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泰勒氏鼠脑脊髓炎病毒引起的心脏和骨骼肌疾病。

Theiler's murine encephalomyelitis virus-induced cardiac and skeletal muscle disease.

作者信息

Gómez R M, Rinehart J E, Wollmann R, Roos R P

机构信息

Department of Neurology, University of Chicago Pritzker School of Medicine, Illinois 60637, USA.

出版信息

J Virol. 1996 Dec;70(12):8926-33. doi: 10.1128/JVI.70.12.8926-8933.1996.

Abstract

The DA strain of Theiler's murine encephalomyelitis virus, a member of the cardiovirus genus of picornaviruses, induces a restricted and persistent infection associated with a demyelinating process following intracerebral inoculation of mice; both virus infection and the immune response are believed to contribute to the late white matter disease. We now report that intraperitoneal inoculation with DA produces an acute myositis that progresses to a chronic inflammatory muscle disease in CD-1 mice as well as several inbred mouse strains. Some mouse strains also develop central nervous system white matter disease and a focal myocarditis. Infectious virus in skeletal muscle falls to undetectable levels 3 weeks postinoculation (p.i.), although viral genome persists for at least 12 weeks p.i., the longest period of observation. Severe combined immunodeficient animals have evidence of muscle pathology as long as 5 weeks p.i., suggesting that DA virus is capable of inducing chronic muscle disease in the absence of an immune response. The presence in immunocompetent mice, however, of prominent muscle inflammation in the absence of infectious virus suggests that the immune system also contributes to the pathology. T lymphocytes are the predominant cell type infiltrating the skeletal muscle during the chronic disease. This murine model may further our understanding of virus-induced chronic myositis and help to clarify the pathogenesis of human inflammatory myopathies.

摘要

泰勒小鼠脑脊髓炎病毒的DA株是微小核糖核酸病毒科心病毒属的成员,在小鼠脑内接种后会引发与脱髓鞘过程相关的局限性持续性感染;病毒感染和免疫反应均被认为与晚期白质疾病有关。我们现在报告,在CD-1小鼠以及几种近交系小鼠品系中,腹腔接种DA会引发急性肌炎,并进展为慢性炎症性肌肉疾病。一些小鼠品系还会发展为中枢神经系统白质疾病和局灶性心肌炎。接种后3周(p.i.),骨骼肌中的传染性病毒降至无法检测的水平,尽管病毒基因组在接种后至少持续存在12周,这是观察的最长时间。严重联合免疫缺陷动物在接种后长达5周都有肌肉病理学证据,这表明DA病毒在没有免疫反应的情况下也能够诱发慢性肌肉疾病。然而,在有免疫能力的小鼠中,在没有传染性病毒的情况下出现明显的肌肉炎症,这表明免疫系统也与病理学有关。在慢性疾病期间,T淋巴细胞是浸润骨骼肌的主要细胞类型。这个小鼠模型可能会增进我们对病毒诱导的慢性肌炎的理解,并有助于阐明人类炎症性肌病的发病机制。

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本文引用的文献

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