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新型RIDA qLine Allergy多参数免疫印迹法与ImmunoCAP特异性IgE检测法在鉴定临床相关食物和吸入性过敏原过敏方面的比较。

Comparison of the new RIDA qLine Allergy multiparameter immunoblot and the ImmunoCAP Specific IgE test for the identification of clinically relevant food and aeroallergen allergies.

作者信息

Hahn Katharina K, Schuppe Marie C, Hollstein Moritz M, Forkel Susann, Buhl Timo

机构信息

Department of Dermatology, Venereology and Allergology, University Medical Centre Goettingen, Goettingen, Germany.

出版信息

Front Allergy. 2025 Jan 10;5:1496882. doi: 10.3389/falgy.2024.1496882. eCollection 2024.

Abstract

BACKGROUND

Multiparameter immunoblot testing is increasingly used as an alternative to multiple individual IgE analyses for type 1 allergies. This study investigated the performance of an inexpensive immunoblot method, the RIDA qLine allergy test system (R-Biopharm AG), vs. the current gold standard.

METHODS

Three study-specific panels with 57 individual allergens (food and aeroallergens) were analyzed in serum samples from 200 patients with signs and symptoms of IgE-mediated allergies, using both the RIDA qLine Allergy and the reference method, the ImmunoCAP Specific IgE test (Thermo Fisher Scientific). In case of divergent results, corresponding allergens were remeasured using the secondary reference method, the 3gAllergy Specific IgE Universal Kit (Siemens). The clinical diagnoses of the 200 patients were included. In addition, a cross-reactive carbohydrate determinant (CCD)-inhibitor was used in the testing to decrease the incidence of positive CCD bands.

RESULTS

The mean overall agreement of all food and aeroallergens with the reference methods was 94.9%. Qualitative evaluation showed an average negative percent agreement of 98.9% and an average positive percent agreement of 75.1% for all individual allergens after testing with both reference methods. The additional treatment of samples with the CCD inhibitor successfully reduced the occurrence of positive CCD reactivity after retesting.

CONCLUSION

The comparative analysis of RIDA qLine Allergy with the reference methods for specific IgE detection revealed a strong correlation between serum IgE levels measured across these platforms and clinical presentations, while also highlighting the necessity for careful contextual interpretation of results. Standardized allergen extracts would improve independent comparisons of different allergy testing methods.

摘要

背景

多参数免疫印迹检测越来越多地被用作1型过敏多种个体IgE分析的替代方法。本研究调查了一种廉价的免疫印迹方法——RIDA qLine过敏检测系统(R - 生物制药公司)与当前金标准方法的性能。

方法

使用RIDA qLine过敏检测法和参考方法免疫CAP特异性IgE检测法(赛默飞世尔科技公司),对来自200例有IgE介导过敏体征和症状患者的血清样本中的三个含有57种个体过敏原(食物和吸入性过敏原)的特定研究面板进行分析。若结果存在差异,则使用二级参考方法——3gAllergy特异性IgE通用试剂盒(西门子公司)对相应过敏原进行重新检测。纳入了200例患者的临床诊断结果。此外,检测中使用了一种交叉反应性碳水化合物决定簇(CCD)抑制剂以降低阳性CCD条带的发生率。

结果

所有食物和吸入性过敏原与参考方法的总体平均一致性为94.9%。定性评估显示,在两种参考方法检测后,所有个体过敏原的平均阴性百分一致性为98.9%,平均阳性百分一致性为75.1%。用CCD抑制剂对样本进行额外处理成功降低了重新检测后阳性CCD反应性的发生率。

结论

RIDA qLine过敏检测法与特异性IgE检测参考方法的对比分析显示,这些平台检测的血清IgE水平与临床表现之间存在很强的相关性,同时也强调了对结果进行仔细背景解读的必要性。标准化的过敏原提取物将改善不同过敏检测方法的独立比较。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2103/11757282/3f067b5cbf67/falgy-05-1496882-g001.jpg

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