白质营养不良症的基因疗法:从临床前动物研究到临床试验

IF 8.3 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
Jasna Metovic , Yedda Li , Yi Gong , Florian Eichler
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引用次数: 0

摘要

白质营养不良症是一种影响脑白质的进行性单基因疾病。目前正在进行多项基因治疗试验,以满足这一患者群体尚未得到满足的迫切需求。我们对 www.clinicaltrials.gov 中列出的截至 2024 年 8 月的所有基因治疗临床试验以及促成临床转化的相关临床前研究进行了全面的文献综述。在迄今为止描述的约 50 种白质营养不良症中,只有 8 种存在基因疗法临床试验:变色斑性白质营养不良症、X 连锁肾上腺白质营养不良症、球形细胞白质营养不良症、卡纳万病、巨轴索神经病、GM2 神经节苷脂病、亚历山大病和佩利泽斯-梅尔茨巴赫病。是什么导致了针对这些特定疾病的基因治疗试验的出现?是什么临床前数据或疾病背景促成了这些试验?对于这八种疾病中的每一种,我们首先描述其病理生理学和临床表现。我们讨论了基因治疗给药途径、靶细胞类型、给药方式、剂量和时间对疗效的影响。我们注意到,在某些白质营养不良症中使用异体造血干细胞移植,即使在缺乏可用动物模型的情况下,也能加快临床路径。在其他白质营养不良症中,小型和大型动物模型研究使实验性基因疗法得以临床转化。针对白质营养不良症的人体临床试验包括体内外慢病毒基因递送、体内 AAV 介导的基因递送以及鞘内反义寡核苷酸方法。我们概述了与每种方法相关的不良事件,尤其侧重于基因毒性和免疫毒性。我们回顾了与插入突变和免疫反应相关事件的监测和管理。本综述提供的数据表明,基因疗法虽然前景广阔,但需要进行系统监测,以考虑到不稳定的疾病生物学特性以及与新技术相关的不良事件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gene therapy for the leukodystrophies: From preclinical animal studies to clinical trials

Leukodystrophies are progressive single gene disorders affecting the white matter of the brain. Several gene therapy trials are in progress to address the urgent unmet need for this patient population. We performed a comprehensive literature review of all gene therapy clinical trials listed in www.clinicaltrials.gov through August 2024, and the relevant preclinical studies that enabled clinical translation. Of the approximately 50 leukodystrophies described to date, only eight have existing gene therapy clinical trials: metachromatic leukodystrophy, X-linked adrenoleukodystrophy, globoid cell leukodystrophy, Canavan disease, giant axonal neuropathy, GM2 gangliosidoses, Alexander disease and Pelizaeus-Merzbacher disease. What led to the emergence of gene therapy trials for these specific disorders? What preclinical data or disease context was enabling? For each of these eight disorders, we first describe its pathophysiology and clinical presentation. We discuss the impact of gene therapy delivery route, targeted cell type, delivery modality, dosage, and timing on therapeutic efficacy. We note that use of allogeneic hematopoietic stem cell transplantation in some leukodystrophies allowed for an accelerated path to clinic even in the absence of available animal models. In other leukodystrophies, small and large animal model studies enabled clinical translation of experimental gene therapies. Human clinical trials for the leukodystrophies include ex vivo lentiviral gene delivery, in vivo AAV-mediated gene delivery, and intrathecal antisense oligonucleotide approaches. We outline adverse events associated with each modality focusing specifically on genotoxicity and immunotoxicity. We review monitoring and management of events related to insertional mutagenesis and immune responses. The data presented in this review show that gene therapy, while promising, requires systematic monitoring to account for the precarious disease biology and the adverse events associated with new technology.

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来源期刊
ACS Applied Materials & Interfaces
ACS Applied Materials & Interfaces 工程技术-材料科学:综合
CiteScore
16.00
自引率
6.30%
发文量
4978
审稿时长
1.8 months
期刊介绍: ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.
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