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用于快速检测HIV-1 p24抗原的纳米机械系统。

Nanomechanical systems for the rapid detection of HIV-1 p24 antigen.

作者信息

Samuel Angel Green, Cornish Daphne, Simons Lacy M, Agarwal Dilip, Shekhawat Gajendra S, Hultquist Judd F, Dravid Vinayak P

机构信息

Department of Material Science and Engineering and NUANCE Center, Northwestern University, Evanston, IL, 60208, USA.

Department of Medicine, Division of Infectious Diseases, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA; Center for Pathogen Genomics and Microbial Evolution, Robert J. Havey Institute for Global Health, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA.

出版信息

Biosens Bioelectron. 2025 Jul 15;280:117395. doi: 10.1016/j.bios.2025.117395. Epub 2025 Mar 22.

Abstract

Early detection of HIV is crucial for reducing transmission and ensuring timely initiation of antiretroviral therapy (ART), significantly improving patient outcomes. Although diagnostic tests have advanced from first-generation antibody detection assays to fourth-generation immunoassays that detect both HIV antibodies and the p24 antigen, these are limited to clinical labs. Their longer processing times, high costs, and the requirement for multiple patient visits highlight the need for rapid, affordable point-of-care (POC) diagnostics. This study introduces a nanomechanical cantilever-based biosensor for the rapid detection of HIV-1 p24 antigen, a key marker for early diagnosis. The platform demonstrated remarkable sensitivity, detecting p24 at concentrations as low as 100 fg/mL in solution and 1 pg/mL in human serum, and was quantitative within several orders of magnitude. After functionalizing the microcantilevers with two broadly cross-reactive monoclonal antibodies (ANT-152 and C65690M), the system was able to detect p24 from a wide range of HIV-1 subtypes. Furthermore, this biosensor was found to be compatible with various blood processing methods and with a direct electronic output. This platform's high sensitivity, specificity, and applicability across multiple HIV subtypes underscores its potential for future development into a next-generation POC diagnostic tool.

摘要

早期检测HIV对于减少传播和确保及时开始抗逆转录病毒疗法(ART)至关重要,这能显著改善患者的治疗效果。尽管诊断测试已从第一代抗体检测试验发展到可同时检测HIV抗体和p24抗原的第四代免疫测定法,但这些方法仅限于临床实验室。它们处理时间长、成本高且需要患者多次就诊,这凸显了对快速、经济的即时检测(POC)诊断方法的需求。本研究介绍了一种基于纳米机械悬臂的生物传感器,用于快速检测HIV-1 p24抗原,这是早期诊断的关键标志物。该平台表现出卓越的灵敏度,能在溶液中检测低至100 fg/mL、在人血清中检测低至1 pg/mL的p24抗原,并且在几个数量级范围内具有定量能力。在用两种广泛交叉反应的单克隆抗体(ANT-152和C65690M)对微悬臂进行功能化后,该系统能够检测多种HIV-1亚型的p24抗原。此外,发现这种生物传感器与各种血液处理方法兼容,并具有直接的电子输出。该平台的高灵敏度、特异性以及对多种HIV亚型的适用性,突出了其未来发展成为下一代POC诊断工具的潜力。

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