About this trial
The goal of this observational study is to evaluate the role of IgE proteoforms in healthy volunteers and in patients with type I allergy, patients with chronic spontaneous urticaria, patients with a recent history of anaphylaxis, patients with mastocytosis, patients with hereditary alpha tryptasemia, patients with X-linked agammaglobulinemia (XLA), and patients undergoing desensitization for venom or medication allergy.
Eligibility criteria
Qualifiers
CSU and type I allergic diseases (including anaphylaxis and desensitization), atopic dermatitis, mastocytosis, XLA and HaT (informed consent, age: any available adult subject, gender: any available subject, clinical phenotype and specific information about the allergy (e.g. severity, medication, medical history, laboratory testing)
Healthy controls (informed consent, age matched to the allergic patients, gender matched to the allergic patients, patient-reported symptoms related to allergy to aeroallergens, food, drugs, hymenoptera venom, CSU)
Disqualifiers
Absence of informed consent
Age < 18 years old
Trial design
Treatments tested in this trial
- Blood sample collection
Treatment groups
9
Treatment groupsSee each treatment group below.
Sponsors and collaborators
KU Leuven
Lead sponsor
Universitaire Ziekenhuizen KU Leuven
Sponsor institution