Evidence map›Paper›PMID 26924728›Full record

ArticleImmunology2016

Mouse and human CD8(+) CD28(low) regulatory T lymphocytes differentiate in the thymus.

Yirajen Vuddamalay, Mehdi Attia, Rita Vicente, Céline Pomié, Geneviève Enault, Bertrand Leobon, Olivier Joffre, Paola Romagnoli, Joost P M van Meerwijk

Open access · bronzeAbstract read
In one paragraph

Article in Immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. CD8+ Regulatory T Cells.Annual review of immunology · 2026
    Review
  3. Review
  4. Circulating CD4Medicina (Kaunas, Lithuania) · 2023
    Article
  5. Review
  6. Review
  7. Cytolytic CD4Frontiers in immunology · 2022
    Review
  8. CXCR5Journal of immunology (Baltimore, Md. : 1950) · 2021
    Review
  9. Galectin-1 fosters an immunosuppressive microenvironment in colorectal cancer by reprogramming CD8Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  10. Review
  11. Review
  12. Review
  13. Future prospects for CD8Immunological reviews · 2019
    Review
  14. Article
  15. Description of CD8Journal of immunology research · 2018
    Review
  16. Disequilibrium in the CD8Digestive diseases and sciences · 2017
    Article
  17. CD28Frontiers in immunology · 2017
    Review
  18. Review
  19. Review
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 4 institutions in 1 country.

Yirajen VuddamalayInstitut National de la Santé et de la Recherche Médicale (Inserm) U1043, Toulouse, France.
Mehdi AttiaInstitut National de la Santé et de la Recherche Médicale (Inserm) U1043, Toulouse, France.
Rita VicenteInstitut National de la Santé et de la Recherche Médicale (Inserm) U1043, Toulouse, France.
Céline PomiéInstitut National de la Santé et de la Recherche Médicale (Inserm) U1043, Toulouse, France.
Geneviève EnaultInstitut National de la Santé et de la Recherche Médicale (Inserm) U1043, Toulouse, France.
Bertrand LeobonDepartment of Pediatric Cardiology and Cardiovascular surgery, Children Hospital, University Hospital of Toulouse, Toulouse, France.
Olivier JoffreInstitut National de la Santé et de la Recherche Médicale (Inserm) U1043, Toulouse, France.
Paola RomagnoliInstitut National de la Santé et de la Recherche Médicale (Inserm) U1043, Toulouse, France.
Joost P M van MeerwijkInstitut National de la Santé et de la Recherche Médicale (Inserm) U1043, Toulouse, France.
Centre National de la Recherche Scientifique · FRUniversité Fédérale de Toulouse Midi-Pyrénées · FRInserm · FRCentre de Physiopathologie de Toulouse-Purpan · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regulatory T (Treg) lymphocytes play a central role in the control of immune responses and so maintain immune tolerance and homeostasis. In mice, expression of the CD8 co-receptor and low levels of the co-stimulatory molecule CD28 characterizes a Treg cell population that exerts potent suppressive function in vitro and efficiently controls experimental immunopathology in vivo. It has remained unclear if CD8(+) CD28(low) Treg cells develop in the thymus or represent a population of chronically activated conventional T cells differentiating into Treg cells in the periphery, as suggested by their CD28(low) phenotype. We demonstrate that functional CD8(+) CD28(low) Treg cells are present in the thymus and that these cells develop locally and are not recirculating from the periphery. Differentiation of CD8(+) CD28(low) Treg cells requires MHC class I expression on radioresistant but not on haematopoietic thymic stromal cells. In contrast to other Treg cells, CD8(+) CD28(low) Treg cells develop simultaneously with CD8(+) CD28(high) conventional T cells. We also identified a novel homologous naive CD8(+) CD28(low) T-cell population with immunosuppressive properties in human blood and thymus. Combined, our data demonstrate that CD8(+) CD28(low) cells can develop in the thymus of mice and suggest that the same is true in humans.

Indexed as

AnimalsCD28 AntigensCD8 AntigensCell DifferentiationCell LineageCells, CulturedHumansImmune ToleranceImmunosuppression TherapyMiceMice, Inbred C57BLThymus GlandT-Lymphocytes, RegulatoryT-Lymphocyte SubsetsCD28 AntigensCD8 Antigensregulatory T lymphocytesthymustolerance

Identifiers

PMID26924728
PMCPMC4863570
OpenAlexW2279142707

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.