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Updated: Oct 25, 2026

Basophil Activation Test for Allergy Diagnosis
Published on: May 31, 2021
Development and Early Evaluation of a Streamlined, Miniaturized and Multi-Allergen Basophil Activation Test Platform
Megan Ullrich1, Alexander Grishin2, Jarad Beers3
1Division of Allergy & Immunology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Background:
While the basophil activation test (BAT) holds increasing potential in food allergy diagnosis, major challenges impede its widespread use in clinical settings.
Objective:
To assess the feasibility and provide proof-of-concept for a newly developed 96-well plate-based, streamlined, miniaturized and multi-allergen basophil activation test (SMMABAT), using dry, room temperature-stable, ready-to-use reagents. This objective was pursued through a pilot study implemented across three US food allergy clinical centers.
Methods:
Whole blood samples from 81 participants (1-36 years of age) were tested with prototypes that assessed 87 conditions with <2 mL blood. In addition to negative and positive controls, samples were tested against 11 foods at 7 concentrations and 7 individual components at 1000 ng/mL.
Results:
891 dose responses were generated. Significant correlations (p<0.0001) were observed between SMMABAT reactivities and allergic (n=245) or tolerant (n=465) clinical statuses. Across 11 allergens (including nuts, tree nuts, milk and egg), most informative doses (1-1000 ng/mL) yielded 97% specificity (1 ng/mL) and 82% sensitivity (1000 ng/mL). For a subset of 322 clinical statuses with available IgE levels, specific IgE (sIgEs) to raw extracts exhibited 97.1% sensitivity but 39.7% specificity. By combining SMMABAT and sIgEs with optimized thresholds, a significant complementarity was demonstrated, yielding 98% sensitivity, 85.3% specificity, 90.6% PPV, and 96.7% NPV. Allergic patients undergoing oral immunotherapy (OIT) exhibited significantly lower SMMABAT reactivities (p<0.0001) than untreated allergic patients, despite similar sIgE levels.
Conclusion:
SMMABAT can be implemented in clinical research to complement sIgE. It can thus contribute to enhanced management of allergic patients, especially those at risk of multi-food allergies.

