Two Different Composite Markers Predict Severity and Threshold Dose in Peanut Allergy.

Basophil activation test FcεRI-positive control Oral food challenge Peanut allergy

Journal

The journal of allergy and clinical immunology. In practice
ISSN: 2213-2201
Titre abrégé: J Allergy Clin Immunol Pract
Pays: United States
ID NLM: 101597220

Informations de publication

Date de publication:
01 2021
Historique:
received: 20 01 2020
revised: 17 09 2020
accepted: 18 09 2020
pubmed: 11 10 2020
medline: 22 5 2021
entrez: 10 10 2020
Statut: ppublish

Résumé

Safe and cost-effective biological surrogate markers to evaluate the severity and threshold dose of peanut allergy (PA) reactions during an oral food challenge (OFC) are lacking. To evaluate biological markers associated with the severity and threshold dose of an allergic reaction during an OFC in a population of children with PA. Demographic and biological parameters of children with peanut OFC and basophil activation test (BAT) results were collected. Patients were stratified into 2 severity groups (mild-to-moderate and severe) and 2 cumulative threshold dose groups: low (LCTG) ≤100 mg crushed peanut and high >100 mg. Among the 68 children included, there was a 96% concordance between the OFC and BAT result for the diagnosis of PA. Of the 56 children with a positive OFC and BAT to peanut (median age: 8.8 years), the severity of an allergic reaction and the cumulative threshold dose were not correlated (P = .24). Higher Ara h 2-specific IgE and FcεRI-positive control values were both associated with severe reactions to peanut. Combining these 2 markers led to a 92% sensitivity (84%-97%) and an 82% specificity (71%-89%) for severe reactions in all subjects. For children in the LCTG, a 4-variable composite marker, including age, normalized basophil sensitivity (EC Distinct composite markers including BAT allergen-specific and non-allergen-specific parameters appear to be associated with severity and cumulative threshold dose in children with PA.

Sections du résumé

BACKGROUND
Safe and cost-effective biological surrogate markers to evaluate the severity and threshold dose of peanut allergy (PA) reactions during an oral food challenge (OFC) are lacking.
OBJECTIVE
To evaluate biological markers associated with the severity and threshold dose of an allergic reaction during an OFC in a population of children with PA.
METHODS
Demographic and biological parameters of children with peanut OFC and basophil activation test (BAT) results were collected. Patients were stratified into 2 severity groups (mild-to-moderate and severe) and 2 cumulative threshold dose groups: low (LCTG) ≤100 mg crushed peanut and high >100 mg.
RESULTS
Among the 68 children included, there was a 96% concordance between the OFC and BAT result for the diagnosis of PA. Of the 56 children with a positive OFC and BAT to peanut (median age: 8.8 years), the severity of an allergic reaction and the cumulative threshold dose were not correlated (P = .24). Higher Ara h 2-specific IgE and FcεRI-positive control values were both associated with severe reactions to peanut. Combining these 2 markers led to a 92% sensitivity (84%-97%) and an 82% specificity (71%-89%) for severe reactions in all subjects. For children in the LCTG, a 4-variable composite marker, including age, normalized basophil sensitivity (EC
CONCLUSION
Distinct composite markers including BAT allergen-specific and non-allergen-specific parameters appear to be associated with severity and cumulative threshold dose in children with PA.

Identifiants

pubmed: 33038591
pii: S2213-2198(20)31092-8
doi: 10.1016/j.jaip.2020.09.043
pii:
doi:

Substances chimiques

Allergens 0
Antigens, Plant 0
Biomarkers 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

275-282.e1

Informations de copyright

Copyright © 2020 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.

Auteurs

Nathalie Cottel (N)

Allergology Department, Hôpital A. Trousseau, Sorbonne Université, AP-HP, Paris, France.

Sarah Saf (S)

Allergology Department, Hôpital A. Trousseau, Sorbonne Université, AP-HP, Paris, France.

Melisande Bourgoin-Heck (M)

Allergology Department, Hôpital A. Trousseau, Sorbonne Université, AP-HP, Paris, France; Epidemiology of Allergic and Respiratory Diseases, IPLESP, INSERM and Sorbonne Université, Paris, France.

Nathalie Lambert (N)

Allergology Department, Hôpital A. Trousseau, Sorbonne Université, AP-HP, Paris, France.

Flore Amat (F)

Allergology Department, Hôpital A. Trousseau, Sorbonne Université, AP-HP, Paris, France; Epidemiology of Allergic and Respiratory Diseases, IPLESP, INSERM and Sorbonne Université, Paris, France.

Pascal Poncet (P)

Immunology Department, Biological Allergology Unit, Hôpital A. Trousseau, Sorbonne Université, AP-HP, Paris, France; Immunology Department, Institut Pasteur, Paris, France.

Helene Senechal (H)

Immunology Department, Biological Allergology Unit, Hôpital A. Trousseau, Sorbonne Université, AP-HP, Paris, France.

Rémy Couderc (R)

Immunology Department, Biological Allergology Unit, Hôpital A. Trousseau, Sorbonne Université, AP-HP, Paris, France.

Jocelyne Just (J)

Allergology Department, Hôpital A. Trousseau, Sorbonne Université, AP-HP, Paris, France; Epidemiology of Allergic and Respiratory Diseases, IPLESP, INSERM and Sorbonne Université, Paris, France. Electronic address: jocelyne.just@aphp.fr.

Yannick Chantran (Y)

Immunology Department, Biological Allergology Unit, Hôpital A. Trousseau, Sorbonne Université, AP-HP, Paris, France.

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Classifications MeSH