Abstract

BackgroundJunín 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 FindingsTo 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/SignificanceThe 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.

Highlights

  • Several New World (Junın, Machupo, Guanarito, Sabia, and Chapare) and Old World (Lassa and Lujo) arenaviruses cause viral hemorrhagic fever (HF) with case fatality rates generally in the range of 15–30% [1]

  • Two of the 10 guinea pigs treated with favipiravir survived the infection, and those that succumbed survived, on average, .4 days longer than the animals treated with placebo (20.362.6 days and 16.261.2 days, respectively)

  • The efficacy of oral and i.p. favipiravir treatment was evaluated in the guinea pig Junın virus (JUNV) challenge model

Read more

Summary

Introduction

Several New World (Junın, Machupo, Guanarito, Sabia, and Chapare) and Old World (Lassa and Lujo) arenaviruses cause viral hemorrhagic fever (HF) with case fatality rates generally in the range of 15–30% [1]. They are rodent-borne viruses that can be transmitted via the aerosol route making them potential bioterror agents. Of the New World arenaviral HFs endemic in different regions of the South America, Junın virus (JUNV), the etiologic agent of Argentine HF (AHF), causes the greatest morbidity and mortality. Antiviral therapy for AHF is limited to immune plasma, which is readily available only in the endemic regions of Argentina. We have previously reported on the in vitro activity of favipiravir against several strains of JUNV and other pathogenic New World arenaviruses

Methods
Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call