NOVEOS™ and ImmunoCAP™ have similar performances for diagnosing food allergies.

allergen extract clinical performance cross-reactive carbohydrate determinant food allergy molecular allergen specific IgE platforms

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:
06 Mar 2024
Historique:
received: 28 03 2023
revised: 15 02 2024
accepted: 28 02 2024
medline: 9 3 2024
pubmed: 9 3 2024
entrez: 8 3 2024
Statut: aheadofprint

Résumé

The clinical interest of newly available platforms for specific IgE measurement must be evaluated. However, data are lacking for NOVEOS™ (Hycor), in particular for food allergens. We compared technical and clinical performance of two platforms (ImmunoCAP™ and NOVEOS™) for the measurement of specific IgE to 10 food allergens. Sera from 289 clinically-characterized patients were tested for IgE specific for six food allergen extracts (egg white, cow's milk, peanut, hazelnut, fish, shrimp) and four molecular allergens (Gal d 1, Bos d 8, Ara h 2, Cor a 14). Specific IgE measurements were carried out using ImmunoCAP™ and NOVEOS™ methods. Food allergy diagnosis was established according to international guidelines. A strong correlation (rho>0.9) was present between the two platforms, while specific IgE concentrations measured with NOVEOS™ were consistently lower (mean -15%) than with ImmunoCAP™. NOVEOS™ and ImmunoCAP™ provided similar overall odds ratios and relative risks for food allergy diagnosis, with both allergen extracts and molecular allergens. When all 10 allergens were considered, NOVEOS™ provided better ROC curves (p=0.04). Finally, we found that the most discordant results were observed with hazelnut and peanut extracts, and were related to cross-reactive carbohydrate determinants on these two ImmunoCAP™. Specific IgE determination by either ImmunoCAP™ or NOVEOS™ (odd-ratios of allergy were 25.1 or 33.0, respectively) is highly informative on the risk of allergy in the selected population. The NOVEOS™ platform presents the advantage of being less affected by unwanted reactivity due to carbohydrate determinants-specific IgE, while requiring a ten-fold lower test sample volume.

Sections du résumé

BACKGROUND BACKGROUND
The clinical interest of newly available platforms for specific IgE measurement must be evaluated. However, data are lacking for NOVEOS™ (Hycor), in particular for food allergens.
OBJECTIVE OBJECTIVE
We compared technical and clinical performance of two platforms (ImmunoCAP™ and NOVEOS™) for the measurement of specific IgE to 10 food allergens.
METHODS METHODS
Sera from 289 clinically-characterized patients were tested for IgE specific for six food allergen extracts (egg white, cow's milk, peanut, hazelnut, fish, shrimp) and four molecular allergens (Gal d 1, Bos d 8, Ara h 2, Cor a 14). Specific IgE measurements were carried out using ImmunoCAP™ and NOVEOS™ methods. Food allergy diagnosis was established according to international guidelines.
RESULTS RESULTS
A strong correlation (rho>0.9) was present between the two platforms, while specific IgE concentrations measured with NOVEOS™ were consistently lower (mean -15%) than with ImmunoCAP™. NOVEOS™ and ImmunoCAP™ provided similar overall odds ratios and relative risks for food allergy diagnosis, with both allergen extracts and molecular allergens. When all 10 allergens were considered, NOVEOS™ provided better ROC curves (p=0.04). Finally, we found that the most discordant results were observed with hazelnut and peanut extracts, and were related to cross-reactive carbohydrate determinants on these two ImmunoCAP™.
CONCLUSIONS CONCLUSIONS
Specific IgE determination by either ImmunoCAP™ or NOVEOS™ (odd-ratios of allergy were 25.1 or 33.0, respectively) is highly informative on the risk of allergy in the selected population. The NOVEOS™ platform presents the advantage of being less affected by unwanted reactivity due to carbohydrate determinants-specific IgE, while requiring a ten-fold lower test sample volume.

Identifiants

pubmed: 38458433
pii: S2213-2198(24)00262-9
doi: 10.1016/j.jaip.2024.02.037
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Auteurs

Benjamin Trouche-Estival (B)

Institut Fédératif de Biologie, CHU de Toulouse, Toulouse, France.

Joana Vitte (J)

INSERM UMR-S 1250, University of Reims-Champagne Ardenne, Reims, France.

Audrey Martin-Blondel (A)

Pneumologie & Allergologie, Hôpital des Enfants, CHU de Toulouse, Toulouse, France.

Marine Michelet (M)

Pneumologie & Allergologie, Hôpital des Enfants, CHU de Toulouse, Toulouse, France.

Vianney Gruzelle (V)

Pneumologie & Allergologie, Hôpital des Enfants, CHU de Toulouse, Toulouse, France.

Alain Didier (A)

Pneumo-Allergologie, Hôpital Larrey, CHU de Toulouse, Toulouse, France.

Laurent Guilleminault (L)

Pneumo-Allergologie, Hôpital Larrey, CHU de Toulouse, Toulouse, France.

Claire Mailhol (C)

Pneumo-Allergologie, Hôpital Larrey, CHU de Toulouse, Toulouse, France.

Silvia Martinez Rivera (S)

Institut Fédératif de Biologie, CHU de Toulouse, Toulouse, France.

Anaïs De Lima Correia (A)

Institut Fédératif de Biologie, CHU de Toulouse, Toulouse, France.

Camille Taurus (C)

Institut Fédératif de Biologie, CHU de Toulouse, Toulouse, France.

Antoine Blancher (A)

Institut Fédératif de Biologie, CHU de Toulouse, Toulouse, France.

Julien Goret (J)

Laboratoire d'Immunologie, CHU de Bordeaux, France.

Caroline Klingebiel (C)

Synlab Provence, Marseille, France.

Pol André Apoil (PA)

Institut Fédératif de Biologie, CHU de Toulouse, Toulouse, France; INSERM INFINITy, U1291, Toulouse, France. Electronic address: apoil.p@chu-toulouse.fr.

Classifications MeSH