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泰勒氏病毒诱导的脱髓鞘疾病作为进行性多发性硬化症的感染模型。

Theiler's virus-induced demyelinating disease as an infectious model of progressive multiple sclerosis.

作者信息

Pike Steven C, Welsh Nora, Linzey Michael, Gilli Francesca

机构信息

Department of Neurology, Dartmouth Hitchcock Medical Center and Geisel School of Medicine, Lebanon, NH, United States.

Integrative Neuroscience at Dartmouth, Dartmouth College, Hanover, NH, United States.

出版信息

Front Mol Neurosci. 2022 Oct 13;15:1019799. doi: 10.3389/fnmol.2022.1019799. eCollection 2022.

Abstract

Multiple sclerosis (MS) is a neuroinflammatory and neurodegenerative disease of unknown etiology. However, several studies suggest that infectious agents, e.g., Human Herpes Viruses (HHV), may be involved in triggering the disease. Molecular mimicry, bystander effect, and epitope spreading are three mechanisms that can initiate immunoreactivity leading to CNS autoimmunity in MS. Theiler's murine encephalomyelitis virus (TMEV)-induced demyelinating disease (TMEV-IDD) is a pre-clinical model of MS in which intracerebral inoculation of TMEV results in a CNS autoimmune disease that causes demyelination, neuroaxonal damage, and progressive clinical disability. Given the spectra of different murine models used to study MS, this review highlights why TMEV-IDD represents a valuable tool for testing the viral hypotheses of MS. We initially describe how the main mechanisms of CNS autoimmunity have been identified across both MS and TMEV-IDD etiology. Next, we discuss how adaptive, innate, and CNS resident immune cells contribute to TMEV-IDD immunopathology and how this relates to MS. Lastly, we highlight the sexual dimorphism observed in TMEV-IDD and MS and how this may be tied to sexually dimorphic responses to viral infections. In summary, TMEV-IDD is an underutilized murine model that recapitulates many unique aspects of MS; as we learn more about the nature of viral infections in MS, TMEV-IDD will be critical in testing the future therapeutics that aim to intervene with disease onset and progression.

摘要

多发性硬化症(MS)是一种病因不明的神经炎症性和神经退行性疾病。然而,多项研究表明,感染因子,如人类疱疹病毒(HHV),可能参与引发该疾病。分子模拟、旁观者效应和表位扩展是三种可引发免疫反应,导致MS中枢神经系统自身免疫的机制。泰勒氏鼠脑脊髓炎病毒(TMEV)诱导的脱髓鞘疾病(TMEV-IDD)是MS的一种临床前模型,其中脑内接种TMEV会导致一种中枢神经系统自身免疫性疾病,引起脱髓鞘、神经轴突损伤和进行性临床残疾。鉴于用于研究MS的不同小鼠模型的情况,本综述强调了为什么TMEV-IDD是检验MS病毒假说的一个有价值的工具。我们首先描述了如何在MS和TMEV-IDD病因中识别中枢神经系统自身免疫的主要机制。接下来,我们讨论适应性免疫、先天性免疫和中枢神经系统驻留免疫细胞如何促成TMEV-IDD的免疫病理学,以及这与MS的关系。最后,我们强调了在TMEV-IDD和MS中观察到的性别差异,以及这可能如何与对病毒感染的性别差异反应相关联。总之,TMEV-IDD是一种未得到充分利用的小鼠模型,它概括了MS的许多独特方面;随着我们对MS中病毒感染性质的了解越来越多,TMEV-IDD对于测试旨在干预疾病发作和进展的未来疗法至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfc0/9606571/dd79fb88e5e4/fnmol-15-1019799-g001.jpg

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