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基于 IBMP-8.1 和 IBMP-8.4 嵌合抗原的新型侧向流动检测法的开发,用于诊断恰加斯病。

Development of a New Lateral Flow Assay Based on IBMP-8.1 and IBMP-8.4 Chimeric Antigens to Diagnose Chagas Disease.

机构信息

Immunobiological Technology Institute (Fiocruz/RJ), Rio de Janeiro, Brazil.

Gonçalo Moniz Institute (Fiocruz/BA), Salvador, Brazil.

出版信息

Biomed Res Int. 2020 Aug 17;2020:1803515. doi: 10.1155/2020/1803515. eCollection 2020.

Abstract

Despite several available methodologies for Chagas disease (CD) serological screening, the main limitation of chronic CD diagnosis is the lack of effective tools for large-scale screening and point-of-care diagnosis to be used in different CD epidemiological scenarios. Taking into account that developing such a diagnostic tool will significantly improve the ability to identify CD carriers, we aimed at performing a proof-of-concept study (phase I study) to assess the use of these proteins in a point-of-care platform using serum samples from different geographical settings of Brazil and distinct clinical presentations. The diagnostic accuracy study was conducted on a panel of two WHO International Standards (IS) and 14 sera from -positive and 16 from -negative individuals. The results obtained with the test strips were converted to digital images, allowing quantitative comparison expressed as a relative band intensity ratio (RBI). The diagnostic potential and performance were also determined. Regardless of the geographical origin or clinical presentation, all sera with antibodies returned positive both for IBMP-8.1 and IBMP-8.4 chimeric antigens. The area under the ROC curve (AUC) values was 100% for both antigens, demonstrating an outstanding overall diagnostic accuracy (100%). Based on the data, we believe that the lateral flow assays based on these antigens are promising methodologies for screening CD.

摘要

尽管有几种可用的方法可用于恰加斯病(CD)血清学筛查,但慢性 CD 诊断的主要限制是缺乏用于大规模筛查和即时诊断的有效工具,以便在不同的 CD 流行病学情况下使用。考虑到开发这种诊断工具将显著提高识别 CD 携带者的能力,我们旨在进行概念验证研究(I 期研究),以使用来自巴西不同地理环境和不同临床特征的血清样本,在即时检测平台上评估这些蛋白质的使用情况。该诊断准确性研究使用了两个世界卫生组织国际标准(IS)和 14 份阳性血清以及 16 份阴性血清进行。测试条的结果转换为数字图像,允许以相对带强度比(RBI)表示的定量比较。还确定了诊断潜力和性能。无论地理起源或临床特征如何,所有具有 抗体的血清对 IBMP-8.1 和 IBMP-8.4 嵌合抗原均呈阳性反应。两种抗原的 ROC 曲线下面积(AUC)值均为 100%,表明总体诊断准确性非常出色(100%)。基于这些数据,我们相信基于这些抗原的横向流动分析是筛查 CD 的有前途的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9963/7450325/7b6d382c57fc/BMRI2020-1803515.001.jpg

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