Evidence of an affinity threshold for IgE-allergen binding in the percutaneous skin test reaction

Authors

  • L. K. Pierson-Mullany,

    1. The Asthma and Allergy Program, University of Minnesota Medical School, Minneapolis, Minnesota, USA
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  • D. R. Jackola,

    Corresponding author
    1. The Asthma and Allergy Program, University of Minnesota Medical School, Minneapolis, Minnesota, USA
      D. R. Jackola, The Asthma and Allergy Center, Department of Medicine, University of Minnesota Medical School, Mayo Mail Code 434, 420 Delaware Street SE, Minneapolis, MN 55455, USA. E-mail: jacko001@tc.umn.edu
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  • M. N. Blumenthal,

    1. The Asthma and Allergy Program, University of Minnesota Medical School, Minneapolis, Minnesota, USA
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  • A. Rosenberg

    1. The Asthma and Allergy Program, University of Minnesota Medical School, Minneapolis, Minnesota, USA
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D. R. Jackola, The Asthma and Allergy Center, Department of Medicine, University of Minnesota Medical School, Mayo Mail Code 434, 420 Delaware Street SE, Minneapolis, MN 55455, USA. E-mail: jacko001@tc.umn.edu

Abstract

Background Atopy is an aberrant immune response involving allergen-specific IgE production, though serum IgE concentration is not an entirely reliable diagnostic tool, particularly for epidemiological and genetic studies. There is no clear correlation between IgE and other indicators of atopy such as skin prick tests (SPT)s, and physiological associations are difficult to justify in cases with detectable IgE but negative SPT results.

Objective IgE reflects the number of molecules available to produce an atopic response, but the degree of the response is determined by the binding strength (affinity) between receptor-bound IgE and the allergen. We sought to determine if there was an association between binding affinity and SPT results in people with histories of atopy.

Methods Standard SPTs (whole allergen extracts) were administered to people with histories of sensitivities to ragweed and house dust mite. The concentrations and affinities of serum allergen-specific IgEs were determined using the purified allergens Amb a 1 and Der p 1.

Results There was a positive correlation between weal area and allergen-specific IgE among SPT-positive donors. However, for those individuals with detectable amounts of allergen-specific IgE, there was considerable overlap of IgE values between SPT-positive and -negative groups. Among sensitized donors, IgE–allergen interactions were characterized by two or three specific reactions of very high affinity (KA range 108−1011 M). Negative SPT reactions were associated with lowered IgE binding affinities to major allergens. This delimited two groups with atopic disorders: specific IgE(+)/SPT(+) and specific IgE(+)/SPT().

Conclusion The product of antibody affinity and concentration, which we define as antibody capacity (CAP = KA × IgE), is more informative with regard to describing allergen sensitivity than antibody concentration alone. Antibody binding capacity provides physiological evidence of atopy in some subjects who do not test positively by common methods and suggests an affinity threshold to produce a positive SPT reaction.

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