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Basophil Activation Test for Investigation of IgE-Mediated Mechanisms in Drug Hypersensitivity
Published on: September 16, 2011
Basal serum tryptase is not a risk factor for immediate-type drug hypersensitivity during childhood
Ozlem Cavkaytar1, Betul Karaatmaca1, Ebru Arik Yilmaz1
1Department of Pediatric Allergy, Hacettepe University School of Medicine, Ankara, Turkey.
Insights
Serum basal tryptase (sBT) levels are not a risk factor for severe drug hypersensitivity reactions in children. Unlike venom or food allergies, sBT does not predict severe systemic reactions in pediatric drug hypersensitivity.
Area of Science:
- Immunology
- Allergy and Immunology
- Pediatric Allergy
Background:
- High serum basal tryptase (sBT) levels are known risk factors for severe allergic reactions to venom and food.
- The role of sBT in drug hypersensitivity reactions (DHRs), particularly in children, requires further investigation.
Purpose of the Study:
- To compare serum basal tryptase (sBT) levels in children with varying severities of drug hypersensitivity reactions (DHRs).
- To assess if sBT levels correlate with the severity of DHRs in pediatric patients.
Main Methods:
- Included children aged 0-18 years with immediate-type DHRs within 0-6 hours of drug intake.
- Evaluated patients using skin and/or provocation tests to confirm drug hypersensitivity.
- Measured serum basal tryptase (sBT) levels in patients and age-/sex-matched controls.
Main Results:
- No significant difference in sBT levels was observed between drug-hypersensitive children (with or without anaphylaxis) and controls.
- sBT levels did not correlate with the severity of DHRs, including sole cutaneous symptoms, mild anaphylaxis, or moderate-to-severe anaphylaxis.
- Factors such as reaction onset time, skin test results, and age groups did not show a correlation with sBT levels.
Conclusions:
- Serum basal tryptase (sBT) levels are not a risk factor for severe systemic reactions in children with actual drug hypersensitivity.
- This finding contrasts with the established role of sBT in severe reactions to food and insect venom allergies.
Background:
High serum basal tryptase (sBT) levels have been identified as a risk factor for both venom- and food-induced severe allergic reactions. The aim of this study was to compare sBT levels in children with different severity of actual drug hypersensitivity reactions (DHRs) with those of age- and sex-matched controls without any history of DHRs.
Method:
Patients between 0 and 18 years of age with a history of immediate-type DHRs manifested in 0-6 h after the culprit drug intake were included. Following ENDA (European Network for Drug Allergy) inquiries, patients were evaluated with skin and/or provocation tests to define the actual drug-hypersensitive patients. Serum BT levels were determined for both patients and controls.
Results:
Of 345 children, 106 patients (30.7%) [(58.5% male), median age (interquartile range) 8.0 years (4.2-12.2)] were diagnosed as drug hypersensitive. Ninety-eight controls were also included. The sBT levels of drug-hypersensitive patients with and without anaphylaxis and the control group were similar [2.6 (2.0-3.6) μg/l vs. 2.8 (1.6-4.3) μg/l vs. 2.6 (1.8-3.6) μg/l, respectively, (p > 0.05)]. The sBT levels of the patients with sole cutaneous symptoms 2.8 (1.6-4.3) μg/l, mild anaphylaxis 3.0 (1.9-4.9) μg/l, and moderate-to-severe anaphylaxis 2.6 (2.0-3.6) μg/l were also comparable (p > 0.05). The onset of DHRs [those occurring in 1 h (n = 87) or in 1-6 h (n = 19) after the drug intake], positive results with skin tests with the culprit drug, or the classification of the patients according to different age groups [(0-2 years), (2-6 years), (6-12 years), (12-18 years)] did not correlate with sBT levels.
Conclusion:
The sBT levels in children with actual drug hypersensitivity would not be a risk factor for severe systemic reactions on the contrary to children with allergic reactions to food or insect venom.
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