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Discovery and Description of Ebola Zaire Virus in 1976 and Relevance to the West African Epidemic During 2013-2016.1976年埃博拉-扎伊尔病毒的发现与描述及其与2013 - 2016年西非疫情的关联
J Infect Dis. 2016 Oct 15;214(suppl 3):S93-S101. doi: 10.1093/infdis/jiw207. Epub 2016 Jun 29.
2
Late Ebola virus relapse causing meningoencephalitis: a case report.晚期埃博拉病毒复发致脑膜脑炎:一例报告
Lancet. 2016 Jul 30;388(10043):498-503. doi: 10.1016/S0140-6736(16)30386-5. Epub 2016 May 18.
3
Experimental Treatment of Ebola Virus Disease with TKM-130803: A Single-Arm Phase 2 Clinical Trial.TKM-130803用于埃博拉病毒病的实验性治疗:一项单臂2期临床试验。
PLoS Med. 2016 Apr 19;13(4):e1001997. doi: 10.1371/journal.pmed.1001997. eCollection 2016 Apr.
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Therapeutic efficacy of the small molecule GS-5734 against Ebola virus in rhesus monkeys.小分子GS-5734对恒河猴体内埃博拉病毒的治疗效果。
Nature. 2016 Mar 17;531(7594):381-5. doi: 10.1038/nature17180. Epub 2016 Mar 2.
5
Experimental Treatment with Favipiravir for Ebola Virus Disease (the JIKI Trial): A Historically Controlled, Single-Arm Proof-of-Concept Trial in Guinea.法匹拉韦治疗埃博拉病毒病的实验性治疗(JIKI试验):在几内亚进行的一项历史对照单臂概念验证试验。
PLoS Med. 2016 Mar 1;13(3):e1001967. doi: 10.1371/journal.pmed.1001967. eCollection 2016 Mar.
6
Clinical Management of Ebola Virus Disease in the United States and Europe.美国和欧洲埃博拉病毒病的临床管理
N Engl J Med. 2016 Feb 18;374(7):636-46. doi: 10.1056/NEJMoa1504874.
7
Differential Regulation of Interferon Responses by Ebola and Marburg Virus VP35 Proteins.埃博拉和马尔堡病毒 VP35 蛋白对干扰素反应的差异调节。
Cell Rep. 2016 Feb 23;14(7):1632-1640. doi: 10.1016/j.celrep.2016.01.049. Epub 2016 Feb 11.
8
Real-time, portable genome sequencing for Ebola surveillance.用于埃博拉监测的实时便携式基因组测序
Nature. 2016 Feb 11;530(7589):228-232. doi: 10.1038/nature16996. Epub 2016 Feb 3.
9
Nanopore Sequencing as a Rapidly Deployable Ebola Outbreak Tool.纳米孔测序作为一种可快速部署的埃博拉疫情应对工具。
Emerg Infect Dis. 2016 Feb;22(2):331-4. doi: 10.3201/eid2202.151796.
10
Specific neutralizing response in plasma from convalescent patients of Ebola Virus Disease against the West Africa Makona variant of Ebola virus.埃博拉病毒病恢复期患者血浆中针对西非马科纳变异株埃博拉病毒的特异性中和反应。
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传播、人口和致病性:以埃博拉病例为例。

Transmission, Human Population, and Pathogenicity: the Ebola Case in Point.

机构信息

Department of Microbiology and Instituto de Investigación i+12, Hospital Universitario 12 de Octubre, Madrid, Spain.

Center for Health Alerts and Emergencies Coordination, Ministry of Health and CIBERESP, Madrid, Spain.

出版信息

Microbiol Spectr. 2018 Mar;6(2). doi: 10.1128/microbiolspec.MTBP-0003-2016.

DOI:10.1128/microbiolspec.MTBP-0003-2016
PMID:29573259
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11633569/
Abstract

The 2013-2016 Ebola outbreak in West Africa has been the largest ever of a known disease in a new context that produced an unprecedented impact and is changing the international approach to responding to public health emergencies. The unprecedented scale of the outbreak, the use of advanced technology for detecting and characterizing the infectious agent, along with the opportunity to treat patients in modern facilities have greatly increased our knowledge of the disease and its transmission. Also, for the first time, an important international effort has been deployed to control the spread of the epidemic by providing care to patients and by adopting basic measures of public health control. Apart from supportive treatment and intensive therapy with fluids and electrolytes, no new compounds have been proved to be clinically effective to treat Ebola virus disease; however, a specific vaccine has shown significant protection in clinical trials in Guinea, opening an expectation for controlling future outbreaks.

摘要

2013 年至 2016 年期间在西非爆发的埃博拉疫情是在新环境中出现的已知疾病中规模最大的一次,其产生了前所未有的影响,正在改变国际社会应对突发公共卫生事件的方式。疫情规模空前,利用先进技术检测和描述病原体,以及在现代化设施中治疗患者的机会,极大地增加了我们对该疾病及其传播方式的了解。此外,这也是首次开展重要的国际努力,通过为患者提供护理和采取基本的公共卫生控制措施来控制疫情的传播。除了支持性治疗和使用液体和电解质的强化疗法外,没有新的化合物被证明对治疗埃博拉病毒病具有临床疗效;然而,一种特定的疫苗在几内亚的临床试验中显示出了显著的保护作用,为控制未来的疫情爆发带来了希望。