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过敏原微阵列用于体外过敏诊断:与 ImmunoCAP 和 AdvanSure 的比较。

Allergen Microarrays for In Vitro Diagnostics of Allergies: Comparison with ImmunoCAP and AdvanSure.

机构信息

Department of Biomedical Engineering (BK21 Plus), Dongguk University, Seoul, Korea.

Department of Otolaryngology, Gil Medical Center, Gachon University, Incheon, Korea.

出版信息

Ann Lab Med. 2018 Jul;38(4):338-347. doi: 10.3343/alm.2018.38.4.338.

Abstract

BACKGROUND

In vitro detection of the allergen-specific IgE antibody (sIgE) is a useful tool for the diagnosis and treatment of allergies. Although multiple simultaneous allergen tests offer simple and low-cost screening methods, these platforms also have limitations with respect to multiplexibility and analytical performance. As an alternative assay platform, we developed and validated a microarray using allergen extracts that we termed "GOLD" chip.

METHODS

Serum samples of 150 allergic rhinitis patients were used in the study, and the diagnostic performance of the microarray was compared with that of AdvanSure (LG Life Sciences, Daejun, Korea) and ImmunoCAP (Phadia, Uppsala, Sweden). Standard IgE samples were used for the quantitative measurement of sIgEs.

RESULTS

The microarray-based assay showed excellent performance in the quantitative measurement of sIgEs, demonstrating a linear correlation within the range of sIgE concentrations tested. The limit of detection (LOD) was lower than 0.35 IU/mL, which is the current standard for the LOD cut-off. The assay also provided highly reproducible sets of data. The total agreement percentage of positive and negative calls was 92.2% compared with ImmunoCAP. Moreover, an outstanding correlation was observed between the microarray and the ImmunoCAP results, with Cohen's kappa and Pearson correlation coefficient values of 0.80 and 0.79, respectively.

CONCLUSIONS

The microarray-based in vitro diagnostic platform offers a sensitive, reproducible, and highly quantitative method to detect sIgEs. The results showed strong correlations with that of ImmunoCAP. These results suggest that the new allergen microarray can serve as a useful alternative to current screening platforms, ultimately becoming a first-line screening method.

摘要

背景

体外检测过敏原特异性 IgE 抗体(sIgE)是诊断和治疗过敏的有用工具。尽管多个同时进行的过敏原测试提供了简单且低成本的筛选方法,但这些平台在多重性和分析性能方面也存在局限性。作为替代检测平台,我们开发并验证了一种使用过敏原提取物的微阵列,我们称之为“GOLD”芯片。

方法

本研究使用了 150 例过敏性鼻炎患者的血清样本,并将微阵列的诊断性能与 AdvanSure(LG Life Sciences,大邱,韩国)和 ImmunoCAP(Phadia,乌普萨拉,瑞典)进行了比较。标准 IgE 样本用于 sIgE 的定量测量。

结果

基于微阵列的检测方法在 sIgE 的定量测量中表现出优异的性能,在测试的 sIgE 浓度范围内显示出线性相关性。检测限(LOD)低于 0.35 IU/mL,这是当前 LOD 截止值的标准。该检测方法还提供了高度可重复的数据。与 ImmunoCAP 相比,阳性和阴性检测的总一致率为 92.2%。此外,微阵列与 ImmunoCAP 结果之间观察到极好的相关性,Cohen's kappa 和 Pearson 相关系数值分别为 0.80 和 0.79。

结论

基于微阵列的体外诊断平台提供了一种敏感、可重复和高度定量的方法来检测 sIgE。结果与 ImmunoCAP 具有很强的相关性。这些结果表明,新的过敏原微阵列可以作为当前筛选平台的有用替代方案,最终成为一线筛选方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43f0/5895863/65265628f23a/alm-38-338-g001.jpg

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