Moosavi Seyedeh Ghazal, Rahiman Niloufar, Jaafari Mahmoud Reza, Arabi Leila
School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran; Student Research Committee, Mashhad University of Medical Sciences, Mashhad, Iran.
Nanotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran; Department of Pharmaceutical Nanotechnology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.
J Control Release. 2025 May 10;381:113641. doi: 10.1016/j.jconrel.2025.113641. Epub 2025 Mar 20.
Neurodegenerative diseases (NDD) are characterized by the progressive loss of neurons and the impairment of cellular functions. Messenger RNA (mRNA) has emerged as a promising therapy for treating NDD, as it can encode missing or dysfunctional proteins and anti-inflammatory cytokines or neuroprotective proteins to halt the progression of these diseases. However, effective mRNA delivery to the central nervous system (CNS) remains a significant challenge due to the limited penetration of the blood-brain barrier (BBB). Lipid nanoparticles (LNPs) offer an efficient solution by encapsulating and protecting mRNA, facilitating transfection and intracellular delivery. This review discusses the pathophysiological mechanisms of neurological disorders, including Parkinson's disease (PD), Alzheimer's disease (AD), multiple sclerosis (MS), Huntington's disease (HD), ischemic stroke, spinal cord injury, and Friedreich's ataxia. Additionally, it explores the potential of LNP-mediated mRNA delivery as a therapeutic strategy for these diseases. Various approaches to overcoming BBB-related challenges and enhancing the delivery and efficacy of mRNA-LNPs are discussed, including non-invasive methods with strong potential for clinical translation. With advancements in artificial intelligence (AI)-guided mRNA and LNP design, targeted delivery, gene editing, and CAR-T cell therapy, mRNA-LNPs could significantly transform the treatment landscape for NDD, paving the way for future clinical applications.
神经退行性疾病(NDD)的特征是神经元逐渐丧失和细胞功能受损。信使核糖核酸(mRNA)已成为治疗NDD的一种有前景的疗法,因为它可以编码缺失或功能失调的蛋白质以及抗炎细胞因子或神经保护蛋白,以阻止这些疾病的进展。然而,由于血脑屏障(BBB)的穿透有限,将mRNA有效递送至中枢神经系统(CNS)仍然是一项重大挑战。脂质纳米颗粒(LNP)通过包裹和保护mRNA、促进转染和细胞内递送提供了一种有效的解决方案。本综述讨论了神经疾病的病理生理机制,包括帕金森病(PD)、阿尔茨海默病(AD)、多发性硬化症(MS)、亨廷顿病(HD)、缺血性中风、脊髓损伤和弗里德赖希共济失调。此外,还探讨了LNP介导的mRNA递送作为这些疾病治疗策略的潜力。讨论了克服与BBB相关挑战以及提高mRNA-LNP递送和疗效的各种方法,包括具有强大临床转化潜力的非侵入性方法。随着人工智能(AI)指导的mRNA和LNP设计、靶向递送、基因编辑和嵌合抗原受体T细胞疗法的进展,mRNA-LNP可能会显著改变NDD的治疗格局,为未来的临床应用铺平道路。