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Evaluation of a novel automated allergy microarray platform compared with three other allergy test methods
P Williams1, A Önell2, F Baldracchini2
1Department of Immunology, University Hospital of Wales, Cardiff.
Clinical and Experimental Immunology
|October 7, 2015
Summary
Microarray allergy tests offer a powerful way to measure specific immunoglobulin (Ig)E profiles. This study found the automated Microtest system comparable to established methods like skin prick tests (SPT) and ImmunoCAP.
Area of Science:
- Immunology
- Allergy Diagnostics
- Medical Technology
Background:
- Microarray platforms allow simultaneous measurement of multiple allergens from small serum samples, showing promise for allergy diagnostics.
- Current allergy diagnostics include skin prick tests (SPT), ImmunoCAP, and manual microarray platforms like Immuno-Solid phase Allergen Chip (ISAC).
Purpose of the Study:
- To compare the diagnostic performance of a fully automated microarray system (Microtest) against a manual microarray (ISAC) and established singleplex tests (SPT, ImmunoCAP).
- To evaluate the agreement between different allergy testing methods in a cohort of adult allergic patients.
Main Methods:
- A comparative study involving 103 adult allergic patients.
- All patients underwent testing with four methods: SPT, ImmunoCAP, Microtest, and ISAC 112.
- Analysis of 3485 pairwise test results to assess agreement and correlation coefficients for common allergens and components.
Main Results:
- All four methods demonstrated comparable results, with a positive/negative agreement ranging from 81% to 88%.
- High agreement (correlation coefficients 0.73–0.95) was observed between methods for prevalent allergens and their components.
- The automated Microtest system showed results consistent with established diagnostic tests.
Conclusions:
- Microarray platforms are efficient and valuable tools for characterizing specific immunoglobulin (Ig)E profiles in allergic patients using minimal serum.
- The Microtest automated system aligns with current diagnostic standards.
- Further validation is recommended across diverse populations, regions, and allergen panels.

