Evidence map›Paper›PMID 29982696›Full record

ArticleThe Journal of infectious diseases2018

Postexposure Protective Efficacy of T-705 (Favipiravir) Against Sudan Virus Infection in Guinea Pigs.

Md N Rahim, Zirui Zhang, Shihua He, Wenjun Zhu, Logan Banadyga, David Safronetz, Xiangguo Qiu

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
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  6. Development of an antibody cocktail for treatment of Sudan virus infection.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  7. Article
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

7 authors at 2 institutions in 1 country.

Md N RahimSpecial Pathogens Program, National Microbiology laboratory, Public Health Agency of Canada.
Zirui ZhangSpecial Pathogens Program, National Microbiology laboratory, Public Health Agency of Canada.
Shihua HeSpecial Pathogens Program, National Microbiology laboratory, Public Health Agency of Canada.
Wenjun ZhuSpecial Pathogens Program, National Microbiology laboratory, Public Health Agency of Canada.
Logan BanadygaSpecial Pathogens Program, National Microbiology laboratory, Public Health Agency of Canada.
David SafronetzSpecial Pathogens Program, National Microbiology laboratory, Public Health Agency of Canada.
Xiangguo QiuSpecial Pathogens Program, National Microbiology laboratory, Public Health Agency of Canada.
University of Manitoba · CAPublic Health Agency of Canada · CA

Funding

Mechanistic Virology CoreU19AI109762 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI SAPHIRE, ERICA OLLMANN · 2014 to 2018
$29.6M
CIHR IER-143487NIAID NIH HHS U19 AI109762
6 · The paper itself

Abstract

Filoviruses such as Ebola virus (EBOV), Marburg virus (MARV), and Sudan virus (SUDV) cause deadly viral hemorrhagic fever in humans, with high case-fatality rates; however, no licensed therapeutic agent or vaccine has been clinically approved to treat or prevent infection. T-705 (favipiravir) is a novel antiviral drug that has been approved for the treatment of influenza in Japan. T-705 exhibits broad-spectrum antiviral activity against different viruses, including MARV and EBOV, and here, we are the first to report the in vitro and in vivo antiviral activity of T-705 against SUDV. T-705 treatment reduced SUDV replication in Vero E6 cells. Subcutaneous administration of T-705, beginning 1-4 days after infection and continuing for 7 days, significantly protected SUDV-infected guinea pigs, with a survival rate of 83%-100%. Viral RNA replication and infectious virus production were also significantly reduced in the blood, spleen, liver, lungs, and kidney. Moreover, early administration of low-dose T-705 and late administration (at 5 days after infection) of higher-dose T-705 also showed partial protection. Overall, our study is the first to demonstrate the antiviral activity of T-705 against SUDV, suggesting that T-705 may be a potential drug candidate for use during outbreaks.

Indexed as

AmidesAnimalsAntiviral AgentsBlood Cell CountChlorocebus aethiopsFemaleFiloviridae InfectionsGuinea PigsPyrazinesRNA, ViralVero CellsVirus ReplicationAmidesAntiviral AgentsfavipiravirPyrazinesRNA, Viral

Identifiers

PMID29982696
PMCPMC6249569
OpenAlexW2811240989

What OpenQuestion holds

Textmetadata
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.