Madelain V, Oestereich L, Graw F, Thi Huyen Tram Nguyen , De Lamballerie X, Mentre F, Guenther S, Guedj J (2015)
Publication Type: Journal article
Publication year: 2015
Book Volume: 123
Pages Range: 70-77
DOI: 10.1016/j.antiviral.2015.08.015
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 8 days post infection. This approach provided estimates of kinetic parameters of Ebola virus reproduction, such as the half-life of productively infected cells, of about 6 h, 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 6 days after initiation of treatment, respectively. The model could be particularly helpful to guide future studies evaluating favipiravir in larger animals.
APA:
Madelain, V., Oestereich, L., Graw, F., Thi Huyen Tram Nguyen, ., De Lamballerie, X., Mentre, F.,... Guedj, J. (2015). Ebola virus dynamics in mice treated with favipiravir. Antiviral Research, 123, 70-77. https://doi.org/10.1016/j.antiviral.2015.08.015
MLA:
Madelain, Vincent, et al. "Ebola virus dynamics in mice treated with favipiravir." Antiviral Research 123 (2015): 70-77.
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