于中枢神经系统的细胞中表达,特别是在星形胶质细胞和小胶质细胞中。通过合成双链 RNA(poly I:C)触发 TLR3 可有效诱导先天抗病毒反应,并增强适应性免疫反应。其他实验表明,TLRs(3、7/8 和 9)之间的协同反应在外周形成有效的抗病毒免疫反应。也许最令人兴奋的数据来自于患者群体,这些数据记录了特定 TLR 在特定中枢神经系统感染中的关键作用。研究还表明,TLRs 的不当激活可能导致致病性结果,而不是保护性结果。由于 TLR 配体因其抗病毒和潜在佐剂作用而被积极考虑,因此这将是一个重要问题,需要在中枢神经系统环境中加以解决。

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