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Combining polymeric devices and stem cells for the treatment of neurological disorders: a promising therapeutic approach.

机译:结合聚合物设备和干细胞治疗神经系统疾病:一种有前途的治疗方法。

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Cell therapy will probably become a major therapeutic strategy for neuronal disorders in the coming years. Nevertheless, due to poor survival of grafted cells and limited differentiation and integration in the host tissue, certain ameliorations must be envisaged. To address these difficulties, several strategies have been developed and among them, two methods seem particularly promising : in situ controlled drug delivery and implantation of cells adhered on biomaterial-based scaffolds. Indeed, the ability of drugs, such as growth factors, to regulate neuronal survival and/or plasticity infers the use of these molecules to treat neurodegeneration associated with human diseases. Moreover, the synthesis of cell scaffolds which mimic the extra-cellular matrix can help guide morphogenesis and tissue repair. Furthermore, cells can be cultivated on these matrices that may eventually make graft therapy a more practical approach for the treatment of neurological diseases. Nevertheless, for those two encouragingapproaches multiple parameters have to be considered, such as the drug targeting strategy, but also the physical and morphological characteristics of the scaffold and the type of cells to be conveyed. This review thus focuses on those two promising strategies and also on their possible association to improve stem cell therapy of neurodegenerative disorders. Indeed, tissue replacement by grafting cells within or adhered onto drug delivering biomaterial-based devices, has recently been reported and seems to be very promising.
机译:在未来几年中,细胞疗法可能会成为神经元疾病的主要治疗策略。然而,由于移植细胞的存活率低以及宿主组织中有限的分化和整合,必须考虑某些改善措施。为了解决这些困难,已经开发了几种策略,其中,两种方法似乎特别有前途:原位控制药物递送和粘附在基于生物材料的支架上的细胞的植入。实际上,诸如生长因子之类的药物调节神经元存活和/或可塑性的能力推断出这些分子用于治疗与人类疾病有关的神经变性的用途。此外,模拟细胞外基质的细胞支架的合成可以帮助指导形态发生和组织修复。此外,可以在这些基质上培养细胞,这最终可能使移植疗法成为治疗神经系统疾病的更实用方法。然而,对于这两种令人鼓舞的方法,必须考虑多个参数,例如药物靶向策略,还需要考虑支架的物理和形态特征以及要转运的细胞类型。因此,本综述着眼于这两种有前途的策略,以及它们在改善神经退行性疾病的干细胞治疗方面的可能联系。实际上,近来已经报道了通过将细胞移植到或粘附在基于生物材料的药物输送装置上的组织替代组织,这似乎非常有希望。

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