Zonouz Aidin Mohammadi, Rahbardar Mahboobeh Ghasemzadeh, Alibolandi Mona
Pharmaceutical Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran; Student Research Committee, Mashhad University of Medical Sciences, Mashhad, Iran.
Applied Biomedical Research Center, Mashhad University of Medical Sciences, Mashhad 9177948564, Iran.
Brain Res Bull. 2025 Mar;222:111256. doi: 10.1016/j.brainresbull.2025.111256. Epub 2025 Feb 12.
Multiple sclerosis (MS) is a chronic autoimmune illness characterized by inflammation and demyelination of the central nervous system (CNS). The effective delivery of therapeutic agents to the CNS continues to be an important barrier in MS treatment due to the blood-brain barrier and limited access to the affected areas. Exosome-based drug delivery systems have become an attractive option for targeted therapy in MS. Exosomes, small extracellular vesicles derived from various cell types, possess unique biological properties that make them ideal nanocarriers for delivering therapeutic cargo to specific cell populations in the CNS. In this study, we supply a comprehensive overview of the current advances and future perspectives of exosome-based drug delivery systems for MS. We discuss the biogenesis of exosomes, strategies for cargo loading, engineering approaches to enhance their targeting capabilities, and the potential clinical applications of exosome-mediated drug delivery in MS therapy. Additionally, we explore preclinical studies and animal models that demonstrate the effectiveness of exosome-based drug delivery in ameliorating MS pathology. By highlighting the challenges and opportunities in utilizing exosomes as drug delivery vehicles, this review aims to contribute to the growing body of knowledge in the field of nanomedicine for MS. Considering the potential of exosome-based drug delivery systems to enhance the accessibility, specificity, and effectiveness of therapies while minimizing off-target effects might change the therapeutic scenario for MS.
多发性硬化症(MS)是一种慢性自身免疫性疾病,其特征是中枢神经系统(CNS)发生炎症和脱髓鞘。由于血脑屏障以及难以到达受影响区域,将治疗药物有效递送至中枢神经系统仍然是MS治疗中的一个重要障碍。基于外泌体的药物递送系统已成为MS靶向治疗的一个有吸引力的选择。外泌体是源自各种细胞类型的小细胞外囊泡,具有独特的生物学特性,使其成为向中枢神经系统中的特定细胞群体递送治疗性货物的理想纳米载体。在本研究中,我们全面概述了基于外泌体的药物递送系统在MS方面的当前进展和未来前景。我们讨论了外泌体的生物发生、货物装载策略、增强其靶向能力的工程方法,以及外泌体介导的药物递送在MS治疗中的潜在临床应用。此外,我们探索了临床前研究和动物模型,这些研究证明了基于外泌体的药物递送在改善MS病理学方面的有效性。通过强调将外泌体用作药物递送载体的挑战和机遇,本综述旨在为MS纳米医学领域不断增长的知识体系做出贡献。考虑到基于外泌体的药物递送系统有可能提高治疗的可及性、特异性和有效性,同时将脱靶效应降至最低,这可能会改变MS的治疗局面。