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
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.