A New Era in the Ethics of Human Embryonic Stem Cell Research

Author:

Lo Bernard1,Zettler Patricia1,Cedars Marcelle I.2,Gates Elena2,Kriegstein Arnold R.3,Oberman Michelle4,Reijo Pera Renee25,Wagner Richard M.6,Wuerth Mary T.7,Wolf Leslie E.1,Yamamoto Keith R.8

Affiliation:

1. Program in Medical Ethics and Division of General Internal Medicine, at the University of California San Francisco, San Francisco, California, USA

2. Department of Medicine and Department of Obstetrics, Gynecology, and Reproductive Sciences, at the University of California San Francisco, San Francisco, California, USA

3. Program in Development and Stem Cell Biology and Department of Neurology at the University of California San Francisco, San Francisco, California, USA

4. School of Law at Santa Clara University, Santa Clara, California, USA

5. Program in Human Embryonic Stem Cell Biology, San Francisco, California, USA

6. Human Subjects Protection Program, San Francisco, California, USA

7. Community member of the UCSF Committee on Gamete, Embryo, and Stem Cell Research, San Francisco, California, USA

8. Department of Cellular and Molecular Pharmacology at the University of California San Francisco, San Francisco, California, USA

Abstract

Abstract Scientific progress in human embryonic stem cell (hESC) research and increased funding make it imperative to look ahead to the ethical issues generated by the expected use of hESCs for transplantation. Several issues should be addressed now, even though phase I clinical trials of hESC transplantation are still in the future. To minimize the risk of hESC transplantation, donors of materials used to derive hESC lines will need to be recontacted to update their medical history and screening. Because of privacy concerns, such recontact needs to be discussed and agreed to at the time of donation, before new hESC lines are derived. Informed consent for phase I clinical trials of hESC transplantation also raises ethical concerns. In previous phase I trials of highly innovative interventions, allegations that trial participants had not really understood the risk and benefits caused delays in subsequent trials. Thus, researchers should consider what information needs to be discussed during the consent process for hESC clinical trials and how to verify that participants have a realistic understanding of the study. Lack of attention to the special ethical concerns raised by clinical trials of hESC transplantation and their implications for the derivation of new hESC lines may undermine or delay progress toward stem cell therapies.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

Reference38 articles.

1. Human embryonic stem cells express an immunogenic nonhuman sialic acid;Martin;Nat Med,2005

2. 3 City Institutions to Get $50 Million for Stem Cell Research;Perez-Pena;The New York Times,2005

3. Hospital Receives $6M for Stem Cell Research;Schworm;The Boston Globe,2005

Cited by 31 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3