溶酶体贮积症基因治疗临床试验的生物标志物。

IF 12.1 1区 医学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Molecular Therapy Pub Date : 2024-09-04 Epub Date: 2024-06-06 DOI:10.1016/j.ymthe.2024.06.003
Alessandro Rossi, Sabrina Malvagia, Giancarlo la Marca, Giancarlo Parenti, Nicola Brunetti-Pierri
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引用次数: 0

摘要

溶酶体储积症(LSDs)是一种多系统进行性疾病,由参与溶酶体功能的蛋白质缺陷引起。目前正在对几种溶酶体贮积症采用不同的基因治疗策略进行临床研究,以克服现有治疗方法的局限性。然而,LSD 是一种进展缓慢的疾病,需要进行长期研究才能确定实验性治疗的疗效。生物标志物可以可靠地替代临床反应,提高临床试验的效率,尤其是在评估长期疾病干预时。在这篇综述中,我们总结了现有和未来的 LSD 生物标记物,并讨论了它们的优缺点。
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Biomarkers for gene therapy clinical trials of lysosomal storage disorders.

Lysosomal storage disorders (LSDs) are multisystemic progressive disorders caused by defects in proteins involved in lysosomal function. Different gene therapy strategies are under clinical investigation in several LSDs to overcome the limitations of available treatments. However, LSDs are slowly progressive diseases that require long-term studies to establish the efficacy of experimental treatments. Biomarkers can be reliable substitutes for clinical responses and improve the efficiency of clinical trials, especially when long-term disease interventions are evaluated. In this review, we summarize both available and future biomarkers for LSDs and discuss their strengths and weaknesses.

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来源期刊
Molecular Therapy
Molecular Therapy 医学-生物工程与应用微生物
CiteScore
19.20
自引率
3.20%
发文量
357
审稿时长
3 months
期刊介绍: Molecular Therapy is the leading journal for research in gene transfer, vector development, stem cell manipulation, and therapeutic interventions. It covers a broad spectrum of topics including genetic and acquired disease correction, vaccine development, pre-clinical validation, safety/efficacy studies, and clinical trials. With a focus on advancing genetics, medicine, and biotechnology, Molecular Therapy publishes peer-reviewed research, reviews, and commentaries to showcase the latest advancements in the field. With an impressive impact factor of 12.4 in 2022, it continues to attract top-tier contributions.
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