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削减层级——降低特定病原体风险的动机与手段

Trimming tiers - Motivations and means for de-risking select agents.

作者信息

Wells Elizabeth, Grisham Christopher, Parker Michael T

机构信息

Department of Biology, Georgetown University, Washington, DC, United States.

College of Arts & Sciences, Georgetown University, Washington, DC, United States.

出版信息

Front Bioeng Biotechnol. 2025 Jun 27;13:1630609. doi: 10.3389/fbioe.2025.1630609. eCollection 2025.

Abstract

In the United States, pathogens and toxins that pose a significant threat to public health are regulated via the Select Agents and Toxins list (SATL). Of those on the list, biological select agents and toxins (BSAT) deemed especially dangerous are designated "Tier 1", and are subject to more stringent regulations. While general criteria for the addition of BSAT to the SATL have been published, along with criteria for Tier 1 designation, there are no clearly defined, publicly available steps for de-tiering or de-listing BSAT, making it difficult to decipher paths to risk reduction. We set out to better understand how the government has historically chosen to list and tier BSAT, to create a generalized profile of Tier 1 and non-Tier 1 BSAT, and to design a methodology that the government can utilize in efforts of de-risking BSAT. To these ends, we conducted a literature review compiling key information on all BSAT, with a specific focus on development and availability of vaccines and therapeutics, as well as evidence and/or reports of prior weaponization efforts. We then performed statistical analyses to compare Tier 1 BSAT to non-Tier 1 BSAT, allowing us to develop a "prototype" that describes the characteristics that are typical of each. Finally, we used these results to design a set of "priority" experiments and threshold goals for perceived risk criteria, the results of which enable clearer avenues to de-risking, and potentially also de-tiering and de-listing, of BSAT. Our results represent a call to action to bolster biosecurity through the utilization of BSAT prototyping, key experiments, and threshold implementation, all in an effort to enable evidence-based risk reduction of select agents.

摘要

在美国,对公众健康构成重大威胁的病原体和毒素通过《特定生物制剂和毒素清单》(SATL)进行监管。在该清单所列的物质中,被认为特别危险的生物特定制剂和毒素(BSAT)被指定为“1级”,并受到更严格的监管。虽然已公布了将BSAT添加到SATL的一般标准以及1级指定标准,但对于BSAT的降等级或除名,没有明确界定且公开可用的步骤,这使得难以解读降低风险的途径。我们着手更好地了解政府历来如何选择列出和划分BSAT等级,以创建1级和非1级BSAT的通用概况,并设计一种政府可用于降低BSAT风险的方法。为此,我们进行了文献综述,汇编了所有BSAT的关键信息,特别关注疫苗和治疗方法的研发与可用性,以及先前武器化努力的证据和/或报告。然后,我们进行统计分析,将1级BSAT与非1级BSAT进行比较,从而能够开发出一个描述每种类型典型特征的“原型”。最后,我们利用这些结果设计了一组针对感知风险标准的“优先”实验和阈值目标,其结果为降低BSAT风险,以及可能的降等级和除名,开辟了更清晰的途径。我们的结果呼吁采取行动,通过利用BSAT原型设计、关键实验和阈值实施来加强生物安全,所有这些都是为了实现基于证据的特定制剂风险降低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33b0/12246755/7efeff9f1ba7/fbioe-13-1630609-g001.jpg

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