Evidence map›Paper›PMID 25939024›Full record

ArticleNature immunology2015

Peripheral regulatory T lymphocytes recirculating to the thymus suppress the development of their precursors.

Nicolas Thiault, Julie Darrigues, Véronique Adoue, Marine Gros, Bénédicte Binet, Corine Perals, Bertrand Leobon, Nicolas Fazilleau, Olivier P Joffre, Ellen A Robey and 2 more

Registry-linked trialAbstract read
PubMed Publisher
In one paragraph

Article in Nature immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03236558 (Thymic Generation of Regulatory T Lymphocytes in Type I Diabetes Patients.), which is not on this map. Cited by 112 papers.

0numbers the graph read from it
0cells of the map it votes in
112citing 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.

NCT03236558 nawithdrawnnot on this mapstarted 2018, after this paper: background citation

Thymic Generation of Regulatory T Lymphocytes in Type I Diabetes Patients.

TypeinterventionalSponsorUniversity Hospital, ToulouseRan2018 to 2019Enrolled0ConditionsType1 DiabetesArmsBlood collection
3 · Its place in the literature

Who cites it

112 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Rag1-based time-stamp tracing of T-cell developmental origins.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Features of Peripheral T Cell Remigration into the Thymus.International journal of molecular sciences · 2025
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review

52 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

12 authors.

Nicolas Thiault1] Institut National de la Santé et de la Recherche Médicale U1043, Toulouse, France. [2] Centre National de la Recherche Scientifique U5282, Toulouse, France. [3] Université de Toulouse, Université Paul Sabatier, Centre de Physiopathologie de Toulouse Purpan, Toulouse, France.
Julie Darrigues1] Institut National de la Santé et de la Recherche Médicale U1043, Toulouse, France. [2] Centre National de la Recherche Scientifique U5282, Toulouse, France. [3] Université de Toulouse, Université Paul Sabatier, Centre de Physiopathologie de Toulouse Purpan, Toulouse, France.
Véronique Adoue1] Institut National de la Santé et de la Recherche Médicale U1043, Toulouse, France. [2] Centre National de la Recherche Scientifique U5282, Toulouse, France. [3] Université de Toulouse, Université Paul Sabatier, Centre de Physiopathologie de Toulouse Purpan, Toulouse, France.
Marine Gros1] Institut National de la Santé et de la Recherche Médicale U1043, Toulouse, France. [2] Centre National de la Recherche Scientifique U5282, Toulouse, France. [3] Université de Toulouse, Université Paul Sabatier, Centre de Physiopathologie de Toulouse Purpan, Toulouse, France. [4] Ecole Normale Supérieure de Lyon, Department of Biology, 69007 Lyon, France.
Bénédicte Binet1] Institut National de la Santé et de la Recherche Médicale U1043, Toulouse, France. [2] Centre National de la Recherche Scientifique U5282, Toulouse, France. [3] Université de Toulouse, Université Paul Sabatier, Centre de Physiopathologie de Toulouse Purpan, Toulouse, France.
Corine Perals1] Institut National de la Santé et de la Recherche Médicale U1043, Toulouse, France. [2] Centre National de la Recherche Scientifique U5282, Toulouse, France. [3] Université de Toulouse, Université Paul Sabatier, Centre de Physiopathologie de Toulouse Purpan, Toulouse, France.
Bertrand LeobonDepartment of Pediatric Cardiology and Cardiovascular surgery, Children Hospital, University Hospital of Toulouse, Toulouse, France.
Nicolas Fazilleau1] Institut National de la Santé et de la Recherche Médicale U1043, Toulouse, France. [2] Centre National de la Recherche Scientifique U5282, Toulouse, France. [3] Université de Toulouse, Université Paul Sabatier, Centre de Physiopathologie de Toulouse Purpan, Toulouse, France.
Olivier P Joffre1] Institut National de la Santé et de la Recherche Médicale U1043, Toulouse, France. [2] Centre National de la Recherche Scientifique U5282, Toulouse, France. [3] Université de Toulouse, Université Paul Sabatier, Centre de Physiopathologie de Toulouse Purpan, Toulouse, France.
Ellen A RobeyDepartment of Molecular and Cell Biology, Division of Immunology and Pathogenesis, University of California, Berkeley, California, USA.
Joost P M van Meerwijk1] Institut National de la Santé et de la Recherche Médicale U1043, Toulouse, France. [2] Centre National de la Recherche Scientifique U5282, Toulouse, France. [3] Université de Toulouse, Université Paul Sabatier, Centre de Physiopathologie de Toulouse Purpan, Toulouse, France.
Paola Romagnoli1] Institut National de la Santé et de la Recherche Médicale U1043, Toulouse, France. [2] Centre National de la Recherche Scientifique U5282, Toulouse, France. [3] Université de Toulouse, Université Paul Sabatier, Centre de Physiopathologie de Toulouse Purpan, Toulouse, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Most T lymphocytes, including regulatory T cells (Treg cells), differentiate in the thymus. The age-dependent involution of this organ leads to decreasing production of T cells. Here we found that the output of new Treg cells from the thymus decreased substantially more than that of conventional T cells. Peripheral mouse and human Treg cells recirculated back to the thymus, where they constituted a large proportion of the pool of Treg cells and displayed an activated and differentiated phenotype. In the thymus, the recirculating cells exerted their regulatory function by inhibiting interleukin 2 (IL-2)-dependent de novo differentiation of Treg cells. Thus, Treg cell development is controlled by a negative feedback loop in which mature progeny cells return to the thymus and restrain development of precursors of Treg cells.

Indexed as

AgingAnimalsBlood CirculationCell DifferentiationCells, CulturedChildFeedback, PhysiologicalForkhead Transcription FactorsHumansImmune ToleranceInterleukin-2MiceMice, Inbred C57BLMice, TransgenicPrecursor Cells, T-LymphoidThymus GlandForkhead Transcription FactorsFoxp3 protein, mouseInterleukin-2

Identifiers

PMID25939024

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.