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Monoclonal Antibodies for Early Treatment of COVID-19 in a World of Evolving SARS-CoV-2 Mutations and Variants

dc.contributor.authorPogue, JM
dc.contributor.authorLauring, AS
dc.contributor.authorGandhi, TN
dc.contributor.authorMarshall, VD
dc.contributor.authorEschenauer, GA
dc.contributor.authorNagel, JL
dc.contributor.authorBaang, JH
dc.contributor.authorZhou, S
dc.contributor.authorValesano, AL
dc.contributor.authorPetty, LA
dc.coverage.spatialUnited States
dc.date.accessioned2022-08-26T19:22:14Z
dc.date.available2022-08-26T19:22:14Z
dc.date.issued2021-07-01
dc.identifier.issn2328-8957
dc.identifier.issn2328-8957
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pubmed/34291118
dc.identifier.urihttps://hdl.handle.net/2027.42/174136en
dc.description.abstractMonoclonal antibodies targeting the receptor binding domain (RBD) of severe acute respiratory syndrome coronavirus 2 spike protein are important outpatient treatment options in coronavirus disease 2019 to mitigate progression of disease and prevent hospitalization. The impact of different RBD mutations on the efficacy of the available monoclonal antibodies and processes for incorporating this impact into treatment algorithms are ill defined. Herein, we synthesize the data surrounding the impact of key RBD mutations on the efficacy of US Food and Drug Administration Emergency Use Authorized monoclonal antibodies and describe our approach at Michigan Medicine at monitoring mutation frequency in circulating virus and developing an algorithm that incorporates these data into outpatient treatment pathways.
dc.format.mediumElectronic-eCollection
dc.languageeng
dc.publisherOxford University Press (OUP)
dc.relation.haspartARTN ofab268
dc.rightsLicence for published version: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectCOVID-19
dc.subjectSARS-CoV-2
dc.subjectbamlanivimab
dc.subjectbamlanivimab and etesevimab
dc.subjectcasirivimab and imdevimab
dc.subjectvariants
dc.titleMonoclonal Antibodies for Early Treatment of COVID-19 in a World of Evolving SARS-CoV-2 Mutations and Variants
dc.typeArticle
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/174136/2/Monoclonal Antibodies for Early Treatment of COVID-19 in a World of Evolving SARS-CoV-2 Mutations and Variants.pdf
dc.identifier.doi10.1093/ofid/ofab268
dc.identifier.doihttps://dx.doi.org/10.7302/5867
dc.identifier.sourceOpen Forum Infectious Diseases
dc.description.versionPublished version
dc.date.updated2022-08-26T19:22:13Z
dc.identifier.orcid0000-0003-4780-6215
dc.identifier.orcid0000-0003-2906-8335
dc.identifier.orcid0000-0001-5971-0531
dc.identifier.orcid0000-0002-5925-4289
dc.identifier.orcid0000-0001-5635-405X
dc.description.filedescriptionDescription of Monoclonal Antibodies for Early Treatment of COVID-19 in a World of Evolving SARS-CoV-2 Mutations and Variants.pdf : Accepted version
dc.identifier.volume8
dc.identifier.issue7
dc.identifier.startpageofab268
dc.identifier.name-orcidPogue, JM; 0000-0003-4780-6215
dc.identifier.name-orcidLauring, AS; 0000-0003-2906-8335
dc.identifier.name-orcidGandhi, TN
dc.identifier.name-orcidMarshall, VD
dc.identifier.name-orcidEschenauer, GA; 0000-0001-5971-0531
dc.identifier.name-orcidNagel, JL
dc.identifier.name-orcidBaang, JH; 0000-0002-5925-4289
dc.identifier.name-orcidZhou, S; 0000-0001-5635-405X
dc.identifier.name-orcidValesano, AL
dc.identifier.name-orcidPetty, LA
dc.working.doi10.7302/5867en
dc.owningcollnamePharmacy, College of


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Licence for published version: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International
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