Evidence map›Paper›PMID 31354726›Full record

ArticleFrontiers in immunology2019

Generation of Foxp3

Marc Schuster, Carlos Plaza-Sirvent, Alexander Visekruna, Jochen Huehn, Ingo Schmitz

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Regulation and Function of the Atypical IκBs-Bcl-3, IκBEuropean journal of immunology · 2025
    Review
  3. Lymphotoxin limits Foxp3Nature communications · 2024
    Article
  4. Article
  5. Review
  6. Artesunate targets cellular metabolism to regulate the Th17/Treg cell balance.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Review
  7. Article
  8. Article
  9. NF-κB in control of regulatory T cell development, identity, and function.Journal of molecular medicine (Berlin, Germany) · 2022
    Review
  10. Review
  11. Review
  12. Mechanisms of exTreg induction.European journal of immunology · 2021
    Review
  13. Review
  14. Article
  15. Article
  16. 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

5 authors at 3 institutions in 1 country.

Marc SchusterSystems-Oriented Immunology and Inflammation Research Group, Department of Experimental Immunology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Carlos Plaza-SirventSystems-Oriented Immunology and Inflammation Research Group, Department of Experimental Immunology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Alexander VisekrunaInstitute for Medical Microbiology and Hygiene, Biomedical Research Center (BMFZ), Philipps University of Marburg, Marburg, Germany.
Jochen HuehnDepartment of Experimental Immunology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Ingo SchmitzSystems-Oriented Immunology and Inflammation Research Group, Department of Experimental Immunology, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Otto-von-Guericke University Magdeburg · DEHelmholtz Centre for Infection Research · DEPhilipps University of Marburg · DE

Funding

Deutsche Forschungsgemeinschaft
6 · The paper itself

Abstract

Next to the classical developmental route, in which first CD25 and subsequently Foxp3 are induced to generate thymic regulatory T (Treg) cells, an alternative route has been described. This alternative route is characterized by reciprocal induction of Foxp3 and CD25, with CD25 induction being required to rescue developing Treg cells from Foxp3-induced apoptosis. NF-κB has been demonstrated to be crucial for the development of thymic Treg cells via the classical route. However, its impact on the alternative route is poorly characterized. Using single and double deficient mice for key regulators of the classical route, c-Rel and IκB

Indexed as

AnimalsCell DifferentiationCells, CulturedForkhead Transcription FactorsI-kappa B ProteinsInterleukin-2 Receptor alpha SubunitIntracellular Signaling Peptides and ProteinsLymphocyte ActivationMiceMice, KnockoutProto-Oncogene Proteins c-relThymocytesT-Lymphocytes, RegulatoryForkhead Transcription FactorsFoxp3 protein, mouseI-kappa B ProteinsInterleukin-2 Receptor alpha SubunitIntracellular Signaling Peptides and ProteinsNfkbid protein, mouseProto-Oncogene Proteins c-relcell differentiationcommon γ-chain cytokinesNF-κBregulatory T cellthymustranscription factor

Identifiers

PMID31354726
PMCPMC6635800
OpenAlexW2957039377

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.