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首页> 外文期刊>The Journal of investigative dermatology. >Component-resolved diagnosis (CRD) of type I allergy with recombinant grass and tree pollen allergens by skin testing.
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Component-resolved diagnosis (CRD) of type I allergy with recombinant grass and tree pollen allergens by skin testing.

机译:通过皮肤测试对重组草和花粉过敏原进行I型过敏的成分分辨诊断(CRD)。

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摘要

The diagnosis of Type I allergy is based on the measurement of allergen-specific IgE antibodies and on provocation with allergens, most frequently conducted by skin testing. Both forms of diagnosis are currently performed with allergen extracts that are difficult to standardize regarding their allergen contents, and which contain additional undefined nonallergenic components. We report the expression in Escherichia coli and purification of some of the most relevant timothy grass- and birch pollen allergens. Recombinant timothy grass- (rPhl p 1, rPhl p 2, rPhl p 5) and birch pollen (rBet v 1, rBet v 2) allergens were purified and used for the measurement of allergen-specific IgE and IgG subclass responses as well as for skin prick testing in 55 pollen allergic patients and 10 nonatopic individuals. Results obtained showed that the recombinant allergens allowed in vivo allergy diagnosis in 52 of 54 of the grass pollen and in 35 of 36 of the birch pollen allergic patients. Positive skin reactions were observed almost exclusively in patients containing detectable allergen-specific IgE antibodies but not in the nonatopic group; however, sensitivity to a given allergen as measured by skin reactivity was weakly correlated with the levels of allergen-specific IgE. Our results demonstrate that recombinant allergens can be used for component-resolved skin test diagnosis (CRD) of the patients' allergen sensitization profile, whereas allergen extracts at best allow to identify allergen-containing sources. CRD may thus represent the basis for novel forms of patient-tailored immunotherapy.
机译:I型过敏的诊断是基于对过敏原特异性IgE抗体的测量以及对过敏原的激发(通常是通过皮肤测试进行的)。目前,两种诊断方法都是使用变应原提取物进行的,这些变应原的变应原含量很难标准化,并且包含其他未定义的非变应原成分。我们报告在大肠杆菌中的表达和一些最相关的提摩西草和桦树花粉过敏原的纯化。纯化了重组提摩西草(rPhl p 1,rPhl p 2,rPhl p 5)和桦树花粉(rBet v 1,rBet v 2)过敏原,并将其用于测量过敏原特异性IgE和IgG亚类,以及用于对55名花粉过敏患者和10名非特应性个体进行皮肤点刺测试。获得的结果表明,重组变应原允许对54名草粉花粉中的52名患者和36名桦树花粉过敏性患者中的35名进行体内过敏诊断。几乎只在含有可检测到的过敏原特异性IgE抗体的患者中观察到阳性皮肤反应,而在非特应性人群中则未观察到。然而,通过皮肤反应性对给定过敏原的敏感性与过敏原特异性IgE的水平弱相关。我们的结果表明,重组变应原可用于患者变应原致敏特性的成分分辨皮肤测试诊断(CRD),而变应原提取物充其量只能确定含变应原的来源。因此,CRD可能代表了针对患者量身定制的新型免疫疗法的基础。

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