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基于纳米颗粒的生物条形码扩增检测法(BCA)用于灵敏且早期检测1型人类免疫缺陷病毒衣壳(p24)抗原

Nanoparticle-Based biobarcode amplification assay (BCA) for sensitive and early detection of human immunodeficiency type 1 capsid (p24) antigen.

作者信息

Tang Shixing, Zhao Jiangqin, Storhoff James J, Norris Philip J, Little Richard F, Yarchoan Robert, Stramer Susan L, Patno Tim, Domanus Marc, Dhar Arindam, Mirkin Chad A, Hewlett Indira K

机构信息

Lab of Molecular Virology, Center for Biologics Evaluation and Research, Food and Drug Administration, Bethesda, MD 20892, USA.

出版信息

J Acquir Immune Defic Syndr. 2007 Oct 1;46(2):231-7. doi: 10.1097/QAI.0b013e31814a554b.

Abstract

Nanotechnology-based techniques are being widely evaluated in medical testing and could provide a new generation of diagnostic assays due to their high degrees of sensitivity, high specificity, multiplexing capabilities, and ability to operate without enzymes. In this article, we have modified a nanoparticle-based biobarcode amplification (BCA) assay for early and sensitive detection of HIV-1 capsid (p24) antigen by using antip24 antibody-coated microplates to capture viral antigen (p24) and streptavidin-coated nanoparticle-based biobarcode DNAs for signal amplification, followed by detection using a chip-based scanometric method. The modified BCA assay exhibited a linear dose-dependent pattern within the detection range of 0.1 to 500 pg/ml and was approximately 150-fold more sensitive than conventional enzyme-linked immunosorbent assay (ELISA). No false positive results were observed in 30 HIV-1-negative samples, while all 45 HIV-1 RNA positive samples were found HIV-1 p24 antigen positive by the BCA assay. In addition, the BCA assay detected HIV-1 infection 3 days earlier than ELISA in seroconversion samples. Preliminary evaluation based on testing a small number of samples indicates that the HIV-1 p24 antigen BCA may provide a new tool for sensitive and early detection of HIV-1 p24 antigen in settings where HIV-1 RNA testing is currently not routinely performed.

摘要

基于纳米技术的方法正在医学检测中得到广泛评估,由于其具有高度的敏感性、高特异性、多重检测能力以及无需酶即可操作的特性,有望提供新一代诊断检测方法。在本文中,我们改进了一种基于纳米颗粒的生物条形码扩增(BCA)检测方法,用于早期、灵敏地检测HIV-1衣壳(p24)抗原。该方法使用包被抗p24抗体的微孔板捕获病毒抗原(p24),并使用包被链霉亲和素的基于纳米颗粒的生物条形码DNA进行信号放大,随后采用基于芯片的扫描检测法进行检测。改进后的BCA检测方法在0.1至500 pg/ml的检测范围内呈现线性剂量依赖性模式,其灵敏度比传统酶联免疫吸附测定(ELISA)高约150倍。在30份HIV-1阴性样本中未观察到假阳性结果,而BCA检测法发现所有45份HIV-1 RNA阳性样本的HIV-1 p24抗原均为阳性。此外,在血清转化样本中,BCA检测法比ELISA提前3天检测到HIV-1感染。基于少量样本检测的初步评估表明,HIV-1 p24抗原BCA检测法可能为在目前不常规进行HIV-1 RNA检测的环境中灵敏、早期检测HIV-1 p24抗原提供一种新工具。

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