Evidence map›Paper›PMID 36661220›Full record

ArticleeLife2023

Quantifying changes in the T cell receptor repertoire during thymic development.

Francesco Camaglia, Arie Ryvkin, Erez Greenstein, Shlomit Reich-Zeliger, Benny Chain, Thierry Mora, Aleksandra M Walczak, Nir Friedman

Open access · goldAbstract read
In one paragraph

Article in eLife, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
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  6. Development of αβ and γδ T Cells in the Thymus and Methods of Analysis.International journal of molecular sciences · 2025
    Review
  7. Article
  8. Basic interactions responsible for thymus function explain the convoluted medulla shape.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  9. Review
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  11. Article
  12. Article
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  15. Innate-like T cell subset commitment in the murine thymus is independent of TCR characteristics and occurs during proliferation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  16. How persistent infection overcomes peripheral tolerance mechanisms to cause T cell-mediated autoimmune disease.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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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

8 authors at 3 institutions in 5 countries.

Francesco Camaglia *Laboratoire de physique de l'École normale supérieure, CNRS, PSL University, Sorbonne Université, and Université de Paris, Paris, France.ORCID 0000-0003-4810-2631
Arie Ryvkin *Department of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Erez GreensteinDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0002-6923-8469
Shlomit Reich-ZeligerDepartment of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Benny ChainDivision of Infection and Immunity, University College London, London, United Kingdom.ORCID 0000-0002-7417-3970
Thierry Mora *Laboratoire de physique de l'École normale supérieure, CNRS, PSL University, Sorbonne Université, and Université de Paris, Paris, France.ORCID 0000-0002-5456-9361
Aleksandra M Walczak *Laboratoire de physique de l'École normale supérieure, CNRS, PSL University, Sorbonne Université, and Université de Paris, Paris, France.ORCID 0000-0002-2686-5702
Nir Friedman *Department of Immunology, Weizmann Institute of Science, Rehovot, Israel.
Weizmann Institute of Science · ILCentre National de la Recherche Scientifique · FRInstitute of Infection and Immunity · CA

Funding

European Research Council COG 724208
6 · The paper itself

Abstract

One of the feats of adaptive immunity is its ability to recognize foreign pathogens while sparing the self. During maturation in the thymus, T cells are selected through the binding properties of their antigen-specific T-cell receptor (TCR), through the elimination of both weakly (positive selection) and strongly (negative selection) self-reactive receptors. However, the impact of thymic selection on the TCR repertoire is poorly understood. Here, we use transgenic Nur77-mice expressing a T-cell activation reporter to study the repertoires of thymic T cells at various stages of their development, including cells that do not pass selection. We combine high-throughput repertoire sequencing with statistical inference techniques to characterize the selection of the TCR in these distinct subsets. We find small but significant differences in the TCR repertoire parameters between the maturation stages, which recapitulate known differentiation pathways leading to the CD4

Indexed as

Thymus GlandT-LymphocytesAnimalsCell DifferentiationMiceMice, TransgenicReceptors, Antigen, T-CellReceptors, Antigen, T-Cellimmune repertoiresimmunologyinflammationmousephysics of living systemsstatistical analysisthymic selection

Identifiers

PMID36661220
PMCPMC9934861
OpenAlexW4317536028

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.