Evidence map›Paper›PMID 19454707›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2009

Airway delivery of silica increases susceptibility to mycobacterial infection in mice: potential role of repopulating macrophages.

Rajamouli Pasula, Bradley E Britigan, Joanne Turner, William J Martin

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
0.2field-weighted citation impact, top 34% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
  2. Silicotuberculosis: a critical narrative review.European respiratory review : an official journal of the European Respiratory Society · 2024
    Review
  3. Article
  4. Article
  5. Review
  6. Mycobacterium abscessus Displays Fitness for Fomite Transmission.Applied and environmental microbiology · 2017
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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

4 authors at 4 institutions in 1 country.

Rajamouli PasulaDepartment of Internal Medicine, University of Cincinnati, Cincinnati, OH 45267, USA. pasular@ucmail.uc.edu
Bradley E Britigan
Joanne Turner
William J Martin
Interface (United States) · USNational Institutes of Health · USUniversity of Cincinnati · USVeterans Health Administration · US

Funding

Alveolar Tissuegenesis in Murine Acute Lung InjuryZ01ES102085 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI MARTIN, WILLIAM J. · 2006 to 2008
$1.9M
Alveolar macrophage and mycobacteriaR01HL076955 · NHLBI · UNIVERSITY OF CINCINNATI · PI PASULA, RAJAMOULI · 2003 to 2007
$1.7M
Alveolar Tissuegenesis in Murine Acute Lung InjuryZIAES102085 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI MARTIN, WILLIAM J. · 2009 to 2009
$963k
Intramural NIH HHS Z01 ES102085NHLBI NIH HHS R01 HL076955
6 · The paper itself

Abstract

Silica exposure results in an increased lifelong risk of developing mycobacterial pulmonary infections. To date, there are no animal models that replicate this finding to permit assessment of the mechanisms underlying susceptibility to mycobacterial infection. To test the hypothesis that prior silica exposure increases risk of mycobacterial infection, we intratracheally (I.T.) administered silica, a control dust (Al(2)O(3)) or saline into mechanically ventilated C57BL/6 mice. Later, the mice received Mycobacterium avium or Mycobacterium tuberculosis I.T. Mice were sacrificed at defined time points and mycobacteria in lung homogenates were quantified. M. avium or M. tuberculosis infection was markedly increased in silica-exposed mice compared with mice exposed to either Al(2)O(3) or saline beginning 3 wk after silica exposure. Similarly, lung sections from silica-exposed mice had many more acid fast bacilli(+) (AFB(+)) organisms than from control mice. Alveolar macrophages (AMs) from bronchoalveolar lavage of silica-exposed mice also revealed a higher number of mycobacteria compared with mice treated with Al(2)O(3) or saline. In addition, passive transfer of AMs from silica-exposed mice to control mice increased M. tuberculosis susceptibility. These results indicate that silica exposure converts mycobacteria-resistant mice into mycobacteria-susceptible mice via a process that likely involves a new population of AMs that are more susceptible to mycobacterial infection.

Indexed as

Aluminum OxideAnimalsDisease SusceptibilityInhalation ExposureMacrophages, AlveolarMiceMycobacterium aviumMycobacterium InfectionsMycobacterium tuberculosisRespiratory SystemSilicon DioxideAluminum OxideSilicon Dioxide

Identifiers

PMID19454707
PMCPMC2748844
OpenAlexW2155785370

What OpenQuestion holds

Textmetadata
LicenceTDM
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.