PropertyValue
?:abstract
  • Coronavirus disease 2019 (COVID-19) is a declared pandemic that is spreading all over the world at a dreadfully fast rate. Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), the pathogen of COVID-19, infects the human body using angiotensin-converting enzyme 2 (ACE2) as a receptor identical to the severe acute respiratory syndrome (SARS) pandemic that occurred in 2002–2003. SARS-CoV-2 has a higher binding affinity to human ACE2 than to that of other species. Animal models that mimic the human disease are highly essential to develop therapeutics and vaccines against COVID-19. Here, we review transgenic mice that express human ACE2 in the airway and other epithelia and have shown to develop a rapidly lethal infection after intranasal inoculation with SARS-CoV, the pathogen of SARS. This literature review aims to present the importance of utilizing the human ACE2 transgenic mouse model to better understand the pathogenesis of COVID-19 and develop both therapeutics and vaccines.
?:creator
?:doi
  • 10.1186/s40246-020-00272-6
?:doi
?:journal
  • Hum_Genomics
?:license
  • cc-by
?:pdf_json_files
  • document_parses/pdf_json/aca0d44933c96e5adb59427e0daa503707274523.json
?:pmc_json_files
  • document_parses/pmc_json/PMC7269898.xml.json
?:pmcid
?:pmid
?:pmid
  • 32498696.0
?:publication_isRelatedTo_Disease
?:sha_id
?:source
  • Medline; PMC
?:title
  • COVID-19 preclinical models: human angiotensin-converting enzyme 2 transgenic mice
?:type
?:year
  • 2020-06-04

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