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The Potential of Stem Cell Therapy

机译:干细胞疗法的潜力

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Given their expected capacity to self-renew and differentiate efficiently into the desired cell type, clonal populations of stem cells (SC) promise to produce beneficial effects in a number of diseases [1]. Several studies already indicate the therapeutic potential of SC transplantation in ischemic lesions, with sources of SC that include embryonic (ESC), foetal and adult SC, and embryonal carcinoma (EC) cell lines [2]. These studies confirm the potential of the lesioned adult brain to host immature cell species, already demonstrated in the 80s, and that led to clinical trials for Parkinson's and Huntington's [3] diseases. However, much crucial information is still lacking before SC transplantation becomes a clinical reality for ischemic brain lesions. For instance, the standardization of the conditions to regulate SC proliferation and differentiation to produce region-specific grafts need to be better defined; changes in their properties induced by transplantation into lesioned brain structures are poorly understood, as is the full extent of functional improvement at long-term post-stroke delays. These are important steps to define the actual potential and limitation of the approach and to standardize the grafting procedures for routine clinical applications.
机译:鉴于其自我更新和有效分化为所需细胞类型的预期能力,干细胞(SC)的克隆种群有望在多种疾病中产生有益的作用[1]。一些研究已经表明SC移植在缺血性病变中的治疗潜力,其SC来源包括胚胎(ESC),胎儿和成年SC以及胚胎癌(EC)细胞系[2]。这些研究证实了患病的成年大脑具有容纳80年代未成熟细胞物种的潜力,从而导致了针对帕金森氏症和亨廷顿氏症[3]的临床试验。然而,在SC移植成为缺血性脑损伤的临床现实之前,仍然缺少许多关键信息。例如,需要更好地定义调节SC增殖和分化以产生特定区域移植物的条件的标准化;人们对中风后长期延误后功能的全面改善尚不甚了解,因为它们被移植到病变的脑部结构中引起的特性改变。这些是定义方法的实际潜力和局限性以及标准化常规临床应用移植程序的重要步骤。

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