IgE antibody repertoire in nasal secretions of children and adults with seasonal allergic rhinitis: A molecular analysis.


Journal

Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology
ISSN: 1399-3038
Titre abrégé: Pediatr Allergy Immunol
Pays: England
ID NLM: 9106718

Informations de publication

Date de publication:
04 2020
Historique:
received: 02 07 2019
accepted: 25 10 2019
revised: 24 10 2019
pubmed: 5 11 2019
medline: 5 3 2021
entrez: 3 11 2019
Statut: ppublish

Résumé

There is growing interest both in testing IgE in nasal secretions (NS) and in molecular diagnosis of seasonal allergic rhinitis (SAR). Yet, the reliability of nasal IgE detection with the newest molecular assays has never been assessed in a large cohort of pollen allergic patients. To investigate with microarray technology and compare the repertoires of specific IgE (sIgE) antibodies in NS and sera of a large population of children and adults with SAR. Nasal secretions were collected with an absorbent device (Merocel 2000 Nasal sIgE was detectable in 68.3% of the patients. The detected nasal sIgE antibodies recognized airborne (88%), vegetable (10%), and animal food or other (<1%) allergen molecules. The prevalence and average levels of sIgE in NS and serum were highly interrelated at population level. A positive nasal sIgE antibody to a given molecule predicted the detection of the same antibody in the patient's serum with a specificity of 99.7% and a sensitivity of 40%. The concentration of sIgE is much lower in nasal secretions than in the serum. sIgE assays with very high analytical sensitivity and sampling methods with minimal dilution will be therefore needed to validate nasal secretions as alternative to serum in testing the sIgE repertoire.

Sections du résumé

BACKGROUND
There is growing interest both in testing IgE in nasal secretions (NS) and in molecular diagnosis of seasonal allergic rhinitis (SAR). Yet, the reliability of nasal IgE detection with the newest molecular assays has never been assessed in a large cohort of pollen allergic patients.
OBJECTIVE
To investigate with microarray technology and compare the repertoires of specific IgE (sIgE) antibodies in NS and sera of a large population of children and adults with SAR.
METHODS
Nasal secretions were collected with an absorbent device (Merocel 2000
RESULTS
Nasal sIgE was detectable in 68.3% of the patients. The detected nasal sIgE antibodies recognized airborne (88%), vegetable (10%), and animal food or other (<1%) allergen molecules. The prevalence and average levels of sIgE in NS and serum were highly interrelated at population level. A positive nasal sIgE antibody to a given molecule predicted the detection of the same antibody in the patient's serum with a specificity of 99.7% and a sensitivity of 40%.
CONCLUSIONS
The concentration of sIgE is much lower in nasal secretions than in the serum. sIgE assays with very high analytical sensitivity and sampling methods with minimal dilution will be therefore needed to validate nasal secretions as alternative to serum in testing the sIgE repertoire.

Identifiants

pubmed: 31677297
doi: 10.1111/pai.13148
doi:

Substances chimiques

Allergens 0
Immunoglobulin E 37341-29-0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

273-280

Informations de copyright

© 2019 The Authors. Pediatric Allergy and Immunology published by John Wiley & Sons Ltd.

Références

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Auteurs

Sveva Castelli (S)

Department of Pediatric Pneumology, Immunology and Intensive Care Medicine, Charité Universitätsmedizin Berlin, Berlin, Germany.

Stefania Arasi (S)

Division of Allergy, University Department of Pediatrics, Pediatric Hospital Bambino Gesù (IRCCS), Rome, Italy.

Salvatore Tripodi (S)

Department of Pediatrics and Pediatric Allergy Unit, Sandro Pertini Hospital, Rome, Italy.

Danilo Villalta (D)

Immunology and Allergy Unit, "S.Maria degli Angeli" Hospital, Pordenone, Italy.

Paola Martelli (P)

Immunology and Allergy Unit, "S.Maria degli Angeli" Hospital, Pordenone, Italy.

Mariaelisabetta Conte (M)

Immunology and Allergy Unit, "S.Maria degli Angeli" Hospital, Pordenone, Italy.

Valentina Panetta (V)

L'altrastatistica srl, Consultancy & Training, Biostatistics Office, Rome, Italy.

Ilaria Simonelli (I)

L'altrastatistica srl, Consultancy & Training, Biostatistics Office, Rome, Italy.

Alexander Rohrbach (A)

Department of Pediatric Pneumology, Immunology and Intensive Care Medicine, Charité Universitätsmedizin Berlin, Berlin, Germany.

Marco Di Fraia (M)

Department of Pediatric Pneumology, Immunology and Intensive Care Medicine, Charité Universitätsmedizin Berlin, Berlin, Germany.

Ifigenia Sfika (I)

Department of Pediatrics and Pediatric Allergy Unit, Sandro Pertini Hospital, Rome, Italy.

Valeria Villella (V)

Department of Pediatrics and Pediatric Allergy Unit, Sandro Pertini Hospital, Rome, Italy.

Andrea Di Rienzo Businco (A)

Department of Pediatrics and Pediatric Allergy Unit, Sandro Pertini Hospital, Rome, Italy.

Serena Perna (S)

Department of Pediatric Pneumology, Immunology and Intensive Care Medicine, Charité Universitätsmedizin Berlin, Berlin, Germany.

Stephanie Dramburg (S)

Department of Pediatric Pneumology, Immunology and Intensive Care Medicine, Charité Universitätsmedizin Berlin, Berlin, Germany.

Ekaterina Potapova (E)

Department of Pediatric Pneumology, Immunology and Intensive Care Medicine, Charité Universitätsmedizin Berlin, Berlin, Germany.

Paolo Maria Matricardi (PM)

Department of Pediatric Pneumology, Immunology and Intensive Care Medicine, Charité Universitätsmedizin Berlin, Berlin, Germany.

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