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人类嗜神经JC病毒在中枢神经系统中的分子生物学与免疫调节

Molecular biology and immunoregulation of human neurotropic JC virus in CNS.

作者信息

Sweet Thersa M, Del Valle Luis, Khalili Kamel

机构信息

Center for Neurovirology and Cancer Biology, Temple University, Philadelphia, Pennsylvania 19122, USA.

出版信息

J Cell Physiol. 2002 Jun;191(3):249-56. doi: 10.1002/jcp.10096.

Abstract

The human polyomavirus, JC virus (JCV), provides an excellent model system to investigate the reciprocal interaction of the immune and nervous systems. Infection with JCV occurs during childhood and the virus remains in the latent state with no apparent clinical symptoms. However, under immunosuppressed conditions, the virus enters the lytic cycle and upon cytolytic destruction of glial cells, causes the fatal demyelinating disease of the central nervous system (CNS), named progressive multifocal leukoencephalopathy (PML). In this short review, we discuss the molecular pathogenesis of PML by highlighting the role of the immune system in modulating JCV gene activation and replication, and the latency/reactivation of this virus upon immunosuppression. Further, due to the higher incidence of PML among AIDS patients, we further elaborate on the cross-talk between JCV and HIV-1 by direct and indirect pathways that lead to enhanced expression of the JCV genome.

摘要

人类多瘤病毒JC病毒(JCV)为研究免疫系统与神经系统之间的相互作用提供了一个出色的模型系统。JCV感染发生在儿童期,病毒处于潜伏状态,无明显临床症状。然而,在免疫抑制条件下,病毒进入裂解周期,在神经胶质细胞发生溶细胞性破坏后,引发中枢神经系统(CNS)致命的脱髓鞘疾病,即进行性多灶性白质脑病(PML)。在这篇简短的综述中,我们通过强调免疫系统在调节JCV基因激活和复制中的作用以及该病毒在免疫抑制时的潜伏/再激活,来探讨PML的分子发病机制。此外,由于艾滋病患者中PML的发病率较高,我们进一步阐述JCV与HIV-1之间通过直接和间接途径导致JCV基因组表达增强的相互作用。

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