Biochemical and immunological analysis of mould skin prick test solution: current status of standardization. Issue 11 (24th October 2013)

• Record Type: Journal Article
• Authors: Kespohl, S.; Maryska, S.; Zahradnik, E.; Sander, I.; Brüning, T.; Raulf‐Heimsoth, M.
• Is Part Of: Clinical & experimental allergy. Volume 43:Issue 11(2013:Nov.)
• Page Start: 1286
• Page End: 1296
• Publication Date: 2013-10-24
• Subjects: allergy -- allergen content -- mould allergen extracts -- skin prick test -- standardization; Allergy -- Periodicals; Immunology -- Periodicals; 616.97
• DOI: 10.1111/cea.12186
• Languages: English
• ISSNs: 0954-7894

Abstract

Summary: Background: Sensitization prevalence to moulds reached from less than 10% in the general population to more than 25% in atopic and/or asthmatic subjects. To diagnose IgE‐mediated mould sensitization, skin prick test (SPT) and specific IgE (sIgE) measurement are recommended. However, concordance of SPT and sIgE results is often less than 50% and standardization of the extracts is required to achieve reliable test results. Objective: The aim of our study was to analyse mould SPT solutions (SPTs) with respect to quantity and quality of protein, antigen and human IgE‐binding content as a prerequisite for further in vivo studies. Methods: Commercial SPTs of Alternaria alternata, Aspergillus fumigatus, Cladosporium herbarum and Penicillium chrysogenum from six manufacturers as well as two in‐house extracts from Aspergillus versicolor were investigated. Protein‐, antigen‐ and IgE‐binding contents were quantified by Bradford assay, sandwich ELISA and IgE‐ImmunoCAP‐inhibition tests. Protein composition and IgE and IgG binding were analysed by SDS‐PAGE and immunoblotting, respectively. Results: Median protein concentrations were similar in all mould SPT extracts (90–110 μg/mL). In contrast, antigen contents and IgE‐binding capacity showed a high variability with median antigen values from 4 to 118 μg/mL and IgE inhibition results between 30 to 95%. Whereas almost all SPTs of A. alternata and A. versicolor showed complete sIgE inhibition with mean values > 80%, only three extracts for A. fumi gatus, two extracts for C. herbarum and none of the tested extracts for P. chrysogenum exceeded 50% sIgE reduction. Quantitative amounts of protein, antigenic and IgE‐binding structures were not comparable with the quality of the corresponding protein or immunoblot pattern, with the exception of A. alternata SPTs. Conclusions and Clinical Relevance: Commercially available mould SPT extracts showed high variability raising the question of comparability and reliability of SPT results. Possible consequences for diagnostic test outcome will be investigated in the next step.