疼痛管理的基因疗法。

S P Wilson, D C Yeomans
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引用次数: 23

摘要

最近在疼痛动物模型中研究了两种用于慢性疼痛管理的基因治疗方法。首先,通过将工程细胞系移植到蛛网膜下腔和重组腺病毒转导硬膜细胞,通过转基因介导将抗伤感受性分子递送到脑脊液中。其次,伤害性神经元的表型已经被过表达抗伤害性肽或减少内源性伤害性分子表达的重组疱疹病毒所改变。这两种方法都可以减轻或逆转持续的伤害性状态,这表明基因疗法可以用于人类疼痛管理的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic therapy for pain management.

Two approaches to genetic therapy for the management of chronic pain have recently been investigated in animal models of pain. First, transgene-mediated delivery of antinociceptive molecules to the cerebrospinal fluid has been performed with engineered cell lines transplanted to the subarachnoid space and with recombinant adenoviruses that transduce pia mater cells. Second, the phenotype of nociceptive neurons has been altered by recombinant herpes viruses overexpressing antinociceptive peptides or reducing expression of endogenous nociceptive molecules. Both approaches attenuate or reverse persistent nociceptive states, suggesting use in the development of genetic therapy for pain management in humans.

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