| Literature DB >> 26343011 |
Vincent Madelain1, Lisa Oestereich2, Frederik Graw3, Thi Huyen Tram Nguyen1, Xavier de Lamballerie4, France Mentré1, Stephan Günther2, Jeremie Guedj5.
Abstract
The polymerase inhibitor favipiravir is a candidate for the treatment of Ebola virus disease. Here, we designed a mathematical model to characterize the viral dynamics in 20 mice experimentally infected with Ebola virus, which were either left untreated or treated with favipiravir at 6 or 8days post infection. This approach provided estimates of kinetic parameters of Ebola virus reproduction, such as the half-life of productively infected cells, of about 6h, and the basic reproductive number which indicates that virus produced by a single infected cell productively infects about 9 new cells. Furthermore, the model predicted that favipiravir efficiently blocks viral production, reaching an antiviral effectiveness of 95% and 99.6% at 2 and 6days after initiation of treatment, respectively. The model could be particularly helpful to guide future studies evaluating favipiravir in larger animals.Entities:
Keywords: Ebola; Favipiravir; Modeling; Viral kinetics
Mesh:
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Year: 2015 PMID: 26343011 DOI: 10.1016/j.antiviral.2015.08.015
Source DB: PubMed Journal: Antiviral Res ISSN: 0166-3542 Impact factor: 5.970