遗传增强
基因转移
失明
基因组编辑
不利影响
重症监护医学
疾病
医学
生物信息学
生物
基因
清脆的
病理
内科学
遗传学
验光服务
作者
Cynthia E. Dunbar,Katherine A. High,J. Keith Joung,Donald B. Kohn,Keiya Ozawa,Michel Sadelain
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2018-01-12
卷期号:359 (6372)
被引量:1064
标识
DOI:10.1126/science.aan4672
摘要
Gene therapy: The power of persistence Nearly 50 years after the concept was first proposed, gene therapy is now considered a promising treatment option for several human diseases. The path to success has been long and tortuous. Serious adverse effects were encountered in early clinical studies, but this fueled basic research that led to safer and more efficient gene transfer vectors. Gene therapy in various forms has produced clinical benefits in patients with blindness, neuromuscular disease, hemophilia, immunodeficiencies, and cancer. Dunbar et al. review the pioneering work that led the gene therapy field to its current state, describe gene-editing technologies that are expected to play a major role in the field's future, and discuss practical challenges in getting these therapies to patients who need them. Science , this issue p. eaan4672
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