jeremiahmetzger讲座:将基因转化为药物:遗传病基因治疗发展的亮点和障碍。

Q2 Medicine
Katherine A High
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引用次数: 0

摘要

从将基因体外转移到哺乳动物细胞,到获得批准的基因治疗产品,这一过程已经跨越了几十年。本文总结了在开发成功的腺相关病毒(AAV)载体治疗血友病B和由RPE65基因突变引起的遗传性视网膜营养不良过程中遇到的障碍和克服的障碍。在血友病B的情况下,对第一次失败尝试的仔细分析导致人们意识到,人类对AAV载体的免疫反应正在阻止持久表达;对重组病毒粒子反应的阐明导致了能够成功进行长期基因转移的策略。对于RPE65缺乏症,成功的关键是开发和验证一种以前缺乏药物治疗的疾病的新临床终点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
THE JEREMIAH METZGER LECTURE: TURNING GENES INTO MEDICINES: HIGHLIGHTS AND HURDLES IN THE DEVELOPMENT OF GENE THERAPY FOR GENETIC DISEASE.

The journey from in vitro transfer of genes into mammalian cells to approved gene therapy products has spanned decades. This manuscript summarizes hurdles encountered and obstacles overcome in the development of successful adeno-associated viral (AAV) vectors for hemophilia B and for an inherited retinal dystrophy caused by mutations in the RPE65 gene. In the case of hemophilia B, careful analysis of the first unsuccessful attempts led to the realization that the human immune response to AAV vectors was preventing durable expression; elucidation of the response to the recombinant virion led to strategies that enabled successful long-lasting gene transfer. For RPE65 deficiency, a key to success was development and validation of a novel clinical endpoint for a disease that previously lacked a pharmacologic treatment.

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CiteScore
1.70
自引率
0.00%
发文量
57
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