Evidence map›Paper›PMID 23945544›Full record

ArticleMucosal immunology2014

Amelioration of ovalbumin-induced allergic airway disease following Der p 1 peptide immunotherapy is not associated with induction of IL-35.

D M Moldaver, M S Bharhani, J N Wattie, R Ellis, H Neighbour, C M Lloyd, M D Inman, M Larché

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Mucosal immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Immunology of allergen immunotherapy.Immunotherapy advances · 2022
    Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Adenovirus-mediated interleukin-35 gene transfer suppresses allergic airway inflammation in a murine model of asthma.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2015
    Article
  10. Article
  11. Mechanisms of peptide immunotherapy in allergic airways disease.Annals of the American Thoracic Society · 2014
    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

8 authors at 3 institutions in 2 countries.

D M MoldaverDivisions of Respirology and Clinical Immunology and Allergy, Department of Medicine, McMaster Immunology Research Centre, Firestone Institute for Respiratory Health, St. Joseph's Healthcare, McMaster University, Hamilton, Ontario, Canada.
M S BharhaniDivisions of Respirology and Clinical Immunology and Allergy, Department of Medicine, McMaster Immunology Research Centre, Firestone Institute for Respiratory Health, St. Joseph's Healthcare, McMaster University, Hamilton, Ontario, Canada.
J N WattieDivisions of Respirology and Clinical Immunology and Allergy, Department of Medicine, McMaster Immunology Research Centre, Firestone Institute for Respiratory Health, St. Joseph's Healthcare, McMaster University, Hamilton, Ontario, Canada.
R EllisDivisions of Respirology and Clinical Immunology and Allergy, Department of Medicine, McMaster Immunology Research Centre, Firestone Institute for Respiratory Health, St. Joseph's Healthcare, McMaster University, Hamilton, Ontario, Canada.
H NeighbourDivisions of Respirology and Clinical Immunology and Allergy, Department of Medicine, McMaster Immunology Research Centre, Firestone Institute for Respiratory Health, St. Joseph's Healthcare, McMaster University, Hamilton, Ontario, Canada.
C M LloydLeukocyte Biology Section, National Heart and Lung Institute, Faculty of Medicine, Imperial College London and MRC/Asthma UK Centre in Allergic Mechanisms of Asthma, London, UK.
M D InmanDivisions of Respirology and Clinical Immunology and Allergy, Department of Medicine, McMaster Immunology Research Centre, Firestone Institute for Respiratory Health, St. Joseph's Healthcare, McMaster University, Hamilton, Ontario, Canada.
M LarchéDivisions of Respirology and Clinical Immunology and Allergy, Department of Medicine, McMaster Immunology Research Centre, Firestone Institute for Respiratory Health, St. Joseph's Healthcare, McMaster University, Hamilton, Ontario, Canada.
St. Joseph’s Healthcare Hamilton · CAMcMaster University · CAImperial College London · GB

Funding

Medical Research Council G1000758Wellcome Trust 087618
6 · The paper itself

Abstract

In the present study, we show therapeutic amelioration of established ovalbumin (OVA)-induced allergic airway disease following house dust mite (HDM) peptide therapy. Mice were sensitized and challenged with OVA and HDM protein extract (Dermatophagoides species) to induce dual allergen sensitization and allergic airway disease. Treatment of allergic mice with peptides derived from the major allergen Der p 1 suppressed OVA-induced airway hyperresponsiveness, tissue eosinophilia, and goblet cell hyperplasia upon rechallenge with allergen. Peptide treatment also suppressed OVA-specific T-cell proliferation. Resolution of airway pathophysiology was associated with a reduction in recruitment, proliferation, and effector function of T(H)2 cells and decreased interleukin (IL)-17⁺ T cells. Furthermore, peptide immunotherapy induced the regulatory cytokine IL-10 and increased the proportion of Fox p3⁺ cells among those expressing IL-10. Tolerance to OVA was not associated with increased IL-35. In conclusion, our results provide in vivo evidence for the creation of a tolerogenic environment following HDM peptide immunotherapy, leading to the therapeutic amelioration of established OVA-induced allergic airway disease.

Indexed as

AllergensAnimalsAntigens, DermatophagoidesArthropod ProteinsCysteine EndopeptidasesDesensitization, ImmunologicDisease Models, AnimalEpitopes, T-LymphocyteFemaleForkhead Transcription FactorsInterleukin-10Interleukin-17Interleukin-5InterleukinsLymphocyte ActivationLymphocyte SubsetsAllergensAntigens, DermatophagoidesArthropod ProteinsCysteine EndopeptidasesDermatophagoides pteronyssinus antigen p 1Epitopes, T-LymphocyteForkhead Transcription FactorsFoxp3 protein, mouseInterleukin-10Interleukin-17interleukin-35, mouseInterleukin-5InterleukinsOvalbuminPeptide Fragments

Identifiers

PMID23945544
OpenAlexW1990621471

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.