首页> 美国卫生研究院文献>International Journal of Molecular Sciences >Cell Therapies under Clinical Trials and Polarized Cell Therapies in Pre-Clinical Studies to Treat Ischemic Stroke and Neurological Diseases: A Literature Review
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Cell Therapies under Clinical Trials and Polarized Cell Therapies in Pre-Clinical Studies to Treat Ischemic Stroke and Neurological Diseases: A Literature Review

机译:在临床前试验中的细胞疗法和偏振细胞疗法治疗缺血性卒中和神经疾病的临床研究:文献综述

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摘要

Stroke remains a major cause of serious disability because the brain has a limited capacity to regenerate. In the last two decades, therapies for stroke have dramatically changed. However, half of the patients cannot achieve functional independence after treatment. Presently, cell-based therapies are being investigated to improve functional outcomes. This review aims to describe conventional cell therapies under clinical trial and outline the novel concept of polarized cell therapies based on protective cell phenotypes, which are currently in pre-clinical studies, to facilitate functional recovery after post-reperfusion treatment in patients with ischemic stroke. In particular, non-neuronal stem cells, such as bone marrow-derived mesenchymal stem/stromal cells and mononuclear cells, confer no risk of tumorigenesis and are safe because they do not induce rejection and allergy; they also pose no ethical issues. Therefore, recent studies have focused on them as a cell source for cell therapies. Some clinical trials have shown beneficial therapeutic effects of bone marrow-derived cells in this regard, whereas others have shown no such effects. Therefore, more clinical trials must be performed to reach a conclusion. Polarized microglia or peripheral blood mononuclear cells might provide promising therapeutic strategies after stroke because they have pleiotropic effects. In traumatic injuries and neurodegenerative diseases, astrocytes, neutrophils, and T cells were polarized to the protective phenotype in pre-clinical studies. As such, they might be useful therapeutic targets. Polarized cell therapies are gaining attention in the treatment of stroke and neurological diseases.
机译:中风仍然是严重残疾的主要原因,因为大脑具有有限的再生能力。在过去的二十年中,卒中的疗法大大改变。然而,一半患者在治疗后无法达到功能独立性。目前,正在研究基于细胞的疗法以改善功能性结果。本综述旨在描述临床试验下的常规细胞疗法,概述基于目前在临床前研究中的保护性细胞表型的偏振细胞疗法的新颖概念,以促进缺血性卒中患者再灌注治疗后的功能恢复。特别地,非神经元干细胞,例如骨髓衍生的间充质茎/基质细胞和单核细胞,赋予肿瘤发生的风险,并且是安全的,因为它们不会诱导排斥和过敏;他们也没有道德问题。因此,最近的研究将它们集中在它们中作为细胞疗法的细胞来源。在这方面,一些临床试验表明骨髓衍生细胞的有益治疗效果,而其他临床试验则显示出没有这样的效果。因此,必须进行更多的临床试验以得出结论。偏振片微胶质或外周血单核细胞可能在中风后提供有前途的治疗策略,因为它们具有抗脂肪效应。在创伤性损伤和神经变性疾病中,星形胶质细胞,中性粒细胞和T细胞被临床研究中的保护表型偏振。因此,它们可能是有用的治疗目标。偏振细胞疗法正在治疗中风和神经疾病的治疗中。

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