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多发性硬化的病毒模型:感染 Theiler 病毒的小鼠的神经退行性变和脱髓鞘。

Viral models of multiple sclerosis: neurodegeneration and demyelination in mice infected with Theiler's virus.

机构信息

Neuroimmunology Group, Functional and System Neurobiology Department, Instituto Cajal, Consejo Superior de Investigaciones Científicas, Madrid, Spain.

出版信息

Prog Neurobiol. 2013 Feb-Mar;101-102:46-64. doi: 10.1016/j.pneurobio.2012.11.003. Epub 2012 Nov 29.

Abstract

Multiple sclerosis (MS) is a complex inflammatory disease of unknown etiology that affects the central nervous system (CNS) white matter, and for which no effective cure exists. Indeed, whether the primary event in MS pathology affects myelin or axons of the CNS remains unclear. Animal models are necessary to identify the immunopathological mechanisms involved in MS and to develop novel therapeutic and reparative approaches. Specifically, viral models of chronic demyelination and axonal damage have been used to study the contribution of viruses in human MS, and they have led to important breakthroughs in our understanding of MS pathology. The Theiler's murine encephalomyelitis virus (TMEV) model is one of the most commonly used MS models, although other viral models are also used, including neurotropic strains of mouse hepatitis virus (MHV) that induce chronic inflammatory demyelination with similar histological features to those observed in MS. This review will discuss the immunopathological mechanisms involved in TMEV-induced demyelinating disease (TMEV-IDD). The TMEV model reproduces a chronic progressive disease due to the persistence of the virus for the entire lifespan in susceptible mice. The evolution and significance of the axonal damage and neuroinflammation, the importance of epitope spread from viral to myelin epitopes, the presence of abortive remyelination and the existence of a brain pathology in addition to the classical spinal cord demyelination, are some of the findings that will be discussed in the context of this TMEV-IDD model. Despite their limitations, viral models remain an important tool to study the etiology of MS, and to understand the clinical and pathological variability associated with this disease.

摘要

多发性硬化症(MS)是一种病因不明的复杂炎症性疾病,影响中枢神经系统(CNS)的白质,目前尚无有效的治疗方法。事实上,MS 病理学中的主要事件是否影响 CNS 的髓鞘或轴突仍不清楚。动物模型对于确定 MS 中涉及的免疫病理学机制以及开发新的治疗和修复方法是必要的。具体来说,慢性脱髓鞘和轴突损伤的病毒模型已被用于研究病毒在人类 MS 中的作用,它们在我们对 MS 病理学的理解方面取得了重要突破。Theiler 鼠脑脊髓炎病毒(TMEV)模型是最常用的 MS 模型之一,尽管也使用了其他病毒模型,包括具有类似组织学特征的致神经毒力的小鼠肝炎病毒(MHV)株,可诱导慢性炎症性脱髓鞘。这篇综述将讨论 TMEV 诱导的脱髓鞘疾病(TMEV-IDD)中涉及的免疫病理学机制。TMEV 模型由于在易感小鼠中病毒在整个寿命期内持续存在,因此可复制出慢性进行性疾病。轴突损伤和神经炎症的演变和意义、从病毒到髓鞘表位的抗原表位扩展的重要性、不完全性髓鞘再生的存在以及除了经典的脊髓脱髓鞘之外的脑病理学的存在,都是将在 TMEV-IDD 模型的背景下讨论的一些发现。尽管存在局限性,但病毒模型仍然是研究 MS 病因以及了解与该疾病相关的临床和病理变异性的重要工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b1ae/7117056/8ac620278ee8/gr1_lrg.jpg

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