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Safety, tolerability, and immunogenicity of the Ebola Sudan chimpanzee adenovirus vector vaccine (cAd3-EBO S) in healthy Ugandan adults: a phase 1, open-label, dose-escalation clinical trial.在健康的乌干达成年人中,使用埃博拉苏丹黑猩猩腺病毒载体疫苗(cAd3-EBO S)的安全性、耐受性和免疫原性:一项 1 期、开放性、剂量递增的临床试验。
Lancet Infect Dis. 2023 Dec;23(12):1408-1417. doi: 10.1016/S1473-3099(23)00344-4. Epub 2023 Aug 3.
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The rVSV-EBOV vaccine provides limited cross-protection against Sudan virus in guinea pigs.rVSV-EBOV疫苗对豚鼠体内的苏丹病毒提供有限的交叉保护。
NPJ Vaccines. 2023 Jun 10;8(1):91. doi: 10.1038/s41541-023-00685-z.
3
A reflection on the Marburg virus outbreak in Tanzania: the importance of preparedness and prevention in public health - a correspondence.关于坦桑尼亚马尔堡病毒疫情的思考:公共卫生防范与预防的重要性——一封通信
Ann Med Surg (Lond). 2023 Apr 11;85(5):2247-2249. doi: 10.1097/MS9.0000000000000596. eCollection 2023 May.
4
A Highly Attenuated Panfilovirus VesiculoVax Vaccine Rapidly Protects Nonhuman Primates Against Marburg Virus and 3 Species of Ebola Virus.一种高度减毒的潘菲洛病毒水疱性口炎疫苗可快速保护非人灵长类动物免受马尔堡病毒和 3 种埃博拉病毒的感染。
J Infect Dis. 2023 Nov 15;228(Suppl 7):S660-S670. doi: 10.1093/infdis/jiad157.
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Species-specific immunogenicity and protective efficacy of a vesicular stomatitis virus-based Sudan virus vaccine: a challenge study in macaques.基于水疱性口炎病毒的苏丹病毒疫苗的种属特异性免疫原性和保护效力:猕猴挑战研究。
Lancet Microbe. 2023 Mar;4(3):e171-e178. doi: 10.1016/S2666-5247(23)00001-0. Epub 2023 Feb 2.
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Vaccines (Basel). 2022 Nov 15;10(11):1935. doi: 10.3390/vaccines10111935.
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Nonhuman Primates Are Protected against Marburg Virus Disease by Vaccination with a Vesicular Stomatitis Virus Vector-Based Vaccine Prepared under Conditions to Allow Advancement to Human Clinical Trials.通过接种在允许推进至人体临床试验的条件下制备的基于水疱性口炎病毒载体的疫苗,非人灵长类动物可免受马尔堡病毒病的侵害。
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JCI Insight. 2022 May 23;7(10):e159090. doi: 10.1172/jci.insight.159090.

推进丝状病毒病对策的观点:多部门会议报告。

Perspectives on Advancing Countermeasures for Filovirus Disease: Report From a Multisector Meeting.

机构信息

Médecins Sans Frontières, Brussels, Belgium.

Galveston National Laboratory, University of Texas Medical Branch, Galveston.

出版信息

J Infect Dis. 2023 Nov 13;228(Suppl 7):S474-S478. doi: 10.1093/infdis/jiad354.

DOI:10.1093/infdis/jiad354
PMID:37596837
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10651188/
Abstract

Although there are now approved treatments and vaccines for Ebola virus disease, the case fatality rate remains unacceptably high even when patients are treated with the newly approved therapeutics. Furthermore, these countermeasures are not expected to be effective against disease caused by other filoviruses. A meeting of subject-matter experts was held during the 10th International Filovirus Symposium to discuss strategies to address these gaps. Several investigational therapeutics, vaccine candidates, and combination strategies were presented. The greatest challenge was identified to be the implementation of well-designed clinical trials of safety and efficacy during filovirus disease outbreaks. Preparing for this will require agreed-upon common protocols for trials intended to bridge multiple outbreaks across all at-risk countries. A multinational research consortium including at-risk countries would be an ideal mechanism to negotiate agreement on protocol design and coordinate preparation. Discussion participants recommended a follow-up meeting be held in Africa to establish such a consortium.

摘要

尽管现在已有针对埃博拉病毒病的批准治疗方法和疫苗,但即使患者接受新批准的疗法治疗,病死率仍高得令人无法接受。此外,这些对策预计对其他丝状病毒引起的疾病无效。在第十届国际丝状病毒研讨会上举行了一次主题专家会议,讨论应对这些空白的策略。提出了几种研究性治疗方法、疫苗候选物和联合策略。最大的挑战被确定为在丝状病毒病暴发期间实施安全和疗效的精心设计的临床试验。为此做好准备需要就旨在跨越所有高危国家的多次暴发的试验达成一致的共同方案。包括高危国家在内的跨国研究联盟将是就方案设计进行谈判和协调筹备工作的理想机制。讨论参与者建议在非洲举行后续会议,以建立这样一个联盟。