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腺相关病毒载体介导的神经退行性疾病基因治疗的特点与优势

Characteristics and advantages of adeno-associated virus vector-mediated gene therapy for neurodegenerative diseases.

作者信息

Qu Yuan, Liu Yi, Noor Ahmed Fayyaz, Tran Johnathan, Li Rui

机构信息

Department of Hand Surgery, the Second Hospital of Jilin University, Changchun, Jilin Province, China.

Department of Orthopedics, Qilu Hospital of Shandong University, Jinan, Shandong Province, China.

出版信息

Neural Regen Res. 2019 Jun;14(6):931-938. doi: 10.4103/1673-5374.250570.

Abstract

Common neurodegenerative diseases of the central nervous system are characterized by progressive damage to the function of neurons, even leading to the permanent loss of function. Gene therapy via gene replacement or gene correction provides the potential for transformative therapies to delay or possibly stop further progression of the neurodegenerative disease in affected patients. Adeno-associated virus has been the vector of choice in recent clinical trials of therapies for neurodegenerative diseases due to its safety and efficiency in mediating gene transfer to the central nervous system. This review aims to discuss and summarize the progress and clinical applications of adeno-associated virus in neurodegenerative disease in central nervous system. Results from some clinical trials and successful cases of central neurodegenerative diseases deserve further study and exploration.

摘要

中枢神经系统常见的神经退行性疾病的特征是神经元功能逐渐受损,甚至导致功能永久性丧失。通过基因替代或基因校正进行的基因治疗为变革性疗法提供了潜力,可延缓或可能阻止受影响患者神经退行性疾病的进一步发展。腺相关病毒因其在介导基因转移至中枢神经系统方面的安全性和有效性,已成为近期神经退行性疾病治疗临床试验中的首选载体。本综述旨在讨论和总结腺相关病毒在中枢神经系统神经退行性疾病中的进展和临床应用。一些中枢神经退行性疾病的临床试验结果和成功案例值得进一步研究和探索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf45/6404499/0a2576387f26/NRR-14-931-g001.jpg

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