Molecular allergen sensitization drives phenotypes of severe asthma in children: Evidence from a megacity cohort (SAMP)
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Updated: Jun 5, 2025

Murine Model of Allergen Induced Asthma
Published on: May 14, 2012
Mélisande Bourgoin-Heck1,2,3, Victoria Wolff-Goldnadel1, Yannick Chantran2,4
1Allergology Department, Hospital A. Trousseau, Sorbonne Université AP-HP, Paris, France.
Insights
Severe childhood asthma is linked to multiple allergies, including to tropomyosin, a new finding. Understanding these allergic sensitization profiles helps identify severe asthma phenotypes in children.
Area of Science:
- Pediatric Allergy and Immunology
- Asthma Research
- Immunology
Background:
- Asthma in children presents diverse sensitization profiles, but their link to specific asthma phenotypes is not fully understood.
- Identifying these profiles is crucial for understanding disease heterogeneity.
Purpose of the Study:
- To investigate and characterize allergenic sensitization profiles in a cohort of children with asthma in a megacity.
- To correlate sensitization patterns with asthma severity and phenotypes.
Main Methods:
- Cross-sectional analysis of 367 children (preschool and school-age) with moderate to severe asthma from the SAMP cohort (2011-2015).
- Utilized ALEX multiplex array for allergen detection and cluster analysis to identify sensitization profiles.
Main Results:
- At preschool age, three clusters emerged: few inhaled allergens/non-T2 inflammation, HDM sensitization, and severe asthma with multiple inhaled/food allergen sensitization.
- At school age, five clusters were identified, including those with HDM, PR-10, tropomyosin, and multiple inhaled/food allergen sensitizations.
Conclusions:
- Significant heterogeneity exists in sensitization profiles among children with severe allergic asthma.
- Severe asthma phenotypes are associated with multiple inhaled and food allergen sensitizations, and notably, with tropomyosin sensitization.
Background:
Several major sensitization profiles have been described in children with asthma, but it remains unclear how these profiles relate to asthma phenotypes. The aim of this study was to determine allergenic sensitization profiles in a megacity cohort (SAMP).
Methods:
This was a cross-sectional analysis performed from 2011 to 2015 including preschool and school-age children with severe and moderate asthma from the SAMP cohort. We performed ALEX multiplex array and carried out cluster analysis.
Results:
Data from 367 children were analyzed: 224 of preschool age and 143 of school age, respectively 84 (38%) and 114 (80%) presented at least one allergic sensitization. At preschool age, three clusters were identified: Cluster 1, Few sensitizations to inhaled allergen molecular families and non-type 2 (T2) inflammation (n = 61); Cluster 2, Predominant sensitization to HDM molecular families (n = 16); Cluster 3, Severe asthma with multiple sensitizations to inhaled and food allergen molecular families (n = 7). At school age, five clusters were identified: Cluster 1, Few sensitizations to inhaled allergen molecular families and non-T2 inflammation (n = 43); Cluster 2, Predominant sensitization to HDM molecular families (n = 31); Cluster 3, Predominant sensitization to PR-10 protein family (n = 25); Cluster 4, Severe asthma with predominant sensitization to tropomyosin family (n = 11); Cluster 5, Severe asthma with multiple sensitizations to inhaled and food allergen molecular families (n = 4).
Conclusion:
These results underline the heterogeneity of sensitization profiles in severe allergic childhood asthma. The most severe asthma phenotypes were associated with multiple sensitizations to both inhaled and food allergen molecular families as expected, and to the tropomyosin molecular family, a novel finding.
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