CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Ultrasound Control of Genomic Regulatory Toolboxes for Cancer Immunotherapy.
Ultrasound Control of Genomic Regulatory Toolboxes for Cancer Immunotherapy.
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CRISPR(成簇规律间隔短回文重复序列)技术需要实现精准调控。为此,我们构建了一套可由聚焦超声(FUS)控制的诱导型CRISPR工具,FUS能够穿透深部组织并诱导局部高热,从而激活转基因。
我们展示了FUS诱导的CRISPR、CRISPR激活系统(CRISPRa)和CRISPR表观遗传编辑器(CRISPRee)调控基因组和表观基因组的能力。
我们发现,FUS-CRISPR介导的端粒破坏可使实体瘤预先对嵌合抗原受体(CAR)T细胞疗法敏感。我们进一步使用腺相关病毒(AAV)在体内递送FUS-CRISPR,随后通过FUS诱导端粒破坏,并在部分肿瘤细胞亚群中表达经临床验证的抗原。这些细胞充当“训练中心”,激活合成Notch(synNotch)CAR-T 细胞,使其产生靶向通用肿瘤抗原的CAR,以清除邻近肿瘤细胞。
因此,FUS-CRISPR(a/ee)工具箱可非侵入性、按时空精准控制基因组/表观基因组重编程,用于癌症治疗。
There remains a critical need for the precise control of CRISPR (clustered regularly interspaced short palindromic repeats)-based technologies.
Here, we engineer a set of inducible CRISPR-based tools controllable by focused ultrasound (FUS), which can penetrate deep and induce localized hyperthermia for transgene activation.
We demonstrate the capabilities of FUS-inducible CRISPR, CRISPR activation (CRISPRa), and CRISPR epigenetic editor (CRISPRee) in modulating the genome and epigenome.
We show that FUS-CRISPR-mediated telomere disruption primes solid tumours for chimeric antigen receptor (CAR)-T cell therapy.
We further deliver FUS-CRISPR in vivo using adeno-associated viruses (AAVs), followed by FUS-induced telomere disruption and the expression of a clinically validated antigen in a subpopulation of tumour cells, functioning as "training centers" to activate synthetic Notch (synNotch) CAR-T cells to produce CARs against a universal tumour antigen to exterminate neighboring tumour cells. The FUS-CRISPR(a/ee) toolbox hence allows the noninvasive and spatiotemporal control of genomic/epigenomic reprogramming for cancer treatment.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
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