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Published on: May 31, 2021
Ara h 2 and Ara h 6 sensitization predicts peanut allergy in Mediterranean pediatric patients
Chantal Agabriel1, Ouafeh Ghazouani, Joëlle Birnbaum
1Multidisciplinary Pediatrics Department, APHM Assistance Publique Hôpitaux de Marseille, La Timone Hospital, Marseille, France.
Insights
Peanut component-resolved diagnosis is effective for children in Southern France. Ara h 6 and Ara h 2 are key predictors for diagnosing peanut allergy (PA) and assessing its persistence.
Area of Science:
- Immunology
- Allergology
- Pediatrics
Background:
- Molecular allergology has advanced peanut allergy (PA) management.
- Guidelines for Mediterranean pediatric patients are needed.
- This study evaluates peanut component-resolved diagnosis in Southern France.
Purpose of the Study:
- To assess peanut component-resolved diagnosis as a diagnostic and prognostic tool in pediatric patients.
- To identify key peanut allergens for diagnosis and persistence prediction.
- To establish diagnostic criteria for Mediterranean children.
Main Methods:
- 181 pediatric patients underwent medical history, skin prick testing, serum-specific IgE testing (extract and components), and oral food challenges.
- Allergen microarray was performed on 68 patients.
- Specific IgE to Arachis hypogea components like Ara h 1, 2, 6, 8, 9, and Pru p 4 were analyzed.
Main Results:
- In 117 peanut-allergic children, IgE to Ara h 6 (64%), Ara h 2 (63%), Ara h 1 (60%), and Ara h 9 (52%) were most prevalent.
- Ara h 6 was the strongest predictor of PA, followed by the Ara h 2/peanut IgE ratio.
- Complex molecular profiles and IgE to Ara h 1, 8 were associated with persistent childhood PA.
Conclusions:
- Ara h 6 and Ara h 2 are the primary predictors for diagnosing PA in Mediterranean pediatric patients.
- Ara h 1, Ara h 8, and molecular complexity correlate with PA persistence.
- Component-resolved diagnosis aids in understanding PA in this population.
Background:
Peanut allergy (PA) management was improved by the introduction of molecular allergology, but guidelines for Mediterranean patients are lacking. We aimed at evaluating peanut component-resolved diagnosis as a diagnostic and prognostic tool in children from Southern France.
Methods:
In 181 pediatric patients, PA diagnosis was founded on medical history, skin prick testing, serum-specific IgE to Arachis hypogea extract and components, Pru p 4, and plant carbohydrates, and oral food challenge. Allergen microarray was also performed in 68 of these patients.
Results:
In peanut-allergic children (n = 117), IgE to Ara h 6 were most prevalent (64%), followed by Ara h 2 (63%), Ara h 1 (60%), and Ara h 9 (52%). Ara h 6 was the best predictor of PA. The second best predictor was the ratio of Ara h 2 IgE to peanut IgE (cutoff 0.113). Persistent childhood PA was associated with complex molecular profiles. Comparison of singleplex and microarray results showed poor concordance for Ara h 2 and Ara h 9.
Conclusion:
Ara h 6 and Ara h 2 are the best predictors of PA at diagnosis in Mediterranean pediatric patients. Ara h 1, Ara h 8, and molecular complexity are associated with PA persistence.
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