Tianjin University of Science and Technology, Tianjin, China.
Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, China.
CRISPR J. 2024 Oct;7(5):272-282. doi: 10.1089/crispr.2024.0016. Epub 2024 Oct 16.
Lentiviral vectors (LVs) are crucial tools in gene therapy and bioproduction, but high-yield LV production systems are urgently needed. Using clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated protein 9 high-throughput screening, we identified nine critical genes (, and ) from 17,501 genes that limit LV packaging and formation. Knocking out these genes in HEK293T cells significantly increased virus production, with knockout exhibiting a 6.63-fold increase. Studies on multigene knockouts demonstrated that the cumulative effects of different gene knockouts can significantly enhance lentivirus production in HEK293T cells. Triple knockout of , and increased LV titer by ∼8.33-fold, and knockout (or knockdown) of and increased LV titer by ∼6.53-fold. This study established HEK293T cell lines with multiple genes knockout for efficient LV production, providing reliable technical support for LV production and application and offering new perspectives for studying LV packaging mechanisms and related virus research.
慢病毒载体 (LV) 是基因治疗和生物生产的重要工具,但迫切需要高产的 LV 生产系统。我们使用成簇规律间隔短回文重复 (CRISPR)-CRISPR 相关蛋白 9 高通量筛选,从 17501 个限制 LV 包装和形成的基因中鉴定出九个关键基因 (、和 )。敲除 HEK293T 细胞中的这些基因可显著提高病毒产量,敲除 基因可使产量增加 6.63 倍。对多基因敲除的研究表明,不同基因敲除的累积效应可显著提高 HEK293T 细胞中的慢病毒产量。敲除 、和 可使 LV 滴度增加约 8.33 倍,敲除 (或敲低) 、和 可使 LV 滴度增加约 6.53 倍。本研究建立了具有多个基因敲除的 HEK293T 细胞系,可高效生产 LV,为 LV 生产和应用提供了可靠的技术支持,并为研究 LV 包装机制和相关病毒研究提供了新的视角。