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美国针对使用具有更高大流行潜力病原体的研究的治理政策演变

The Evolution of United States Governance Policies for Research Using Pathogens with Enhanced Pandemic Potential.

作者信息

Epstein Gerald L

机构信息

RAND Corporation, Arlington, Virginia, USA.

出版信息

Appl Biosaf. 2025 Jun 5;30(2):79-96. doi: 10.1089/apb.2024.0049. eCollection 2025 Jun.

DOI:10.1089/apb.2024.0049
PMID:40548091
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12179363/
Abstract

BACKGROUND

Prompted by publications in 2012 involving the enhancement of a highly virulent but poorly transmissible human pathogen to make it more transmissible, the research community and the U.S. government have implemented policies to oversee research involving enhanced pathogens that pose the risk of causing a pandemic.

METHOD

This article reviews the evolution of policies governing high consequence, government-funded research that has been called "gain-of-function-research-of-concern," research with "enhanced potential pandemic pathogens" (ePPPs), and research with "pathogens with enhanced pandemic potential" (PEPPs). It analyzes features that these policies share and points out some of their shortcomings, challenges, and ambiguities.

RESULTS

These policies, culminating in the 2024 United States Government Policy for Oversight of Dual-Use Research of Concern and Pathogens with Enhanced Pandemic Potential, all define a set of consequential research activities that trigger the need for additional high-level review, and they all set out principles that must be satisfied before the research can be funded.

CONCLUSION

The 2024 policy, like its predecessors, only applies to government-funded research. Extending it to cover privately funded research would require either new regulations under existing statutory authority or new legislation. Like its predecessors, the 2024 policy requires that the benefits of PEPP research justify its potential pandemic risk. Unlike its predecessors, however, the 2024 policy is missing an important principle that prevents construction of a pandemic pathogen that-were it not for its creation in the proposed research-would have little likelihood of ever causing an actual pandemic.

摘要

背景

2012年有出版物报道了对一种高致病性但传播性差的人类病原体进行增强使其更具传播性,受此推动,研究界和美国政府已实施政策来监督涉及可能引发大流行风险的增强病原体的研究。

方法

本文回顾了管理高风险、政府资助研究的政策演变,这些研究被称为“具有潜在风险的功能获得性研究”、“具有增强大流行潜力病原体”(ePPP)的研究以及“具有增强大流行潜力的病原体”(PEPP)的研究。分析了这些政策的共同特征,并指出了它们的一些缺点、挑战和模糊之处。

结果

这些政策最终形成了《2024年美国政府对两用关注研究和具有增强大流行潜力病原体的监督政策》,所有政策都定义了一系列引发额外高级别审查需求的重要研究活动,并且都规定了在研究能够获得资助之前必须满足的原则。

结论

2024年政策与其前身一样,仅适用于政府资助的研究。将其扩展到涵盖私人资助的研究需要依据现有法定权限制定新法规或出台新立法。与前身一样,2024年政策要求PEPP研究的益处能够证明其潜在的大流行风险是合理的。然而,与前身不同的是,2024年政策缺少一项重要原则,该原则可防止构建一种大流行病原体——若不是在拟议研究中创造出来——几乎不可能引发实际大流行。