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基于 Halo 的通用荧光读取仪的威胁病原体检测平台——使用 SARS-CoV-2 检测的概念验证研究。

Halo-A Universal Fluorescence Reader Based Threat Agent Detection Platform-A Proof of Concept Study Using SARS-CoV-2 Assays.

机构信息

C2Sense, Inc., Watertown, MA, United States.

MRIGlobal, Kansas City, MO, United States.

出版信息

Front Public Health. 2022 Apr 12;10:852083. doi: 10.3389/fpubh.2022.852083. eCollection 2022.

DOI:10.3389/fpubh.2022.852083
PMID:35493369
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9039038/
Abstract

Polymerase chain reaction (PCR) remains the gold standard in disease diagnostics due to its extreme sensitivity and specificity. However, PCR tests are expensive and complex, require skilled personnel and specialized equipment to conduct the tests, and have long turnaround times. On the other hand, lateral flow immunoassay-based antigen tests are rapid, relatively inexpensive, and can be performed by untrained personnel at the point of care or even in the home. However, rapid antigen tests are less sensitive than PCR since they lack the inherent target amplification of PCR. It has been argued that rapid antigen tests are better indicators of infection in public health decision-making processes to test, trace, and isolate infected people to curtail further transmission. Hence, there is a critical need to increase the sensitivity of rapid antigen tests and create innovative solutions to achieve that goal. Herein, we report the development of a low-cost diagnostic platform, enabling rapid detection of SARS-CoV-2 under field or at-home conditions. This platform (Halo™) is a small, highly accurate, consumer-friendly diagnostic reader paired with fluorescently labeled lateral flow assays and custom software for collection and reporting of results. The focus of this study is to compare the analytical performance of Halo against comparable tests that use either colloidal gold nanoparticles or fluorescence-based reporters in simulated nasal matrix and not in clinical samples. Live virus data has demonstrated limit of detection performance of 1.9 TCID/test in simulated nasal matrix for the delta variant, suggesting that single-assay detection of asymptomatic SARS-CoV-2 infections may be feasible. Performance of the system against all tested SARS CoV-2 virus variants showed comparable sensitivities indicating mutations in SARS-CoV-2 variants do not negatively impact the assay.

摘要

聚合酶链式反应(PCR)因其极高的灵敏度和特异性仍然是疾病诊断的金标准。然而,PCR 测试昂贵且复杂,需要熟练的人员和专门的设备进行测试,并且周转时间长。另一方面,基于侧向流动免疫测定的抗原测试快速、相对便宜,并且可以由未经训练的人员在护理点甚至家中进行。然而,快速抗原测试的灵敏度不如 PCR,因为它们缺乏 PCR 的固有靶标扩增。有人认为,快速抗原测试在公共卫生决策过程中是更好的感染指标,用于测试、追踪和隔离受感染的人,以遏制进一步的传播。因此,迫切需要提高快速抗原测试的灵敏度,并创造创新的解决方案来实现这一目标。在这里,我们报告了一种低成本诊断平台的开发,该平台能够在现场或家庭条件下快速检测 SARS-CoV-2。该平台(Halo™)是一个小型、高度精确、面向消费者的诊断读取器,与荧光标记的侧向流动测定法和用于收集和报告结果的定制软件配对。本研究的重点是比较 Halo 与使用胶体金纳米粒子或荧光报告器在模拟鼻腔基质中而不是在临床样本中的类似测试的分析性能。活病毒数据表明,在模拟鼻腔基质中,针对 delta 变体的检测限性能为 1.9 TCID/测试,表明可能可以通过单次检测无症状 SARS-CoV-2 感染来实现。该系统对所有测试的 SARS CoV-2 病毒变体的性能表明,敏感性相当,表明 SARS-CoV-2 变体中的突变不会对检测产生负面影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21cb/9039038/1ab5a943a73b/fpubh-10-852083-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21cb/9039038/809050315714/fpubh-10-852083-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21cb/9039038/1ab5a943a73b/fpubh-10-852083-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21cb/9039038/809050315714/fpubh-10-852083-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21cb/9039038/1ab5a943a73b/fpubh-10-852083-g0002.jpg

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