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
Lab of Molecular Virology, Center for Biologics Evaluation and Research, Food and Drug Administration, Bethesda, MD 20892, USA.
J Acquir Immune Defic Syndr. 2007 Oct 1;46(2):231-7. doi: 10.1097/QAI.0b013e31814a554b.
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.
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。