Volume 121, Issue 3 , Pages 737-743.e10, March 2008
Peanut epitopes for IgE and IgG4 in peanut-sensitized children in relation to severity of peanut allergy
Background
Better understanding of the relationship between antibody response to peanut and clinical sensitivity might lead to more accurate prognostication.
Objective
We sought to investigate peanut-specific IgE and IgG4 epitope diversity in relation to challenge-defined clinical sensitivity to peanut in a group of peanut-sensitized children.
Methods
Clinical sensitivity was determined by means of double-blind, placebo-controlled peanut challenges in 24 sensitized children. Six atopic control subjects were included. Specific IgE and IgG4 binding to 419 overlapping 15-amino-acid peptides representing the sequence of recombinant Ara h 1, Ara h 2, and Ara h3 was analyzed by means of microarray immunoassay.
Results
Peanut-sensitized patient sera bound significantly more IgE and IgG4 epitopes than control sera. This patient group reacted to the same Ara h 1, Ara h 2, and Ara h 3 epitopes as reported previously. There was a positive correlation between IgE epitope diversity (ie, number of epitopes recognized) and clinical sensitivity (r = 0.6), such that patients with the greatest epitope diversity were significantly more sensitive than those with the lowest diversity (P = .021). No specific epitopes were associated with severe reactions to peanut. IgG4 binding was observed to largely similar epitopes but was less pronounced than IgE binding and did not relate to the clinical sensitivity to peanut. IgE and IgG4 epitope-recognition patterns were largely stable over a 20-month period.
Conclusion
Clinical sensitivity, as determined by means of double-blind, placebo-controlled peanut challenge, is positively related to a more polyclonal IgE response, which remains stable over time.
Key words: Peanut allergy, children, peptides, IgE, IgG4, severity of allergic reactions, diversity
Abbreviations used: DBPCFC, Double-blind, placebo-controlled food challenge, ED, Eliciting dose, HSA, Human serum albumin, MIA, Microarray immunoassay, PBS-T, PBS containing 0.5% Tween 20, SNR, Signal-to-noise ratio
Supported in part by a research grant obtained from the Wilhelmina Children's Research Foundation, The Netherlands. W.G.S. was supported by NIH K12HD052890 and the Pediatric Research NIH-LRP.
Disclosure of potential conflict of interest: L. Bardina has received research support from the National Institutes of Health and the Food Allergy Research Initiative. H. A. Sampson has consulting arrangements with and owns stock in Allertein. The rest of the authors have declared that they have no conflict of interest.
PII: S0091-6749(07)03579-8
doi:10.1016/j.jaci.2007.11.039
© 2008 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.
Volume 121, Issue 3 , Pages 737-743.e10, March 2008
