Evidence map›Paper›PMID 32281944›Full record

ArticleThe Journal of clinical investigation2020

The neonatal microenvironment programs innate γδ T cells through the transcription factor STAT5.

Darshana Kadekar, Rasmus Agerholm, John Rizk, Heidi A Neubauer, Tobias Suske, Barbara Maurer, Monica Torrellas Viñals, Elena M Comelli, Amel Taibi, Richard Moriggl and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2020. 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
1.4field-weighted citation impact, top 19% 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, 31 citations in OpenAlex.

  1. Review
  2. Role of Bile Acid Receptors in Non-Infectious Diarrhea: A Narrative Review.Medical science monitor : international medical journal of experimental and clinical research · 2026
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  8. Restriction of innate Tγδ17 cell plasticity by an AP-1 regulatory axis.bioRxiv : the preprint server for biology · 2024
    Article
  9. IL-27 maintains cytotoxic Ly6CThe EMBO journal · 2024
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. A RecurrentCancers · 2021
    Article
  17. Review
  18. Article
  19. Article
  20. Review
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

11 authors at 3 institutions in 3 countries.

Darshana KadekarDepartment of Health Technology, Technical University of Denmark, Kongens Lyngby, Denmark.
Rasmus AgerholmDepartment of Health Technology, Technical University of Denmark, Kongens Lyngby, Denmark.
John RizkDepartment of Health Technology, Technical University of Denmark, Kongens Lyngby, Denmark.
Heidi A NeubauerInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria.
Tobias SuskeInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria.
Barbara MaurerInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria.
Monica Torrellas ViñalsDepartment of Health Technology, Technical University of Denmark, Kongens Lyngby, Denmark.
Elena M ComelliDepartment of Nutritional Sciences and.
Amel TaibiDepartment of Nutritional Sciences and.
Richard MorigglInstitute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria.
Vasileios BekiarisDepartment of Health Technology, Technical University of Denmark, Kongens Lyngby, Denmark.
Technical University of Denmark · DKUniversity of Veterinary Medicine Vienna · ATThe Wilson Centre · CA

Funding

Austrian Science Fund FWF I 4157Austrian Science Fund FWF I 4218
6 · The paper itself

Abstract

IL-17-producing RORγt+ γδ T cells (γδT17 cells) are innate lymphocytes that participate in type 3 immune responses during infection and inflammation. Herein, we show that γδT17 cells rapidly proliferate within neonatal lymph nodes and gut, where, upon entry, they upregulate T-bet and coexpress IL-17, IL-22, and IFN-γ in a STAT3- and retinoic acid-dependent manner. Neonatal expansion was halted in mice conditionally deficient in STAT5, and its loss resulted in γδT17 cell depletion from all adult organs. Hyperactive STAT5 mutant mice showed that the STAT5A homolog had a dominant role over STAT5B in promoting γδT17 cell expansion and downregulating gut-associated T-bet. In contrast, STAT5B preferentially expanded IFN-γ-producing γδ populations, implying a previously unknown differential role of STAT5 gene products in lymphocyte lineage regulation. Importantly, mice lacking γδT17 cells as a result of STAT5 deficiency displayed a profound resistance to experimental autoimmune encephalomyelitis. Our data identify that the neonatal microenvironment in combination with STAT5 is critical for post-thymic γδT17 development and tissue-specific imprinting, which is essential for infection and autoimmunity.

Indexed as

Immunity, InnateAnimalsAnimals, NewbornCellular MicroenvironmentCytokinesIntestinesMiceMice, TransgenicOrgan SpecificityReceptors, Antigen, T-Cell, gamma-deltaSTAT3 Transcription FactorSTAT5 Transcription FactorT-LymphocytesCytokinesReceptors, Antigen, T-Cell, gamma-deltaStat3 protein, mouseSTAT3 Transcription FactorStat5a protein, mouseStat5b protein, mouseSTAT5 Transcription FactorCellular immune responseImmunologyT cell developmentT cells

Identifiers

PMID32281944
PMCPMC7190909
OpenAlexW3016087872

What OpenQuestion holds

Textmetadata
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.