基因组编辑
嵌合抗原受体
转录激活物样效应核酸酶
清脆的
遗传增强
锌指核酸酶
Cas9
细胞疗法
免疫疗法
计算生物学
生物
癌症研究
基因
医学
细胞
免疫学
免疫系统
遗传学
作者
In-Young Jung,Jungmin Lee
出处
期刊:PubMed
[National Institutes of Health]
日期:2018-08-31
卷期号:41 (8): 717-723
被引量:48
标识
DOI:10.14348/molcells.2018.0242
摘要
Chimeric antigen receptor (CAR) T-cell therapy, an emerging immunotherapy, has demonstrated promising clinical results in hematological malignancies including B-cell malignancies. However, accessibility to this transformative medicine is highly limited due to the complex process of manufacturing, limited options for target antigens, and insufficient anti-tumor responses against solid tumors. Advances in gene-editing technologies, such as the development of Zinc Finger Nucleases (ZFNs), Transcription Activator-Like Effector Nucleases (TALENs), and Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR/Cas9), have provided novel engineering strategies to address these limitations. Development of next-generation CAR-T cells using gene-editing technologies would enhance the therapeutic potential of CAR-T cell treatment for both hematologic and solid tumors. Here we summarize the unmet medical needs of current CAR-T cell therapies and gene-editing strategies to resolve these challenges as well as safety concerns of gene-edited CAR-T therapies.
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