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基于基因的运动神经元疾病治疗。

Gene-based treatment of motor neuron diseases.

作者信息

Federici Thais, Boulis Nicholas M

机构信息

Department of Neuroscience, Cleveland Clinic Foundation, NB2-126A, 9500 Euclid Avenue, Cleveland, Ohio 44195, USA.

出版信息

Muscle Nerve. 2006 Mar;33(3):302-23. doi: 10.1002/mus.20439.

Abstract

Motor neuron diseases (MND), such as amyotrophic lateral sclerosis (ALS) and spinal muscular atrophy (SMA), are progressive neurodegenerative diseases that share the common characteristic of upper and/or lower motor neuron degeneration. Therapeutic strategies for MND are designed to confer neuroprotection, using trophic factors, anti-apoptotic proteins, as well as antioxidants and anti-excitotoxicity agents. Although a large number of therapeutic clinical trials have been attempted, none has been shown satisfactory for MND at this time. A variety of strategies have emerged for motor neuron gene transfer. Application of these approaches has yielded therapeutic results in cell culture and animal models, including the SOD1 models of ALS. In this study we describe the gene-based treatment of MND in general, examining the potential viral vector candidates, gene delivery strategies, and main therapeutic approaches currently attempted. Finally, we discuss future directions and potential strategies for more effective motor neuron gene delivery and clinical translation.

摘要

运动神经元疾病(MND),如肌萎缩侧索硬化症(ALS)和脊髓性肌萎缩症(SMA),是进行性神经退行性疾病,具有上运动神经元和/或下运动神经元变性的共同特征。MND的治疗策略旨在通过使用神经营养因子、抗凋亡蛋白以及抗氧化剂和抗兴奋毒性剂来提供神经保护作用。尽管已经尝试了大量的治疗性临床试验,但目前尚无一种对MND显示出令人满意的效果。运动神经元基因转移已经出现了多种策略。这些方法的应用在细胞培养和动物模型中产生了治疗效果,包括ALS的SOD1模型。在本研究中,我们总体描述了基于基因的MND治疗方法,研究了潜在的病毒载体候选物、基因递送策略以及目前尝试的主要治疗方法。最后,我们讨论了未来的方向以及更有效的运动神经元基因递送和临床转化的潜在策略。

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