Show simple item record

dc.contributor.authorRosenke, K
dc.contributor.authorHansen, F
dc.contributor.authorSchwarz, B
dc.contributor.authorFeldmann, F
dc.contributor.authorHaddock, E
dc.contributor.authorRosenke, R
dc.contributor.authorBarbian, K
dc.contributor.authorMeade-White, K
dc.contributor.authorOkumura, A
dc.contributor.authorLeventhal, S
dc.contributor.authorHawman, DW
dc.contributor.authorRicotta, E
dc.contributor.authorBosio, CM
dc.contributor.authorMartens, C
dc.contributor.authorSaturday, G
dc.contributor.authorFeldmann, H
dc.contributor.authorJarvis, Michael A
dc.date.accessioned2021-08-09T12:36:20Z
dc.date.issued2021-04-16
dc.identifier.issn2041-1723
dc.identifier.issn2041-1723
dc.identifier.other2295
dc.identifier.urihttp://hdl.handle.net/10026.1/17496
dc.description.abstract

<jats:title>Abstract</jats:title><jats:p>The COVID-19 pandemic progresses unabated in many regions of the world. An effective antiviral against SARS-CoV-2 that could be administered orally for use following high-risk exposure would be of substantial benefit in controlling the COVID-19 pandemic. Herein, we show that MK-4482, an orally administered nucleoside analog, inhibits SARS-CoV-2 replication in the Syrian hamster model. The inhibitory effect of MK-4482 on SARS-CoV-2 replication is observed in animals when the drug is administered either beginning 12 h before or 12 h following infection in a high-risk exposure model. These data support the potential utility of MK-4482 to control SARS-CoV-2 infection in humans following high-risk exposure as well as for treatment of COVID-19 patients.</jats:p>

dc.format.extent2295-
dc.format.mediumElectronic
dc.languageen
dc.language.isoen
dc.publisherNature Research (part of Springer Nature)
dc.subjectAdministration, Oral
dc.subjectAnimals
dc.subjectAntiviral Agents
dc.subjectCOVID-19
dc.subjectChlorocebus aethiops
dc.subjectCytidine
dc.subjectDisease Models, Animal
dc.subjectHumans
dc.subjectHydroxylamines
dc.subjectMesocricetus
dc.subjectSARS-CoV-2
dc.subjectVero Cells
dc.subjectVirus Replication
dc.subjectCOVID-19 Drug Treatment
dc.titleOrally delivered MK-4482 inhibits SARS-CoV-2 replication in the Syrian hamster model
dc.typejournal-article
dc.typeJournal Article
dc.typeResearch Support, N.I.H., Intramural
dc.typeResearch Support, Non-U.S. Gov't
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000641850500003&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.issue1
plymouth.volume12
plymouth.publication-statusPublished online
plymouth.journalNature Communications
dc.identifier.doi10.1038/s41467-021-22580-8
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Health
plymouth.organisational-group/Plymouth/Faculty of Health/School of Biomedical Sciences
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA01 Clinical Medicine
plymouth.organisational-group/Plymouth/Research Groups
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)/CBR
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
dc.publisher.placeEngland
dcterms.dateAccepted2021-02-18
dc.rights.embargodate2021-8-14
dc.identifier.eissn2041-1723
dc.rights.embargoperiodNot known
rioxxterms.versionofrecord10.1038/s41467-021-22580-8
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2021-04-16
rioxxterms.typeJournal Article/Review


Files in this item

Thumbnail
Thumbnail

This item appears in the following Collection(s)

Show simple item record


All items in PEARL are protected by copyright law.
Author manuscripts deposited to comply with open access mandates are made available in accordance with publisher policies. Please cite only the published version using the details provided on the item record or document. In the absence of an open licence (e.g. Creative Commons), permissions for further reuse of content should be sought from the publisher or author.
Theme by 
Atmire NV