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Cor a 14:榛子过敏分子诊断中的缺失环节?

Cor a 14: missing link in the molecular diagnosis of hazelnut allergy?

作者信息

Faber Margaretha A, De Graag Maaike, Van Der Heijden Catherina, Sabato Vito, Hagendorens Margo M, Bridts Chris H, De Clerck Luc S, Ebo Didier G

机构信息

Department of Immunology-Allergology-Rheumatology, Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.

出版信息

Int Arch Allergy Immunol. 2014;164(3):200-6. doi: 10.1159/000365050. Epub 2014 Jul 15.

Abstract

BACKGROUND

Hazelnut allergy shows distinct clinical patterns that can be predicted through component-resolved diagnosis. However, identification of sensitization profiles remains incomplete.

METHODS

Sera of 75 patients allergic to hazelnuts, 14 infants with atopic dermatitis (AD) sensitized to hazelnuts, 15 hazelnut-tolerant individuals with specific IgE (sIgE) to hazelnuts and 15 healthy control individuals were tested for sIgE reactivity to rCor a 1.04, rCor a 8, nCor a 9, nCor a 11, rCor a 14, rBet v 1, rBet v 2 and cross-reactive carbohydrate determinants (CCDs).

RESULTS

Sensitization to Cor a 14 was observed in 18 out of 20 preschool children, 8 out of 10 school-aged children and 2 out of 7 adults with generalized reactions and in 3 out of 14 infants with AD. Only 2 out of 38 patients with an oral allergy syndrome (OAS) were sensitized to Cor a 14. No sensitization to Cor a 14 was observed in the group of hazelnut-tolerant and healthy control individuals. Sensitization to Cor a 1.04 was seen in 36 out of 38 OAS patients and in 14 out of 37 patients with generalized reactions. However, only 3 patients with generalized reactions were monosensitized to Cor a 1.04. Sensitization to Cor a 9 was observed in 26 out of 37 patients with generalized reactions and in 4 out of 14 infants with AD. Sensitization to Cor a 11, Cor a 8, rBet v 2 and CCDs was rare.

CONCLUSIONS

Sensitization to Cor a 14 can have early onset and shows age-related variations. Together with Cor a 9, Cor a 14 enables us to correctly identify almost 90% of children with generalized reactions to hazelnut.

摘要

背景

榛子过敏表现出不同的临床模式,可通过组分分辨诊断进行预测。然而,致敏谱的识别仍不完整。

方法

检测了75例对榛子过敏的患者、14例对榛子致敏的特应性皮炎(AD)婴儿、15例对榛子有特异性IgE(sIgE)的榛子耐受个体以及15例健康对照个体的血清对rCor a 1.04、rCor a 8、nCor a 9、nCor a 11、rCor a 14、rBet v 1、rBet v 2和交叉反应性碳水化合物决定簇(CCD)的sIgE反应性。

结果

在20名学龄前儿童中有18名、10名学龄儿童中有8名、7名有全身性反应的成人中有2名以及14名AD婴儿中有3名对Cor a 14致敏。在38例口腔过敏综合征(OAS)患者中只有2名对Cor a 14致敏。在榛子耐受组和健康对照组中未观察到对Cor a 14的致敏。在38例OAS患者中有36名以及37例有全身性反应的患者中有14名对Cor a 1.04致敏。然而,只有3例有全身性反应的患者对Cor a 1.04单致敏。在37例有全身性反应的患者中有26名以及14名AD婴儿中有4名对Cor a 9致敏。对Cor a 11、Cor a 8、rBet v 2和CCD的致敏很少见。

结论

对Cor a 14的致敏可早发并表现出与年龄相关的差异。与Cor a 9一起,Cor a 14使我们能够正确识别近90%对榛子有全身性反应的儿童。

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