Evidence map›Paper›PMID 25173802›Full record

Trial reportClinical immunology (Orlando, Fla.)2014

Modulation of dendritic cell innate and adaptive immune functions by oral and sublingual immunotherapy.

Pamela A Frischmeyer-Guerrerio, Corinne A Keet, Anthony L Guerrerio, Kristin L Chichester, Anja P Bieneman, Robert G Hamilton, Robert A Wood, John T Schroeder

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Clinical immunology (Orlando, Fla.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
2.9field-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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Dendritic cells in food allergy, treatment, and tolerance.The Journal of allergy and clinical immunology · 2024
    Review
  6. Review
  7. Review
  8. Observational
  9. Review
  10. Article
  11. Article
  12. Review
  13. [The research progress of mechanism of allergen immunotherapy in allergic rhinitis].Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2021
    Review
  14. Review
  15. Review
  16. Immune mechanisms of oral immunotherapy.The Journal of allergy and clinical immunology · 2018
    Review
  17. Review
  18. Immunotherapy for cow's milk allergy.Human vaccines & immunotherapeutics · 2017
    Review
  19. Innate and adaptive dendritic cell responses to immunotherapy.Current opinion in allergy and clinical immunology · 2015
    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

8 authors at 2 institutions in 1 country.

Pamela A Frischmeyer-GuerrerioDivision of Allergy and Immunology, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA. Electronic address: pguerrerio@jhmi.edu.
Corinne A KeetDivision of Allergy and Immunology, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA. Electronic address: ckeet1@jhmi.edu.
Anthony L GuerrerioDivision of Gastroenterology, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA. Electronic address: aguerrerio@jhmi.edu.
Kristin L ChichesterDivision of Allergy and Immunology, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA. Electronic address: kchiches@jhmi.edu.
Anja P BienemanDivision of Allergy and Clinical Immunology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA. Electronic address: abienema@jhmi.edu.
Robert G HamiltonDivision of Allergy and Clinical Immunology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA. Electronic address: rhamilto@jhmi.edu.
Robert A WoodDivision of Allergy and Immunology, Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, MD, USA. Electronic address: rwood@jhmi.edu.
John T SchroederDivision of Allergy and Clinical Immunology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA. Electronic address: schray@jhmi.edu.
Johns Hopkins Medicine · USJohns Hopkins University · US

Funding

Genetic and Environmental Determinants of Food AllergyK23AI103187 · NIAID · JOHNS HOPKINS UNIVERSITY · PI KEET, CORINNE · 2012 to 2016
$684k
Investigation of the Role of TGF Beta in TH2-Mediated DiseaseK23AI091869 · NIAID · JOHNS HOPKINS UNIVERSITY · PI GUERRERIO, PAMELA ANN · 2011 to 2014
$537k
Immune Cell Responses in Food HypersensitivityR21AI079853 · NIAID · JOHNS HOPKINS UNIVERSITY · PI SCHROEDER, JOHN T. · 2008 to 2009
$451k
Development of a Dissolving Film for Allergen Immunotherapy in ChildrenR21HD073557 · NICHD · JOHNS HOPKINS UNIVERSITY · PI KEET, CORINNE · 2013 to 2014
$445k
NIAID NIH HHS K23 AI091869NIAID NIH HHS K23AI091869NIAID NIH HHS K23 AI103187NIAID NIH HHS R21 AI079853NIAID NIH HHS R21AI079853NICHD NIH HHS R21 HD073557PHS HHS 101872
6 · The paper itself

Abstract

Sublingual (SLIT) and oral immunotherapy (OIT) are promising treatments for food allergy, but underlying mechanisms are poorly understood. Dendritic cells (DCs) induce and maintain Th2-type allergen-specific T cells, and also regulate innate immunity through their expression of Toll-like receptors (TLRs). We examined how SLIT and OIT influenced DC innate and adaptive immune responses in children with IgE-mediated cow's milk (CM) allergy. SLIT, but not OIT, decreased TLR-induced IL-6 secretion by myeloid DCs (mDCs). SLIT and OIT altered mDC IL-10 secretion, a potent inhibitor of FcεRI-dependent pro-inflammatory responses. OIT uniquely augmented IFN-α and decreased IL-6 secretion by plasmacytoid DCs (pDCs), which was associated with reduced TLR-induced IL-13 release in pDC-T cell co-cultures. Both SLIT and OIT decreased Th2 cytokine secretion to CM in pDC-T, but not mDC-T, co-cultures. Therefore, SLIT and OIT exert unique effects on DC-driven innate and adaptive immune responses, which may inhibit allergic inflammation and promote tolerance.

Indexed as

Administration, OralAdministration, SublingualAdolescentAllergensCells, CulturedChildCoculture TechniquesCytokinesDendritic CellsDouble-Blind MethodGene Expression RegulationHumansMilk HypersensitivityPeptidoglycanReceptors, IgET-LymphocytesAllergensCytokinesPeptidoglycanReceptors, IgETLR2 protein, humanToll-Like Receptor 2Adaptive immunity;Dendritic cell;Food allergy;Immunotherapy;Innate immunity;Tolerance

Identifiers

PMID25173802
PMCPMC4252363
OpenAlexW2015486369

What OpenQuestion holds

Textmetadata
LicenceTDM
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.