Antiviral immunity and nucleic acid sensing in haematopoietic stem cell gene engineering

被引:17
|
作者
Piras, Francesco [1 ]
Kajaste-Rudnitski, Anna [1 ]
机构
[1] IRCCS San Raffaele Sci Inst, San Raffaele Telethon Inst Gene Therapy, Milan, Italy
基金
欧洲研究理事会;
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; DOUBLE-STRANDED-RNA; WEST NILE VIRUS; CYCLIC GMP-AMP; NF-KAPPA-B; DNA-DAMAGE; LENTIVIRAL VECTOR; TRANSDUCTION EFFICIENCY; SAMHD1; RESTRICTS; PROGENITOR CELLS;
D O I
10.1038/s41434-020-0175-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The low gene manipulation efficiency of human hematopoietic stem and progenitor cells (HSPC) remains a major hurdle for sustainable and broad clinical application of innovative therapies for a wide range of disorders. Given that all current and emerging gene transfer and editing technologies are bound to expose HSPC to exogenous nucleic acids and most often also to viral vectors, we reason that host antiviral factors and nucleic acid sensors play a pivotal role in the efficacy of HSPC genetic manipulation. Here, we review recent progress in our understanding of vector-host interactions and innate immunity in HSPC upon gene engineering and discuss how dissecting this crosstalk can guide the development of more stealth and efficient gene therapy approaches in the future.
引用
收藏
页码:16 / 28
页数:13
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