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Favipiravir (T-705) Inhibits Junín Virus Infection and Reduces Mortality in a Guinea Pig Model of Argentine Hemorrhagic Fever

BACKGROUND: Junín virus (JUNV), the etiologic agent of Argentine hemorrhagic fever (AHF), is classified by the NIAID and CDC as a Category A priority pathogen. Presently, antiviral therapy for AHF is limited to immune plasma, which is readily available only in the endemic regions of Argentina. T-705...

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Autores principales: Gowen, Brian B., Juelich, Terry L., Sefing, Eric J., Brasel, Trevor, Smith, Jennifer K., Zhang, Lihong, Tigabu, Bersabeh, Hill, Terence E., Yun, Tatyana, Pietzsch, Colette, Furuta, Yousuke, Freiberg, Alexander N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3873268/
https://www.ncbi.nlm.nih.gov/pubmed/24386500
http://dx.doi.org/10.1371/journal.pntd.0002614
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author Gowen, Brian B.
Juelich, Terry L.
Sefing, Eric J.
Brasel, Trevor
Smith, Jennifer K.
Zhang, Lihong
Tigabu, Bersabeh
Hill, Terence E.
Yun, Tatyana
Pietzsch, Colette
Furuta, Yousuke
Freiberg, Alexander N.
author_facet Gowen, Brian B.
Juelich, Terry L.
Sefing, Eric J.
Brasel, Trevor
Smith, Jennifer K.
Zhang, Lihong
Tigabu, Bersabeh
Hill, Terence E.
Yun, Tatyana
Pietzsch, Colette
Furuta, Yousuke
Freiberg, Alexander N.
author_sort Gowen, Brian B.
collection PubMed
description BACKGROUND: Junín virus (JUNV), the etiologic agent of Argentine hemorrhagic fever (AHF), is classified by the NIAID and CDC as a Category A priority pathogen. Presently, antiviral therapy for AHF is limited to immune plasma, which is readily available only in the endemic regions of Argentina. T-705 (favipiravir) is a broadly active small molecule RNA-dependent RNA polymerase inhibitor presently in clinical evaluation for the treatment of influenza. We have previously reported on the in vitro activity of favipiravir against several strains of JUNV and other pathogenic New World arenaviruses. METHODOLOGY/PRINCIPAL FINDINGS: To evaluate the efficacy of favipiravir in vivo, guinea pigs were challenged with the pathogenic Romero strain of JUNV, and then treated twice daily for two weeks with oral or intraperitoneal (i.p.) favipiravir (300 mg/kg/day) starting 1–2 days post-infection. Although only 20% of animals treated orally with favipiravir survived the lethal challenge dose, those that succumbed survived considerably longer than guinea pigs treated with placebo. Consistent with pharmacokinetic analysis that showed greater plasma levels of favipiravir in animals dosed by i.p. injection, i.p. treatment resulted in a substantially higher level of protection (78% survival). Survival in guinea pigs treated with ribavirin was in the range of 33–40%. Favipiravir treatment resulted in undetectable levels of serum and tissue viral titers and prevented the prominent thrombocytopenia and leucopenia observed in placebo-treated animals during the acute phase of infection. CONCLUSIONS/SIGNIFICANCE: The remarkable protection afforded by i.p. favipiravir intervention beginning 2 days after challenge is the highest ever reported for a small molecule antiviral in the difficult to treat guinea pig JUNV challenge model. These findings support the continued development of favipiravir as a promising antiviral against JUNV and other related arenaviruses.
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spelling pubmed-38732682014-01-02 Favipiravir (T-705) Inhibits Junín Virus Infection and Reduces Mortality in a Guinea Pig Model of Argentine Hemorrhagic Fever Gowen, Brian B. Juelich, Terry L. Sefing, Eric J. Brasel, Trevor Smith, Jennifer K. Zhang, Lihong Tigabu, Bersabeh Hill, Terence E. Yun, Tatyana Pietzsch, Colette Furuta, Yousuke Freiberg, Alexander N. PLoS Negl Trop Dis Research Article BACKGROUND: Junín virus (JUNV), the etiologic agent of Argentine hemorrhagic fever (AHF), is classified by the NIAID and CDC as a Category A priority pathogen. Presently, antiviral therapy for AHF is limited to immune plasma, which is readily available only in the endemic regions of Argentina. T-705 (favipiravir) is a broadly active small molecule RNA-dependent RNA polymerase inhibitor presently in clinical evaluation for the treatment of influenza. We have previously reported on the in vitro activity of favipiravir against several strains of JUNV and other pathogenic New World arenaviruses. METHODOLOGY/PRINCIPAL FINDINGS: To evaluate the efficacy of favipiravir in vivo, guinea pigs were challenged with the pathogenic Romero strain of JUNV, and then treated twice daily for two weeks with oral or intraperitoneal (i.p.) favipiravir (300 mg/kg/day) starting 1–2 days post-infection. Although only 20% of animals treated orally with favipiravir survived the lethal challenge dose, those that succumbed survived considerably longer than guinea pigs treated with placebo. Consistent with pharmacokinetic analysis that showed greater plasma levels of favipiravir in animals dosed by i.p. injection, i.p. treatment resulted in a substantially higher level of protection (78% survival). Survival in guinea pigs treated with ribavirin was in the range of 33–40%. Favipiravir treatment resulted in undetectable levels of serum and tissue viral titers and prevented the prominent thrombocytopenia and leucopenia observed in placebo-treated animals during the acute phase of infection. CONCLUSIONS/SIGNIFICANCE: The remarkable protection afforded by i.p. favipiravir intervention beginning 2 days after challenge is the highest ever reported for a small molecule antiviral in the difficult to treat guinea pig JUNV challenge model. These findings support the continued development of favipiravir as a promising antiviral against JUNV and other related arenaviruses. Public Library of Science 2013-12-26 /pmc/articles/PMC3873268/ /pubmed/24386500 http://dx.doi.org/10.1371/journal.pntd.0002614 Text en © 2013 Gowen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Gowen, Brian B.
Juelich, Terry L.
Sefing, Eric J.
Brasel, Trevor
Smith, Jennifer K.
Zhang, Lihong
Tigabu, Bersabeh
Hill, Terence E.
Yun, Tatyana
Pietzsch, Colette
Furuta, Yousuke
Freiberg, Alexander N.
Favipiravir (T-705) Inhibits Junín Virus Infection and Reduces Mortality in a Guinea Pig Model of Argentine Hemorrhagic Fever
title Favipiravir (T-705) Inhibits Junín Virus Infection and Reduces Mortality in a Guinea Pig Model of Argentine Hemorrhagic Fever
title_full Favipiravir (T-705) Inhibits Junín Virus Infection and Reduces Mortality in a Guinea Pig Model of Argentine Hemorrhagic Fever
title_fullStr Favipiravir (T-705) Inhibits Junín Virus Infection and Reduces Mortality in a Guinea Pig Model of Argentine Hemorrhagic Fever
title_full_unstemmed Favipiravir (T-705) Inhibits Junín Virus Infection and Reduces Mortality in a Guinea Pig Model of Argentine Hemorrhagic Fever
title_short Favipiravir (T-705) Inhibits Junín Virus Infection and Reduces Mortality in a Guinea Pig Model of Argentine Hemorrhagic Fever
title_sort favipiravir (t-705) inhibits junín virus infection and reduces mortality in a guinea pig model of argentine hemorrhagic fever
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3873268/
https://www.ncbi.nlm.nih.gov/pubmed/24386500
http://dx.doi.org/10.1371/journal.pntd.0002614
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