[通过全基因组CRISPR筛选鉴定人类CAR-T细胞增殖调控基因]。

Yoshitaka Adachi
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引用次数: 0

摘要

CAR-T细胞的体内扩增和长期维持被认为是CD19 CAR-T细胞治疗后治疗成功的标志。全基因组CRISPR筛选已经成为大规模基因筛选的有力工具。全基因组CRISPR筛选显示,CUL5基因敲除(KO)改善了CD19 CAR-T细胞的增殖。CUL5KO不仅能提高CAR-T细胞的增殖能力,还能提高CAR-T细胞的效应功能。CUL5KO CAR-T细胞中JAK-STAT通路上调,CUL5通过IL-2信号通路激活后与JAK3降解相关。与对照CD19 CAR-T细胞相比,CUL5KO CD19 CAR-T细胞能有效抑制体内肿瘤进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Identification of genes regulating human CAR-T cell proliferation by genome-wide CRISPR screening].

In vivo expansion and long-term maintenance of CAR-T cells are considered to be the hallmark of treatment success after CD19 CAR-T cell therapy. Genome-wide CRISPR screening has emerged as a powerful tool for large-scale gene screens. Genome-wide CRISPR screening revealed that CUL5 gene knockout (KO) improved the proliferation of CD19 CAR-T cells. CUL5KO improved not only the proliferation but also the effector function of CAR-T cells. The JAK-STAT pathway was upregulated in CUL5KO CAR-T cells, and CUL5 was associated with the degradation of JAK3 upon activation through IL-2 signaling. CUL5KO CD19 CAR-T cells efficiently suppressed in vivo tumor progression as compared to control CD19 CAR-T cells.

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