The Journal of Allergy and Clinical Immunology
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

  • Annebeth E. Flinterman, MD

      Affiliations

    • Department of Dermatology/Allergology, University Medical Centre Utrecht, Utrecht, The Netherlands
  • ,
  • Edward F. Knol, PhD

      Affiliations

    • Department of Dermatology/Allergology, University Medical Centre Utrecht, Utrecht, The Netherlands
    • Corresponding Author InformationReprint requests: Edward F. Knol, PhD, University Medical Centre, G02.124, PO Box 85500, 3508 GA Utrecht, The Netherlands.
  • ,
  • Doerthe A. Lencer, MD

      Affiliations

    • Department of Pediatrics, Division of Allergy and Immunology, and the Immunology Institute, Mount Sinai School of Medicine, New York, NY
  • ,
  • Ludmilla Bardina, MS

      Affiliations

    • Department of Pediatrics, Division of Allergy and Immunology, and the Immunology Institute, Mount Sinai School of Medicine, New York, NY
  • ,
  • Constance F. den Hartog Jager, BSc

      Affiliations

    • Department of Dermatology/Allergology, University Medical Centre Utrecht, Utrecht, The Netherlands
  • ,
  • Jing Lin, PhD

      Affiliations

    • Department of Pediatrics, Division of Allergy and Immunology, and the Immunology Institute, Mount Sinai School of Medicine, New York, NY
  • ,
  • Suzanne G.M.A. Pasmans, MD, PhD

      Affiliations

    • Department of Dermatology/Allergology, University Medical Centre Utrecht, Utrecht, The Netherlands
  • ,
  • Carla A.F.M. Bruijnzeel-Koomen, MD, PhD

      Affiliations

    • Department of Dermatology/Allergology, University Medical Centre Utrecht, Utrecht, The Netherlands
  • ,
  • Hugh A. Sampson, MD

      Affiliations

    • Department of Pediatrics, Division of Allergy and Immunology, and the Immunology Institute, Mount Sinai School of Medicine, New York, NY
  • ,
  • Els van Hoffen, PhD

      Affiliations

    • Department of Dermatology/Allergology, University Medical Centre Utrecht, Utrecht, The Netherlands
  • ,
  • Wayne G. Shreffler, MD, PhD

      Affiliations

    • Department of Pediatrics, Division of Allergy and Immunology, and the Immunology Institute, Mount Sinai School of Medicine, New York, NY

Received 15 July 2007; received in revised form 27 November 2007; accepted 28 November 2007. published online 31 January 2008.

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

The Journal of Allergy and Clinical Immunology
Volume 121, Issue 3 , Pages 737-743.e10, March 2008