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基于成分的猕猴桃过敏原微阵列在猕猴桃过敏诊断中的性能。

The performance of a component-based allergen microarray for the diagnosis of kiwifruit allergy.

机构信息

Department of Pathophysiology and Allergy Research, Medical University of Vienna, Vienna, Austria.

出版信息

Clin Exp Allergy. 2011 Jan;41(1):129-36. doi: 10.1111/j.1365-2222.2010.03619.x. Epub 2010 Nov 17.

Abstract

BACKGROUND

Allergy to kiwifruit is increasingly reported across Europe. Currently, the reliability of its diagnosis by the measurement of allergen-specific IgE with extracts or by skin testing with fresh fruits is unsatisfying.

OBJECTIVE

To evaluate the usefulness of a component-based allergen microarray for the diagnosis of kiwifruit allergy in a large group of patients.

METHODS

With an allergen microarray, we measured specific IgE and IgG4 levels to a panel of nine kiwifruit allergens in sera of 237 individuals with kiwifruit allergy. Sera from 198 allergic patients without kiwifruit allergy served as controls. Furthermore, we determined the extent of sensitization to latex.

RESULTS

The panel of kiwifruit allergens showed a diagnostic sensitivity of 66%, a specificity of 56% and a positive predictive value of 73%. Sera from kiwifruit-allergic patients contained significantly more frequently Act d 1-specific IgE than sera from control patients. Furthermore, 51% of the positive sera contained IgE directed to a single allergen, namely Act d 1 (45%), Act d 9 (27%) or Act d 7 (13%). Within the control group, 36% sera recognized a single allergen. Out of those, 48% were positive to the cross-reactive glycoallergen Act d 7, 43% to the profilin Act d 9 and only 5% to Act d 1. Allergen-specific IgG4 levels did not differ between kiwifruit-allergic and -tolerant patients. Kiwifruit- and latex-allergic patients contained Hev b 11-specific IgE significantly more frequently than latex-allergic patients without kiwifruit allergy.

CONCLUSIONS

Act d 1 can be considered a marker allergen for genuine sensitization to kiwifruit. We demonstrated that a component-based kiwifruit allergen microarray would improve the prognostic value of in vitro diagnostic tests.

摘要

背景

猕猴桃过敏在整个欧洲的报道越来越多。目前,通过提取的过敏原特异性 IgE 测量或通过新鲜水果进行皮肤测试来诊断猕猴桃过敏的可靠性并不令人满意。

目的

评估基于成分的过敏原微阵列在一大组患者中诊断猕猴桃过敏的有用性。

方法

使用过敏原微阵列,我们测量了 237 名猕猴桃过敏患者血清中 9 种猕猴桃过敏原的特异性 IgE 和 IgG4 水平。198 名无猕猴桃过敏的过敏患者的血清作为对照。此外,我们还确定了乳胶致敏的程度。

结果

猕猴桃过敏原组显示诊断敏感性为 66%,特异性为 56%,阳性预测值为 73%。与对照患者相比,猕猴桃过敏患者的血清中含有更多的 Act d 1 特异性 IgE。此外,51%的阳性血清含有针对单一过敏原的 IgE,即 Act d 1(45%)、Act d 9(27%)或 Act d 7(13%)。在对照组中,36%的血清识别出单一过敏原。其中,48%对交叉反应性糖蛋白过敏原 Act d 7 呈阳性,43%对丝状蛋白 Act d 9 呈阳性,只有 5%对 Act d 1 呈阳性。猕猴桃过敏和耐受患者的过敏原特异性 IgG4 水平与过敏患者之间没有差异。猕猴桃和乳胶过敏患者比没有猕猴桃过敏的乳胶过敏患者更频繁地含有 Hev b 11 特异性 IgE。

结论

Act d 1 可以被认为是真正对猕猴桃过敏的标志物过敏原。我们证明了基于成分的猕猴桃过敏原微阵列将提高体外诊断测试的预后价值。

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