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10.1016/j.chom.2020.09.016

http://scihub22266oqcxt.onion/10.1016/j.chom.2020.09.016
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33152279!7528903!33152279
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suck abstract from ncbi


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pmid33152279      Cell+Host+Microbe 2020 ; 28 (5): 646-659
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  • ACTIVating Resources for the COVID-19 Pandemic: In Vivo Models for Vaccines and Therapeutics #MMPMID33152279
  • Hewitt JA; Lutz C; Florence WC; Pitt MLM; Rao S; Rappaport J; Haigwood NL
  • Cell Host Microbe 2020[Nov]; 28 (5): 646-659 PMID33152279show ga
  • 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.
  • |*Coronavirus[MESH]
  • |*Coronavirus Infections/epidemiology[MESH]
  • |*Pandemics/prevention & control[MESH]
  • |*Pneumonia, Viral[MESH]
  • |*Vaccines[MESH]
  • |Animals[MESH]
  • |Betacoronavirus[MESH]
  • |COVID-19[MESH]
  • |Cricetinae[MESH]
  • |Guinea Pigs[MESH]
  • |Humans[MESH]
  • |Mice[MESH]


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