慢病毒
遗传增强
Cas9
基因组编辑
造血干细胞
基因
生物
干细胞
造血
遗传学
计算生物学
生物信息学
清脆的
病毒性疾病
病毒
作者
Andrés Lamsfus‐Calle,Alberto Daniel-Moreno,Guillermo Ureña-Bailén,Janani Raju,Justin S. Antony,Rupert Handgretinger,Markus Mezger
出处
期刊:Blood Reviews
[Elsevier BV]
日期:2019-11-15
卷期号:40: 100641-100641
被引量:20
标识
DOI:10.1016/j.blre.2019.100641
摘要
Due to pioneering in vitro investigations on gene modification, gene engineering platforms have incredibly improved to a safer and more powerful tool for the treatment of multiple blood and immune disorders. Likewise, several clinical trials have been initiated combining autologous hematopoietic stem cell transplantation (auto-HSCT) with gene therapy (GT) tools. As several GT modalities such as lentivirus and gene editing tools have a long developmental path ahead to diminish its negative side effects, it is hard to decide which modality is optimal for treating a specific disease. Gene transfer by lentiviruses is the platform of choice for loss-of-mutation diseases, whereas gene correction/addition or gene disruption by gene editing tools, mainly CRISPR/Cas9, is likely to be more efficient in diseases where tight regulation is needed. Therefore, in this review, we compiled pertinent information about lentiviral gene transfer and CRISPR/Cas9 gene editing, their evolution to a safer platform for HSCT, and their applications on other types of gene disorders based on the etiology of the disease and cell fitness.
科研通智能强力驱动
Strongly Powered by AbleSci AI