Evidence map›Paper›PMID 31619554›Full record

ArticleJournal of virology2019

Distinct Roles of Interferon Alpha and Beta in Controlling Chikungunya Virus Replication and Modulating Neutrophil-Mediated Inflammation.

Lindsey E Cook, Marissa C Locke, Alissa R Young, Kristen Monte, Matthew L Hedberg, Raeann M Shimak, Kathleen C F Sheehan, Deborah J Veis, Michael S Diamond, Deborah J Lenschow

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2019. 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
8.0field-weighted citation impact, top 2% 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, 65 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

10 authors at 2 institutions in 1 country.

Lindsey E CookDepartment of Pathology and Immunology, Washington University School of Medicine, Saint Louis, Missouri, USA.
Marissa C LockeDepartment of Pathology and Immunology, Washington University School of Medicine, Saint Louis, Missouri, USA.
Alissa R YoungDepartment of Molecular Microbiology, Washington University School of Medicine, Saint Louis, Missouri, USA.
Kristen MonteDepartment of Medicine, Washington University School of Medicine, Saint Louis, Missouri, USA.
Matthew L HedbergDepartment of Pathology and Immunology, Washington University School of Medicine, Saint Louis, Missouri, USA.
Raeann M ShimakDepartment of Pathology and Immunology, Washington University School of Medicine, Saint Louis, Missouri, USA.
Kathleen C F SheehanDepartment of Pathology and Immunology, Washington University School of Medicine, Saint Louis, Missouri, USA.
Deborah J VeisDepartment of Pathology and Immunology, Washington University School of Medicine, Saint Louis, Missouri, USA.
Michael S DiamondDepartment of Pathology and Immunology, Washington University School of Medicine, Saint Louis, Missouri, USA.
Deborah J LenschowDepartment of Pathology and Immunology, Washington University School of Medicine, Saint Louis, Missouri, USA dlenschow@wustl.edu.
Washington University in St. Louis · USShriners Hospitals for Children - St. Louis · US

Funding

TRAINING PROGRAM IN CELLULAR AND MOLECULAR BIOLOGYT32GM007067 · NIGMS · WASHINGTON UNIVERSITY · PI TRUE-KROB, HEATHER L · 1985 to 2020
$20.4M
TRAINING PROGRAM IN IMMUNOLOGY AND IMMUNOGENETICST32AI007163 · NIAID · WASHINGTON UNIVERSITY · PI Kenneth M Murphy, Kodi S Ravichandran · 1985 to 2026
$14.8M
TRAINING IN THE IMMUNOBIOLOGY AND MOLECULAR CELL BIOLOGY OF CANCERT32CA009547 · NCI · WASHINGTON UNIVERSITY · PI ROBERT DAVID SCHREIBER · 1986 to 2026
$12.1M
Washington University Rheumatic DiseasesResearch Resource-based CenterP30AR073752 · NIAMS · WASHINGTON UNIVERSITY · PI Alfred Hyoungju Kim · 2018 to 2026
$7.6M
Resource Based Center for Musculoskeletal Biology and Medicine (Overall Application)P30AR074992 · NIAMS · WASHINGTON UNIVERSITY · PI MATTHEW J SILVA · 2019 to 2026
$6.8M
Structure-Function Analysis of Mxra8 Interaction with Alphaviruses.R01AI143673 · NIAID · WASHINGTON UNIVERSITY · PI DIAMOND, MICHAEL S, FREMONT, DAVED H. · 2019 to 2025
$6.5M
The Role of the Osteoblast Secretome in Bone FormationP30AR057235 · NIAMS · WASHINGTON UNIVERSITY · PI JOHNSON, AARON N · 2009 to 2018
$5.7M
Chikungunya Virus Replication and PathogenesisR01AI123348 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DERMODY, TERENCE S., DIAMOND, MICHAEL S · 2016 to 2020
$3.7M
IFN Dependent Control of Acute and Chronic Chikungunya Virus Induced DiseaseR01AI127513 · NIAID · WASHINGTON UNIVERSITY · PI DIAMOND, MICHAEL S, LENSCHOW, DEBORAH J · 2017 to 2020
$2.1M
Role of Mitochondrial Dynamics In Bone HomeostasisR01AR070030 · NIAMS · WASHINGTON UNIVERSITY · PI VEIS, DEBORAH J · 2016 to 2020
$1.8M
IDENTIFICATION OF MECHANISMS CONTRIBUTING TO CHIKUNGUNYA VIRUS INDUCED CHRONIC ARTHRITISR21AI135490 · NIAID · WASHINGTON UNIVERSITY · PI LENSCHOW, DEBORAH J · 2018 to 2019
$419k
Mouse Models of Pediatric OsteomyelitisR21AR073507 · NIAMS · WASHINGTON UNIVERSITY · PI VEIS, DEBORAH J · 2018 to 2019
$377k
NCI NIH HHS T32 CA009547NIAID NIH HHS F31 AI149999NIAID NIH HHS R01 AI123348NIAID NIH HHS R01 AI127513NIAID NIH HHS R01 AI143673NIAID NIH HHS R21 AI135490NIAID NIH HHS T32 AI007163NIAMS NIH HHS P30 AR057235NIAMS NIH HHS P30 AR073752NIAMS NIH HHS P30 AR074992NIAMS NIH HHS R01 AR070030NIAMS NIH HHS R21 AR073507NIGMS NIH HHS T32 GM007067
6 · The paper itself

Abstract

Type I interferons (IFNs) are key mediators of the innate immune response. Although members of this family of cytokines signal through a single shared receptor, biochemical and functional variation exists in response to different IFN subtypes. While previous work has demonstrated that type I IFNs are essential to control infection by chikungunya virus (CHIKV), a globally emerging alphavirus, the contributions of individual IFN subtypes remain undefined. To address this question, we evaluated CHIKV pathogenesis in mice lacking IFN-β (IFN-β knockout [IFN-β-KO] mice or mice treated with an IFN-β-blocking antibody) or IFN-α (IFN regulatory factor 7 knockout [IRF7-KO] mice or mice treated with a pan-IFN-α-blocking antibody). Mice lacking either IFN-α or IFN-β developed severe clinical disease following infection with CHIKV, with a marked increase in foot swelling compared to wild-type mice. Virological analysis revealed that mice lacking IFN-α sustained elevated infection in the infected ankle and in distant tissues. In contrast, IFN-β-KO mice displayed minimal differences in viral burdens within the ankle or at distal sites and instead had an altered cellular immune response. Mice lacking IFN-β had increased neutrophil infiltration into musculoskeletal tissues, and depletion of neutrophils in IFN-β-KO but not IRF7-KO mice mitigated musculoskeletal disease caused by CHIKV. Our findings suggest disparate roles for the IFN subtypes during CHIKV infection, with IFN-α limiting early viral replication and dissemination and IFN-β modulating neutrophil-mediated inflammation.

Indexed as

AnimalsAntibodies, NeutralizingBone and BonesChikungunya FeverChikungunya virusFemaleGene ExpressionHost-Pathogen InteractionsImmunity, InnateInflammationInterferon-alphaInterferon-betaInterferon Regulatory Factor-7MaleMiceMice, KnockoutAntibodies, NeutralizingInterferon-alphaInterferon-betaInterferon Regulatory Factor-7Irf7 protein, mousechikungunya virushost-pathogen interactionsinnate immunityinterferons

Identifiers

PMID31619554
PMCPMC6912113
OpenAlexW2981075877

What OpenQuestion holds

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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.