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dc.contributor.authorTran, Trung The
dc.contributor.authorVaage, Eline Benno
dc.contributor.authorMehta, Adi
dc.contributor.authorChopra, Adity
dc.contributor.authorTietze, Lisa
dc.contributor.authorKolderup, Anette
dc.contributor.authorAnthi, Aina Karen
dc.contributor.authorKönig, Marton
dc.contributor.authorNygaard, Gro Owren
dc.contributor.authorLind, Andreas
dc.contributor.authorMüller, Fredrik
dc.contributor.authorNissen-Meyer, Lise Sofie Haug
dc.contributor.authorMagnus, Per Minor
dc.contributor.authorTrogstad, Lill
dc.contributor.authorMjaaland, Siri
dc.contributor.authorSøraas, Arne Vasli
dc.contributor.authorMidtvedt, Karsten
dc.contributor.authorÅsberg, Anders
dc.contributor.authorBarratt-Due, Andreas
dc.contributor.authorMedhus, Asle Wilhelm
dc.contributor.authorHøivik, Marte Lie
dc.contributor.authorLundin, Knut
dc.contributor.authorKarlsen, Randi Fuglaas
dc.contributor.authorDahle, Reidun
dc.contributor.authorDanielsson, Karin
dc.contributor.authorThomassen, Kristine Stien
dc.contributor.authorKro, Grete Anette Birkeland
dc.contributor.authorCox, Rebecca Jane
dc.contributor.authorZhou, Fan
dc.contributor.authorLangeland, Nina
dc.contributor.authorAukrust, Pål
dc.contributor.authorMelum, Espen
dc.contributor.authorÅvitsland, Tone Lise
dc.contributor.authorWiencke, Kristine
dc.contributor.authorHolter, Jan Cato
dc.contributor.authorMunthe, Ludvig Andre
dc.contributor.authorGrødeland, Gunnveig
dc.contributor.authorAndersen, Jan Terje
dc.contributor.authorVaage, John T.
dc.contributor.authorLund-Johansen, Fridtjof
dc.date.accessioned2023-01-13T09:32:11Z
dc.date.available2023-01-13T09:32:11Z
dc.date.created2023-01-04T16:05:38Z
dc.date.issued2022
dc.identifier.issn2059-0105
dc.identifier.urihttps://hdl.handle.net/11250/3043266
dc.description.abstractDiagnostic assays currently used to monitor the efficacy of COVID-19 vaccines measure levels of antibodies to the receptor-binding domain of ancestral SARS-CoV-2 (RBDwt). However, the predictive value for protection against new variants of concern (VOCs) has not been firmly established. Here, we used bead-based arrays and flow cytometry to measure binding of antibodies to spike proteins and receptor-binding domains (RBDs) from VOCs in 12,000 serum samples. Effects of sera on RBD-ACE2 interactions were measured as a proxy for neutralizing antibodies. The samples were obtained from healthy individuals or patients on immunosuppressive therapy who had received two to four doses of COVID-19 vaccines and from COVID-19 convalescents. The results show that anti-RBDwt titers correlate with the levels of binding- and neutralizing antibodies against the Alpha, Beta, Gamma, Delta, Epsilon and Omicron variants. The benefit of multiplexed analysis lies in the ability to measure a wide range of anti-RBD titers using a single dilution of serum for each assay. The reactivity patterns also yield an internal reference for neutralizing activity and binding antibody units per milliliter (BAU/ml). Results obtained with sera from vaccinated healthy individuals and patients confirmed and extended results from previous studies on time-dependent waning of antibody levels and effects of immunosuppressive agents. We conclude that anti-RBDwt titers correlate with levels of neutralizing antibodies against VOCs and propose that our method may be implemented to enhance the precision and throughput of immunomonitoring.en_US
dc.language.isoengen_US
dc.publisherNature Researchen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleTiters of antibodies against ancestral SARS-CoV-2 correlate with levels of neutralizing antibodies to multiple variantsen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright The Author(s) 2022en_US
dc.source.articlenumber174en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1038/s41541-022-00586-7
dc.identifier.cristin2100792
dc.source.journalnpj Vaccinesen_US
dc.identifier.citationnpj Vaccines. 2022, 7, 174.en_US
dc.source.volume7en_US


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