Screening asthmatics for atopic status using the ALergy EXplorer (ALEX 2 ) macroarray

• Published in: The Journal of asthma Vol. 61; no. 9; p. 1050
• Main Authors: Hamilton, Robert G, Holbreich, Mark, Bronzert, Charles, Anderson, Rebecca L, Schoettler, Nathan, Ober, Carole
• Format: Journal Article
• Language: English
• Published: England 01.09.2024
• Subjects: Adolescent; Allergens - immunology; Animals; Asthma - blood; Asthma - diagnosis; Asthma - immunology; Child; Child, Preschool; Female; Humans; Hypersensitivity, Immediate - diagnosis; Hypersensitivity, Immediate - immunology; Immunoglobulin E - blood; Immunoglobulin E - immunology; Male; Mass Screening - methods; atopy; Phadiatop; macroarray; ALEX2; multiallergen screen; singleplex
• ISSN: 1532-4303
• DOI: 10.1080/02770903.2024.2324839

Screening asthma patients for atopy facilitates management. Since 2010, the core biomarker for screening asthma subjects for atopic status has been the qualitative Phadiatop. multi-aeroallergen screen. A more quantitative macroarray, the Allergy Explorer (ALEX ), shows promise as an alternative. The study's goal was to examine the pros and cons of the use of ALEX in the screening of asthma patients for atopic status. We evaluated the atopic (IgE-sensitization) status in asthmatic Amish and Hutterite farm children using the ImmunoCAP and ALEX assays in Phadiatop equivocal and positive subjects. All 42 asthmatic children were analyzed by Phadiatop and total serum IgE. Of these, 22 had a negative Phadiatop (<0.1 kUa/L) and total IgE <100 kU/L which defined them as non-atopic and they were excluded from ALEX testing. Of six children with equivocal Phadiatops (0.1-0.2 kUa/L-Group 1) and three children with a negative Phadiatop but total IgE >100 kUa/L (group 3), 44% (  = 4) had detectable IgE antibody by ALEX to mite, tree pollen, and other allergens not detected by Phadiatop, but confirmed by allergen-specific ImmunoCAP testing. In 11 Phadiatop positive subjects (>0.2 kUa/L-group 2), all but one were positive by ALEX . IgE antibody specific for mold and rabbit aeroallergens matched their agricultural and pet exposure history. Three children were positive for IgE antibody to allergens in the profilin, nsLTP, or PR-10 cross-reactive protein families. Judicious use of ALEX 's enhanced specificity data not provided by the Phadiatop can aid in the interpretation of sensitization patterns and planning management of atopic asthmatics, but sensitization relevance must be confirmed by the patient's clinical history.