Chattopadhyay Munmun, Goss James, Wolfe Darren, Goins William C, Huang Shaohua, Glorioso Joseph C, Mata Marina, Fink David J
Department of Neurology, University of Pittsburgh, Pittsburgh, PA 15213, USA.
Brain. 2004 Apr;127(Pt 4):929-39. doi: 10.1093/brain/awh103. Epub 2004 Jan 28.
Attempts to develop clinical treatments for neuropathy using neurotrophins have not been successful. We tested whether neurotrophin gene delivery to dorsal root ganglia (DRGs) using non-replicating herpes simplex virus (HSV)-based vectors could prevent the development of neuropathy caused by administration of cisplatin. Following subcutaneous inoculation of HSV vectors expressing nerve growth factor (NGF) or neurotrophin-3 (NT-3), neurons in the DRG were transduced to produce NGF or NT-3 in vivo. Inoculation of either the NGF- or the NT-3-expressing vectors 3 days before the start of a 6-week course of cisplatin treatment protected against cisplatin-induced neuropathy assessed by electrophysiological, histological and behavioural measures 2 months later. Iatrogenic neuropathy caused by administration of chemotherapeutic drugs represents an excellent target for a human trial to assess the potential of gene therapy to prevent neuropathy.
尝试使用神经营养因子开发用于治疗神经病变的临床疗法尚未成功。我们测试了使用基于非复制型单纯疱疹病毒(HSV)的载体将神经营养因子基因导入背根神经节(DRG)是否可以预防由顺铂给药引起的神经病变的发展。在皮下接种表达神经生长因子(NGF)或神经营养因子-3(NT-3)的HSV载体后,DRG中的神经元在体内被转导以产生NGF或NT-3。在为期6周的顺铂治疗开始前3天接种表达NGF或NT-3的载体,可预防2个月后通过电生理、组织学和行为学测量评估的顺铂诱导的神经病变。由化疗药物给药引起的医源性神经病变是人体试验评估基因疗法预防神经病变潜力的理想靶点。