柯萨奇病毒b3致远交系NMRI小鼠慢性心肌炎。

Journal of human virology Pub Date : 1999-11-01
I Merkle, M Tonew, B Glück, M Schmidtke, R Egerer, A Stelzner
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引用次数: 0

摘要

目的:探讨柯萨奇病毒B3 (CVB3)诱发成年汉族NMRI小鼠心肌炎的发病机制。近交系模型比近交系模型更能反映人类群体的自然变量敏感性。研究设计/方法:我们分析了复制病毒滴度、疾病急性期和慢性期的抗体反应、心肌损伤组织学和病毒RNA的持久性。结果:NMRI小鼠感染5000斑块形成单位(PFU)的CVB3变体“P”D(人成纤维细胞系的裂解变体),在第14天出现病毒复制高峰,并发生严重的急性心肌炎。慢性心肌炎的特征是进行性纤维化,浸润灶小,心脏持续存在病毒RNA,感染后98天可检测到抗cvb3 IgG产生和中和抗体反应。结论:CVB3“P”D具有诱导NMRI小鼠慢性心肌炎的作用。该模型为检验和证明心肌发病机制和制定治疗策略提供了一种方法。
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Coxsackievirus B3-induced chronic myocarditis in outbred NMRI mice.

Objectives: The pathogenesis of coxsackievirus B3 (CVB3)-induced myocarditis was investigated in adult Han:NMRI mice. The outbred model, in comparison with inbred models, represents better the natural variable susceptibility of the human population.

Study design/methods: We analyzed the replicating virus titer, the antibody response in the acute and chronic phase of disease, the histology of myocardial injury, and the persistence of viral RNA.

Results: NMRI mice infected with 5000 plaque-forming units (PFU) of the CVB3 variant "P"D, a lytic variant to human fibroblast lines, showed a peak of virus replication at day 14 and developed a severe acute myocarditis. The chronic myocarditis was characterized by progressive fibrosis, small foci of infiltrates, persistent viral RNA in the heart, and detectable anti-CVB3 IgG production and neutralizing antibody response up to day 98 postinfection.

Conclusions: CVB3"P"D is able to induce chronic myocarditis in NMRI mice. This model provides a method for examining and proving the mechanisms of myocardial pathogenesis and of developing therapeutic strategies.

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