Evidence map›Paper›PMID 26562011›Full record

ArticlePLoS pathogens2015

Interferon-γ Inhibits Ebola Virus Infection.

Bethany A Rhein, Linda S Powers, Kai Rogers, Manu Anantpadma, Brajesh K Singh, Yasuteru Sakurai, Thomas Bair, Catherine Miller-Hunt, Patrick Sinn, Robert A Davey and 2 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

63 citing papers in PubMed, 97 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. IFNγ Expression Correlates with Enhanced Cytotoxicity in CD8+ T Cells.International journal of molecular sciences · 2025
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. International journal of molecular sciences · 2024
    Article
  15. Review
  16. The Infection Properties ofAnimals : an open access journal from MDPI · 2023
    Article
  17. Article
  18. The TIGITScientific reports · 2023
    Article
  19. Article
  20. Article

3 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Bethany A RheinDepartment of Microbiology, The University of Iowa, Iowa City, Iowa, United States of America.
Linda S PowersDepartment of Internal Medicine, The University of Iowa, Iowa City, Iowa, United States of America.
Kai RogersDepartment of Microbiology, The University of Iowa, Iowa City, Iowa, United States of America.
Manu AnantpadmaDepartment of Virology and Immunology, Texas Biomedical Research Institute, San Antonio, Texas, United States of America.
Brajesh K SinghDepartment of Pediatrics, The University of Iowa, Iowa City, Iowa, United States of America.
Yasuteru SakuraiDepartment of Virology and Immunology, Texas Biomedical Research Institute, San Antonio, Texas, United States of America.
Thomas BairIowa Institute for Human Genetics, The University of Iowa, Iowa City, Iowa, United States of America.
Catherine Miller-HuntDepartment of Microbiology, The University of Iowa, Iowa City, Iowa, United States of America.
Patrick SinnDepartment of Pediatrics, The University of Iowa, Iowa City, Iowa, United States of America.
Robert A DaveyDepartment of Virology and Immunology, Texas Biomedical Research Institute, San Antonio, Texas, United States of America.
Martha M MonickDepartment of Internal Medicine, The University of Iowa, Iowa City, Iowa, United States of America.
Wendy MauryDepartment of Microbiology, The University of Iowa, Iowa City, Iowa, United States of America.
University of Iowa · USTexas Biomedical Research Institute · US

Funding

Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI Brandi Janssen · 1990 to 2026
$40.5M
Vector Core-Core 2P30DK054759 · NIDDK · UNIVERSITY OF IOWA · PI Alejandro Antonio Pezzulo · 1998 to 2026
$30.5M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007337 · NIGMS · UNIVERSITY OF IOWA · PI GEYER, PAMELA K., LENTZ, STEVEN R · 1985 to 2020
$15.9M
Filoviral glycoprotein/cellular protein interactionsR01AI077519 · NIAID · UNIVERSITY OF IOWA · PI MAURY, WENDY JEAN · 2010 to 2014
$1.7M
Cigarette Smoke and Autophagy/Lysosomal Pathway DysfunctionR01HL096625 · NHLBI · UNIVERSITY OF IOWA · PI MONICK, MARTHA M · 2010 to 2013
$1.5M
Cigarette Smoking Alters the Genomic Tone of Alveolar MacrophagesR21HL109589 · NHLBI · UNIVERSITY OF IOWA · PI GROSS, THOMAS J, MONICK, MARTHA M · 2012 to 2013
$406k
NHLBI NIH HHS R01 HL096625NHLBI NIH HHS R21 HL109589NHLBI NIH HHS R21HL109589NIAID NIH HHS R01 AI077519NIAID NIH HHS R01AI077519NIEHS NIH HHS P30 ES005605NIEHS NIH HHS P30ES005605PHS HHS T32AU996343
6 · The paper itself

Abstract

Ebola virus outbreaks, such as the 2014 Makona epidemic in West Africa, are episodic and deadly. Filovirus antivirals are currently not clinically available. Our findings suggest interferon gamma, an FDA-approved drug, may serve as a novel and effective prophylactic or treatment option. Using mouse-adapted Ebola virus, we found that murine interferon gamma administered 24 hours before or after infection robustly protects lethally-challenged mice and reduces morbidity and serum viral titers. Furthermore, we demonstrated that interferon gamma profoundly inhibits Ebola virus infection of macrophages, an early cellular target of infection. As early as six hours following in vitro infection, Ebola virus RNA levels in interferon gamma-treated macrophages were lower than in infected, untreated cells. Addition of the protein synthesis inhibitor, cycloheximide, to interferon gamma-treated macrophages did not further reduce viral RNA levels, suggesting that interferon gamma blocks life cycle events that require protein synthesis such as virus replication. Microarray studies with interferon gamma-treated human macrophages identified more than 160 interferon-stimulated genes. Ectopic expression of a select group of these genes inhibited Ebola virus infection. These studies provide new potential avenues for antiviral targeting as these genes that have not previously appreciated to inhibit negative strand RNA viruses and specifically Ebola virus infection. As treatment of interferon gamma robustly protects mice from lethal Ebola virus infection, we propose that interferon gamma should be further evaluated for its efficacy as a prophylactic and/or therapeutic strategy against filoviruses. Use of this FDA-approved drug could rapidly be deployed during future outbreaks.

Indexed as

AnimalsAntiviral AgentsCells, CulturedEbolavirusHemorrhagic Fever, EbolaHumansInterferon-gammaMacrophagesMice, Inbred BALB CRNA, ViralVirus ReplicationAntiviral AgentsIFNG protein, humanInterferon-gammaRNA, Viral

Identifiers

PMID26562011
PMCPMC4643030
OpenAlexW2175122451

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.