Lin Xinrou, Wei Lingyu, Li Xiangpen, Zeng Ling, Tang Yingsen, Wang Hongjin, Lu Hengjian, Li Chenguang, Wang Hongxuan, Chen Jinjin, Peng Ying
Department of Neurology, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou, 510000, China.
Nanhai Translational Innovation Center of Precision Immunology, Sun Yat-Sen Memorial Hospital, Foshan, 528200, China.
Adv Sci (Weinh). 2025 Jun;12(23):e2500362. doi: 10.1002/advs.202500362. Epub 2025 May 13.
Paclitaxel (PTX) is a commonly used chemotherapeutic agent for treating various solid tumors; however, it often leads to a severe side effect known as paclitaxel-induced peripheral neuropathy (PIPN), for which effective treatments are limited. Although mRNA therapies have shown promise in addressing central nervous system (CNS) disorders, the successful delivery of mRNA therapeutics to the nervous system is still hindered by many biological barriers. In this study, it is demonstrated that, compared with commercial MC3 lipid nanoparticles (MC3 LNPs), mRNA-loaded P6CIT-derived lipopolymer nanoparticles (P6CIT LPNPs), which are delivered via intrathecal injection, achieve effective penetration through the pia mater. More importantly, this P6CIT LPNP demonstrates the ability to achieve highly targeted mRNA transfection in gliocytes within the spinal cord and dorsal root ganglia (DRG), which is essential for the regulation of neuroinflammation. Furthermore, two intrathecal injections of P6CIT LPNPs encapsulating mIL-10 (P6CIT/mIL-10) significantly alleviate PIPN by reducing proinflammatory cytokine production, gliocyte activation, and presynaptic NMDA receptor hyperactivity in both male and female mice. This study presents a promising and clinically translatable platform for using mRNA-loaded LPNPs to treat PIPN.
紫杉醇(PTX)是一种常用于治疗各种实体瘤的化疗药物;然而,它常常会导致一种名为紫杉醇诱导的周围神经病变(PIPN)的严重副作用,对此有效的治疗方法有限。尽管mRNA疗法在治疗中枢神经系统(CNS)疾病方面已显示出前景,但mRNA治疗药物向神经系统的成功递送仍受到许多生物屏障的阻碍。在本研究中,结果表明,与市售的MC3脂质纳米颗粒(MC3 LNPs)相比,通过鞘内注射递送的负载mRNA的P6CIT衍生的脂聚合物纳米颗粒(P6CIT LPNPs)能够有效穿透软脑膜。更重要的是,这种P6CIT LPNP显示出在脊髓和背根神经节(DRG)内的神经胶质细胞中实现高度靶向的mRNA转染的能力,这对于神经炎症的调节至关重要。此外,两次鞘内注射包裹mIL-10的P6CIT LPNPs(P6CIT/mIL-10)可通过减少促炎细胞因子的产生、神经胶质细胞的激活以及雄性和雌性小鼠突触前NMDA受体的亢进,显著减轻PIPN。本研究提出了一个有前景且可临床转化的平台,用于使用负载mRNA的LPNPs治疗PIPN。