Evidence map›Paper›PMID 27791035›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

miRNA92a targets KLF2 and the phosphatase PTEN signaling to promote human T follicular helper precursors in T1D islet autoimmunity.

Isabelle Serr, Rainer W Fürst, Verena B Ott, Martin G Scherm, Alexei Nikolaev, Füsun Gökmen, Stefanie Kälin, Stephanie Zillmer, Melanie Bunk, Benno Weigmann and 10 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
2.8field-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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Article
  6. The immunology of type 1 diabetes.Nature reviews. Immunology · 2024
    Review
  7. Article
  8. Review
  9. Review
  10. Self-Antigens Targeted by Regulatory T Cells in Type 1 Diabetes.International journal of molecular sciences · 2022
    Review
  11. An update on epigenetic regulation in autoimmune diseases.Journal of translational autoimmunity · 2022
    Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. The Many Faces of CD4International journal of molecular sciences · 2020
    Review
  20. B cell helper T cells and type 1 diabetes.Scandinavian journal of immunology · 2020
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 8 institutions in 2 countries.

Isabelle SerrInstitute for Diabetes Research, Independent Young Investigator Group Immune Tolerance in Type 1 Diabetes, Helmholtz Diabetes Center at Helmholtz Zentrum München, 80939 Munich, Germany; Deutsches Zentrum für Diabetesforschung, 85764 Munich, Germany.
Rainer W FürstDeutsches Zentrum für Diabetesforschung, 85764 Munich, Germany; Institute for Diabetes Research, Helmholtz Diabetes Center at Helmholtz Zentrum München, 80939 Munich, Germany; Klinikum rechts der Isar, Technische Universität München, 80939 Munich, Germany.
Verena B OttDeutsches Zentrum für Diabetesforschung, 85764 Munich, Germany; Institute for Diabetes and Obesity, Helmholtz Diabetes Center at Helmholtz Zentrum München, 80939 Munich, Germany; Division of Metabolic Diseases, Technische Universität München, 85748 Munich, Germany.
Martin G SchermInstitute for Diabetes Research, Independent Young Investigator Group Immune Tolerance in Type 1 Diabetes, Helmholtz Diabetes Center at Helmholtz Zentrum München, 80939 Munich, Germany; Deutsches Zentrum für Diabetesforschung, 85764 Munich, Germany.
Alexei NikolaevInstitute for Molecular Medicine, Universitätsmedizin der Johannes Gutenberg-Universität, 55131 Mainz, Germany.
Füsun GökmenInstitute for Diabetes Research, Independent Young Investigator Group Immune Tolerance in Type 1 Diabetes, Helmholtz Diabetes Center at Helmholtz Zentrum München, 80939 Munich, Germany; Deutsches Zentrum für Diabetesforschung, 85764 Munich, Germany.
Stefanie KälinDeutsches Zentrum für Diabetesforschung, 85764 Munich, Germany; Institute for Diabetes and Obesity, Helmholtz Diabetes Center at Helmholtz Zentrum München, 80939 Munich, Germany; Division of Metabolic Diseases, Technische Universität München, 85748 Munich, Germany.
Stephanie ZillmerDeutsches Zentrum für Diabetesforschung, 85764 Munich, Germany; Institute for Diabetes Research, Helmholtz Diabetes Center at Helmholtz Zentrum München, 80939 Munich, Germany; Klinikum rechts der Isar, Technische Universität München, 80939 Munich, Germany.
Melanie BunkDeutsches Zentrum für Diabetesforschung, 85764 Munich, Germany; Institute for Diabetes Research, Helmholtz Diabetes Center at Helmholtz Zentrum München, 80939 Munich, Germany; Klinikum rechts der Isar, Technische Universität München, 80939 Munich, Germany.
Benno WeigmannDepartment of Medicine 1, University of Erlangen-Nuremberg, Kussmaul Campus for Medical Research, 91052 Erlangen, Germany.
Nicole KunschkeDepartment of Drug Delivery, Helmholtz Institute for Pharmaceutical Research Saarland, Helmholtz Centre for Infection Research, 66123 Saarbruecken, Germany.
Brigitta LoretzDepartment of Drug Delivery, Helmholtz Institute for Pharmaceutical Research Saarland, Helmholtz Centre for Infection Research, 66123 Saarbruecken, Germany.
Claus-Michael LehrDepartment of Drug Delivery, Helmholtz Institute for Pharmaceutical Research Saarland, Helmholtz Centre for Infection Research, 66123 Saarbruecken, Germany; Department of Pharmacy, Saarland University, 66123 Saarbruecken, Germany.ORCID 0000-0002-5864-8462
Benedikt KirchnerPhysiology Weihenstephan, Technische Universität München, 85354 Freising, Germany.
Bettina HaaseGenomics Core Facility, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.
Michael PfafflPhysiology Weihenstephan, Technische Universität München, 85354 Freising, Germany.
Ari WaismanInstitute for Molecular Medicine, Universitätsmedizin der Johannes Gutenberg-Universität, 55131 Mainz, Germany.
Richard A WillisEmory Vaccine Center, NIH Tetramer Core Facility, Atlanta, GA 30322.
Anette-G ZieglerDeutsches Zentrum für Diabetesforschung, 85764 Munich, Germany; Institute for Diabetes Research, Helmholtz Diabetes Center at Helmholtz Zentrum München, 80939 Munich, Germany; Klinikum rechts der Isar, Technische Universität München, 80939 Munich, Germany.
Carolin DanielInstitute for Diabetes Research, Independent Young Investigator Group Immune Tolerance in Type 1 Diabetes, Helmholtz Diabetes Center at Helmholtz Zentrum München, 80939 Munich, Germany; Deutsches Zentrum für Diabetesforschung, 85764 Munich, Germany; carolin.daniel@helmholtz-muenchen.de.
Helmholtz Zentrum München · DETUM Klinikum · DEHelmholtz Centre for Infection Research · DEJohannes Gutenberg University Mainz · DETechnical University of Munich · DEEmory Healthcare · USEuropean Molecular Biology Laboratory · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aberrant immune activation mediated by T effector cell populations is pivotal in the onset of autoimmunity in type 1 diabetes (T1D). T follicular helper (TFH) cells are essential in the induction of high-affinity antibodies, and their precursor memory compartment circulates in the blood. The role of TFH precursors in the onset of islet autoimmunity and signaling pathways regulating their differentiation is incompletely understood. Here, we provide direct evidence that during onset of islet autoimmunity, the insulin-specific target T-cell population is enriched with a C-X-C chemokine receptor type 5 (CXCR5)

Indexed as

AutoimmunityAdolescentAnimalsAntagomirsAutoantibodiesChildDiabetes Mellitus, Type 1FemaleForkhead Box Protein O1Gene Expression RegulationHumansIslets of LangerhansKruppel-Like Transcription FactorsMaleMiceMice, Inbred NODAntagomirsAutoantibodiesCXCR5 protein, humanForkhead Box Protein O1FOXO1 protein, humanKLF2 protein, humanKruppel-Like Transcription FactorsMicroRNAsMIRN92 microRNA, humanPhosphatidylinositol 3-KinasesPTEN PhosphohydrolasePTEN protein, humanReceptors, CXCR5KLF2miRNA92aPTEN-PI3K signalingT follicular helper cellstype 1 diabetes

Identifiers

PMID27791035
PMCPMC5087025
OpenAlexW2530721136

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.