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The ethics of biosafety considerations in gain-of-function research resulting in the creation of potential pandemic pathogens

机译:功能获得研究中的生物安全伦理考虑因素导致了潜在的大流行病原体的产生

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This paper proposes an ethical framework for evaluating biosafety risks of gain-of-function (GOF) experiments that create novel strains of influenza expected to be virulent and transmissible in humans, so-called potential pandemic pathogens (PPPs). Such research raises ethical concerns because of the risk that accidental release from a laboratory could lead to extensive or even global spread of a virulent pathogen. Biomedical research ethics has focused largely on human subjects research, while biosafety concerns about accidental infections, seen largely as a problem of occupational health, have been ignored. GOF/PPP research is an example of a small but important class of research where biosafety risks threaten public health, well beyond the small number of persons conducting the research. We argue that bioethical principles that ordinarily apply only to human subjects research should also apply to research that threatens public health, even if, as in GOF/PPP studies, the research involves no human subjects. Specifically we highlight the Nuremberg Code's requirements of fruitful results for the good of society, unprocurable by other methods', and proportionality of risk and humanitarian benefit, as broad ethical principles that recur in later documents on research ethics and should also apply to certain types of research not involving human subjects. We address several potential objections to this view, and conclude with recommendations for bringing these ethical considerations into policy development.
机译:本文提出了一个伦理框架,用于评估功能获得(GOF)实验的生物安全风险,该实验可创造出新型流感毒株,这些毒株有望在人类体内产生强毒和传染性,即所谓的潜在大流行病原体(PPPs)。此类研究引起了伦理上的关注,因为存在从实验室意外释放可能导致有毒病原体广泛传播甚至全球传播的风险。生物医学研究伦理学主要集中在人体研究上,而对意外感染的生物安全问题(主要被视为职业健康问题)却被忽略了。 GOF / PPP研究只是一小部分但很重要的研究的例子,其中生物安全风险威胁着公共健康,远远超出了少数从事研究的人员。我们认为,通常仅适用于人体研究的生物伦理原则也应适用于威胁公共卫生的研究,即使像GOF / PPP研究中那样,该研究不涉及人体研究。具体而言,我们强调《纽伦堡守则》要求取得有益成果,以造福社会,不能通过其他方法进行采购,以及风险和人道主义收益的比例性,因为广泛的道德原则在以后有关研究伦理的文件中都有提及,并且也应适用于某些类型的不涉及人类受试者的研究。我们针对该观点提出了一些潜在的反对意见,并提出了将这些道德考量纳入政策制定的建议。

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