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Published on: April 21, 2019
Molecular sIgE profile in infants and young children with peanut sensitization and eczema
Valérie Trendelenburg1, Alexander Rohrbach1, Gabriele Schulz1
1Department of Pediatric Pneumology and Immunology, Charité-Universitätsmedizin, Berlin, Germany.
Insights
Infants with eczema sensitized to peanut before dietary exposure primarily react to seed storage proteins like Ara h 1 and Ara h 2. This suggests early sensitization patterns in young children, even before peanut consumption.
Area of Science:
- Allergy and Immunology
- Pediatrics
- Molecular Allergology
Background:
- Early peanut sensitization is common in infants, especially those with eczema, often before dietary introduction.
- Limited data exists on specific peanut allergen sensitization profiles in this high-risk group.
- Understanding these profiles is crucial for early diagnosis and management of peanut allergy.
Purpose of the Study:
- To investigate the specific peanut allergen sensitization patterns in infants and young children diagnosed with eczema and peanut sensitization.
- To identify the prevalence of specific immunoglobulin E (sIgE) to different peanut allergens in this cohort.
- To explore the relationship between allergen sensitization and clinical peanut allergy.
Main Methods:
- Analysis of sera from 53 infants (≤ 20 months) with eczema and peanut sensitization, who had no prior peanut consumption.
- Utilized microarray immunoassay (ImmunoCAP ISAC) to detect specific IgE against various peanut allergens.
- Clinical relevance data was assessed for a subset of participants.
Main Results:
- 63% of peanut-sensitized children showed sIgE to at least one peanut allergen.
- Prevalent sensitizations included Ara h 1 (7S globulin, 40%), Ara h 2 (2S albumin, 30%), and Ara h 3 (11S globulin, 23%).
- Sensitization to pollen-related Ara h 8 was rare (1 child). Ara h 2 was absent in 43% of children with confirmed peanut allergy.
Conclusions:
- Infants with eczema and peanut sensitization predominantly recognize peanut seed storage proteins (Ara h 1, Ara h 2, Ara h 3) before dietary exposure.
- Pollen-related allergen sensitization appears uncommon in this age group.
- Both Ara h 1 and Ara h 2 sensitization are potentially linked to clinical relevance in early childhood peanut allergy.
Background:
Many children develop a sensitization to peanut in early infancy, even before peanut is introduced in their diet. Sensitization is particularly common in young children with eczema. There have been scant data available to date on the sensitization pattern for specific peanut allergens in this patient group. The aim of this study was to investigate the allergen profile of infants and young children with peanut sensitization and eczema.
Methods:
Sera from 53 children aged ≤ 20 months with eczema and sensitization to peanut but who had not yet consumed products containing peanuts were included in the analysis. Sera were analyzed using microarray immunoassay (ImmunoCAP ISAC).
Results:
In total, 63 % of peanut-sensitized children showed specific immunoglobulin E (sIgE) against at least one peanut allergen on the microarray. Specific IgE to the 7S globulin Ara h 1 was detected in 40 % of the children, to the 2S albumin Ara h 2 in 30 % and to the 11S globulin Ara h 3 in 23 %. Only one child had sIgE to Arah 8, the homologoue of Bet-v-1. Data on clinical relevance were available for 24 of 53 children: 14 of 24 patients had objective allergic reactions to peanut, while 10 children were peanut-tolerant. The seed storage protein Ara h 2 was not detected on microarray in 43 % (6 of 14) of children with peanut allergy. Two of these six children were mono-sensitized to Ara h 1 and two to Ara h 3, while in three children none of these seed storage proteins was detected.
Discussion:
It could be shown that infants and young children with eczema and sensitization to peanut recognize predominantly seed storage proteins from peanut, even before the introduction of peanut into their diet. Sensitization to pollen-related food allergens seems to be rare at this age. At this age not only Ara h 2, but also Ara h 1 seems to be related to clinical relevance.
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