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利用肽的神经治疗潜力:使用单纯疱疹病毒载体进行靶向递送。

Exploiting the neurotherapeutic potential of peptides: targeted delivery using HSV vectors.

作者信息

Glorioso Joseph C, Mata Marina, Fink David J

机构信息

Department of Neurology, University of Pittsburgh School of Medicine, 200 Lothrop Street, Pittsburgh, PA 15213, USA.

出版信息

Expert Opin Biol Ther. 2003 Dec;3(8):1233-9. doi: 10.1517/14712598.3.8.1233.

Abstract

Neurotrophic factors and peptide neurotransmitters represent two classes of potent macromolecules whose therapeutic use in the treatment of neurologic disease is limited by unwanted effects that result from the widespread distribution of cognate receptors within and beyond the neuraxis. Targeted gene delivery to sensory neurons of the dorsal root ganglion (DRG) by subcutaneous inoculation of herpes simplex virus (HSV)-based gene transfer vectors may be used to achieve local expression and release of these pleiotropic, short-lived molecules in a restricted area. Recent studies demonstrate that HSV-mediated transfer of genes coding for neurotrophic factors prevents the progression of disease in animal models of drug-induced or diabetic polyneuropathy and that HSV-mediated transfer of genes coding for inhibitory neurotransmitters provides a regional analgesic effect in animal models of chronic pain. The first human trial of HSV-mediated gene transfer to DRG is about to commence. HSV-mediated gene transfer may allow the therapeutic potential of these peptides for the treatment of neurologic disease to be realised.

摘要

神经营养因子和肽类神经递质代表了两类强大的大分子,它们在治疗神经疾病中的应用受到限制,因为其同源受体在神经轴内外广泛分布会产生不良影响。通过皮下接种基于单纯疱疹病毒(HSV)的基因转移载体,将基因靶向递送至背根神经节(DRG)的感觉神经元,可用于在受限区域实现这些多效性、短寿命分子的局部表达和释放。最近的研究表明,HSV介导的编码神经营养因子的基因转移可预防药物诱导或糖尿病性多发性神经病动物模型中的疾病进展,并且HSV介导的编码抑制性神经递质的基因转移在慢性疼痛动物模型中具有局部镇痛作用。HSV介导的基因转移至DRG的首次人体试验即将开始。HSV介导的基因转移可能使这些肽在治疗神经疾病方面的治疗潜力得以实现。

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