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纯化变应原与完整提取物在悬铃木花粉过敏诊断中的比较

Purified allergens vs. complete extract in the diagnosis of plane tree pollen allergy.

作者信息

Asturias J A, Ibarrola I, Amat P, Tella R, Malet A, Cisteró-Bahíma A, Enrique E, Malek T, Martínez A

机构信息

Bial-Arístegui, R&D Department, Bilbao, Spain.

出版信息

Clin Exp Allergy. 2006 Dec;36(12):1505-12. doi: 10.1111/j.1365-2222.2006.02591.x.

Abstract

BACKGROUND

Plane tree pollen allergy is a clinical disorder affecting human population in cities of Europe, North America, South Africa, and Australia.

OBJECTIVE

To compare IgE-reactivity of the natural and recombinant forms of two major plane allergens, Pla a 1 and Pla a 2, with the reactivity of Platanus acerifolia pollen extract.

METHODS

Forty-seven patients with P. acerifolia allergy, 15 of them monosensitized, and 24 control subjects were included in the study. Natural Pla a 1 and Pla a 2 were purified by standard chromatographic methods and recombinant proteins were expressed in Escherichia coli. Skin prick test and determination of specific IgE were performed with commercial P. acerifolia extract and natural and recombinant purified allergens.

RESULTS

Pla a 1 and Pla a 2 were responsible for 79% of the IgE-binding capacity against P. acerifolia pollen extract. A high correlation has been found between the IgE response to nPla a 1 (R = 0.80; P < 0.001) or nPla a 2 (R = 0.79; P < 0.001) vs. P. acerifolia extract as well as between natural and recombinant Pla a 1 (R = 0.89; P < 0.001). Skin testing showed no significant differences between extract and nPla a 2, whereas a higher reactivity was found with nPla a 1. In contrast, rPla a 1 revealed markedly reduced sensitivity in comparison with extract by skin prick test and specific IgE. The sensitivity of the mix Pla a 1+Pla a 2 was 100% and 87.5% for monosensitized and polysensitized patients, respectively, with no false-positive reactions detected. Conclusion Pla a 1 and Pla 2 are sufficient for a reliable diagnosis of P. acerifolia in most patients and induce comparable skin test reactivity as a whole extract.

摘要

背景

悬铃木花粉过敏是一种影响欧洲、北美、南非和澳大利亚城市人群的临床病症。

目的

比较两种主要悬铃木过敏原天然形式和重组形式的Pla a 1和Pla a 2与二球悬铃木花粉提取物的IgE反应性。

方法

47例二球悬铃木过敏患者(其中15例为单敏患者)和24例对照受试者纳入本研究。天然Pla a 1和Pla a 2通过标准色谱方法纯化,重组蛋白在大肠杆菌中表达。使用市售二球悬铃木提取物以及天然和重组纯化过敏原进行皮肤点刺试验和特异性IgE测定。

结果

Pla a 1和Pla a 2占针对二球悬铃木花粉提取物的IgE结合能力的79%。发现对天然Pla a 1(R = 0.80;P < 0.001)或天然Pla a 2(R = 0.79;P < 0.001)与二球悬铃木提取物的IgE反应之间以及天然和重组Pla a 1之间(R = 0.89;P < 0.001)存在高度相关性。皮肤试验显示提取物与天然Pla a 2之间无显著差异,而天然Pla a 1的反应性更高。相比之下,重组Pla a 1通过皮肤点刺试验和特异性IgE显示与提取物相比敏感性明显降低。Pla a 1 + Pla a 2混合物对单敏和多敏患者的敏感性分别为100%和87.5%,未检测到假阳性反应。结论Pla a 1和Pla 2足以对大多数患者进行可靠的二球悬铃木诊断,并诱导与全提取物相当的皮肤试验反应性。

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