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Gene therapy approaches to enhance regeneration of the injured peripheral nerve

机译:基因疗法可增强受伤的周围神经的再生

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Peripheral nerve injury in humans often leads to incomplete functional recovery. In this review we discuss the potential for gene therapy to be used as a strategy alongside surgical repair techniques for the study of peripheral nerve regeneration in rodent models and with a view to its eventual use for the promotion of successful regeneration in the clinic. Gene therapy can be defined as the introduction of a foreign, therapeutic gene into living cells in order to treat a disease. The first attempts to express a foreign gene in peripheral neurons date back more than 25 years. The vectors used at that time were imperfect - mainly because they contained viral genes that were expressed in the target cells and elicited an immunological response. Fortunately significant progress has been made: today adeno-associated viral vectors can be produced completely free of viral genes and Phase I and II clinical studies have shown that these vectors are well tolerated. The technology for gene delivery has reached a state of readiness for clinical translation in many fields of neurology, including peripheral nerve repair. The current range of potential therapeutic genes for the repair of the traumatized peripheral nerve has also grown over the years and now includes neurotrophic factors with specificities for various subtypes of peripheral neurons, cell adhesion and extracellular matrix molecules and transcription factors. This review for this Festschrift, published to celebrate the 70th birthday of Willem Hendrik Gispen, contains many "footprints" from the time the senior author (JV) worked with Willem Hendrik, first as a student intern, then as a Ph.D. student (1983-1987) and later as a postdoctoral fellow (1989-1993). The preface of this article highlights personal memories of a time that will never come back.
机译:人体周围神经损伤通常会导致功能恢复不完全。在这篇综述中,我们讨论了基因疗法与啮齿动物模型中研究周围神经再生的外科修复技术以及外科修复技术一起使用的可能性,以期最终将其用于促进临床成功再生。基因治疗可以定义为将外源的治疗性基因引入活细胞以治疗疾病。在周围神经元中表达外源基因的首次尝试可以追溯到25年前。当时使用的载体是不完善的-主要是因为它们含有在靶细胞中表达并引发免疫应答的病毒基因。幸运的是,已经取得了重大进展:如今,腺相关病毒载体可以完全不含病毒基因,并且I和II期临床研究表明这些载体具有良好的耐受性。基因递送技术已经在神经系统学的许多领域,包括周围神经修复领域,准备好进行临床翻译。多年来,用于修复受创伤的周围神经的潜在治疗基因的范围也在增长,现在包括对周围神经元的各种亚型具有特异性的神经营养因子,细胞粘附,细胞外基质分子和转录因子。为庆祝Willem Hendrik Gispen诞辰70周年而出版的本Festschrift的这篇评论包含了许多“足迹”,从高级作者(JV)与Willem Hendrik一起工作(最初是作为一名实习生,然后是博士学位)开始。研究生(1983年至1987年)和博士后(1989年至1993年)。本文的序言强调了一个永远不会回来的个人记忆。

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