Nano Delivery Systems for In Vivo CRISPR/Cas-Based Gene Therapy: From Vectors to Clinical Outcomes

IF 17.3 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ACS Nano Pub Date : 2026-10-20 Epub Date: 2026-10-06 DOI:10.1021/acsnano.6c12154
Ruhan Chen, Haimei Zhou, Qinjie Wu, Changyang Gong
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引用次数: 0

Abstract

As a powerful gene-editing tool, the clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated (Cas) system features simple construction, precise targeting, and higher editing efficiency, bringing prospects of radical cures for numerous critical illnesses at the genomic level. To date, ex vivo CRISPR/Cas-based gene therapies represented by Casgevy have achieved significant clinical advances. Nevertheless, cumbersome operational workflows and prohibitive treatment costs severely hinder their widespread clinical accessibility. In contrast, in vivo CRISPR/Cas-based gene therapies stand out with convenient administration procedures and reduced overall costs, endowing them with enormous translational potential. Although it holds great promise, the clinical translation of in vivo CRISPR/Cas-based gene therapies remains hampered by a number of factors. Among those multiple obstacles restricting the clinical translation of in vivo CRISPR/Cas-based gene therapies, delivery systems constitute the core bottleneck dominating in vivo editing efficiency and therapeutic potency. Centered on delivery platforms for in vivo CRISPR/Cas-based gene therapies, this review systematically summarizes prevailing in vivo CRISPR/Cas nano delivery systems, recapitulates relevant preclinical and clinical outcomes, discusses translational hurdles, and prospects the evolution of next-generation delivery systems, aiming to facilitate further development of in vivo CRISPR/Cas-based gene therapies.

体内CRISPR/ cas基因治疗的纳米递送系统:从载体到临床结果
聚类规则间隔短回文重复序列(CRISPR)/CRISPR-associated (Cas)系统作为一种强大的基因编辑工具,具有构建简单、靶向精确、编辑效率高的特点,在基因组水平上为许多危重疾病的根治带来了前景。迄今为止,以Casgevy为代表的体外CRISPR/ cas基因疗法已经取得了重大的临床进展。然而,繁琐的操作流程和高昂的治疗费用严重阻碍了它们在临床的广泛应用。相比之下,基于CRISPR/ cas的体内基因疗法因其方便的给药程序和降低的总体成本而脱颖而出,赋予了它们巨大的转化潜力。尽管它有很大的希望,但基于CRISPR/ cas的体内基因疗法的临床翻译仍然受到许多因素的阻碍。在限制基于CRISPR/ cas的体内基因疗法临床翻译的诸多障碍中,递送系统是制约体内编辑效率和治疗效力的核心瓶颈。本文围绕基于CRISPR/Cas的体内基因治疗的递送平台,系统总结了目前流行的体内CRISPR/Cas纳米递送系统,概述了相关的临床前和临床结果,讨论了转化障碍,并展望了下一代递送系统的发展,旨在促进基于CRISPR/Cas的体内基因治疗的进一步发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Nano
ACS Nano 工程技术-材料科学:综合
CiteScore
26.00
自引率
4.10%
发文量
1627
审稿时长
1.7 months
期刊介绍: ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.
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