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本文引用的文献

1
A recombinant Hendra virus G glycoprotein-based subunit vaccine protects ferrets from lethal Hendra virus challenge.一种基于重组亨德拉病毒 G 糖蛋白的亚单位疫苗可保护雪貂免受致命性亨德拉病毒的攻击。
Vaccine. 2011 Aug 5;29(34):5623-30. doi: 10.1016/j.vaccine.2011.06.015. Epub 2011 Jul 1.
2
A novel model of lethal Hendra virus infection in African green monkeys and the effectiveness of ribavirin treatment.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。
J Virol. 2010 Oct;84(19):9831-9. doi: 10.1128/JVI.01163-10. Epub 2010 Jul 21.
3
Development of an acute and highly pathogenic nonhuman primate model of Nipah virus infection.建立急性高致病性尼帕病毒感染非人灵长类动物模型。
PLoS One. 2010 May 18;5(5):e10690. doi: 10.1371/journal.pone.0010690.
4
Human Hendra virus encephalitis associated with equine outbreak, Australia, 2008.2008 年,澳大利亚亨德拉病毒脑炎与人感染马相关的疫情爆发。
Emerg Infect Dis. 2010 Feb;16(2):219-23. doi: 10.3201/eid1602.090552.
5
A neutralizing human monoclonal antibody protects against lethal disease in a new ferret model of acute nipah virus infection.一种中和性人源单克隆抗体可预防新型雪貂急性尼帕病毒感染模型中的致死性疾病。
PLoS Pathog. 2009 Oct;5(10):e1000642. doi: 10.1371/journal.ppat.1000642. Epub 2009 Oct 30.
6
Recurrent zoonotic transmission of Nipah virus into humans, Bangladesh, 2001-2007.2001 - 2007年,孟加拉国尼帕病毒反复出现人畜共患传播至人类的情况。
Emerg Infect Dis. 2009 Aug;15(8):1229-35. doi: 10.3201/eid1508.081237.
7
Targeted strategies for henipavirus therapeutics.亨尼帕病毒治疗的靶向策略。
Open Virol J. 2007;1:14-25. doi: 10.2174/1874357900701010014. Epub 2007 Sep 28.
8
Acute Hendra virus infection: Analysis of the pathogenesis and passive antibody protection in the hamster model.急性亨德拉病毒感染:仓鼠模型中的发病机制及被动抗体保护分析
Virology. 2009 May 10;387(2):459-65. doi: 10.1016/j.virol.2009.03.001. Epub 2009 Mar 28.
9
Preparation of recombinant viral glycoproteins for novel and therapeutic antibody discovery.用于新型和治疗性抗体发现的重组病毒糖蛋白的制备。
Methods Mol Biol. 2009;525:31-58, xiii. doi: 10.1007/978-1-59745-554-1_2.
10
A recombinant subunit vaccine formulation protects against lethal Nipah virus challenge in cats.一种重组亚单位疫苗制剂可保护猫免受尼帕病毒致死性攻击。
Vaccine. 2008 Jul 23;26(31):3842-52. doi: 10.1016/j.vaccine.2008.05.016. Epub 2008 Jun 2.

一种中和性人源单克隆抗体可保护非洲绿猴免受亨德拉病毒的攻击。

A neutralizing human monoclonal antibody protects african green monkeys from hendra virus challenge.

机构信息

Department of Microbiology, Boston University School of Medicine, Boston, MA 02118, USA.

出版信息

Sci Transl Med. 2011 Oct 19;3(105):105ra103. doi: 10.1126/scitranslmed.3002901.

DOI:10.1126/scitranslmed.3002901
PMID:22013123
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3313625/
Abstract

Hendra virus (HeV) is a recently emerged zoonotic paramyxovirus that can cause a severe and often fatal disease in horses and humans. HeV is categorized as a biosafety level 4 agent, which has made the development of animal models and testing of potential therapeutics and vaccines challenging. Infection of African green monkeys (AGMs) with HeV was recently demonstrated, and disease mirrored fatal HeV infection in humans, manifesting as a multisystemic vasculitis with widespread virus replication in vascular tissues and severe pathologic manifestations in the lung, spleen, and brain. Here, we demonstrate that m102.4, a potent HeV-neutralizing human monoclonal antibody (hmAb), can protect AGMs from disease after infection with HeV. Fourteen AGMs were challenged intratracheally with a lethal dose of HeV, and 12 subjects were infused twice with a 100-mg dose of m102.4 beginning at either 10, 24, or 72 hours after infection and again about 48 hours later. The presence of viral RNA, infectious virus, and HeV-specific immune responses demonstrated that all subjects were infected after challenge. All 12 AGMs that received m102.4 survived infection, whereas the untreated control subjects succumbed to disease on day 8 after infection. Animals in the 72-hour treatment group exhibited neurological signs of disease, but all animals started to recover by day 16 after infection. These results represent successful post-exposure in vivo efficacy by an investigational drug against HeV and highlight the potential impact a hmAb can have on human disease.

摘要

亨德拉病毒(HeV)是一种新近出现的人畜共患病副粘病毒,可导致马和人类患上严重且常常致命的疾病。HeV 被归类为生物安全 4 级制剂,这使得开发动物模型和测试潜在治疗方法和疫苗变得极具挑战性。最近有研究表明,非洲绿猴(AGM)感染了 HeV,其疾病与人类致命性 HeV 感染相似,表现为多系统血管炎,血管组织中广泛存在病毒复制,并在肺部、脾脏和大脑中出现严重的病理表现。在这里,我们证明 m102.4 是一种有效的 HeV 中和人源单克隆抗体(hmAb),可在 AGM 感染 HeV 后预防疾病。14 只 AGM 通过气管内接种致死剂量的 HeV 进行攻毒,12 只动物在感染后 10、24 或 72 小时开始,分两次给予 100mg 剂量的 m102.4 治疗,两次治疗间隔 48 小时。病毒 RNA、感染性病毒和 HeV 特异性免疫反应的存在表明,所有动物在攻毒后均被感染。接受 m102.4 治疗的 12 只 AGM 全部存活,而未接受治疗的对照组动物在感染后第 8 天死亡。在 72 小时治疗组的动物出现了疾病的神经症状,但所有动物在感染后第 16 天开始恢复。这些结果代表了一种研究性药物在 HeV 暴露后对动物的体内疗效,突出了人源单克隆抗体对人类疾病的潜在影响。