Clinical & Experimental Allergy · 2005 · 77 citations · 33 references
Life SciencesFood ScienceImmunologyAllergyFood ChemistryHypersensitivityAllergic DiseaseFood AllergensFood AllergyIge-mediated AllergyPeanut AllergyPollen AllergyAllergen Component DiagnosticsAllergen Component TestingDiagnostic Test ProceduresEscherichia ColiImmunoassays For Food AllergensMolecular Basis Of AllergenicityPollen Allergen CharacterizationPollen Allergens
BACKGROUND: In Europe, pollen-related food allergy is the most frequent form of food allergy in adults. Reliability of current diagnostic procedures, however, is poor and therapeutic options are not available. OBJECTIVES: In the present study, we created a panel of recombinant allergens from carrot and evaluated its potential in component-resolved in vitro diagnosis of carrot allergy. METHODS: Recombinant (r) Dau c 1.0104, Dau c 1.0201 and Dau c 4 were cloned by a polymerase chain reaction strategy, expressed in Escherichia coli and purified. Carrot lipid transfer protein (LTP) was expressed in the yeast Pichia pastoris. Sera from 40 carrot-allergic patients were investigated. Twenty-one birch pollen-allergic subjects with negative open provocation to carrot and 20 non-allergic subjects were included as controls. IgE binding to recombinant allergens as well as to cross-reactive carbohydrate determinants (CCD) was measured by ELISA. Cross-reactivity between Dau c 1 isoforms and Bet v 1 was assayed by ELISA inhibition. Biological activity of the recombinant carrot allergens was assessed by histamine release assay and peripheral blood mononuclear cells stimulation. RESULTS: Ninety-eight percent of the carrot-allergic patients were positive to at least one recombinant allergen; 98% reacted to rDau c 1.0104, 65% to rDau c 1.0201, 38% to rDau c 4 and 20% had IgE against CCD. Specificity using the recombinant allergens was high when compared with non-allergic controls, but low compared with birch-sensitized subjects without carrot allergy. Sensitization to Dau c 1.0201, however, proved to be highly specific for clinically relevant sensitization. Inhibition assays indicated the absence of LTP in carrot root extract, and epitope diversity between Dau c 1.0104, Dau c 1.0201 and Bet v 1. CONCLUSIONS: Our panel of recombinant allergens from carrot can provide a standardized tool for in vitro diagnosis of carrot allergy, and for epitope studies.
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Long-Term Clinical Efficacy of Grass-Pollen Immunotherapy
Stephen R. Durham, Samantha Walker, Eva‐Maria Varga et al. · New England Journal of Medicine · 1999 · 1.4K citations · Full text
Cell-specific expression of the carrot EP2 lipid transfer protein gene.
Peter Sterk, H. Booij, G A Schellekens et al. · The Plant Cell · 1991 · 498 citations · Full text
Allergy to Apple, Carrot and Potato in Children with Birch Pollen Allergy
Sten Dreborg, Tony Foucard · Allergy · 1983 · 428 citations