Nasal IL-13 production identifies patients with late-phase allergic responses.

Allergic rhinitis allergen biomarker birch pollen allergy cytokine responses late allergic response nasal allergen challenge

Journal

The Journal of allergy and clinical immunology
ISSN: 1097-6825
Titre abrégé: J Allergy Clin Immunol
Pays: United States
ID NLM: 1275002

Informations de publication

Date de publication:
11 2023
Historique:
received: 13 01 2023
revised: 09 05 2023
accepted: 23 06 2023
medline: 7 11 2023
pubmed: 4 8 2023
entrez: 3 8 2023
Statut: ppublish

Résumé

There is limited knowledge on how local cytokine secretion patterns after nasal allergen challenge correlate with clinical symptoms especially with regard to the "late allergic response," which occurs in approximately 40% to 50% of patients with allergy. We sought to characterize the immunologic and clinical nasal responses to birch pollen allergen challenge with a special focus on the late allergic response. In this randomized, double-blind, placebo-controlled trial, birch pollen-allergic participants were challenged with birch pollen extract (n = 20) or placebo (n = 10) on 3 consecutive days. On days 1 and 3, nasal secretions were collected at selected time points over a 24-hour time course for the measurement of 33 inflammatory mediators. Clinical responses were determined through subjective symptom scores and objective nasal airflow measurements. Provoked participants had significantly greater clinical responses and showed significant increases in tryptase and the soluble IL-33 receptor serum stimulation 2 (sST2) in nasal secretions within minutes compared with the placebo group. Eight of 20 provoked participants displayed high IL-13 levels 2 to 8 hours after allergen provocation. This group also showed significant changes in clinical parameters, with a secondary drop in nasal airflow measured by peak nasal inspiratory flow and increased symptoms of nasal obstruction, which significantly differed from IL-13 nonresponders after 6 hours. IL-13 response status correlates with clinical responses and type 2 cytokine responses in the late phase after allergen provocation.

Sections du résumé

BACKGROUND
There is limited knowledge on how local cytokine secretion patterns after nasal allergen challenge correlate with clinical symptoms especially with regard to the "late allergic response," which occurs in approximately 40% to 50% of patients with allergy.
OBJECTIVE
We sought to characterize the immunologic and clinical nasal responses to birch pollen allergen challenge with a special focus on the late allergic response.
METHODS
In this randomized, double-blind, placebo-controlled trial, birch pollen-allergic participants were challenged with birch pollen extract (n = 20) or placebo (n = 10) on 3 consecutive days. On days 1 and 3, nasal secretions were collected at selected time points over a 24-hour time course for the measurement of 33 inflammatory mediators. Clinical responses were determined through subjective symptom scores and objective nasal airflow measurements.
RESULTS
Provoked participants had significantly greater clinical responses and showed significant increases in tryptase and the soluble IL-33 receptor serum stimulation 2 (sST2) in nasal secretions within minutes compared with the placebo group. Eight of 20 provoked participants displayed high IL-13 levels 2 to 8 hours after allergen provocation. This group also showed significant changes in clinical parameters, with a secondary drop in nasal airflow measured by peak nasal inspiratory flow and increased symptoms of nasal obstruction, which significantly differed from IL-13 nonresponders after 6 hours.
CONCLUSIONS
IL-13 response status correlates with clinical responses and type 2 cytokine responses in the late phase after allergen provocation.

Identifiants

pubmed: 37536510
pii: S0091-6749(23)00971-5
doi: 10.1016/j.jaci.2023.06.026
pii:
doi:

Substances chimiques

Interleukin-13 0
Allergens 0
Cytokines 0

Types de publication

Randomized Controlled Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1167-1178.e12

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Nicholas J Campion (NJ)

Department of Otorhinolaryngology, Medical University of Vienna, Vienna, Austria.

Sergio Villazala-Merino (S)

Department of Otorhinolaryngology, Medical University of Vienna, Vienna, Austria.

Ryan S Thwaites (RS)

National Heart and Lung Institute, Imperial College of London, London, United Kingdom.

Victoria Stanek (V)

Department of Otorhinolaryngology, Medical University of Vienna, Vienna, Austria.

Helen Killick (H)

Translational Science and Experimental Medicine, Research and Early Development, Respiratory & Immunology, BioPharmaceuticals R&D, AstraZeneca, Cambridge, United Kingdom.

Eleftheria Pertsinidou (E)

Research and Development, Thermo Fisher Scientific, Uppsala, Sweden.

Mohammed Zghaebi (M)

Department of Otorhinolaryngology, Medical University of Vienna, Vienna, Austria.

Josef Toth (J)

Department of Otorhinolaryngology, Medical University of Vienna, Vienna, Austria.

Renate Fröschl (R)

Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.

Thomas Perkmann (T)

Department of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.

Katharina Gangl (K)

Department of Otorhinolaryngology, Medical University of Vienna, Vienna, Austria.

Sven Schneider (S)

Department of Otorhinolaryngology, Medical University of Vienna, Vienna, Austria.

Robin Ristl (R)

Center for Medical Statistics, Informatics and Intelligent Systems, Medical University of Vienna, Vienna, Austria.

Ian C Scott (IC)

Translational Science and Experimental Medicine, Research and Early Development, Respiratory & Immunology, BioPharmaceuticals R&D, AstraZeneca, Cambridge, United Kingdom.

Emma Suzanne Cohen (ES)

Bioscience Asthma, Research and Early Development, Respiratory & Immunology, BioPharmaceuticals R&D, AstraZeneca, Cambridge, United Kingdom.

Magnus Molin (M)

Research and Development, Thermo Fisher Scientific, Uppsala, Sweden.

Margit Focke-Tejkl (M)

Division of Immunopathology, Department of Pathophysiology and Allergy Research, Medical University of Vienna, Vienna, Austria; Karl Landsteiner University of Health Sciences, Krems, Austria.

Guenther Regelsberger (G)

Division of Neuropathology and Neurochemistry, Department of Neurology, Medical University of Vienna, Vienna, Austria.

Trevor T Hansel (TT)

National Heart and Lung Institute, Imperial College of London, London, United Kingdom.

Rudolf Valenta (R)

Division of Immunopathology, Department of Pathophysiology and Allergy Research, Medical University of Vienna, Vienna, Austria; Karl Landsteiner University of Health Sciences, Krems, Austria.

Verena Niederberger-Leppin (V)

Department of Otorhinolaryngology, Medical University of Vienna, Vienna, Austria. Electronic address: verena.niederberger@meduniwien.ac.at.

Julia Eckl-Dorna (J)

Department of Otorhinolaryngology, Medical University of Vienna, Vienna, Austria.

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Classifications MeSH