| Literature DB >> 27890675 |
Wei Sun1, Shihua He2,3, Carles Martínez-Romero4,5, Jennifer Kouznetsova1, Gregory Tawa1, Miao Xu1, Paul Shinn1, Ethan Fisher1, Yan Long1, Omid Motabar1, Shu Yang1, Philip E Sanderson1, Peter R Williamson6, Adolfo García-Sastre4,5,7, Xiangguo Qiu2,3, Wei Zheng1.
Abstract
Although a group of FDA-approved drugs were previously identified with activity against Ebola virus (EBOV), most of them are not clinically useful because their human blood concentrations are not high enough to inhibit EBOV infection. We screened 795 unique three-drug combinations in an EBOV entry assay. Two sets of three-drug combinations, toremifene-mefloquine-posaconazole and toremifene-clarithromycin-posaconazole, were identified that effectively blocked EBOV entry and were further validated for inhibition of live EBOV infection. The individual drug concentrations in the combinations were reduced to clinically relevant levels. We identified mechanisms of action of these drugs: functional inhibitions of Niemann-Pick C1, acid sphingomyelinase, and lysosomal calcium release. Our findings identify the drug combinations with potential to treat EBOV infection. Published by Elsevier B.V.Entities:
Keywords: Drug combination; Drug repurposing; Ebola prevention; Ebola treatment; Polypharmacology
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Year: 2016 PMID: 27890675 PMCID: PMC5182099 DOI: 10.1016/j.antiviral.2016.11.017
Source DB: PubMed Journal: Antiviral Res ISSN: 0166-3542 Impact factor: 5.970