Evidence map›Paper›PMID 21239529›Full record

ArticleAmerican journal of physiology. Lung cellular and molecular physiology2011

In vivo function of airway epithelial TLR2 in host defense against bacterial infection.

Qun Wu, Di Jiang, Maisha N Minor, Richard J Martin, Hong Wei Chu

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Lung cellular and molecular physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
5.7field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Human lung organoids model for assessing host response toFrontiers in cellular and infection microbiology · 2026
    Article
  3. Journal of thoracic disease · 2023
    Article
  4. Article
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  6. HIV-1 Productively Infects and Integrates in Bronchial Epithelial Cells.Frontiers in cellular and infection microbiology · 2020
    Article
  7. Article
  8. Smoking-induced iron dysregulation in the lung.Free radical biology & medicine · 2019
    Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
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

5 authors at 1 institution in 1 country.

Qun WuDepartment of Medicine, National Jewish Health and University of Colorado Denver, Denver, Colorado 80206, USA.
Di Jiang
Maisha N Minor
Richard J Martin
Hong Wei Chu
National Jewish Health · US

Funding

SPLUNC1 protein in host defense against Mycoplasma pneumoniae infectionR01HL088264 · NHLBI · NATIONAL JEWISH HEALTH · PI CHU, HONG W · 2009 to 2012
$1.8M
Effects of Allergic Inflammation on TLR2 Signaling and Mycoplasma InfectionR01AI070175 · NIAID · NATIONAL JEWISH HEALTH · PI CHU, HONG W · 2008 to 2011
$1.6M
NHLBI NIH HHS R01 HL088264NHLBI NIH HHS R01HL088264NIAID NIH HHS R01 AI070175NIAID NIH HHS R01AI070175
6 · The paper itself

Abstract

Decreased Toll-like receptor 2 (TLR2) expression has been reported in patients with chronic obstructive pulmonary disease and in a murine asthma model, which may predispose the hosts to bacterial infections, leading to disease exacerbations. Since airway epithelial cells serve as the first line of respiratory mucosal defense, the present study aimed to reveal the role of airway epithelial TLR2 signaling to lung bacterial [i.e., Mycoplasma pneumoniae (Mp)] clearance. In vivo TLR2 gene transfer via intranasal inoculation of adenoviral vector was performed to reconstitute TLR2 expression in airway epithelium of TLR2(-/-) BALB/c mice, with or without ensuing Mp infection. TLR2 and lactotransferrin (LTF) expression in airway epithelial cells and lung Mp load were assessed. Adenovirus-mediated TLR2 gene transfer to airway epithelial cells of TLR2(-/-) mice reconstituted 30-40% TLR2 expression compared with TLR2(+/+) cells. Such airway epithelial TLR2 reconstitution in TLR2(-/-) mice significantly reduced lung Mp load (an appropriate 45% reduction), coupled with elevated LTF expression. LTF expression in mice was shown to be mainly dependent on TLR2 signaling in response to Mp infection. Exogenous human LTF protein dose-dependently decreased lung bacterial load in Mp-infected TLR2(-/-) mice. In addition, human LTF protein directly dose-dependently decreased Mp levels in vitro. These data indicate that reconstitution of airway epithelial TLR2 signaling in TLR2(-/-) mice significantly restores lung defense against bacteria (e.g., Mp) via increased lung antimicrobial protein LTF production. Our findings may offer a deliverable approach to attenuate bacterial infections in airways of asthma or chronic obstructive pulmonary disease patients with impaired TLR2 function.

Indexed as

AdenoviridaeAnimalsBacterial InfectionsBacterial LoadEpithelial CellsGene Expression RegulationGene Transfer TechniquesHumansLactoferrinLungMiceMice, Inbred BALB CMycoplasma pneumoniaePneumonia, MycoplasmaToll-Like Receptor 2LactoferrinTlr2 protein, mouseToll-Like Receptor 2

Identifiers

PMID21239529
PMCPMC3075102
OpenAlexW2109532615

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.