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本文引用的文献

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A 40-Month Follow-Up of Ebola Virus Disease Survivors in Guinea (PostEbogui) Reveals Long-Term Detection of Ebola Viral Ribonucleic Acid in Semen and Breast Milk.几内亚埃博拉病毒病幸存者40个月随访(PostEbogui)显示,精液和母乳中长期检测到埃博拉病毒核糖核酸。
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Characterization of Ebola Virus Disease (EVD) in Rhesus Monkeys for Development of EVD Therapeutics.用于埃博拉病毒病(EVD)治疗药物研发的恒河猴 EVD 特征描述。
Viruses. 2020 Jan 13;12(1):92. doi: 10.3390/v12010092.
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Comparative therapeutic efficacy of remdesivir and combination lopinavir, ritonavir, and interferon beta against MERS-CoV.比较瑞德西韦与洛匹那韦利托那韦和干扰素β联合治疗中东呼吸综合征冠状病毒的疗效。
Nat Commun. 2020 Jan 10;11(1):222. doi: 10.1038/s41467-019-13940-6.
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A Randomized, Controlled Trial of Ebola Virus Disease Therapeutics.埃博拉病毒病治疗的随机、对照试验。
N Engl J Med. 2019 Dec 12;381(24):2293-2303. doi: 10.1056/NEJMoa1910993. Epub 2019 Nov 27.
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New Nucleoside Analogues for the Treatment of Hemorrhagic Fever Virus Infections.新型核苷类似物治疗出血热病毒感染。
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Estimating the impact of violent events on transmission in Ebola virus disease outbreak, Democratic Republic of the Congo, 2018-2019.估算 2018-2019 年刚果民主共和国埃博拉疫情中暴力事件对传播的影响。
Epidemics. 2019 Sep;28:100353. doi: 10.1016/j.epidem.2019.100353. Epub 2019 Jul 26.
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Broad spectrum antiviral remdesivir inhibits human endemic and zoonotic deltacoronaviruses with a highly divergent RNA dependent RNA polymerase.广谱抗病毒药物瑞德西韦通过高度分化的 RNA 依赖的 RNA 聚合酶抑制人类地方性和人畜共患的德尔塔冠状病毒。
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Remdesivir (GS-5734) protects African green monkeys from Nipah virus challenge.瑞德西韦(GS-5734)可保护非洲绿猴免受尼帕病毒攻击。
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Medical countermeasures during the 2018 Ebola virus disease outbreak in the North Kivu and Ituri Provinces of the Democratic Republic of the Congo: a rapid genomic assessment.2018 年刚果民主共和国北基伍省和伊图里省爆发埃博拉病毒病期间的医疗对策:快速基因组评估。
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埃博拉病毒病治疗的近期成功:不能自满。

Recent successes in therapeutics for Ebola virus disease: no time for complacency.

机构信息

United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD, USA.

Integrated Research Facility at Fort Detrick, Division of Clinical Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Fort Detrick, Frederick, MD, USA.

出版信息

Lancet Infect Dis. 2020 Sep;20(9):e231-e237. doi: 10.1016/S1473-3099(20)30282-6. Epub 2020 Jun 18.

DOI:10.1016/S1473-3099(20)30282-6
PMID:32563280
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7302789/
Abstract

The PALM trial in the Democratic Republic of the Congo identified a statistically significant survival benefit for two monoclonal antibody-based therapeutics in the treatment of acute Ebola virus disease; however, substantial gaps remain in improving the outcomes of acute Ebola virus disease and for the survivors. Ongoing efforts are needed to develop more effective strategies, particularly for individuals with severe disease, for prevention and treatment of viral persistence in immune-privileged sites, for optimisation of post-exposure prophylaxis, and to increase therapeutic breadth. As antibody-based approaches are identified and advanced, promising small-molecule antivirals currently in clinical stage development should continue to be evaluated for filovirus diseases, with consideration of their added value in combination approaches with bundled supportive care, their penetration in tissues of interest, the absence of interaction with glycoprotein-based vaccines, and filoviral breadth.

摘要

刚果民主共和国的 PALM 试验表明,两种基于单克隆抗体的治疗方法在治疗急性埃博拉病毒病方面具有统计学意义上的生存获益;然而,在改善急性埃博拉病毒病的结局和幸存者的结局方面仍存在很大差距。需要继续努力制定更有效的策略,特别是针对重症患者,预防和治疗免疫特权部位的病毒持续存在,优化暴露后预防,并扩大治疗范围。随着抗体为基础的治疗方法的出现和发展,目前处于临床开发阶段的有前途的小分子抗病毒药物也应继续针对丝状病毒病进行评估,考虑它们与捆绑支持性护理的联合治疗方法的附加值、它们在感兴趣的组织中的渗透能力、与糖蛋白疫苗无相互作用以及丝状病毒的广泛程度。