神经系统疾病的干细胞疗法:当前进展、挑战和未来展望。

IF 2.8 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Ramyar Rahimi Darehbagh, Seyedeh Asrin Seyedoshohadaei, Rojin Ramezani, Nima Rezaei
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引用次数: 0

摘要

干细胞疗法利用干细胞的再生潜力,恢复受损的神经组织和电路,已成为治疗各种神经系统疾病的有前途的方法。这篇综合综述深入分析了干细胞在原发性神经疾病中的应用现状,包括帕金森病(PD)、阿尔茨海默病(AD)、肌萎缩侧索硬化症(ALS)、多发性硬化症(MS)、中风、脊髓损伤(SCI)和其他相关疾病。综述首先详细介绍了干细胞生物学,讨论了干细胞在神经系统疗法中的类型、来源和作用机制。然后,它对来自动物模型和早期人体试验的临床前证据进行了严格审查,调查了不同类型干细胞的安全性、可行性和有效性,如胚胎干细胞(ESC)、间充质干细胞(MSC)、神经干细胞(NSC)和诱导多能干细胞(iPSC)。虽然在临床前模型中对 ESCs 进行了广泛研究,但临床试验主要集中在间充质干细胞和 NSCs 等成体干细胞以及 iPSCs 及其衍生物。我们认真评估了每种细胞类型的研究现状,强调了它们在不同神经系统疾病中的潜在应用和局限性。综述综合了近期针对每种神经疾病的高质量研究的主要发现,讨论了细胞制造、输送方法和治疗结果。文章强调了干细胞替代失去的神经元和直接重建神经回路的潜力,同时也强调了旁分泌和免疫调节机制在介导干细胞对大多数神经系统疾病的治疗效果中的关键作用。文章还探讨了将干细胞疗法转化为临床实践所面临的挑战和限制,包括与细胞来源、可扩展性、安全性和监管考虑有关的问题。此外,文章还讨论了推进干细胞疗法的未来方向和机遇,如基因编辑、生物材料、个性化iPSC衍生疗法和新型递送策略。综述最后强调了干细胞疗法在彻底改变神经系统疾病治疗方面的变革潜力,同时承认需要严格的临床试验、标准化方案和多学科合作,以实现其全部治疗承诺。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Stem cell therapies for neurological disorders: current progress, challenges, and future perspectives.

Stem cell-based therapies have emerged as a promising approach for treating various neurological disorders by harnessing the regenerative potential of stem cells to restore damaged neural tissue and circuitry. This comprehensive review provides an in-depth analysis of the current state of stem cell applications in primary neurological conditions, including Parkinson's disease (PD), Alzheimer's disease (AD), amyotrophic lateral sclerosis (ALS), multiple sclerosis (MS), stroke, spinal cord injury (SCI), and other related disorders. The review begins with a detailed introduction to stem cell biology, discussing the types, sources, and mechanisms of action of stem cells in neurological therapies. It then critically examines the preclinical evidence from animal models and early human trials investigating the safety, feasibility, and efficacy of different stem cell types, such as embryonic stem cells (ESCs), mesenchymal stem cells (MSCs), neural stem cells (NSCs), and induced pluripotent stem cells (iPSCs). While ESCs have been studied extensively in preclinical models, clinical trials have primarily focused on adult stem cells such as MSCs and NSCs, as well as iPSCs and their derivatives. We critically assess the current state of research for each cell type, highlighting their potential applications and limitations in different neurological conditions. The review synthesizes key findings from recent, high-quality studies for each neurological condition, discussing cell manufacturing, delivery methods, and therapeutic outcomes. While the potential of stem cells to replace lost neurons and directly reconstruct neural circuits is highlighted, the review emphasizes the critical role of paracrine and immunomodulatory mechanisms in mediating the therapeutic effects of stem cells in most neurological disorders. The article also explores the challenges and limitations associated with translating stem cell therapies into clinical practice, including issues related to cell sourcing, scalability, safety, and regulatory considerations. Furthermore, it discusses future directions and opportunities for advancing stem cell-based treatments, such as gene editing, biomaterials, personalized iPSC-derived therapies, and novel delivery strategies. The review concludes by emphasizing the transformative potential of stem cell therapies in revolutionizing the treatment of neurological disorders while acknowledging the need for rigorous clinical trials, standardized protocols, and multidisciplinary collaboration to realize their full therapeutic promise.

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来源期刊
European Journal of Medical Research
European Journal of Medical Research 医学-医学:研究与实验
CiteScore
3.20
自引率
0.00%
发文量
247
审稿时长
>12 weeks
期刊介绍: European Journal of Medical Research publishes translational and clinical research of international interest across all medical disciplines, enabling clinicians and other researchers to learn about developments and innovations within these disciplines and across the boundaries between disciplines. The journal publishes high quality research and reviews and aims to ensure that the results of all well-conducted research are published, regardless of their outcome.
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