Evidence map›Paper›PMID 18209084›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2008

Polarized localization of epithelial CXCL11 in chronic obstructive pulmonary disease and mechanisms of T cell egression.

Joanna C Porter, Mary Falzon, Alan Hall

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Adenosine APurinergic signalling · 2023
    Article
  6. Article
  7. Chemokines in COPD: From Implication to Therapeutic Use.International journal of molecular sciences · 2019
    Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Epithelial ICAM-1 and ICAM-2 regulate the egression of human T cells across the bronchial epithelium.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2009
    Article
  14. 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

3 authors at 3 institutions in 2 countries.

Joanna C PorterMedical Research Council Laboratory of Molecular Cell Biology, University College London, London, UK. Joanna.porter@ucl.ac.uk
Mary Falzon
Alan Hall
MRC Laboratory for Molecular Cell Biology · GBRockefeller University · USUniversity College Hospital · GB

Funding

Wellcome Trust 064961
6 · The paper itself

Abstract

The exit of lymphocytes from the interstitium of the lung, across the bronchial epithelium and into the airway lumen, is known as egression, or luminal clearance. Egression is important for immune surveillance and the resolution of inflammation, but the mechanisms involved are unknown. We show that egression of human T cells across the bronchial epithelium is a multistep process, driven in part by a polarized transepithelial gradient of CXCL11 that is up-regulated in patients with chronic obstructive airways disease. Previous studies have shown that T cells can migrate across a disrupted bronchial epithelium, but we provide evidence that egression does not require epithelial injury, and can take place across an intact epithelial barrier. After negotiating the extracellular matrix, the T cell adheres to the basal surface of the bronchial epithelial cell using alpha(4) and leukocyte function associated-1 integrins before crossing the epithelium in an leukocyte function associated-1-dependent way. We demonstrate an egression-dependent decrease in transepithelial resistance across the epithelium without gross alteration in tight-junction proteins. The process of egression has been relatively overlooked when considering the control of leukocyte trafficking in the lung and other epithelial organs. This study highlights the role of the respiratory epithelium in the trafficking of T lymphocytes from the pulmonary interstitium and into the large airways, during the onset and resolution of pulmonary inflammation.

Indexed as

Cell MovementActinsAntibodies, Monoclonalbeta CateninBronchiCell AdhesionCell PolarityCells, CulturedChemokine CXCL11HumansIntegrinsLymphocyte Function-Associated Antigen-1Membrane ProteinsPhosphoproteinsPulmonary Disease, Chronic ObstructiveReceptors, CXCR3ActinsAntibodies, Monoclonalbeta CateninChemokine CXCL11CXCL11 protein, humanCXCR3 protein, humanIntegrinsLymphocyte Function-Associated Antigen-1Membrane ProteinsPhosphoproteinsReceptors, CXCR3TJP1 protein, humanZonula Occludens-1 Protein

Identifiers

PMID18209084
PMCPMC2274894
OpenAlexW1916975147

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.