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Article: SARS-CoV-2 infection and disease outcomes in non-human primate models: advances and implications

TitleSARS-CoV-2 infection and disease outcomes in non-human primate models: advances and implications
Authors
KeywordsSARS-CoV-2
Non-human primates
Severe acute respiratory syndrome
Immunopathogenesis
Vaccine and drug discovery
Issue Date2021
PublisherTaylor & Francis, published in association with Shanghai Shangyixun Cultural Communication Company. The Journal's web site is located at https://www.tandfonline.com/toc/temi20/current
Citation
Emerging Microbes & Infections, 2021, v. 10 n. 1, p. 1881-1889 How to Cite?
AbstractSARS-CoV-2 has been the causative pathogen of the pandemic of COVID-19, resulting in catastrophic health issues globally. It is important to develop human-like animal models for investigating the mechanisms that SARS-CoV-2 uses to infect humans and cause COVID-19. Several studies demonstrated that the non-human primate (NHP) is permissive for SARS-CoV-2 infection to cause typical clinical symptoms including fever, cough, breathing difficulty, and other diagnostic abnormalities such as immunopathogenesis and hyperplastic lesions in the lung. These NHP models have been used for investigating the potential infection route and host immune response to SARS-CoV-2, as well as testing vaccines and drugs. This review aims to summarize the benefits and caveats of NHP models currently available for SARS-CoV-2, and to discuss key topics including model optimization, extended application, and clinical translation.
Persistent Identifierhttp://hdl.handle.net/10722/304166
ISSN
2021 Impact Factor: 19.568
2020 SCImago Journal Rankings: 2.475
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorYuan, L-
dc.contributor.authorTang, Q-
dc.contributor.authorZhu, H-
dc.contributor.authorGuan, Y-
dc.contributor.authorCheng, T-
dc.contributor.authorXia, N-
dc.date.accessioned2021-09-23T08:56:09Z-
dc.date.available2021-09-23T08:56:09Z-
dc.date.issued2021-
dc.identifier.citationEmerging Microbes & Infections, 2021, v. 10 n. 1, p. 1881-1889-
dc.identifier.issn2222-1751-
dc.identifier.urihttp://hdl.handle.net/10722/304166-
dc.description.abstractSARS-CoV-2 has been the causative pathogen of the pandemic of COVID-19, resulting in catastrophic health issues globally. It is important to develop human-like animal models for investigating the mechanisms that SARS-CoV-2 uses to infect humans and cause COVID-19. Several studies demonstrated that the non-human primate (NHP) is permissive for SARS-CoV-2 infection to cause typical clinical symptoms including fever, cough, breathing difficulty, and other diagnostic abnormalities such as immunopathogenesis and hyperplastic lesions in the lung. These NHP models have been used for investigating the potential infection route and host immune response to SARS-CoV-2, as well as testing vaccines and drugs. This review aims to summarize the benefits and caveats of NHP models currently available for SARS-CoV-2, and to discuss key topics including model optimization, extended application, and clinical translation.-
dc.languageeng-
dc.publisherTaylor & Francis, published in association with Shanghai Shangyixun Cultural Communication Company. The Journal's web site is located at https://www.tandfonline.com/toc/temi20/current-
dc.relation.ispartofEmerging Microbes & Infections-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectSARS-CoV-2-
dc.subjectNon-human primates-
dc.subjectSevere acute respiratory syndrome-
dc.subjectImmunopathogenesis-
dc.subjectVaccine and drug discovery-
dc.titleSARS-CoV-2 infection and disease outcomes in non-human primate models: advances and implications-
dc.typeArticle-
dc.identifier.emailZhu, H: zhuhch@hku.hk-
dc.identifier.emailGuan, Y: yguan@hkucc.hku.hk-
dc.identifier.authorityZhu, H=rp01535-
dc.identifier.authorityGuan, Y=rp00397-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1080/22221751.2021.1976598-
dc.identifier.pmid34490832-
dc.identifier.pmcidPMC8451603-
dc.identifier.scopuseid_2-s2.0-85115211855-
dc.identifier.hkuros325410-
dc.identifier.volume10-
dc.identifier.issue1-
dc.identifier.spage1881-
dc.identifier.epage1889-
dc.identifier.isiWOS:000697179700001-
dc.publisher.placeUnited Kingdom-

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