Evidence map›Paper›PMID 24214487›Full record

ReviewEuropean journal of immunology2014

Serial progression of cortical and medullary thymic epithelial microenvironments.

Nuno L Alves, Yousuke Takahama, Izumi Ohigashi, Ana R Ribeiro, Song Baik, Graham Anderson, William E Jenkinson

Erratum issuedAbstract readReview
In one paragraph

Review in European journal of immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing 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.

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

54 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. The Ins and Outs of Thymic Epithelial Cell Differentiation and Function.Advances in experimental medicine and biology · 2025
    Review
  7. Generation and repair of thymic epithelial cells.The Journal of experimental medicine · 2024
    Review
  8. Review
  9. Insm1 regulates mTEC development and immune tolerance.Cellular & molecular immunology · 2023
    Article
  10. Embryonic keratin19Nature communications · 2023
    Article
  11. Article
  12. Central tolerance promoted by cell chimerism.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

7 authors.

Nuno L AlvesInfection and Immunity Unit, Institute for Molecular and Cellular Biology, University of Porto, Porto, Portugal.
Yousuke Takahama
Izumi Ohigashi
Ana R Ribeiro
Song Baik
Graham Anderson
William E Jenkinson

Funding

Medical Research Council G1000213Medical Research Council G1001055
6 · The paper itself

Abstract

Thymic epithelial cells (TECs) provide key instructive signals for T-cell differentiation. Thymic cortical (cTECs) and medullary (mTECs) epithelial cells constitute two functionally distinct microenvironments for T-cell development, which derive from a common bipotent TEC progenitor. While seminal studies have partially elucidated events downstream of bipotent TECs in relation to the emergence of mTECs and their progenitors, the control and timing of the emergence of the cTEC lineage, particularly in relation to that of mTEC progenitors, has remained elusive. In this review, we describe distinct models that explain cTEC/mTEC lineage divergence from common bipotent progenitors. In particular, we summarize recent studies in mice providing evidence that mTECs, including the auto-immune regulator(+) subset, derive from progenitors initially endowed with phenotypic properties typically associated with the cTEC lineage. These observations support a novel "serial progression" model of TEC development, in which progenitors serially acquire cTEC lineage markers, prior to their commitment to the mTEC differentiation pathway. Gaining a better understanding of the phenotypic properties of early stages in TEC progenitor development should help in determining the mechanisms regulating cTEC/mTEC lineage development, and in strategies aimed at thymus reconstitution involving TEC therapy.

Indexed as

Models, ImmunologicalAnimalsAutoimmunityCell CommunicationCell DifferentiationCell LineageEpithelial CellsHumansImmunotherapyLymphoid Progenitor CellsMiceThymus GlandT-Lymphocytes, RegulatoryT-Lymphocyte SubsetsCortexMedullaThymic epithelial cellsThymus

Identifiers

PMID24214487
PMCPMC4253091

What OpenQuestion holds

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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.