Diagnostic Value of Antigen-Specific Immunoglobulin E Immunoassays against Ara h 2 and Ara h 8 Peanut Components in Child Food Allergy

被引:36
作者
Martinet, Jeremie [1 ,3 ,4 ]
Couderc, Laure [2 ,5 ]
Renosi, Florian [1 ]
Bobee, Victor [1 ]
Marguet, Christophe [2 ,5 ]
Boyer, Olivier [1 ,3 ,4 ]
机构
[1] Rouen Univ Hosp, Dept Immunol, Rouen, France
[2] Rouen Univ Hosp, Dept Pediat Pneumol & Allergy, Rouen, France
[3] Normandy Univ, IRIB, Rouen, France
[4] INSERM, U905, Rouen, France
[5] INSERM, CIC 1014, Rouen, France
关键词
Peanut allergy; Pediatric allergy; Ara h 2; Ara h 8; Diagnostic tests; Food allergy; RESOLVED DIAGNOSTICS; CLINICAL IMMUNOLOGY; EUROPEAN ACADEMY; SKIN PRICK; IGE; PREVALENCE; IDENTIFICATION; ANAPHYLAXIS; CHALLENGES; HYPERSENSITIVITY;
D O I
10.1159/000446181
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Peanut allergy is one of the most severe food allergies in children. The diagnostic gold standard is the oral food challenge (OFC). However, OFC has inherent risks and is time consuming. The measurement of specific immunoglobulin E (sIgE) to peanut components in blood detects peanut sensitization, but the decision point predicting allergy is still unclear. The aim of this study was to determine the diagnostic value of these tests for the evaluation of child peanut allergy. Methods : In this retrospective study, 81 children were referred for peanut allergy. The diagnosis of peanut allergy was based on the clinical context and a positive OFC. Levels of sIgE against whole peanuts or peanut components (Ara h 2 and Ara h 8) were determined by immunoassay. Results: The Ara h 2 sIgE assay has the best negative predictive value (0.93) and positive predictive value (1) at a cutoff of 0.1 kU/l. Ara h 2 sIgE titers can predict the risk of anaphylaxis (<0.44 kU/l, low risk; >14 kU/l, high risk). The Ara h 8 sIgE assay is not able to discriminate peanut-allergic patients but can be used to evaluate possible cross-reactions to birch pollen with a low risk of anaphylaxis. The best diagnostic strategy is to first determine the Ara h 2 sIgE level and, if negative, evaluate Ara h 8 sIgE. Conclusions: We propose an algorithm for a better use of peanut component sIgE immunoassays that should improve their diagnostic value and avoid unnecessary OFC. (C) 2016 S. Karger AG, Basel
引用
收藏
页码:216 / 222
页数:7
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