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Mesenchymal stem cells to treat diabetic neuropathy: a long and strenuous way from bench to the clinic

机译:间充质干细胞治疗糖尿病性神经病:从实验台到临床的漫长而艰辛的方式

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As one of the most common complications of diabetes, diabetic neuropathy often causes foot ulcers and even limb amputations. Inspite of continuous development in antidiabetic drugs, there is still no efficient therapy to cure diabetic neuropathy. Diabetic neuropathy shows declined vascularity in peripheral nerves and lack of angiogenic and neurotrophic factors. Mesenchymal stem cells (MSCs) have been indicated as a novel emerging regenerative therapy for diabetic neuropathy because of their multipotency. We will briefly review the pathogenesis of diabetic neuropathy, characteristic of MSCs, effects of MSC therapies for diabetic neuropathy and its related mechanisms. In order to treat diabetic neuropathy, neurotrophic or angiogenic factors in the form of protein or gene therapy are delivered to diabetic neuropathy, but therapeutic efficiencies are very modest if not ineffective. MSC treatment reverses manifestations of diabetic neuropathy. MSCs have an important role to repair tissue and to lower blood glucose level. MSCs even paracrinely secrete neurotrophic factors, angiogenic factors, cytokines, and immunomodulatory substances to ameliorate diabetic neuropathy. There are still several challenges in the clinical translation of MSC therapy, such as safety, optimal dose of administration, optimal mode of cell delivery, issues of MSC heterogeneity, clinically meaningful engraftment, autologous or allogeneic approach, challenges with cell manufacture, and further mechanisms.
机译:糖尿病性神经病是糖尿病最常见的并发症之一,通常会导致足部溃疡甚至截肢。尽管抗糖尿病药物不断发展,但仍没有有效的疗法来治疗糖尿病性神经病。糖尿病性神经病显示周围神经的血管减少以及缺乏血管生成和神经营养因子。间充质干细胞(MSCs)由于其多能性而已被指示为糖尿病神经病的一种新兴的再生疗法。我们将简要回顾一下糖尿病性神经病的发病机制,MSCs的特征,MSC治疗糖尿病性神经病的效果及其相关机制。为了治疗糖尿病性神经病,以蛋白质或基因疗法的形式的神经营养或血管生成因子被递送至糖尿病性神经病,但是即使不是无效的治疗效率也非常适中。 MSC治疗可逆转糖尿病性神经病变的表现。 MSC具有修复组织和降低血糖水平的重要作用。 MSC甚至旁分泌分泌神经营养因子,血管生成因子,细胞因子和免疫调节物质,以改善糖尿病性神经病。 MSC治疗的临床翻译仍然存在一些挑战,例如安全性,最佳给药剂量,最佳细胞递送方式,MSC异质性问题,具有临床意义的植入,自体或同种异体途径,细胞制造挑战以及其他机制。

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