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丑闻之后重新审视人类 germline 编辑的伦理问题。

Reexamining the Ethics of Human Germline Editing in the Wake of Scandal.

机构信息

Biomedical Ethics Research Program, Mayo Clinic, Rochester, MN; Center for Individualized Medicine, Mayo Clinic, Rochester, MN; Division of Health Care Policy and Research, Mayo Clinic, Rochester, MN.

Biomedical Ethics Research Program, Mayo Clinic, Rochester, MN; Division of Health Care Policy and Research, Mayo Clinic, Rochester, MN; Department of Obstetrics and Gynecology, Mayo Clinic, Rochester, MN.

出版信息

Mayo Clin Proc. 2020 Feb;95(2):330-338. doi: 10.1016/j.mayocp.2019.11.018.

Abstract

In November 2018, the announcement that genetically edited human embryos had been used for reproductive purposes caused international uproar; many observers argued that editing the human germline was unethical, particularly given the early stage of the science and the absence of appropriate oversight. We provide an overview of the implications of these events, focusing on the relevant ethical considerations for physicians addressing patient questions and concerns. The editing of the human germline for reproductive purposes should be understood against an historic backdrop of clinical research in assisted reproduction, as well as other exemplars of translational investigation. An important question raised by our growing capacity to genetically alter human embryos is how to understand the implicit social contract between science and society. To ensure that translational research continues to enjoy the historic trust placed in scientists and research organizations, it is critical that scientific and health care institutions proactively engage governments, patient advocacy organizations, and the general public in the formation of policies that guide gene editing.

摘要

2018 年 11 月,一则关于利用基因编辑的人类胚胎进行生殖目的的消息引起了国际社会的轩然大波;许多观察家认为编辑人类生殖细胞系是不道德的,特别是考虑到该科学仍处于早期阶段,且缺乏适当的监督。我们提供了对这些事件的影响的概述,重点关注了医生在处理患者问题和关注时涉及的相关伦理考虑。生殖目的的人类生殖细胞系编辑应该放在辅助生殖临床研究以及其他转化研究的范例的历史背景下理解。我们日益增强的基因编辑人类胚胎的能力引发了一个重要问题,即如何理解科学和社会之间隐含的社会契约。为了确保转化研究继续享有科学家和研究机构所获得的历史信任,至关重要的是,科学和医疗机构要积极与政府、患者倡导组织和公众合作,制定指导基因编辑的政策。

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