B‐Cell Repertoire of Children With Atopic Dermatitis Exhibits Altered <scp>IgE</scp> Maturation Associated With Allergic Food Sensitization

IgE B cells produce antibodies responsible for the inappropriate specificity seen in allergic disease. In this study, we sequence antibody gene repertoires from a large, well-characterized early life cohort at risk for developing food allergy. We found that food allergen sensitization was associated with lower IgE mutation frequencies that was abrogated in children living with a pet dog, suggesting potential molecular mechanisms underlying the hygiene hypothesis (i.e., protective effects of pet ownership and non-antiseptic environs reported for allergic disease). We also observed increased IgE diversity and increased isotype-switching to IgE, suggesting that B-cell development is altered in those with food allergen sensitizations relative to those without. IgE diversity was even more extreme in subjects who were highly likely to be peanut allergic. Unlike food sensitization, we detected no effect of aeroallergen sensitization on IgE mutation levels and diversity. Consistent patterns of antibody rearrangement were associated with food allergen sensitization. These results have important implications for the allergic response driven by mast cells and basophils and the underlying drivers of the atopic march.

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Publication Details

Journal
Allergy
Published
2025-11-11
DOI
https://doi.org/10.1111/all.70150
Primary Topic
Food Allergy and Anaphylaxis Research
Type
article
Field-Weighted Citation Impact
0.00

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article

B‐Cell Repertoire of Children With Atopic Dermatitis Exhibits Altered IgE Maturation Associated With Allergic Food Sensitization

Mariana L. Stevens, Emily R. Miraldi, Justin T. Schwartz, Gurjit K. Khurana Hershey et al.
Allergy
Food Allergy and Anaphylaxis Research
article

B‐Cell Repertoire of Children With Atopic Dermatitis Exhibits Altered IgE Maturation Associated With Allergic Food Sensitization

Mariana L. Stevens, Emily R. Miraldi, Justin T. Schwartz, Gurjit K. Khurana Hershey, Leah C. Kottyan, John Kroner, Krishna M. Roskin, Lisa Joy Martin, Amal Assa’ad, Samuel J. Virolainen, Kirandeep K. Gill, Ashley L. Devonshire, Jeffrey Burkle, Jocelyn M. Biagini Myers, Onyekachi Nwogu, Sandra Andorf, Carolina Moore, Wan‐Chi Chang, Asel Baatyrbek
article en

Abstract

IgE B cells produce antibodies responsible for the inappropriate specificity seen in allergic disease. In this study, we sequence antibody gene repertoires from a large, well-characterized early life cohort at risk for developing food allergy. We found that food allergen sensitization was associated with lower IgE mutation frequencies that was abrogated in children living with a pet dog, suggesting potential molecular mechanisms underlying the hygiene hypothesis (i.e., protective effects of pet ownership and non-antiseptic environs reported for allergic disease). We also observed increased IgE diversity and increased isotype-switching to IgE, suggesting that B-cell development is altered in those with food allergen sensitizations relative to those without. IgE diversity was even more extreme in subjects who were highly likely to be peanut allergic. Unlike food sensitization, we detected no effect of aeroallergen sensitization on IgE mutation levels and diversity. Consistent patterns of antibody rearrangement were associated with food allergen sensitization. These results have important implications for the allergic response driven by mast cells and basophils and the underlying drivers of the atopic march.

AllergyVol. 81(2)
Cincinnati Children's Hospital Medical Center (US), University of Cincinnati Medical Center (US)
Food Allergy Research and Education, Cincinnati Children's Hospital Medical Center, National Institutes of Health, Banting and Best Diabetes Centre, University of Toronto, National Institute of Allergy and Infectious Diseases, National Institute of Arthritis and Musculoskeletal and Skin Diseases
Openalex Percentile: Top 57%
Food Allergy and Anaphylaxis Research
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