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关于意外接触埃博拉病毒后可供人类使用的医学应对措施的最新技术研讨会。

State-of-the-Art Workshops on Medical Countermeasures Potentially Available for Human Use Following Accidental Exposures to Ebola Virus.

作者信息

Jahrling Peter B, Hensley Lisa E, Barrett Kevin, Lane Henry Clifford, Davey Richard T

机构信息

Integrated Research Facility.

Division of Clinical Research, National Institute of Allergy and Infectious Diseases (NIAID), Bethesda, Maryland.

出版信息

J Infect Dis. 2015 Oct 1;212 Suppl 2(Suppl 2):S84-90. doi: 10.1093/infdis/jiv115. Epub 2015 May 9.

DOI:10.1093/infdis/jiv115
PMID:25957962
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4564537/
Abstract

The ongoing outbreak of Ebola in West Africa has raised a general awareness that at present there are no Ebola-specific medical countermeasures (MCMs) with proven effectiveness. This paper recapitulates discussions held at the 6th International Filovirus Symposium in March 2014 as well as the subsequent design of a randomized clinical trial design for treating Ebola virus-infected patients evacuated from West Africa to the United States. A number of different drugs or biologics were critically reviewed and 3 different postexposure strategies were identified as being farthest along in development; passive immunotherapy with monoclonal antibodies, postexposure vaccination with constructs involving viral vectors (such as vesicular stomatitis virus), and antisense compounds directly targeting the viral genome such as modified phosphorodiamidate morpholino oligomer-based compounds and small interfering RNA products. At the time of the meetings, there were no investigational new drugs (INDs) in place for the candidate MCMs. Developers and sponsors of these candidate products were strongly encouraged to prepare pre-IND packets and submit pre-IND meeting requests to the Food and Drug Administration. Some of these investigational products have already been used under emergency authorizations to treat patients in Africa as well as patients evacuated to the United States or Western Europe.

摘要

西非持续爆发的埃博拉疫情使人们普遍意识到,目前尚无经证实有效的针对埃博拉的医学应对措施(MCM)。本文概述了2014年3月第六届国际丝状病毒研讨会的讨论内容以及随后为治疗从西非撤离至美国的埃博拉病毒感染患者而设计的一项随机临床试验。对多种不同的药物或生物制剂进行了严格审查,并确定了3种处于研发最前沿的不同暴露后策略;使用单克隆抗体进行被动免疫治疗、使用涉及病毒载体(如水泡性口炎病毒)的构建体进行暴露后疫苗接种,以及直接靶向病毒基因组的反义化合物,如基于修饰的磷二酰胺吗啉代寡聚物的化合物和小干扰RNA产品。在会议召开之时,这些候选MCM尚无研究性新药(IND)。强烈鼓励这些候选产品的开发者和赞助商准备IND前数据包,并向美国食品药品监督管理局提交IND前会议申请。其中一些研究性产品已在紧急授权下用于治疗非洲患者以及撤离至美国或西欧的患者。

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本文引用的文献

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Evaluation of the potential impact of Ebola virus genomic drift on the efficacy of sequence-based candidate therapeutics.评估埃博拉病毒基因组漂移对基于序列的候选治疗药物疗效的潜在影响。
mBio. 2015 Jan 20;6(1):e02227-14. doi: 10.1128/mBio.02227-14.
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Evaluating Ebola therapies--the case for RCTs.评估埃博拉治疗方法——随机对照试验的必要性
N Engl J Med. 2014 Dec 18;371(25):2350-1. doi: 10.1056/NEJMp1414145. Epub 2014 Dec 3.
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Reversion of advanced Ebola virus disease in nonhuman primates with ZMapp.ZMapp 逆转非人灵长类动物的晚期埃博拉病毒病。
Nature. 2014 Oct 2;514(7520):47-53. doi: 10.1038/nature13777. Epub 2014 Aug 29.
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A model of federal interagency cooperation: the National Interagency Confederation for Biological Research.联邦跨部门合作模式:国家生物研究跨部门联盟。
Biosecur Bioterror. 2014 May-Jun;12(3):144-50. doi: 10.1089/bsp.2013.0084. Epub 2014 May 12.
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Post-exposure therapy of filovirus infections.丝状病毒感染的暴露后治疗。
Trends Microbiol. 2014 Aug;22(8):456-63. doi: 10.1016/j.tim.2014.04.002. Epub 2014 Apr 30.
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Sustained protection against Ebola virus infection following treatment of infected nonhuman primates with ZMAb.用ZMAb治疗受感染的非人灵长类动物后对埃博拉病毒感染的持续保护作用。
Sci Rep. 2013 Nov 28;3:3365. doi: 10.1038/srep03365.
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mAbs and Ad-vectored IFN-α therapy rescue Ebola-infected nonhuman primates when administered after the detection of viremia and symptoms.当在检测到病毒血症和症状后给予单克隆抗体和腺载体 IFN-α 治疗时,可挽救感染埃博拉病毒的非人灵长类动物。
Sci Transl Med. 2013 Oct 16;5(207):207ra143. doi: 10.1126/scitranslmed.3006605.
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Therapeutic intervention of Ebola virus infection in rhesus macaques with the MB-003 monoclonal antibody cocktail.用 MB-003 单克隆抗体鸡尾酒疗法治疗恒河猴的埃博拉病毒感染。
Sci Transl Med. 2013 Aug 21;5(199):199ra113. doi: 10.1126/scitranslmed.3006608.
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