Evidence map›Paper›PMID 17502386›Full record

ArticleInfection and immunity2007

Role of primary human alveolar epithelial cells in host defense against Francisella tularensis infection.

Megan Gentry, Joanna Taormina, Richard B Pyles, Linsey Yeager, Michelle Kirtley, Vsevolod L Popov, Gary Klimpel, Tonyia Eaves-Pyles

Abstract read
In one paragraph

Article in Infection and immunity, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
–field-weighted citation impact
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. Frontiers in cellular and infection microbiology · 2023
    Article
  2. Article
  3. Genetic Determinants of Antibiotic Resistance inFrontiers in microbiology · 2021
    Review
  4. Innate Immune Recognition: Implications for the Interaction ofFrontiers in cellular and infection microbiology · 2017
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. NF-κB RNAi decreases the Bax/Bcl-2 ratio and inhibits TNF-α-induced apoptosis in human alveolar epithelial cells.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2013
    Article
  12. Neutrophils: potential therapeutic targets in tularemia?Frontiers in cellular and infection microbiology · 2013
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Ion transport by pulmonary epithelia.Journal of biomedicine & biotechnology · 2011
    Review
  19. Article
  20. Immunity to Francisella.Frontiers in microbiology · 2011
    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

8 authors.

Megan GentryDepartment of Microbiology and Immunology, University of Texas Medical Branch, 301 University Blvd., Galveston, TX 77555-1070, USA.
Joanna Taormina
Richard B Pyles
Linsey Yeager
Michelle Kirtley
Vsevolod L Popov
Gary Klimpel
Tonyia Eaves-Pyles

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Francisella tularensis, an intracellular pathogen, is highly virulent when inhaled. Alveolar epithelial type I (ATI) and type II (ATII) cells line the majority of the alveolar surface and respond to inhaled pathogenic bacteria via cytokine secretion. We hypothesized that these cells contribute to the lung innate immune response to F. tularensis. Results demonstrated that the live vaccine strain (LVS) contacted ATI and ATII cells by 2 h following intranasal inoculation of mice. In culture, primary human ATI or ATII cells, grown on transwell filters, were stimulated on the apical (AP) surface with virulent F. tularensis Schu 4 or LVS. Basolateral (BL) conditioned medium (CM), collected 6 and 24 h later, was added to the BL surfaces of transwell cultures of primary human pulmonary microvasculature endothelial cells (HPMEC) prior to the addition of polymorphonuclear leukocytes (PMNs) or dendritic cells (DCs) to the AP surface. HPMEC responded to S4- or LVS-stimulated ATII, but not ATI, CM as evidenced by PMN and DC migration. Analysis of the AP and BL ATII CM revealed that both F. tularensis strains induced various levels of a variety of cytokines via NF-kappaB activation. ATII cells pretreated with an NF-kappaB inhibitor prior to F. tularensis stimulation substantially decreased interleukin-8 secretion, which did not occur through Toll-like receptor 2, 2/6, 4, or 5 stimulation. These data indicate a crucial role for ATII cells in the innate immune response to F. tularensis.

Indexed as

AnimalsCell MovementCells, CulturedChemokinesCulture Media, ConditionedCytokinesDendritic CellsDisease Models, AnimalEndothelial CellsEpithelial CellsFemaleFrancisella tularensisHumansImmunity, InnateInterleukin-8LungChemokinesCulture Media, ConditionedCytokinesInterleukin-8NF-kappa BToll-Like Receptors

Identifiers

PMID17502386
PMCPMC1951971

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.