利用装载crispr的功能化纳米载体在体内生成CAR-T细胞治疗b细胞系急性淋巴细胞白血病的综述。

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Tushara Saha, Rudra Prasad Saha, Manoj Kumar Singh, Kanu Priya, Shareen Singh, Mithul Rajeev, Debasmita Bhattacharya, Moupriya Nag, Dibyajit Lahiri
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引用次数: 0

摘要

嵌合抗原受体T (CAR-T)细胞治疗已成为B细胞系急性淋巴细胞白血病治疗的一个里程碑。然而,传统的方法依赖于体外操作、扩增和自体T细胞的回输,这种方法成本高,可扩展性低,并且具有严重的免疫相关毒性。在这里,我们报道了一种新的纳米免疫工程平台,该平台通过使用携带聚集规则间隔短回文重复序列(CRISPR)和CRISPR相关蛋白9 (Cas9)基因编辑元件的功能化纳米颗粒,允许在体内生产嵌合抗原受体T细胞。这些纳米颗粒被设计成专门针对血液循环T淋巴细胞,并传递CRISPR/Cas9复合物,这些复合物具有将嵌合抗原受体构建物整合到TRAC位点的能力,同时敲除免疫检查点基因,如程序性细胞死亡蛋白1 (PD-1)。通过基于金和DNA纳米结构的载体,可以确保靶向递送、内体逃逸和有效的基因组编辑,并具有最小的脱靶效应。临床前模型显示嵌合抗原受体T细胞在体内有效编程,具有强大的抗肿瘤功效,改善持久性,减少细胞因子释放综合征。这种方法是癌症免疫治疗的革命性突破,为传统的嵌合抗原受体T细胞生产提供了可扩展、经济和临床灵活的替代品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An overview on in-vivo generation of CAR-T cells using CRISPR-loaded functionalized nanocarriers for treating B-cell lineage acute lymphoblastic leukemia.

Chimeric antigen receptor T (CAR-T) cell therapy has become a milestone in the management of B cell lineage acute lymphoblastic leukemia. Yet, the traditional method-dependent on ex vivo manipulation, amplification, and reinfusion of autologous T cells-is high-cost, low-scalability, and severely immune-related toxicity. Here, we report a new nano-immunoengineering platform that allows in vivo production of chimeric antigen receptor T cells through the use of functionalized nanoparticles carrying clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated protein 9 (Cas9) gene editing elements. These nanoparticles are engineered to specifically target blood circulating T lymphocytes and deliver CRISPR/Cas9 complexes that have the ability to integrate chimeric antigen receptor constructs into the TRAC locus and knock out immune checkpoint genes like programmed cell death protein 1 (PD-1) simultaneously. Targeted delivery, endosomal escape, and efficient genome editing with minimal off-target effects are ensured through gold-based and DNA nanostructure-based carriers. Preclinical models show effective in vivo programming of functional chimeric antigen receptor T cells with vigorous antitumor efficacy, improved persistence, and decreased cytokine release syndrome. This method is a revolutionary breakthrough in cancer immunotherapy that provides a scalable, economical, and clinically flexible replacement for conventional chimeric antigen receptor T cell production.

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来源期刊
Molecular Biology Reports
Molecular Biology Reports 生物-生化与分子生物学
CiteScore
5.00
自引率
0.00%
发文量
1048
审稿时长
5.6 months
期刊介绍: Molecular Biology Reports publishes original research papers and review articles that demonstrate novel molecular and cellular findings in both eukaryotes (animals, plants, algae, funghi) and prokaryotes (bacteria and archaea).The journal publishes results of both fundamental and translational research as well as new techniques that advance experimental progress in the field and presents original research papers, short communications and (mini-) reviews.
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