榛子皮点刺试验提取物的体内外特性研究。

Jaap H Akkerdaas, Marjolein Wensing, André C Knulst, Rob C Aalberse, Susan L Hefle, Ronald van Ree
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引用次数: 0

摘要

理由:榛子过敏是最常见的食物过敏之一。临床症状范围从口腔过敏综合征到危及生命的过敏反应。榛子过敏的诊断部分依赖于皮肤点刺试验(SPT)的体内试验。本研究的目的是在体外和体内对榛子SPT提取物进行表征。方法:研究榛子SPT提取物的蛋白质含量和组成。采用竞争性免疫印迹法和免疫印迹法检测榛子主要变应原Cor a1、脂质转移蛋白(LTP)和thumatin - likeprotein (TLP)。在一组榛子过敏患者(n = 30)中,分析SPT提取物(n = 6)的皮肤反应性,测定SPT提取物蛋白浓度与平均皮肤反应性(HEIC)的相关性。对于一种SPT提取物,测定了Cor a 1单致敏患者(n = 5)的阈值水平。结果:蛋白质浓度范围为0.2- 14mg /ml。尽管在大多数提取物中存在一些蛋白质(10、22-28、32和48 kDa左右的条带),但在组成上观察到明显的差异(包括内部和内部变异)。主要榛子过敏原Cor 1的浓度差异高达50倍(0.6-32微克/毫升)。在3/9 SPT提取物中几乎不存在LTP,通过免疫印迹检测到不同数量的TLP。部分患者(6/30)使用3/6 SPT提取物时SPT假阴性。蛋白浓度与平均HEIC有明显的相关性(RPearson = 0.87)。根据其中一种产品的评估,Cor a1的阈值水平为+/- 3.2 ng/ml。结论:不同蛋白质浓度/组成的SPT提取物导致不同的皮肤试验反应。缺乏潜在的严重过敏原如LTP可能导致假阴性的SPT结果,危及患者的安全。从这些结果可以看出,SPT产品的标准化是非常必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In vitro and in vivo characterization of hazelnut skin prick test extracts.

Rationale: Hazelnut allergy ranks among the most frequently observed food allergies. Clinical symptoms range from the oral allergy syndrome to life threatening anaphylaxis. Diagnosis of hazelnut allergy partially relies on in vivo testing by means of skin prick testing (SPT). The aim of this study was to characterize hazelnut SPT extracts both in vitro and in vivo.

Methods: Hazelnut SPT extracts were investigated for protein concentration and composition. The major hazelnut allergen Cor a 1, lipid transfer protein (LTP) and thaumatin-like-protein (TLP) were monitored by competitive RIA and immunoblotting. SPT extracts (n = 6) were analyzed for skin reactivity and the correlation between the SPT extract protein concentration and the mean skin reactivity (HEIC) was determined in a group of hazelnut-allergic patients (n = 30). For one SPT extract, the threshold level for Cor a 1 was determined in Cor a 1-monosensitized patients (n = 5).

Results: Protein concentrations ranged from 0.2-14 mg/ml. Although some proteins were present in most extracts (bands at 10, 22-28, 32 and around 48 kDa), clear differences in composition were observed (both intra- and inter-variability). The concentration of the major hazelnut allergen Cor a 1 differed up to a factor 50 (0.6-32 micrograms/ml). LTP was virtually absent in 3/9 SPT extracts and variable quantities of TLP were detected by immunoblotting. Some patients (6/30) had a false-negative SPT with 3/6 SPT extracts. There was a clear correlation between the protein concentration and the mean HEIC (RPearson = 0.87). The threshold level for Cor a 1 was +/- 3.2 ng/ml as assessed with one of the products investigated.

Conclusions: Heterogeneous protein concentration/composition of SPT extracts results in variable skin test responses. The absence of potentially severe allergens like LTP may lead to false-negative SPT results that jeopardize a patient's safety. From these results it can be concluded that there is a strong need for standardization of products for SPT.

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