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可扩展的全球卫生解决方案:唾液直接检测模型。

Scalable solutions for global health: the SalivaDirect model.

机构信息

Department of Global, Environmental, and Occupational Health, University of Maryland School of Public Health, College Park, MD, United States.

SalivaDirect, Inc., New Haven, CT, United States.

出版信息

Front Cell Infect Microbiol. 2024 Oct 29;14:1446514. doi: 10.3389/fcimb.2024.1446514. eCollection 2024.

Abstract

The COVID-19 pandemic caught the world unprepared. Large-scale testing efforts were urgently needed, and diagnostic strategies had to rapidly evolve in response to unprecedented worldwide demand. However, the rollout of diagnostic testing and screening for SARS-CoV-2 was often impeded by logistical challenges, including regulatory delays, workforce shortages, laboratory bottlenecks, and supply chain disruptions. Recognizing these hurdles early on, we developed a testing approach that supported frequent, repeat testing, particularly as communities reopened. We hypothesized and experimentally demonstrated that saliva was a suitable specimen for the detection of SARS-CoV-2. This finding was advanced into the development of open-source, extraction-free reverse transcription polymerase chain reaction protocols using readily available, "off-the-shelf" reagents and equipment for the direct detection of SARS-CoV-2 in saliva ("SalivaDirect''). Working with the US Food and Drug Administration (FDA), we established a novel regulatory framework wherein the FDA granted Emergency Use Authorization to Yale University to offer the SalivaDirect test protocol to high-complexity diagnostic laboratories (as designated by the Clinical Laboratory Improvement Amendments) with quality oversight provided by Yale. This grew into a network of more than 200 labs across the United States that, as of May 2024, resulted in over 6.5 million SARS-CoV-2 tests. By making the protocol flexible and open-source, laboratories were able to rapidly and economically scale testing using a simple, self-collected saliva specimen. Additionally, fostering a national network of laboratories enabled real-time exchanges, problem solving, and the development of community best practices. Preparing for the next pandemic, or simply the next seasonal epidemic, the SalivaDirect model of deploying a readily available, expandable solution and accompanying network provides a proven method for the successful implementation of pathogen testing in the United States and globally.

摘要

COVID-19 大流行让全世界猝不及防。急需开展大规模检测工作,诊断策略必须迅速发展以应对全球前所未有的需求。然而,SARS-CoV-2 的诊断检测和筛查的推出常常受到后勤挑战的阻碍,包括监管延迟、劳动力短缺、实验室瓶颈和供应链中断。我们很早就认识到这些障碍,开发了一种支持频繁、重复检测的测试方法,特别是在社区重新开放时。我们假设并通过实验证明唾液是检测 SARS-CoV-2 的合适标本。这一发现推动了开源、无提取逆转录聚合酶链反应协议的开发,使用现成的、“现成的”试剂和设备直接从唾液中检测 SARS-CoV-2(“SalivaDirect'’)。我们与美国食品和药物管理局 (FDA) 合作,建立了一个新的监管框架,FDA 授予耶鲁大学紧急使用授权,允许耶鲁大学将 SalivaDirect 测试协议提供给高复杂度诊断实验室(由临床实验室改进修正案指定),并由耶鲁大学提供质量监督。这发展成为一个由美国 200 多个实验室组成的网络,截至 2024 年 5 月,该网络进行了超过 650 万次 SARS-CoV-2 检测。通过使协议具有灵活性和开源性,实验室能够使用简单的、自我采集的唾液样本快速、经济地扩大检测规模。此外,建立一个全国性的实验室网络可以实现实时交流、问题解决和社区最佳实践的发展。为应对下一次大流行,或者仅仅是下一次季节性流行,部署现成、可扩展解决方案和配套网络的 SalivaDirect 模式为在美国和全球成功实施病原体检测提供了一种经过验证的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/762e/11554656/03622d9612f9/fcimb-14-1446514-g001.jpg

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