腺相关病毒基因治疗方法的进展:探索新的视野。

F1000 medicine reports Pub Date : 2011-01-01 Epub Date: 2011-09-01 DOI:10.3410/M3-17
Caroline J Aalbers, Paul P Tak, Margriet J Vervoordeldonk
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引用次数: 28

摘要

基因治疗是一种很有前景的新治疗策略,已经在多种疾病中得到了探索,从癌症到血友病,从眼部疾病到自身免疫性疾病,等等。基因转移方法的概念已在100多项疾病动物模型研究中得到证明,尽管只有少数正在开发用于临床应用。到目前为止,美国食品和药物管理局和欧洲药品管理局还没有批准任何病毒人类基因治疗产品的销售,但在美国和欧洲发生的基因相关研究和开发的数量继续以快速的速度增长。本文综述了以腺相关病毒为载体的病毒基因治疗领域的发展现状,并以关节炎为重点。对于类风湿性关节炎,以及较小程度的其他免疫相关炎症性疾病,已经在临床前水平研究了几种细胞和基因转移方法,其中一些已在临床试验中实施。最后,讨论了病毒基因治疗在发展到临床应用过程中所面临的潜力和障碍。
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Advancements in adeno-associated viral gene therapy approaches: exploring a new horizon.

Gene therapy is a promising new therapeutic strategy that has been explored in a wide variety of diseases, ranging from cancer to hemophilia, and ocular disorders to autoimmune diseases, among others. Proof of concept of gene transfer approaches has been shown in over 100 studies of animal models of disease, although only a few are under development for clinical application. The US Food and Drug Administration and the European Medicines Agency have not approved any viral human gene therapy products for sale so far, but the amount of gene-related research and development occurring in the United States and Europe continues to grow at a fast rate. This review summarizes the current status of developments in the field of viral gene therapy using adeno-associated virus as a vector, with a special focus on arthritis. For rheumatoid arthritis, and to a lesser extent for other immune-related inflammatory disorders, several cell and gene transfer approaches have been investigated at the preclinical level and a few have been implemented in clinical trials. Finally, both the potential and the hurdles that are faced during development of a viral gene therapy through to its clinical application are discussed.

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