ISAC测定花生成分:与ImmunoCap比较及其在花生过敏儿童中的临床意义。

Q2 Medicine
H K Brand, M W J Schreurs, J A M Emons, R Gerth van Wijk, H de Groot, N J T Arends
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引用次数: 4

摘要

背景:针对花生成分arachhis hypogaea (Ara h) 2的特异性IgE (sIgE)已被证明是区分花生过敏和花生耐受的最重要的过敏原。几项研究确定了Ara h2的sIgE截止值,由单路测量确定。然而,多路复用数组的截断值定义得不太好。本研究的目的是评估单路与多路测量测定的Ara h 2 sIgE之间的相关性,并评估免疫固相过敏原芯片(ISAC)多路分析中包含的不同花生成分对疑似花生过敏儿童的诊断价值。方法:回顾性分析117例疑似花生过敏儿童的单路荧光酶免疫分析法(FEIA, ImmunoCap)和多路微阵列(ISAC)测定的Ara h 2 sIgE值。同时对ISAC测定的花生其他成分进行了分析。双盲安慰剂对照口服食物挑战作为金标准。结果:在所有花生成分中,FEIA Ara h2 sIgE曲线下面积最大(AUC为0.922),其次是ISAC Ara h2和Ara h2 sIgE, AUC分别为0.906和0.902。FEIA Ara h 2 sIgE诊断花生过敏的最佳截断值为4.40 kU/l, ISAC芯片对Ara h 2和Ara h 6 sIgE的最佳截断值分别为7.43 ISU和8.13 ISU。FEIA与ISAC测定的Ara h2 sIgE呈良好的相关性(r = 0.88;结论:arah6和arah2 sIgE在多重ISAC中均能很好地预测荷兰儿童的临床花生过敏,其表现与arah2在单一FEIA中的表现相当。使用ISAC同时测量不同花生成分是一种优势,对于检测Ara h2阴性但对其他花生蛋白(如Ara h6)敏感的花生过敏儿童具有临床意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Peanut components measured by ISAC: comparison with ImmunoCap and clinical relevance in peanut allergic children.

Peanut components measured by ISAC: comparison with ImmunoCap and clinical relevance in peanut allergic children.

Peanut components measured by ISAC: comparison with ImmunoCap and clinical relevance in peanut allergic children.

Background: Specific IgE (sIgE) against the peanut component Arachis hypogaea (Ara h) 2 has been shown to be the most important allergen to discriminate between peanut allergy and peanut tolerance. Several studies determined sIgE cut off values for Ara h 2, determined by singleplex measurements. However, cut off values for Ara h 2 from multiplex arrays are less well defined. The aim of this study was to evaluate the correlation between Ara h 2 sIgE determined by singleplex versus multiplex measurements and to assess the diagnostic value of the different peanut components included in Immuno Solid-phase Allergen Chip (ISAC) multiplex analysis in children with a suspected peanut allergy.

Methods: In this retrospective study we analyzed Ara h 2 sIgE values with singleplex Fluorescence Enzyme Immunoassay (FEIA, ImmunoCap) and multiplex microarray (ISAC) measurements in 117 children with a suspected peanut allergy. Also, other peanut components measured by ISAC were analyzed. Double blinded placebo controlled oral food challenges were used as golden standard.

Results: Among all studied peanut components FEIA Ara h 2 sIgE showed the highest area under the curve (AUC, 0.922), followed by ISAC Ara h 6 and Ara h 2 sIgE with AUCs of respectively 0.906 and 0.902. Best cut off values to diagnose peanut allergy were 4.40 kU/l for FEIA Ara h 2 sIgE and, 7.43 ISU and 8.13 ISU for respectively Ara h 2 and Ara h 6 sIgE in ISAC microarray. Ara h 2 sIgE determined in FEIA and ISAC showed a good correlation (r = 0.88; p < 0.01).

Conclusion: Ara h 6 and Ara h 2 sIgE in multiplex ISAC are both good predictors of clinical peanut allergy in Dutch children, and their performance is comparable to the use of Ara h 2 in singleplex FEIA. The simultaneous measurement of different peanut components using ISAC is an advantage and clinically useful to detect peanut allergic children that are Ara h 2 negative but sensitized to other peanut proteins such as Ara h 6.

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来源期刊
Clinical and Molecular Allergy
Clinical and Molecular Allergy Medicine-Immunology and Allergy
CiteScore
8.20
自引率
0.00%
发文量
11
审稿时长
13 weeks
期刊介绍: Clinical and Molecular Allergy is an open access, peer-reviewed, online journal that publishes research on human allergic and immunodeficient disease (immune deficiency not related to HIV infection/AIDS). The scope of the journal encompasses all aspects of the clinical, genetic, molecular and inflammatory aspects of allergic-respiratory (Type 1 hypersensitivity) and non-AIDS immunodeficiency disorders. However, studies of allergic/hypersensitive aspects of HIV infection/AIDS or drug desensitization protocols in AIDS are acceptable. At the basic science level, this includes original work and reviews on the genetic and molecular mechanisms underlying the inflammatory response.
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