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dc.contributor.authorIanevski, Aleksandr
dc.contributor.authorZusinaite, Eva
dc.contributor.authorTenson, Tanel
dc.contributor.authorOksenych, Valentyn
dc.contributor.authorWang, Wei
dc.contributor.authorAfset, Jan Egil
dc.contributor.authorBjørås, Magnar
dc.contributor.authorKainov, Denis
dc.date.accessioned2023-02-13T10:06:56Z
dc.date.available2023-02-13T10:06:56Z
dc.date.created2022-10-13T14:37:13Z
dc.date.issued2022
dc.identifier.citationViruses. 2022, 14 (9), .en_US
dc.identifier.issn1999-4915
dc.identifier.urihttps://hdl.handle.net/11250/3050306
dc.description.abstractBackground: Enterovirus infections affect people around the world, causing a range of illnesses, from mild fevers to severe, potentially fatal conditions. There are no approved treatments for enterovirus infections. Methods: We have tested our library of broad-spectrum antiviral agents (BSAs) against echovirus 1 (EV1) in human adenocarcinoma alveolar basal epithelial A549 cells. We also tested combinations of the most active compounds against EV1 in A549 and human immortalized retinal pigment epithelium RPE cells. Results: We confirmed anti-enteroviral activities of pleconaril, rupintrivir, cycloheximide, vemurafenib, remdesivir, emetine, and anisomycin and identified novel synergistic rupintrivir–vemurafenib, vemurafenib–pleconaril and rupintrivir–pleconaril combinations against EV1 infection. Conclusions: Because rupintrivir, vemurafenib, and pleconaril require lower concentrations to inhibit enterovirus replication in vitro when combined, their cocktails may have fewer side effects in vivo and, therefore, should be further explored in preclinical and clinical trials against EV1 and other enterovirus infections.en_US
dc.language.isoengen_US
dc.publisherMDPIen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleNovel Synergistic Anti-Enteroviral Drug Combinationsen_US
dc.title.alternativeNovel Synergistic Anti-Enteroviral Drug Combinationsen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.volume14en_US
dc.source.journalVirusesen_US
dc.source.issue9en_US
dc.identifier.doi10.3390/v14091866
dc.identifier.cristin2061239
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Navngivelse 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse 4.0 Internasjonal