1. Predicting probability of tolerating discrete amounts of peanut protein in allergic children using epitope‐specific <scp>IgE</scp> antibody profiling
- Author
-
Maria Suprun, Paul Kearney, Clive Hayward, Heather Butler, Robert Getts, Scott H. Sicherer, Paul J. Turner, Dianne E. Campbell, Hugh A. Sampson, and Medical Research Council (MRC)
- Subjects
Adult ,MICROARRAY IMMUNOASSAY ,Allergy ,Adolescent ,Arachis ,Immunology ,OFC ,Epitopes ,Young Adult ,Humans ,Immunology and Allergy ,DIAGNOSTIC-ACCURACY ,Peanut Hypersensitivity ,Child ,DBPCFC ,Probability ,epitope ,Science & Technology ,COMPONENTS ,peanut allergy ,Allergens ,Immunoglobulin E ,CTD ,allergy diagnosis ,1107 Immunology ,Child, Preschool ,IgE ,Life Sciences & Biomedicine - Abstract
Background: IgE-epitope profiling can accurately diagnose clinical peanut allergy. Objective: We sought to determine whether sequential (linear) epitope-specific IgE (ses-IgE) profiling can provide probabilities of tolerating discrete doses of peanut protein in allergic subjects undergoing double-blind, placebo-controlled food challenges utilizing PRACTALL dosing. Methods: 64 ses-IgE antibodies were quantified in blood samples using a bead-based epitope assay. A pair of ses-IgEs that predicts Cumulative Tolerated Dose (CTD) was determined using regression in 75 subjects from the discovery cohort. This epitope-based predictor was validated on 331 subjects from five independent cohorts (ages 4-25 years). Subjects were grouped based on their predicted values and probabilities of reactions at each CTD threshold were calculated. Results: In discovery, an algorithm using two ses-IgE antibodies was correlated with CTDs (rho=0.61, p
- Published
- 2022
- Full Text
- View/download PDF