体细胞
遗传学
政治学
生物
基因
工程伦理学
医学
工程类
出处
期刊:Annual Review of Genomics and Human Genetics
[Annual Reviews]
日期:2024-08-27
卷期号:25 (1): 421-438
被引量:1
标识
DOI:10.1146/annurev-genom-021623-104458
摘要
Manipulation of a patient's genome for therapeutic ends is being attempted through numerous methods, some of which have resulted in disease-modifying interventions. The much anticipated promise of somatic gene therapy is starting to pay off; however, there remain many scientific unknowns, including concerns about safety and durability. A significant ethical concern is that of access to these novel interventions, an issue that is normally framed in terms of the high costs of approved products. I describe how access issues permeate gene therapy long before there is any commercial product and how even upstream decisions-such as choices of indication to pursue, viral vector, and where to site a trial-have significant implications for access to resultant products in both the developmental and commercial stages.
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