遗传增强
溶酶体贮存障碍
基质还原疗法
临床试验
医学
溶酶体贮存病
计算生物学
生物
生物信息学
基因
遗传学
病理
酶替代疗法
疾病
作者
Alessandro Rossi,Sabrina Malvagia,Giancarlo la Marca,Giancarlo Parenti,Nicola Brunetti‐Pierri
标识
DOI:10.1016/j.ymthe.2024.06.003
摘要
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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