Correlation of serum allergy (IgE) tests performed by different assay systems

• Published in: Journal of allergy and clinical immunology 2008-05, Vol.121 (5), p.1219-1224
• Main Authors: Wang, Julie, MD, Godbold, James H., PhD, Sampson, Hugh A., MD
• Format: Article
• Language: English
• Subjects: Adolescent; Allergens; Allergic diseases; Allergies; Allergy and Immunology; Arachis hypogaea; Biological and medical sciences; Child; Child, Preschool; Dermatophagoides farinae; Digestive allergic diseases; Food; Food allergies; food allergy; Fundamental and applied biological sciences. Psychology; Fundamental immunology; Humans; Hypersensitivity - blood; Hypersensitivity - diagnosis; IgE; Immulite; ImmunCAP; Immunoassay - methods; Immunoglobulin E - blood; Immunopathology; Laboratories; Medical sciences; Patients; Regression analysis; Reproducibility of Results; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis; Sensitivity and Specificity; Turbo-MP
• ISSN: 0091-6749; 1097-6825
• DOI: 10.1016/j.jaci.2007.12.1150

Background In vitro testing is commonly used to diagnose and manage allergies. Clinical reactivity has been correlated with food-specific IgE levels by using the ImmunoCAP (Phadia, Uppsala, Sweden). Objective To determine whether IgE levels derived from different assays are equivalent to those measured by ImmunoCAP. Methods Fifty patients from the Mount Sinai Pediatric Allergy practice were prospectively enrolled. For each deidentified sample, specific IgE levels were measured to egg, milk, peanut, cat, birch, and Dermatophagoides farinae at different laboratories, each using a different assay system (Phadia ImmunoCAP, Agilent Turbo-MP, and Siemens Immulite 2000). Results were analyzed to determine whether IgE measurements were equivalent. Food allergen–specific IgE levels were correlated with clinical data and around empirically determined thresholds that predict probability of clinical disease in 50% or 95% of subjects. Results Variable degrees of agreement existed among the 3 assays. Immulite 2000 overestimated all specific IgE levels compared with ImmunoCAP. Turbo-MP overestimated for egg but underestimated for birch and D farinae . Differences for milk, peanut, and cat were observed, without a trend toward overestimation or underestimation. Furthermore, several values for the food allergens were discrepant around the 50% and 95% positive predictive values for clinical reactivity. Conclusion Discrepancies in specific IgE values from 3 different assays can potentially lead to altered management and treatment. The predictive values for clinical reactivity associated with food-specific IgE levels determined by ImmunoCAP should not be applied to results from other assays.