Evidence map›Paper›PMID 22966083›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2012

CD31 exhibits multiple roles in regulating T lymphocyte trafficking in vivo.

Liang Ma, Kenneth C P Cheung, Madhav Kishore, Sussan Nourshargh, Claudio Mauro, Federica M Marelli-Berg

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2012. 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
1.1field-weighted citation impact, top 23% 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, 27 citations in OpenAlex.

  1. Article
  2. CD31 as a probable responding and gate-keeping protein of the blood-brain barrier and the risk of Alzheimer's disease.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2023
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Antigen Presentation by Vascular Cells.Frontiers in immunology · 2017
    Review
  9. Article
  10. CD31 signals confer immune privilege to the vascular endothelium.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  11. Review
  12. Article
  13. 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

6 authors at 3 institutions in 1 country.

Liang MaDivision of Medicine, Department of Immunology, Imperial College London, Hammersmith Hospital Campus, London W12 0NN, United Kingdom.
Kenneth C P Cheung
Madhav Kishore
Sussan Nourshargh
Claudio Mauro
Federica M Marelli-Berg
Queen Mary University of London · GBHammersmith Hospital · GBWilliam Harvey Research Institute · GB

Funding

British Heart Foundation FS/11/64/2894British Heart Foundation FS/11/64/28945British Heart Foundation FS/12/38/29640British Heart Foundation PG/05/136/19997British Heart Foundation RG/09/002British Heart Foundation RG/09/002/26425
6 · The paper itself

Abstract

The role of CD31, an Ig-like molecule expressed by leukocytes and endothelial cells (ECs), in the regulation of T lymphocyte trafficking remains contentious. Using CD31-deficient mice, we show that CD31 regulates both constitutive and inflammation-induced T cell migration in vivo. Specifically, T cell:EC interactions mediated by CD31 molecules are required for efficient localization of naive T lymphocytes to secondary lymphoid tissue and constitutive recirculation of primed T cells to nonlymphoid tissues. In inflammatory conditions, T cell:EC CD31-mediated interactions facilitate T cell recruitment to Ag-rich sites. However, endothelial CD31 also provides a gate-keeping mechanism to limit the rate of Ag-driven T cell extravasation. This event contributes to the formation of Ag-specific effector T cell infiltrates and is induced by recognition of Ag on the endothelium. In this context, CD31 engagement is required for restoring endothelial continuity, which is temporarily lost upon MHC molecule ligation by migrating cognate T cells. We propose that integrated adhesive and signaling functions of CD31 molecules exert a complex regulation of T cell trafficking, a process that is differentially adapted depending on cell-specific expression, the presence of inflammatory conditions and the molecular mechanism facilitating T cell extravasation.

Indexed as

AnimalsCell CommunicationCells, CulturedEndothelium, VascularFemaleLymphoid TissueMaleMiceOrgan Culture TechniquesPlatelet Endothelial Cell Adhesion Molecule-1T-LymphocytesTransendothelial and Transepithelial MigrationPlatelet Endothelial Cell Adhesion Molecule-1

Identifiers

PMID22966083
PMCPMC3496211
OpenAlexW2102490214

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.