Evidence map›Paper›PMID 29779209›Full record

ArticleAllergy2019

Gata3 hypermethylation and Foxp3 hypomethylation are associated with sustained protection and bystander effect following epicutaneous immunotherapy in peanut-sensitized mice.

L Mondoulet, V Dioszeghy, F Busato, C Plaquet, V Dhelft, K Bethune, L Leclere, C Daviaud, M Ligouis, H Sampson and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Allergy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
7.0field-weighted citation impact, top 2% 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, 69 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Zéro allergie research clinic: a clinical and research initiative in oral immunotherapy for managing IgE-mediated food allergy.Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology · 2024
    Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Immunology of allergen immunotherapy.Immunotherapy advances · 2022
    Review
  14. Epigenetic Mechanisms in Allergy Development and Prevention.Handbook of experimental pharmacology · 2022
    Article
  15. Review
  16. Review
  17. Pathogenesis of IgE-mediated food allergy and implications for future immunotherapeutics.Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2021
    Review
  18. Article
  19. New Insights in Therapy for Food Allergy.Foods (Basel, Switzerland) · 2021
    Review
  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

12 authors at 3 institutions in 2 countries.

L MondouletDBV Technologies, Montrouge, France.ORCID 0000-0003-0110-0321
V DioszeghyDBV Technologies, Montrouge, France.
F BusatoLaboratory for Epigenetics & Environment, Centre National de Recherche en Génomique Humaine, CEA - Institut de Biologie François Jacob, Evry, France.
C PlaquetDBV Technologies, Montrouge, France.
V DhelftDBV Technologies, Montrouge, France.
K BethuneLaboratory for Epigenetics & Environment, Centre National de Recherche en Génomique Humaine, CEA - Institut de Biologie François Jacob, Evry, France.
L LeclereLaboratory for Epigenetics & Environment, Centre National de Recherche en Génomique Humaine, CEA - Institut de Biologie François Jacob, Evry, France.
C DaviaudLaboratory for Epigenetics & Environment, Centre National de Recherche en Génomique Humaine, CEA - Institut de Biologie François Jacob, Evry, France.
M LigouisDBV Technologies, Montrouge, France.
H SampsonDBV Technologies, Montrouge, France.
C DupontUniversité Paris Descartes, Hôpital Necker-Enfants Malades, Paris, France.
J TostLaboratory for Epigenetics & Environment, Centre National de Recherche en Génomique Humaine, CEA - Institut de Biologie François Jacob, Evry, France.ORCID 0000-0002-2683-0817
DBV Technologies (France) · FRCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRHôpital Necker-Enfants Malades · FR

Funding

DBV Technologies
6 · The paper itself

Abstract

backgroundEpicutaneous immunotherapy (EPIT) is a promising method for treating food allergies. In animal models, EPIT induces sustained unresponsiveness and prevents further sensitization mediated by Tregs. Here, we elucidate the mechanisms underlying the therapeutic effect of EPIT, by characterizing the kinetics of DNA methylation changes in sorted cells from spleen and blood and by evaluating its persistence and bystander effect compared to oral immunotherapy (OIT).

methodsBALB/c mice orally sensitized to peanut proteins (PPE) were treated by EPIT using a PPE-patch or by PPE-OIT. Another set of peanut-sensitized mice treated by EPIT or OIT were sacrificed following a protocol of sensitization to OVA. DNA methylation was analyzed during immunotherapy and 8 weeks after the end of treatment in sorted cells from spleen and blood by pyrosequencing. Humoral and cellular responses were measured during and after immunotherapy.

resultsAnalyses showed a significant hypermethylation of the Gata3 promoter detectable only in Th2 cells for EPIT from the 4th week and a significant hypomethylation of the Foxp3 promoter in CD62L

conclusionsOur study demonstrates that EPIT leads to a unique and stable epigenetic signature in specific T-cell compartments with downregulation of Th2 key regulators and upregulation of Treg transcription factors, likely explaining the sustainability of protection and the observed bystander effect.

Indexed as

DNA MethylationAdministration, CutaneousAdministration, OralAnimalsBystander EffectDrug Administration RoutesEpigenomicsForkhead Transcription FactorsGATA3 Transcription FactorImmunotherapyMiceMice, Inbred BALB CPeanut HypersensitivityTh2 CellsTime FactorsT-Lymphocytes, RegulatoryForkhead Transcription FactorsFoxp3 protein, mouseGata3 protein, mouseGATA3 Transcription FactorTranscription Factorsbystander effectDNA methylationepicutaneous immunotherapyfood allergyTregs

Identifiers

PMID29779209
PMCPMC6585762
OpenAlexW2804930432

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.