Evidence map›Paper›PMID 24386500›Full record

ArticlePLoS neglected tropical diseases2013

Favipiravir (T-705) inhibits Junín virus infection and reduces mortality in a guinea pig model of Argentine hemorrhagic fever.

Brian B Gowen, Terry L Juelich, Eric J Sefing, Trevor Brasel, Jennifer K Smith, Lihong Zhang, Bersabeh Tigabu, Terence E Hill, Tatyana Yun, Colette Pietzsch and 2 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.8field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

52 citing papers in PubMed, 90 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 2 countries.

Brian B GowenDepartment of Animal, Dairy, and Veterinary Sciences, Utah State University, Logan, Utah, United States of America ; Institute for Antiviral Research, Utah State University, Logan, Utah, United States of America ; School of Veterinary Medicine, Utah State University, Logan, Utah, United States of America.
Terry L JuelichDepartment of Pathology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Eric J SefingDepartment of Animal, Dairy, and Veterinary Sciences, Utah State University, Logan, Utah, United States of America ; Institute for Antiviral Research, Utah State University, Logan, Utah, United States of America.
Trevor BraselDepartment of Microbiology and Immunology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Jennifer K SmithDepartment of Pathology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Lihong ZhangDepartment of Pathology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Bersabeh TigabuDepartment of Microbiology and Immunology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Terence E HillDepartment of Pathology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Tatyana YunDepartment of Pathology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Colette PietzschDepartment of Pathology, The University of Texas Medical Branch, Galveston, Texas, United States of America.
Yousuke FurutaResearch Laboratories, Toyama Chemical Company, Ltd., Toyama, Japan.
Alexander N FreibergDepartment of Pathology, The University of Texas Medical Branch, Galveston, Texas, United States of America ; Sealy Center for Vaccine Development, The University of Texas Medical Branch, Galveston, Texas, United States of America ; Center for Biodefense and Emerging Infectious Diseases, The University of Texas Medical Branch, Galveston, Texas, United States of America.
The University of Texas Medical Branch at Galveston · USUtah State University · USToyama College · JP

Funding

Vascular stabilization as a broad theraprutic platform for biodefenseU54AI065357 · NIAID · COLORADO STATE UNIVERSITY-FORT COLLINS · PI SCHWEIZER, HERBERT P. · 2005 to 2013
$77.5M
NIAID NIH HHS U54 AI-065357NIAID NIH HHS U54 AI065357
6 · The paper itself

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/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.

Indexed as

Administration, OralAmidesAnimalsAntiviral AgentsDisease Models, AnimalGuinea PigsHemorrhagic Fever, AmericanInjections, IntraperitonealJunin virusMalePlasmaPyrazinesSurvival AnalysisViremiaAmidesAntiviral AgentsfavipiravirPyrazines

Identifiers

PMID24386500
PMCPMC3873268
OpenAlexW2130394030

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.