Kim Daewook, Kim Kyung-Ran, Kwon Yejin, Kim Minjung, Kim Min-Ju, Sim Yeomoon, Ji Hyelin, Park Jang-Joon, Cho Jong-Ho, Choi Heonsik, Kim Sujeong
Institute of BioInnovation Research, Kolon Life Science, 110 Magokdong-ro, Gangseo-gu, Seoul 07793, Republic of Korea.
Mol Ther Methods Clin Dev. 2020 Jun 25;18:473-483. doi: 10.1016/j.omtm.2020.06.018. eCollection 2020 Sep 11.
Neuropathic pain is a chronic pain state characterized by nerve damage, inflammation, and nociceptive neuron hyperactivity. As the underlying pathophysiology is complex, a more effective therapy for neuropathic pain would be one that targets multiple elements. Here, we generated recombinant adeno-associated viruses (AAVs) encoding three therapeutic genes, namely, , , and , with various combinations. The efficacy for pain relief was evaluated in a rat spared nerve injury model of neuropathic pain. The maximal analgesic effect was achieved when the AAVs expressing all three genes were administered to rats with neuropathic pain. The combination of two virus constructs expressing the three genes was named KLS-2031 and evaluated as a potential novel therapeutic for neuropathic pain. Single transforaminal epidural injections of KLS-2031 into the intervertebral foramen to target the appropriate dorsal root ganglion produced notable long-term analgesic effects in female and male rats. Furthermore, KLS-2031 mitigated the neuroinflammation, neuronal cell death, and dorsal root ganglion hyperexcitability induced by the spared nerve injury. These results suggest that KLS-2031 represents a promising therapeutic option for refractory neuropathic pain.
神经性疼痛是一种以神经损伤、炎症和伤害性神经元活动亢进为特征的慢性疼痛状态。由于其潜在的病理生理学较为复杂,一种更有效的神经性疼痛治疗方法应该是针对多个因素的疗法。在此,我们构建了携带三种治疗基因(即 、 和 )不同组合的重组腺相关病毒(AAV)。在大鼠坐骨神经分支选择性损伤神经性疼痛模型中评估了其缓解疼痛的效果。将表达所有三种基因的AAV注射到患有神经性疼痛的大鼠体内时,可达到最大镇痛效果。表达这三种基因的两种病毒构建体的组合被命名为KLS - 2031,并被评估为一种潜在的神经性疼痛新型治疗方法。通过经椎间孔单次硬膜外注射KLS - 2031至椎间孔以靶向合适的背根神经节,在雌性和雄性大鼠中产生了显著的长期镇痛效果。此外,KLS - 2031减轻了坐骨神经分支选择性损伤诱导的神经炎症、神经元细胞死亡和背根神经节兴奋性过高。这些结果表明,KLS - 2031是难治性神经性疼痛的一种有前景的治疗选择。