Evidence map›Paper›PMID 23853545›Full record

ArticlePLoS biology2013

NKT cell-TCR expression activates conventional T cells in vivo, but is largely dispensable for mature NKT cell biology.

J Christoph Vahl, Klaus Heger, Nathalie Knies, Marco Y Hein, Louis Boon, Hideo Yagita, Bojan Polic, Marc Schmidt-Supprian

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 45 citations in OpenAlex.

  1. Trial
  2. CD1a and Lipids as Mediators of T Cell Activation in the Skin.The Journal of investigative dermatology · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Nur77 controls tolerance induction, terminal differentiation, and effector functions in semi-invariant natural killer T cells.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  10. Article
  11. Article
  12. Review
  13. Differing roles of CD1d2 and CD1d1 proteins in type I natural killer T cell development and function.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  14. Review
  15. Article
  16. T Cells Going Innate.Trends in immunology · 2016
    Review
  17. CD1d-restricted peripheral T cell lymphoma in mice and humans.The Journal of experimental medicine · 2016
    Article
  18. Article
  19. Article
  20. Immune-based Therapy Clinical Trials in Hepatocellular Carcinoma.Journal of clinical & cellular immunology · 2015
    Article
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 5 institutions in 4 countries.

J Christoph VahlMolecular Immunology and Signaltransduction, Max Planck Institute of Biochemistry, Martinsried, Germany.
Klaus Heger
Nathalie Knies
Marco Y Hein
Louis Boon
Hideo Yagita
Bojan Polic
Marc Schmidt-Supprian
Max Planck Institute of Biochemistry · DEJuntendo University · JPMax Planck Society · DEPolpharma Biologics (Netherlands) · NLUniversity of Rijeka · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural killer T (NKT) cell development depends on recognition of self-glycolipids via their semi-invariant Vα14i-TCR. However, to what extent TCR-mediated signals determine identity and function of mature NKT cells remains incompletely understood. To address this issue, we developed a mouse strain allowing conditional Vα14i-TCR expression from within the endogenous Tcrα locus. We demonstrate that naïve T cells are activated upon replacement of their endogenous TCR repertoire with Vα14i-restricted TCRs, but they do not differentiate into NKT cells. On the other hand, induced TCR ablation on mature NKT cells did not affect their lineage identity, homeostasis, or innate rapid cytokine secretion abilities. We therefore propose that peripheral NKT cells become unresponsive to and thus are independent of their autoreactive TCR.

Indexed as

AnimalsCell DifferentiationCell LineageCytokinesGene Knock-In TechniquesHomeostasisImmunity, InnateInflammationLymphocyte ActivationLymphocyte CountMiceMice, TransgenicNatural Killer T-CellsPhenotypeReceptors, Antigen, T-Cell, alpha-betaSignal TransductionCytokinesReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID23853545
PMCPMC3708704
OpenAlexW2087708257

What OpenQuestion holds

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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.