Evidence map›Paper›PMID 27049514›Full record

ArticleAmerican journal of respiratory cell and molecular biology2016

Human and Mouse Eosinophils Have Antiviral Activity against Parainfluenza Virus.

Matthew G Drake, Elizabeth R Bivins-Smith, Becky J Proskocil, Zhenying Nie, Gregory D Scott, James J Lee, Nancy A Lee, Allison D Fryer, David B Jacoby

Open access · greenAbstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

69 citing papers in PubMed, 115 citations in OpenAlex.

  1. Lower viral loads in subjects with rhinovirus-challenged allergy despite reduced innate immunity.Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology · 2022
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9 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

9 authors at 4 institutions in 1 country.

Matthew G Drake1 Division of Pulmonary and Critical Care Medicine, Oregon Health & Science University, Portland, Oregon.
Elizabeth R Bivins-Smith1 Division of Pulmonary and Critical Care Medicine, Oregon Health & Science University, Portland, Oregon.
Becky J Proskocil1 Division of Pulmonary and Critical Care Medicine, Oregon Health & Science University, Portland, Oregon.ORCID 0000-0002-7803-6447
Zhenying Nie1 Division of Pulmonary and Critical Care Medicine, Oregon Health & Science University, Portland, Oregon.
Gregory D Scott2 Department of Pathology, Stanford University School of Medicine, Stanford, California.
James J Lee3 Department of Biochemistry and Molecular Biology, Division of Pulmonary Medicine, and.
Nancy A Lee4 Department of Biochemistry and Molecular Biology, Divisions of Hematology and Oncology, Mayo Clinic in Arizona, Scottsdale, Arizona.
Allison D Fryer1 Division of Pulmonary and Critical Care Medicine, Oregon Health & Science University, Portland, Oregon.
David B Jacoby1 Division of Pulmonary and Critical Care Medicine, Oregon Health & Science University, Portland, Oregon.
Oregon Health & Science University · USMayo Clinic in Arizona · USPulmonary Associates · USStanford University · US

Funding

Multidisciplinary Research Training in Pulmonary MedicineT32HL083808 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI LEWINSOHN, DAVID M., SLATORE, CHRISTOPHER G. · 2008 to 2025
$5.3M
Airway Sensory Nerves in AsthmaR01HL124165 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI JACOBSEN, ELIZABETH A, JACOBY, DAVID B · 2014 to 2017
$3.1M
Eosinophil-nerve Interactions in Mouse Models of DermatitisR01AR061567 · NIAMS · MAYO CLINIC ARIZONA · PI JACOBSEN, ELIZABETH A, JACOBY, DAVID B · 2012 to 2016
$2.9M
ACUTE AIRWAY EFFECTS OF TLR7 AND TLR8 STIMULATION IN HEALTH AND DISEASER01HL113023 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI JACOBY, DAVID B · 2012 to 2016
$2.1M
ANTIVIRAL EFFECTS OF EOSINOPHILS IN THE LUNGSR01HL071795 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI JACOBY, DAVID B · 2004 to 2007
$1.5M
Rapid Toll-like receptor 7-mediated nitric oxide production in the airwayK08HL121254 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI DRAKE, MATTHEW G. · 2014 to 2018
$732k
Eosinophil Mechanisms of Sensory Neuroplasticity in a Murine Model of AsthmaF30HL106930 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI SCOTT, GREGORY DAVID · 2012 to 2014
$95k
NHLBI NIH HHS F30 HL106930NHLBI NIH HHS K08 HL121254NHLBI NIH HHS R01 HL071795NHLBI NIH HHS R01 HL113023NHLBI NIH HHS R01 HL124165NHLBI NIH HHS T32 HL083808NIAMS NIH HHS R01 AR061567
6 · The paper itself

Abstract

Respiratory viruses cause asthma exacerbations. Because eosinophils are the prominent leukocytes in the airways of 60-70% of patients with asthma, we evaluated the effects of eosinophils on a common respiratory virus, parainfluenza 1, in the lung. Eosinophils recruited to the airways of wild-type mice after ovalbumin sensitization and challenge significantly decreased parainfluenza virus RNA in the lungs 4 days after infection compared with nonsensitized animals. This antiviral effect was also seen in IL-5 transgenic mice with an abundance of airway eosinophils (NJ.1726) but was lost in transgenic eosinophil-deficient mice (PHIL) and in IL-5 transgenic mice crossed with eosinophil-deficient mice (NJ.1726-PHIL). Loss of the eosinophil granule protein eosinophil peroxidase, using eosinophil peroxidase-deficient transgenic mice, did not reduce eosinophils' antiviral effect. Eosinophil antiviral mechanisms were also explored in vitro. Isolated human eosinophils significantly reduced parainfluenza virus titers. This effect did not involve degradation of viral RNA by eosinophil granule RNases. However, eosinophils treated with a nitric oxide synthase inhibitor lost their antiviral activity, suggesting eosinophils attenuate viral infectivity through production of nitric oxide. Consequently, eosinophil nitric oxide production was measured with an intracellular fluorescent probe. Eosinophils produced nitric oxide in response to virus and to a synthetic agonist of the virus-sensing innate immune receptor, Toll-like receptor (TLR) 7. IFNγ increased expression of eosinophil TLR7 and potentiated TLR7-induced nitric oxide production. These results suggest that eosinophils promote viral clearance in the lung and contribute to innate immune responses against respiratory virus infections in humans.

Indexed as

AnimalsAntiviral AgentsEosinophilsFemaleHumansInterferon-gammaLungMacaca mulattaMice, Inbred C57BLNitric OxideOvalbuminParamyxoviridae InfectionsParamyxovirinaePeroxidaseRibonucleasesToll-Like Receptor 7Antiviral AgentsInterferon-gammaNitric OxideOvalbuminPeroxidaseRibonucleasesToll-Like Receptor 7asthmaeosinophilnitric oxideparainfluenza virusToll-like receptor 7

Identifiers

PMID27049514
PMCPMC5023029
OpenAlexW2325970945

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.