Evidence map›Paper›PMID 30918005›Full record

ArticleThe Journal of experimental medicine2019

Aire-expressing ILC3-like cells in the lymph node display potent APC features.

Tomoyoshi Yamano, Jan Dobeš, Matouš Vobořil, Madlen Steinert, Tomáš Brabec, Natalia Ziętara, Martina Dobešová, Caspar Ohnmacht, Martti Laan, Part Peterson and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

45 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. RORγt eTACs mediate oral tolerance and Treg induction.The Journal of experimental medicine · 2025
    Article
  8. Review
  9. Article
  10. Article
  11. RORγt-expressing dendritic cells are functionally versatile and evolutionarily conserved antigen-presenting cells.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  12. Mapping of RORγtFrontiers in immunology · 2025
    Article
  13. Review
  14. Microbiota and urinary tumor immunity: Mechanisms, therapeutic implications, and future perspectives.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2024
    Article
  15. Thymic Mimetic Cells: Ontogeny as Immunology.Annual review of cell and developmental biology · 2024
    Review
  16. Aire in Autoimmunity.Annual review of immunology · 2024
    Review
  17. Review
  18. Review
  19. The emerging family of RORγtNature reviews. Immunology · 2024
    Review
  20. Extrathymic AIRE-Expressing Cells: A Historical Perspective.Advances in experimental medicine and biology · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 7 institutions in 4 countries.

Tomoyoshi YamanoInstitute for Immunology, Faculty of Medicine, Ludwig-Maximilans-Universität, Munich, Germany.
Jan DobešLaboratory of Immunobiology, Institute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic.ORCID 0000-0003-1853-1603
Matouš VobořilLaboratory of Immunobiology, Institute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic.ORCID 0000-0002-3672-7629
Madlen SteinertInstitute for Immunology, Faculty of Medicine, Ludwig-Maximilans-Universität, Munich, Germany.
Tomáš BrabecLaboratory of Immunobiology, Institute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic.
Natalia ZiętaraInstitute for Immunology, Faculty of Medicine, Ludwig-Maximilans-Universität, Munich, Germany.
Martina DobešováLaboratory of Immunobiology, Institute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic.
Caspar OhnmachtHelmholtz Zentrum München, Institut für Allergieforschung, Neuherberg, Germany.
Martti LaanInstitute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.
Part PetersonInstitute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.
Vladimir BenesGenomics Core Facility, European Molecular Biology Laboratory, Services and Technology Unit, Heidelberg, Germany.ORCID 0000-0002-0352-2547
Radislav SedláčekCzech Centre for Phenogenomics and Laboratory of Transgenic Models of Diseases, Institute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic.
Rikinari HanayamaDepartment of Immunology, Kanazawa University Graduate School of Medical Sciences, and World Premier International Research Center Initiative Nano Life Science Institute, Kanazawa University, Ishikawa, Japan.
Michal KolářLaboratory of Genomics and Bioinformatics, Institute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic.
Ludger KleinInstitute for Immunology, Faculty of Medicine, Ludwig-Maximilans-Universität, Munich, Germany ludger.klein@med.lmu.de.ORCID 0000-0003-2054-071X
Dominik FilippLaboratory of Immunobiology, Institute of Molecular Genetics of the Czech Academy of Sciences, Prague, Czech Republic dominik.filipp@img.cas.cz.
Czech Academy of Sciences, Institute of Molecular Genetics · CZLudwig-Maximilians-Universität München · DEUniversity of Tartu · EECharles University · CZEuropean Molecular Biology Laboratory · DEHelmholtz Zentrum München · DEKanazawa University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The autoimmune regulator (Aire) serves an essential function for T cell tolerance by promoting the "promiscuous" expression of tissue antigens in thymic epithelial cells. Aire is also detected in rare cells in peripheral lymphoid organs, but the identity of these cells is poorly understood. Here, we report that Aire protein-expressing cells in lymph nodes exhibit typical group 3 innate lymphoid cell (ILC3) characteristics such as lymphoid morphology, absence of "classical" hematopoietic lineage markers, and dependence on RORγt. Aire

Indexed as

AIRE ProteinAnimalsAntigen-Presenting CellsCD11 AntigensEpithelial Cell Adhesion MoleculeGene Expression RegulationHistocompatibility Antigens Class IIImmunity, InnateLymph NodesLymphocytesMiceMice, Inbred BALB CMice, KnockoutNuclear Receptor Subfamily 1, Group F, Member 3PhenotypeTranscription FactorsAIRE ProteinCD11 AntigensEpithelial Cell Adhesion MoleculeHistocompatibility Antigens Class IIItgax protein, mouseNuclear Receptor Subfamily 1, Group F, Member 3Rorc protein, mouseTranscription Factors

Identifiers

PMID30918005
PMCPMC6504225
OpenAlexW2926186791

What OpenQuestion holds

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LicenceCC BY-NC-SA
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Registered trials

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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.