克服病毒感染快速检测的局限性:利用当地现有资源开发 SARS-Cov-2 侧流检测试剂盒

Biosensors Pub Date : 2024-08-27 DOI:10.3390/bios14090416
Estefanía S. Peri Ibáñez, Agostina Mazzeo, Carolina Silva, Maria Juliana Juncos, Guadalupe S. Costa Navarro, Horacio M. Pallarés, Virginia J. Wolos, Gabriel L. Fiszman, Silvia L. Mundo, Julio J. Caramelo, Marcelo J. Yanovsky, Matías Fingermann, Alejandro A. Castello, Andrea V. Gamarnik, Ana S. Peinetti, Daiana A. Capdevila
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引用次数: 0

摘要

COVID-19 大流行凸显了发展中国家检测工作的不公平。缺乏侧流试验(LFT)生产能力是中低收入地区应对 COVID-19 的主要瓶颈。在此,我们报告了用于检测 SARS-CoV-2 的开放式侧流试验的开发情况,该试验与商业试验相当,只需当地供应。主要的关键资源是当地开发的马多克隆抗体(pAb),通过亲和纯化,这种抗体的灵敏度和选择性大大提高。我们证明,这些抗体的性能与商业单克隆抗体(mAbs)以及针对相同抗原开发的 mAbs 和其他 pAbs 相似。我们报告了使用鼻咽拭子进行 RT-qPCR 的测试优化工作流程,其中添加了灭活病毒,以确定检测限等分析性能特征。我们的最终原型显示出与现有测试类似的性能(与 RT-qPCR 相比灵敏度为 83.3%,与商业抗原测试相比灵敏度为 90.9%)。最后,我们讨论了利用亲和纯化 pAbs 作为疫情爆发情况下当地开发抗原检测的替代方法以及作为解决快速检测不平等问题的工具的可能性和挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Overcoming Limited Access to Virus Infection Rapid Testing: Development of a Lateral Flow Test for SARS-Cov-2 with Locally Available Resources
The COVID-19 pandemic highlighted testing inequities in developing countries. Lack of lateral flow test (LFT) manufacturing capacity was a major COVID-19 response bottleneck in low- and middle-income regions. Here we report the development of an open-access LFT for SARS-CoV-2 detection comparable to commercial tests that requires only locally available supplies. The main critical resource is a locally developed horse polyclonal antibody (pAb) whose sensitivity and selectivity are greatly enhanced by affinity purification. We demonstrate that these Abs can perform similarly to commercial monoclonal antibodies (mAbs), as well as mAbs and other pAbs developed against the same antigen. We report a workflow for test optimization using nasopharyngeal swabs collected for RT-qPCR, spiked with the inactivated virus to determine analytical performance characteristics as the limit of detection, among others. Our final prototype showed a performance similar to available tests (sensitivity of 83.3% compared to RT-qPCR, and 90.9% compared to commercial antigen tests). Finally, we discuss the possibility and the challenges of utilizing affinity-purified pAbs as an alternative for the local development of antigen tests in an outbreak context and as a tool to address inequalities in access to rapid tests.
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