ACTIVating Resources for the COVID-19 Pandemic: In Vivo Models for Vaccines and Therapeutics.

ACTIVating Resources for the COVID-19 Pandemic: In Vivo Models for Vaccines and Therapeutics.
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DOI:
10.1016/j.chom.2020.09.016
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发表时间:
2020-11-11
影响因子:
30.3
通讯作者:
Haigwood NL
Haigwood NL
中科院分区:
医学1区
文献类型:
--
作者:
Hewitt JA;Lutz C;Florence WC;Pitt MLM;Rao S;Rappaport J;Haigwood NL

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加速COVID-19治疗干预和疫苗临床前工作组(ACTIV)是由美国国立卫生研究院牵头的公私合作伙伴关系,负责识别、优先考虑和交流SARS-CoV-2临床前资源。审查SARS-CoV-2动物模型数据有助于标准化和协调,并告知知识差距和有限资源的优先次序。迄今为止,已对小鼠、仓鼠、雪貂、豚鼠和非人灵长类动物进行了研究。有几个物种允许SARS-CoV-2复制,通常表现出轻微的疾病并消退,反映了大多数人类COVID-19病例。在一些模型中会出现更严重的疾病,其中一些与高龄有关,这是人类疾病的一个风险因素。这篇综述提供了一个快照,建议用于测试疫苗和治疗方法的模型的适用性,随着我们对COVID-19疾病生物学的理解的提高,这可能会发生变化。COVID-19是一种复杂的疾病,单个模型概括了疾病的某些方面;因此,动物模型的协调和评估势在必行。COVID-19疾病的动物模型得到了迅速发展。休伊特等人代表NIH领导的ACTIV公私合作伙伴关系。将这些小型和大型模型与人类疾病进行比较,并为各类治疗药物和疫苗的临床前测试提出建议。
The Preclinical Working Group of Accelerating COVID-19 Therapeutic Interventions and Vaccines (ACTIV), a public-private partnership spearheaded by the National Institutes of Health, has been charged with identifying, prioritizing, and communicating SARS-CoV-2 preclinical resources. Reviewing SARS-CoV-2 animal model data facilitates standardization and harmonization and informs knowledge gaps and prioritization of limited resources. To date, mouse, hamster, ferret, guinea pig, and non-human primates have been investigated. Several species are permissive for SARS-CoV-2 replication, often exhibiting mild disease with resolution, reflecting most human COVID-19 cases. More severe disease develops in a few models, some associated with advanced age, a risk factor for human disease. This review provides a snapshot that recommends the suitability of models for testing vaccines and therapeutics, which may evolve as our understanding of COVID-19 disease biology improves. COVID-19 is a complex disease, and individual models recapitulate certain aspects of disease; therefore, the coordination and assessment of animal models is imperative. Animal models of COVID-19 disease have been rapidly developed. On behalf of the ACTIV public-private partnership led by NIH, Hewitt et al. compare these small and large models to human disease and make recommendations for preclinical testing of various classes of therapeutics and vaccines.
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