In vitro and in vivo allergenicity of recombinant Bet v 1 compared to the reactivity of natural birch pollen extract

Clin Exp Allergy. 2003 Aug;33(8):1153-8. doi: 10.1046/j.1365-2222.2003.01717.x.

Abstract

Background: Diagnostic procedures using natural extracts show only limited quantitative correlation between in vivo and in vitro results. Highly pure recombinant allergens might show more predictive findings.

Objective: The aim of this study was to compare natural birch pollen extract (BPE) and recombinant Betula verrucosa (rBet v 1) for their diagnostic value comparing skin prick tests (SPTS) and nasal provocation tests (NPTS) with specific IgE in the serum.

Methods: Thirty-four patients allergic to birch pollen and five healthy controls were investigated. SPT and NPT were performed with BPE and rBet v 1 at different concentrations. Specific serum IgE was measured by the Pharmacia CAP system.

Results: Commercial BPE and rBet v 1 (10 micro g/mL) were able to elicit similar allergenic reactions in vivo and IgE binding in vitro. SPT reflects immediate-type allergy as determined by NPT to a higher degree than specific IgE, for both reagents. To cause allergic reactions in NPT, higher amounts of rBet v 1 were needed than for skin tests and the sensitivity was lower than with BPE.

Conclusion: rBet v 1 alone is sufficient for a reliable diagnosis of birch pollen allergy in most patients and induces comparable skin test reactivity as BPE, but less allergic reactions in nasal provocations.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Allergens* / immunology
  • Antigens, Plant
  • Betula / immunology
  • Female
  • Humans
  • Immunoglobulin E / biosynthesis
  • Male
  • Nasal Provocation Tests / methods
  • Plant Extracts / immunology
  • Pollen / immunology*
  • Recombinant Proteins / immunology
  • Rhinitis, Allergic, Seasonal / diagnosis*
  • Skin Tests / methods

Substances

  • Allergens
  • Antigens, Plant
  • Plant Extracts
  • Recombinant Proteins
  • Immunoglobulin E