Evidence map›Paper›PMID 25908537›Full record

ArticleNature communications2015

A dominant role for the methyl-CpG-binding protein Mbd2 in controlling Th2 induction by dendritic cells.

Peter C Cook, Heather Owen, Aimée M Deaton, Jessica G Borger, Sheila L Brown, Thomas Clouaire, Gareth-Rhys Jones, Lucy H Jones, Rachel J Lundie, Angela K Marley and 15 more

Registry-linked trialAbstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03941496 (Phase 1b/2a Safety and Immunogenicity of the DNMT Inhibitor Azacitidine During Anti-Tuberculosis Therapy), which is not on this map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
–field-weighted citation impact
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.

NCT03941496 phase1 / phase2withdrawnnot on this mapstarted 2022, after this paper: background citation

Phase 1b/2a Safety and Immunogenicity of the DNMT Inhibitor Azacitidine During Anti-Tuberculosis Therapy

TypeinterventionalSponsorAndrew DinardoRan2022 to 2023Enrolled0ConditionsTuberculosis, PulmonaryArmsAzacitidine Injection
3 · Its place in the literature

Who cites it

49 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Mgl2Nature communications · 2025
    Article
  6. Review
  7. Review
  8. Weighted gene co-expression network analysis reveals immune evasion related genes inExperimental biology and medicine (Maywood, N.J.) · 2024
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
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  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

25 authors.

Peter C CookManchester Collaborative Centre for Inflammation Research, University of Manchester, Manchester M3 9NT, UK.
Heather OwenInstitute of Immunology and Infection Research, Centre for Immunity, Infection and Evolution, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FL, UK.
Aimée M DeatonWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh EH9 3BF, UK.
Jessica G BorgerInstitute of Immunology and Infection Research, Centre for Immunity, Infection and Evolution, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FL, UK.
Sheila L BrownManchester Collaborative Centre for Inflammation Research, University of Manchester, Manchester M3 9NT, UK.
Thomas ClouaireWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh EH9 3BF, UK.
Gareth-Rhys JonesManchester Collaborative Centre for Inflammation Research, University of Manchester, Manchester M3 9NT, UK.
Lucy H JonesInstitute of Immunology and Infection Research, Centre for Immunity, Infection and Evolution, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FL, UK.
Rachel J LundieInstitute of Immunology and Infection Research, Centre for Immunity, Infection and Evolution, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FL, UK.
Angela K MarleyInstitute of Immunology and Infection Research, Centre for Immunity, Infection and Evolution, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FL, UK.
Vicky L MorrisonMedical Research Institute, Ninewells Hospital and Medical School, University of Dundee, Dundee, DD1 9SY UK.
Alexander T Phythian-AdamsManchester Collaborative Centre for Inflammation Research, University of Manchester, Manchester M3 9NT, UK.
Elisabeth WachterWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh EH9 3BF, UK.
Lauren M WebbManchester Collaborative Centre for Inflammation Research, University of Manchester, Manchester M3 9NT, UK.
Tara E SutherlandInstitute of Immunology and Infection Research, Centre for Immunity, Infection and Evolution, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FL, UK.
Graham D ThomasInstitute of Immunology and Infection Research, Centre for Immunity, Infection and Evolution, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FL, UK.
John R GraingerManchester Collaborative Centre for Inflammation Research, University of Manchester, Manchester M3 9NT, UK.
Jim SelfridgeWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh EH9 3BF, UK.
Andrew N J McKenzieMedical Research Council Laboratory of Molecular Biology, Cambridge, CB2 0QH UK.
Judith E AllenInstitute of Immunology and Infection Research, Centre for Immunity, Infection and Evolution, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FL, UK.
Susanna C FagerholmMedical Research Institute, Ninewells Hospital and Medical School, University of Dundee, Dundee, DD1 9SY UK.
Rick M MaizelsInstitute of Immunology and Infection Research, Centre for Immunity, Infection and Evolution, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FL, UK.
Alasdair C IvensInstitute of Immunology and Infection Research, Centre for Immunity, Infection and Evolution, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3FL, UK.
Adrian BirdWellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh EH9 3BF, UK.
Andrew S MacDonaldManchester Collaborative Centre for Inflammation Research, University of Manchester, Manchester M3 9NT, UK.

Funding

TICK SYSTEMATICS ON A GLOBAL BASISR01AI030026 · NIAID · GEORGIA SOUTHERN UNIVERSITY · PI KEIRANS, JAMES E · 1990 to 1994
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Biotechnology and Biological Sciences Research CouncilMedical Research Council G0701437Medical Research Council G120/822Medical Research Council MC_U105178805Medical Research Council MR/K01207X/1NIAID NIH HHS N01 AI030026Wellcome Trust 106122
6 · The paper itself

Abstract

Dendritic cells (DCs) direct CD4(+) T-cell differentiation into diverse helper (Th) subsets that are required for protection against varied infections. However, the mechanisms used by DCs to promote Th2 responses, which are important both for immunity to helminth infection and in allergic disease, are currently poorly understood. We demonstrate a key role for the protein methyl-CpG-binding domain-2 (Mbd2), which links DNA methylation to repressive chromatin structure, in regulating expression of a range of genes that are associated with optimal DC activation and function. In the absence of Mbd2, DCs display reduced phenotypic activation and a markedly impaired capacity to initiate Th2 immunity against helminths or allergens. These data identify an epigenetic mechanism that is central to the activation of CD4(+) T-cell responses by DCs, particularly in Th2 settings, and reveal methyl-CpG-binding proteins and the genes under their control as possible therapeutic targets for type-2 inflammation.

Indexed as

AllergensAnimalsCD4-Positive T-LymphocytesCell PolarityChromatin ImmunoprecipitationDendritic CellsDNA-Binding ProteinsDNA MethylationEnzyme-Linked Immunosorbent AssayEpigenesis, GeneticFlow CytometryGene Expression RegulationHypersensitivityLymphocyte ActivationMiceMice, KnockoutAllergensDNA-Binding ProteinsMbd2 protein, mouseRNA, Messenger

Identifiers

PMID25908537
PMCPMC4413429

What OpenQuestion holds

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Registered trials

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.