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Safeguarding against Ebola: Vaccines and therapeutics to be stockpiled for future outbreaks

机译:预防埃博拉病毒:库存疫苗和治疗剂以备将来爆发

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The Ebola virus outbreak of 2014 to 2016 had severe and devastating consequences for the people of West Africa, with more than 28,000 cases and 11,000 deaths across Liberia, Sierra Leone,and Guinea [1]. This epidemic exposed inadequacies in the medical countermeasure preparedness of international governments and organizations that limited their ability to effectivelyaddress the spread of the Ebola virus. Although Ebola virus had been circulating in Africa fordecades with periodic outbreaks [1], funding for filoviruses has been limited to preclinicalevaluation and establishment of assays and reagents that were necessary to quickly evaluatevaccine and therapeutic candidates. The few medical countermeasures that existed were stalledin early stages of development, a consequence of several factors, including insufficient fundingto advance candidates, an uncertain regulatory path for development, and constraints associated with Biosafety Level 4 containment suites for research using Ebola viruses [2, 3, 4]. As theWest Africa Ebola epidemic grew in scale, governments, international organizations, nongovernment organizations, and industry scrambled to mount an effective response to contain theoutbreak [5]. The United States government (USG) and others invested millions of dollars toaccelerate the development of vaccine, therapeutic, and diagnostic candidates from early preclinical development into manufacturing scale-up and clinical trials [2]. Several of these clinical trials were conducted in West Africa, which offered the potential to have a direct impact onthe ongoing outbreak and demonstrate clinical efficacy of the medical countermeasures. Ultimately, the early development of these medical countermeasures was led by collaborativeefforts across multiple organizations and countries. For example, early development of bothvaccines and therapeutics can be attributed to organizations such as the National Institutes ofAllergy and Infectious Diseases (NIAID), the US Army Medical Research Institute of Infectious Diseases (USAMRIID), the Defense Threat Reduction Agency (DTRA), the MedicalCountermeasure Systems-Joint Vaccine Acquisition Program (MCS-JVAP), and the PublicHealth Agency Canada (PHAC). During the international response to the outbreak, numerousorganizations, institutions, and international governments contributed to the evaluation ofthese medical countermeasures in the field, including the Ministries of Health in Guinea andLiberia, the Ministry of Health and Sanitation in Sierra Leone, the World Health Organization(WHO), and the Wellcome Trust, United Kingdom, to name a few.
机译:2014年至2016年的埃博拉病毒爆发对西非人民造成了严重的破坏性后果,利比里亚,塞拉利昂和几内亚各地共发生28,000多起病例,造成11,000例死亡[1]。这种流行病暴露了国际政府和组织在医疗对策准备方面的不足,从而限制了它们有效应对埃博拉病毒传播的能力。尽管埃博拉病毒已经在非洲爆发了数十年,并有周期性暴发[1],但丝状病毒的资金仅限于临床前评估以及建立快速评估疫苗和治疗候选药物所必需的测定和试剂。现有的几种医学对策在开发的早期阶段就陷入了停滞状态,这是多种因素的结果,其中包括缺乏足够的资金来晋升候选人,不确定的监管发展路径以及与埃博拉病毒研究用的生物安全4级遏制套件相关的限制[2,3 ,4]。随着西非埃博拉疫情规模的扩大,政府,国际组织,非政府组织和行业争相采取有效措施应对疫情[5]。美国政府(USG)等投资了数百万美元,以加快从早期临床前开发到生产规模扩大和临床试验的疫苗,治疗和诊断候选药物的开发[2]。这些临床试验中有几项是在西非进行的,这有可能直接影响正在爆发的疾病并证明医疗对策的临床疗效。最终,这些医疗对策的早期发展是由多个组织和国家之间的协作努力所主导的。例如,疫苗和治疗剂的早期开发可归因于以下组织:美国国家过敏和传染病研究所(NIAID),美国陆军传染病医学研究所(USAMRIID),美国国防威胁减少局(DTRA), MedicalCountermeasure Systems-联合疫苗采购计划(MCS-JVAP)和加拿大公共卫生署(PHAC)。在国际社会对疫情的应对中,许多组织,机构和国际政府为评估这些医疗对策做出了贡献,包括几内亚和利比里亚的卫生部,塞拉利昂卫生和卫生部,世界卫生组织(世卫组织)和联合王国的惠康基金会等等。

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