Diamyd Inc., Pittsburgh, PA, USA.
Neurosci Lett. 2012 Oct 11;527(2):85-9. doi: 10.1016/j.neulet.2012.04.047. Epub 2012 Apr 27.
Gene transfer to target delivery of neurotrophic factors to the primary sensory afferent for treatment of polyneuropathy, or of inhibitory neurotransmitters for relief of chronic pain, offers the possibility of a highly selective targeted release of bioactive molecules within the nervous system. Preclinical studies with non-replicating herpes simplex virus (HSV)-based vectors injected into the skin to transduce neurons in the dorsal root ganglion have demonstrated efficacy in reducing-pain related behaviors in animal models of inflammatory pain, neuropathic pain, and pain caused by cancer, and in preventing progression of sensory neuropathy caused by toxins, chemotherapeutic drugs or resulting from diabetes. Successful completion of the first phase 1 clinical trial of HSV-mediated gene transfer in patients with intractable pain from cancer has set the stage for further clinical trials of this approach.
将基因转移到目标部位,以向初级感觉传入神经输送神经营养因子来治疗多发性神经病,或输送抑制性神经递质来缓解慢性疼痛,为在神经系统内高度选择性地靶向释放生物活性分子提供了可能。将非复制型单纯疱疹病毒(HSV)载体注入皮肤,以转导背根神经节中的神经元,这种方法在动物炎症性疼痛、神经性疼痛和癌症引起的疼痛模型中,已显示出减轻与疼痛相关行为的功效,而且还能预防毒素、化疗药物或糖尿病引起的感觉神经病变的进展。在癌症难治性疼痛患者中进行的 HSV 介导的基因转移的 I 期临床试验的成功完成,为该方法的进一步临床试验奠定了基础。