Evidence map›Paper›PMID 21282653›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2011

Human endothelial cells generate Th17 and regulatory T cells under inflammatory conditions.

Cécile Taflin, Benoit Favier, Jeremy Baudhuin, Alain Savenay, Patrice Hemon, Armand Bensussan, Dominique Charron, Denis Glotz, Nuala Mooney

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

67 citing papers in PubMed, 109 citations in OpenAlex.

  1. Article
  2. Article
  3. Regulatory T cell and endothelial cell crosstalk.Nature reviews. Immunology · 2025
    Review
  4. Immune and inflammatory mechanisms in hypertension.Nature reviews. Cardiology · 2024
    Review
  5. Article
  6. Review
  7. Review
  8. Endothelial Cells Activated by Extracellular Histones Promote Foxp3International journal of molecular sciences · 2022
    Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Failing Heart Transplants and Rejection-A Cellular Perspective.Journal of cardiovascular development and disease · 2021
    Review
  14. Article
  15. Article
  16. Endothelial cell, myeloid, and adaptive immune responses in SARS-CoV-2 infection.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Review
  17. Review
  18. Regulatory T Cells in Chronic Heart Failure.Frontiers in immunology · 2021
    Review
  19. Article
  20. Review

7 more citing papers are in PubMed but not listed here.

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

9 authors at 6 institutions in 1 country.

Cécile TaflinInstitut National de la Santé et de la Recherche Médicale, Unité Mixte de Recherche Santé 940, Hôpital Saint Louis, 75010 Paris, France.
Benoit Favier
Jeremy Baudhuin
Alain Savenay
Patrice Hemon
Armand Bensussan
Dominique Charron
Denis Glotz
Nuala Mooney
Commissariat à l'Énergie Atomique et aux Énergies Alternatives · FRDélégation Paris 7 · FRUniversité Paris Cité · FRAssistance Publique – Hôpitaux de Paris · FRHôpital Saint-Louis · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Organ transplantation represents a unique therapeutic option for irreparable organ dysfunction and rejection of transplants results from a breakdown in operational tolerance. Although endothelial cells (ECs) are the first target in graft rejection following kidney transplantation, their capacity to alloactivate and generate particular T lymphocyte subsets that could intervene in this process remains unknown. By using an experimental model of microvascular endothelium, we demonstrate that, under inflammatory conditions, human ECs induced proliferation of memory CD4(+)CD45RA(-) T cells and selectively amplified proinflammatory Th17 and suppressive CD45RA(-)HLA-DR(+)FoxP3(bright) regulatory CD4(+) T lymphocytes (Tregs). Although HLA-DR expression on resting microvascular ECs was sufficient to induce proliferation of memory CD4(+) T cells, Treg amplification was dependent on the interaction with CD54, highly expressed only under inflammatory conditions. Moreover, expansion of Th17 cells was dependent on IL-6 and STAT-3, and inhibition of either specifically impaired Th17, without altering Treg expansion. Collectively these data reveal that the HLA-DR(+) ECs regulate the local inflammatory allogeneic response, promoting either an IL-6/STAT-3-dependent Th17 response or a contact-CD54-dependent regulatory response according to the cytokine environment. Finally, these data open therapeutic perspectives in human organ transplantation based on targeting the IL-6/STAT-3 pathway and/or promoting CD54 dependent Treg proliferation.

Indexed as

Cell ProliferationEndothelial CellsEnzyme-Linked Immunosorbent AssayFlow CytometryHLA-DR AntigensHumansInflammationIntercellular Adhesion Molecule-1Interleukin-6OligonucleotidesPolymerase Chain ReactionSTAT3 Transcription FactorStatistics, NonparametricTh17 CellsT-Lymphocytes, RegulatoryHLA-DR AntigensIntercellular Adhesion Molecule-1Interleukin-6OligonucleotidesSTAT3 protein, humanSTAT3 Transcription Factor

Identifiers

PMID21282653
PMCPMC3041137
OpenAlexW2082184328

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.