Evidence map›Paper›PMID 25482432›Full record

ArticleCell host & microbe2015

Type I interferons link viral infection to enhanced epithelial turnover and repair.

Lulu Sun, Hiroyuki Miyoshi, Sofia Origanti, Timothy J Nice, Alexandra C Barger, Nicholas A Manieri, Leslie A Fogel, Anthony R French, David Piwnica-Worms, Helen Piwnica-Worms and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell host & microbe, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
3.6field-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

70 citing papers in PubMed, 93 citations in OpenAlex.

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  15. Article
  16. Type I IFN signaling in the absence of IRGM1 promotesbioRxiv : the preprint server for biology · 2023
    Article
  17. iScience · 2023
    Review
  18. Article
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  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 1 country.

Lulu SunDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Hiroyuki MiyoshiDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Sofia OrigantiDepartment of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Timothy J NiceDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Alexandra C BargerDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Nicholas A ManieriDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Leslie A FogelDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Pediatrics, Washington University School of Medicine, St. Louis, MO 63110, USA.
Anthony R FrenchDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Pediatrics, Washington University School of Medicine, St. Louis, MO 63110, USA.
David Piwnica-WormsDepartment of Cancer Systems Imaging, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Helen Piwnica-WormsDepartment of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Herbert W VirginDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Deborah J LenschowDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA; Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Thaddeus S StappenbeckDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: stappenb@pathology.wustl.edu.
Washington University in St. Louis · USThe University of Texas MD Anderson Cancer Center · US

Funding

Washington University Center for Cellular ImagingP30CA091842 · NCI · WASHINGTON UNIVERSITY · PI TIMOTHY J. EBERLEIN · 2001 to 2026
$128.0M
Washington University DDRCC Supplemental Equipment RequestP30DK052574 · NIDDK · WASHINGTON UNIVERSITY · PI Nicholas O. Davidson · 2000 to 2026
$30.8M
WU-MDACC Inter-Institutional Molecular Imaging CenterP50CA094056 · NCI · WASHINGTON UNIVERSITY · PI KOPAN, RAPHAEL · 2002 to 2016
$26.3M
PRINCIPLES IN PULMONARY RESEARCHT32HL007317 · NHLBI · WASHINGTON UNIVERSITY · PI Steven Brody, Michael J Holtzman · 1985 to 2026
$16.1M
TRAINING IN THE IMMUNOBIOLOGY AND MOLECULAR CELL BIOLOGY OF CANCERT32CA009547 · NCI · WASHINGTON UNIVERSITY · PI ROBERT DAVID SCHREIBER · 1986 to 2026
$12.1M
Viral Discovery in Rheumatoid ArthritisP30AR048335 · NIAMS · WASHINGTON UNIVERSITY · PI WEIHL, CONRAD C · 2001 to 2015
$8.9M
RESPONSES OF INTESTINAL STEM CELLS TO EPITHELIAL INJURYR01DK071619 · NIDDK · WASHINGTON UNIVERSITY · PI STAPPENBECK, THADDEUS S · 2008 to 2017
$3.2M
REGULATION OF INFLUENZA VIRUS INFECTION BY ISG15R01AI080672 · NIAID · WASHINGTON UNIVERSITY · PI LENSCHOW, DEBORAH J · 2009 to 2021
$2.9M
SUSCEPTIBILILTY GENE-VIRUS INTERACTIONS IN INFLAMMATORY BOWEL DISEASER01AI084887 · NIAID · WASHINGTON UNIVERSITY · PI STAPPENBECK, THADDEUS S, VIRGIN, HERBERT W · 2010 to 2014
$1.9M
NCI NIH HHS P30CA91842NCI NIH HHS P50 CA094056NCI NIH HHS P50CA94056NCI NIH HHS T32 CA009547NHLBI NIH HHS T32 HL007317NIAID NIH HHS AI056160NIAID NIH HHS AI080672NIAID NIH HHS AI08488702NIAID NIH HHS R01 AI080672NIAID NIH HHS R01 AI084887NIAMS NIH HHS AR048335NIAMS NIH HHS P30 AR048335NIDDK NIH HHS DK071619NIDDK NIH HHS P30 DK052574NIDDK NIH HHS P30DK052574NIDDK NIH HHS R01 DK071619
6 · The paper itself

Abstract

The host immune system functions constantly to maintain chronic commensal and pathogenic organisms in check. The consequences of these immune responses on host physiology are as yet unexplored, and may have long-term implications in health and disease. We show that chronic viral infection increases epithelial turnover in multiple tissues, and the antiviral cytokines type I interferons (IFNs) mediate this response. Using a murine model with persistently elevated type I IFNs in the absence of exogenous viral infection, the Irgm1(-/-) mouse, we demonstrate that type I IFNs act through nonepithelial cells, including macrophages, to promote increased epithelial turnover and wound repair. Downstream of type I IFN signaling, the highly related IFN-stimulated genes Apolipoprotein L9a and b activate epithelial proliferation through ERK activation. Our findings demonstrate that the host immune response to chronic viral infection has systemic effects on epithelial turnover through a myeloid-epithelial circuit.

Indexed as

AnimalsEpithelial CellsEpitheliumFemaleGene Expression ProfilingGTP-Binding ProteinsInterferon Type IMaleMice, KnockoutMolecular Sequence DataSequence Analysis, DNASignal TransductionVirus DiseasesGTP-Binding ProteinsIfi1 protein, mouseInterferon Type I

Identifiers

PMID25482432
PMCPMC4297260
OpenAlexW2101561402

What OpenQuestion holds

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Registered trials

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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.