Evidence map›Paper›PMID 27841874›Full record

ArticleNature medicine2016

Hepatitis-C-virus-induced microRNAs dampen interferon-mediated antiviral signaling.

Abigail Jarret, Adelle P McFarland, Stacy M Horner, Alison Kell, Johannes Schwerk, MeeAe Hong, Samantha Badil, Rochelle C Joslyn, Darren P Baker, Mary Carrington and 3 more

Open access · greenAbstract read
In one paragraph

Article in Nature medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

35 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Synthetic RIG-I-Agonist RNA Induces Death of Hepatocellular Carcinoma Cells.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2025
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Combination of azithromycin and methylprednisolone alleviatesExperimental and therapeutic medicine · 2022
    Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Article
  18. Innate Immunity in Hepatitis C Virus Infection.Cold Spring Harbor perspectives in medicine · 2021
    Review
  19. Review
  20. 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

13 authors at 4 institutions in 1 country.

Abigail JarretDepartment of Immunology, University of Washington, Seattle, Washington, USA.
Adelle P McFarlandDepartment of Immunology, University of Washington, Seattle, Washington, USA.
Stacy M HornerDepartment of Immunology, University of Washington, Seattle, Washington, USA.
Alison KellDepartment of Immunology, University of Washington, Seattle, Washington, USA.
Johannes SchwerkDepartment of Immunology, University of Washington, Seattle, Washington, USA.
MeeAe HongDepartment of Immunology, University of Washington, Seattle, Washington, USA.
Samantha BadilDepartment of Immunology, University of Washington, Seattle, Washington, USA.
Rochelle C JoslynDepartment of Immunology, University of Washington, Seattle, Washington, USA.
Darren P BakerBiogen-Idec Inc., Cambridge, Massachusetts, USA.
Mary CarringtonCancer and Inflammation Program, Laboratory of Experimental Immunology, Leidos Biomedical Research-Frederick, Frederick National Laboratory for Cancer Research, Frederick, Maryland, USA.
Curt H HagedornDepartment of Medicine and Genetics Program, University of Arkansas for Medical Sciences, and The Central Arkansas Veterans Healthcare System, Little Rock, Arkansas, USA.
Michael GaleDepartment of Immunology, University of Washington, Seattle, Washington, USA.
Ram SavanDepartment of Immunology, University of Washington, Seattle, Washington, USA.
University of Washington · USBiogen (United States) · USRagon Institute of MGH, MIT and Harvard · USUniversity of Arkansas for Medical Sciences · US

Funding

Effects of genetic polymorphism in MHC, KIR, and related loci on human diseaseZIABC010791 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI CARRINGTON, MARY N. · 2009 to 2025
$18.2M
Virus-Host Interactions in Hepatitis C Virus (HCV) InfectionsU19AI040035 · NIAID · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI THOMAS, DAVID L · 1996 to 2009
$12.0M
The Host Response to Hepatitis C VirusR01AI060389 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI GALE, MICHAEL · 2003 to 2012
$3.4M
The Host Response to Hepatitis C VirusR01AI118916 · NIAID · UNIVERSITY OF WASHINGTON · PI GALE, MICHAEL · 2016 to 2020
$2.5M
Novel regulatory mechanisms control IFNL3 expression during HCV infectionR01AI108765 · NIAID · UNIVERSITY OF WASHINGTON · PI SAVAN, RAM · 2014 to 2018
$2.3M
The Host Response to Hepatitis C VirusR56AI060389 · NIAID · UNIVERSITY OF WASHINGTON · PI GALE, MICHAEL · 2014 to 2014
$494k
Sentinel Pol II RNAs for Measuring RNA Integrity in BiospecimensR21CA148068 · NCI · UNIVERSITY OF UTAH · PI HAGEDORN, CURT H. · 2011 to 2012
$343k
CCR NIH HHS HHSN261200800001CNCI NIH HHS HHSN261200800001ENCI NIH HHS R21 CA148068NIAID NIH HHS N01 AI040035NIAID NIH HHS R01 AI060389NIAID NIH HHS R01 AI108765NIAID NIH HHS R01 AI118916NIAID NIH HHS R56 AI060389
6 · The paper itself

Abstract

Hepatitis C virus (HCV) infects 200 million people globally, and 60-80% of cases persist as a chronic infection that will progress to cirrhosis and liver cancer in 2-10% of patients. We recently demonstrated that HCV induces aberrant expression of two host microRNAs (miRNAs), miR-208b and miR-499a-5p, encoded by myosin genes in infected hepatocytes. These miRNAs, along with AU-rich-element-mediated decay, suppress IFNL2 and IFNL3, members of the type III interferon (IFN) gene family, to support viral persistence. In this study, we show that miR-208b and miR-499a-5p also dampen type I IFN signaling in HCV-infected hepatocytes by directly down-regulating expression of the type I IFN receptor chain, IFNAR1. Inhibition of these miRNAs by using miRNA inhibitors during HCV infection increased expression of IFNAR1. Additionally, inhibition rescued the antiviral response to exogenous type I IFN, as measured by a marked increase in IFN-stimulated genes and a decrease in HCV load. Treatment of HCV-infected hepatocytes with type I IFN increased expression of myosins over HCV infection alone. Since these miRNAs can suppress type III IFN family members, these data collectively define a novel cross-regulation between type I and III IFNs during HCV infection.

Indexed as

CRISPR-Cas SystemsDown-RegulationGene Expression RegulationGene Knockout TechniquesHepacivirusHepatitis CHepatitis C, ChronicHepatocytesHep G2 CellsHumansInterferon LambdaInterferonsInterferon Type IInterleukinsMicroRNAsMyosinsIFNAR1 protein, humanInterferon Lambdainterferon-lambda, humanInterferonsInterferon Type IInterleukinsMicroRNAsMIRN208 microRNA, humanMIRN499 microRNA, humanMyosinsReceptor, Interferon alpha-beta

Identifiers

PMID27841874
PMCPMC5551900
OpenAlexW2557197752

What OpenQuestion holds

Textmetadata
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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.