Validation of a Multiplex Molecular Macroarray for the Determination of Allergen-Specific IgE Sensitizations in Dogs

被引:1
|
作者
Olivry, Thierry [1 ]
Fontao, Ana Mas [2 ]
Aumayr, Martina [3 ]
Ivanovova, Natalia Paulenka [3 ]
Mitterer, Georg [3 ]
Harwanegg, Christian [3 ]
机构
[1] Nextmune AB, Riddargatan 19, SE-114-56 Stockholm, Sweden
[2] Nextmune Spain, Valentin Beato 24, Madrid 28037, Spain
[3] MacroArray Diagnost, Lembockgasse 59, A-1230 Vienna, Austria
关键词
allergen; allergy; atopic dermatitis; dog; IgE; molecular allergology; serodiagnosis; serology; DUST MITE ALLERGEN; ATOPIC-DERMATITIS; ANTI-IGE; ELISA; IDENTIFICATION; IMMUNOTHERAPY; CLONING;
D O I
10.3390/vetsci11100482
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Simple Summary To determine which allergens allergic dogs are sensitive to, veterinarians can use either skin or blood tests with allergen extracts. However, these extracts can be hard to standardize and may not contain important proteins at high enough levels. Using molecular allergens can offer certain benefits. In this paper, we introduce the Pet Allergy Xplorer (PAX), the first serum test designed and validated for dogs using principles of molecular allergology. This test, based on a leading platform for allergic humans, is accurate and reproducible and provides unique advantages compared with traditional extract-based tests.Abstract Detecting IgE sensitizations in the serum of allergic dogs is commonly performed using allergen extracts, but these are difficult to standardize. This article details the development and validation of the Pet Allergy Xplorer (PAX; Nextmune, Stockholm, Sweden), the first multiplex macroarray for the detection of IgE sensitization in dogs using allergen extracts and molecular components; the PAX is derived from the Allergy Xplorer (ALEX2; MacroArray Diagnostics, Vienna, Austria). The selection of allergens, cartridge processing, strategy for identifying and blocking IgE directed against cross-reactive carbohydrate determinants (CCDs), and the method used for determining the positivity threshold are described. The validation of the PAX included evaluations of the specificity of its anti-IgE monoclonal antibody, specificity of IgE binding to target allergens, assay precision, and internal consistency. Additionally, the influence of possible confounding factors, such as sample type, the influence of hemolysis, lipemia, bilirubinemia, and elevated CCD-IgE, was tested. Finally, the sensitization rates of 23,858 European dogs to 145 environmental and Hymenoptera venom allergens were summarized. The PAX is accurate and reproducible and has a unique CCD-detection and blocking strategy; its molecular allergens offer a unique window on allergen cross-reactivity.
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页数:20
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