Evidence map›Paper›PMID 26378172›Full record

ArticleJournal of virology2015

Differential Susceptibilities of Human Lung Primary Cells to H1N1 Influenza Viruses.

Emily Travanty, Bin Zhou, Hongbo Zhang, Y Peter Di, John F Alcorn, David E Wentworth, Robert Mason, Jieru Wang

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Journal of virology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 12% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Frontiers in immunology · 2021
    Pooled it
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  9. Impact of e-cigarette aerosol on primary human alveolar epithelial type 2 cells.American journal of physiology. Lung cellular and molecular physiology · 2022
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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

8 authors at 3 institutions in 1 country.

Emily TravantyDepartment of Medicine, National Jewish Health, Denver, Colorado, USA.
Bin ZhouJ. Craig Venter Institute, Rockville, Maryland, USA.
Hongbo ZhangDepartment of Environmental and Occupational Health, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Y Peter DiDepartment of Environmental and Occupational Health, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
John F AlcornDepartment of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
David E WentworthJ. Craig Venter Institute, Rockville, Maryland, USA.
Robert MasonDepartment of Medicine, National Jewish Health, Denver, Colorado, USA.
Jieru WangDepartment of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA Jieru.wang@chp.edu.
University of Pittsburgh · USJ. Craig Venter Institute · USUniversity of Colorado Denver · US

Funding

Influenza A Inhibits TH17 Host Defense Against Bacterial PneumoniaR01HL107380 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ALCORN, JOHN F · 2012 to 2024
$5.4M
Alveolar type II cell innate immune response to influenzaU01AI082982 · NIAID · NATIONAL JEWISH HEALTH · PI MASON, ROBERT JAMES · 2009 to 2013
$2.4M
Epithelial PLUNC as a determinant of Airway Mucosal Antimicrobial ActivityR01HL091938 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI DI, YUANPU PETER · 2008 to 2012
$2.3M
SPLUNC1 in Severe AsthmaR01HL125128 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHU, HONG W, DI, YUANPU PETER · 2015 to 2018
$1.9M
Regulation of alveolar epithelial homeostasis in acute lung injuryR01HL113655 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WANG, JIERU · 2012 to 2016
$1.9M
IFN-lambda polymorphisms and host response to respiratory viral infections in humR03AI101953 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WANG, JIERU · 2012 to 2013
$159k
NHLBI NIH HHS R01 HL091938NHLBI NIH HHS R01 HL107380NHLBI NIH HHS R01 HL113655NHLBI NIH HHS R01HL113655NHLBI NIH HHS R01 HL125128NIAID NIH HHS R03 AI101953NIAID NIH HHS R03AI101953NIAID NIH HHS U01 AI082982NIAID NIH HHS U01AI082982
6 · The paper itself

Abstract

unlabelledHuman alveolar epithelial cells (AECs) and alveolar macrophages (AMs) are the first lines of lung defense. Here, we report that AECs are the direct targets for H1N1 viruses that have circulated since the 2009 pandemic (H1N1pdm09). AMs are less susceptible to H1N1pdm09 virus, but they produce significantly more inflammatory cytokines than AECs from the same donor. AECs form an intact epithelial barrier that is destroyed by H1N1pdm09 infection. However, there is significant variation in the cellular permissiveness to H1N1pdm09 infection among different donors. AECs from obese donors appear to be more susceptible to H1N1pdm09 infection, whereas gender, smoking history, and age do not appear to affect AEC susceptibility. There is also a difference in response to different strains of H1N1pdm09 viruses. Compared to A/California04/09 (CA04), A/New York/1682/09 (NY1682) is more infectious and causes more epithelial barrier injury, although it stimulates less cytokine production. We further determined that a single amino acid residue substitution in NY1682 hemagglutinin is responsible for the difference in infectivity. In conclusion, this is the first study of host susceptibility of human lung primary cells and the integrity of the alveolar epithelial barrier to influenza. Further elucidation of the mechanism of increased susceptibility of AECs from obese subjects may facilitate the development of novel protection strategies against influenza virus infection. IMPORTANCE: Disease susceptibility of influenza is determined by host and viral factors. Human alveolar epithelial cells (AECs) form the key line of lung defenses against pathogens. Using primary AECs from different donors, we provided cellular level evidence that obesity might be a risk factor for increased susceptibility to influenza. We also compared the infections of two closely related 2009 pandemic H1N1 strains in AECs from the same donor and identified a key viral factor that affected host susceptibility, the dominance of which may be correlated with disease epidemiology. In addition, primary human AECs can serve as a convenient and powerful model to investigate the mechanism of influenza-induced lung injury and determine the effect of genetic and epigenetic factors on host susceptibility to pandemic influenza virus infection.

Indexed as

AdiposityCytokinesDisease SusceptibilityEpithelial CellsFlow CytometryHemagglutininsHost-Pathogen InteractionsHumansInfluenza A Virus, H1N1 SubtypeInfluenza, HumanLungMacrophagesObesityPulmonary AlveoliSpecies SpecificityStatistics, NonparametricCytokinesHemagglutinins

Identifiers

PMID26378172
PMCPMC4645340
OpenAlexW2270417929

What OpenQuestion holds

Textmetadata
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.