Evidence map›Paper›PMID 31513433›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2019

Antiviral immunity is impaired in COPD patients with frequent exacerbations.

Aran Singanayagam, Su-Ling Loo, Maria Calderazzo, Lydia J Finney, Maria-Belen Trujillo Torralbo, Eteri Bakhsoliani, Jason Girkin, Punnam Veerati, Prabuddha S Pathinayake, Kristy S Nichol and 7 more

Open access · hybridAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
7.3field-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

47 citing papers in PubMed, 68 citations in OpenAlex.

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  19. How inhaled corticosteroids target inflammation in COPD.European respiratory review : an official journal of the European Respiratory Society · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 2 institutions in 2 countries.

Aran SinganayagamNational Heart and Lung Institute, Imperial College London, London, United Kingdom.
Su-Ling LooFaculty of Health and Medicine and Priority Research Centre for Healthy Lungs, Hunter Medical Research Institute and University of Newcastle, Newcastle, New South Wales, Australia.
Maria CalderazzoNational Heart and Lung Institute, Imperial College London, London, United Kingdom.
Lydia J FinneyNational Heart and Lung Institute, Imperial College London, London, United Kingdom.
Maria-Belen Trujillo TorralboNational Heart and Lung Institute, Imperial College London, London, United Kingdom.
Eteri BakhsolianiNational Heart and Lung Institute, Imperial College London, London, United Kingdom.
Jason GirkinFaculty of Health and Medicine and Priority Research Centre for Healthy Lungs, Hunter Medical Research Institute and University of Newcastle, Newcastle, New South Wales, Australia.
Punnam VeeratiFaculty of Health and Medicine and Priority Research Centre for Healthy Lungs, Hunter Medical Research Institute and University of Newcastle, Newcastle, New South Wales, Australia.
Prabuddha S PathinayakeFaculty of Health and Medicine and Priority Research Centre for Healthy Lungs, Hunter Medical Research Institute and University of Newcastle, Newcastle, New South Wales, Australia.
Kristy S NicholFaculty of Health and Medicine and Priority Research Centre for Healthy Lungs, Hunter Medical Research Institute and University of Newcastle, Newcastle, New South Wales, Australia.
Andrew ReidFaculty of Health and Medicine and Priority Research Centre for Healthy Lungs, Hunter Medical Research Institute and University of Newcastle, Newcastle, New South Wales, Australia.ORCID 0000-0001-5751-7025
Joseph FootittNational Heart and Lung Institute, Imperial College London, London, United Kingdom.
Peter A B WarkNational Heart and Lung Institute, Imperial College London, London, United Kingdom.
Christopher L GraingeNational Heart and Lung Institute, Imperial College London, London, United Kingdom.
Sebastian L JohnstonNational Heart and Lung Institute, Imperial College London, London, United Kingdom.
Nathan W BartlettFaculty of Health and Medicine and Priority Research Centre for Healthy Lungs, Hunter Medical Research Institute and University of Newcastle, Newcastle, New South Wales, Australia.ORCID 0000-0002-2715-5163
Patrick MalliaNational Heart and Lung Institute, Imperial College London, London, United Kingdom.
Imperial College London · GBHunter Medical Research Institute · AU

Funding

Medical Research Council G0600879Wellcome TrustWellcome Trust WT096382AIA
6 · The paper itself

Abstract

Patients with frequent exacerbations represent a chronic obstructive pulmonary disease (COPD) subgroup requiring better treatment options. The aim of this study was to determine the innate immune mechanisms that underlie susceptibility to frequent exacerbations in COPD. We measured sputum expression of immune mediators and bacterial loads in samples from patients with COPD at stable state and during virus-associated exacerbations. In vitro immune responses to rhinovirus infection in differentiated primary bronchial epithelial cells (BECs) sampled from patients with COPD were additionally evaluated. Patients were stratified as frequent exacerbators (≥2 exacerbations in the preceding year) or infrequent exacerbators (<2 exacerbations in the preceding year) with comparisons made between these groups. Frequent exacerbators had reduced sputum cell mRNA expression of the antiviral immune mediators type I and III interferons and reduced interferon-stimulated gene (ISG) expression when clinically stable and during virus-associated exacerbation. A role for epithelial cell-intrinsic innate immune dysregulation was identified: induction of interferons and ISGs during in vitro rhinovirus (RV) infection was also impaired in differentiated BECs from frequent exacerbators. Frequent exacerbators additionally had increased sputum bacterial loads at 2 wk following virus-associated exacerbation onset. These data implicate deficient airway innate immunity involving epithelial cells in the increased propensity to exacerbations observed in some patients with COPD. Therapeutic approaches to boost innate antimicrobial immunity in the lung could be a viable strategy for prevention and treatment of frequent exacerbations.

Indexed as

AgedBronchiDisease ProgressionFemaleForced Expiratory VolumeHumansImmunity, InnateLongitudinal StudiesLung Volume MeasurementsMaleMiddle AgedPhenotypePicornaviridae InfectionsProspective StudiesPulmonary Disease, Chronic ObstructiveRespiratory InsufficiencyCOPDinnate immunityviral infection

Identifiers

PMID31513433
PMCPMC6962603
OpenAlexW2972965291

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.