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一种新型致命亨德拉病毒感染非洲绿猴模型及利巴韦林治疗效果。

A novel model of lethal Hendra virus infection in African green monkeys and the effectiveness of ribavirin treatment.

机构信息

Laboratory of Virology, Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, 903 S. 4th Street, Hamilton, Montana, USA.

出版信息

J Virol. 2010 Oct;84(19):9831-9. doi: 10.1128/JVI.01163-10. Epub 2010 Jul 21.

Abstract

The henipaviruses, Hendra virus (HeV) and Nipah virus (NiV), are emerging zoonotic paramyxoviruses that can cause severe and often lethal neurologic and/or respiratory disease in a wide variety of mammalian hosts, including humans. There are presently no licensed vaccines or treatment options approved for human or veterinarian use. Guinea pigs, hamsters, cats, and ferrets, have been evaluated as animal models of human HeV infection, but studies in nonhuman primates (NHP) have not been reported, and the development and approval of any vaccine or antiviral for human use will likely require efficacy studies in an NHP model. Here, we examined the pathogenesis of HeV in the African green monkey (AGM) following intratracheal inoculation. Exposure of AGMs to HeV produced a uniformly lethal infection, and the observed clinical signs and pathology were highly consistent with HeV-mediated disease seen in humans. Ribavirin has been used to treat patients infected with either HeV or NiV; however, its utility in improving outcome remains, at best, uncertain. We examined the antiviral effect of ribavirin in a cohort of nine AGMs before or after exposure to HeV. Ribavirin treatment delayed disease onset by 1 to 2 days, with no significant benefit for disease progression and outcome. Together our findings introduce a new disease model of acute HeV infection suitable for testing antiviral strategies and also demonstrate that, while ribavirin may have some antiviral activity against the henipaviruses, its use as an effective standalone therapy for HeV infection is questionable.

摘要

亨德拉病毒(HeV)和尼帕病毒(NiV)是新兴的人畜共患副粘病毒,可导致广泛的哺乳动物宿主(包括人类)发生严重且常致命的神经和/或呼吸道疾病。目前尚无获准用于人类或兽医用途的疫苗或治疗选择。豚鼠、仓鼠、猫和雪貂已被评估为人类 HeV 感染的动物模型,但尚未报道在非人类灵长类动物(NHP)中的研究,任何用于人类的疫苗或抗病毒药物的开发和批准可能需要在 NHP 模型中进行疗效研究。在这里,我们研究了 HeV 在经气管接种后的非洲绿猴(AGM)中的发病机制。AGM 暴露于 HeV 后会产生一致的致死性感染,观察到的临床症状和病理学与人类中观察到的 HeV 介导的疾病高度一致。利巴韦林曾用于治疗感染 HeV 或 NiV 的患者;然而,其改善预后的效果最多仍不确定。我们在 9 只 AGM 接触 HeV 之前或之后检查了利巴韦林的抗病毒作用。利巴韦林治疗使疾病发作延迟了 1 至 2 天,但对疾病进展和预后没有明显益处。我们的研究结果共同引入了一种新的急性 HeV 感染疾病模型,适用于测试抗病毒策略,也表明尽管利巴韦林可能对亨德拉病毒具有一定的抗病毒活性,但将其作为 HeV 感染的有效单一疗法是值得怀疑的。

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