Ekrani Seyedeh Toktam, Mahmoudi Mahmoud, Haghmorad Dariush, Kheder Ramiar Kamal, Hatami Alireza, Esmaeili Seyed-Alireza
Department of Immunology, Semnan University of Medical Sciences, Semnan, Iran.
Cancer Research Center, Semnan University of Medical Sciences, Semnan, Iran.
Stem Cell Res Ther. 2024 Dec 18;15(1):476. doi: 10.1186/s13287-024-04073-9.
Mesenchymal stem cell (MSC) therapy has been considered a promising approach for the treatment of Parkinson's disease (PD) for several years. PD is a globally prevalent neurodegenerative disease characterized by the accumulation of Lewy bodies and the loss of dopaminergic neurons, leading to severe motor and non-motor complications in patients. As current treatments are unable to halt the progression of neuronal loss and dopamine degradation, MSC therapy has emerged as a highly promising strategy for PD treatment. This promise is due to MSCs' unique properties compared to other types of stem cells, including self-renewal, differentiation potential, immune privilege, secretion of neurotrophic factors, ability to improve damaged tissue, modulation of the immune system, and lack of ethical concerns. MSCs have been employed in numerous pre-clinical and clinical studies for PD treatment with promising results. However, certain aspects of their efficacy in treating PD may benefit from various genetic and epigenetic modifications. In this review article, we assess these approaches to improving MSCs for specialized treatment of PD.
多年来,间充质干细胞(MSC)疗法一直被认为是治疗帕金森病(PD)的一种有前景的方法。帕金森病是一种全球普遍存在的神经退行性疾病,其特征是路易小体的积累和多巴胺能神经元的丧失,导致患者出现严重的运动和非运动并发症。由于目前的治疗方法无法阻止神经元丧失和多巴胺降解的进展,MSC疗法已成为一种极有前景的帕金森病治疗策略。这种前景归因于与其他类型干细胞相比,间充质干细胞具有独特的特性,包括自我更新、分化潜能、免疫特权、神经营养因子分泌、改善受损组织的能力、免疫系统调节以及不存在伦理问题。间充质干细胞已被用于众多治疗帕金森病的临床前和临床研究,并取得了有前景的结果。然而,它们在治疗帕金森病方面的疗效的某些方面可能受益于各种基因和表观遗传修饰。在这篇综述文章中,我们评估这些改善间充质干细胞以专门治疗帕金森病的方法。