观点:帕金森病的疾病修饰和基于细胞分泌组的方法:我们在正确的轨道上吗?

IF 5.3 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Biologics : Targets & Therapy Pub Date : 2021-07-29 eCollection Date: 2021-01-01 DOI:10.2147/BTT.S267281
Thomas Müller
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引用次数: 1

摘要

特发性帕金森氏症这个术语描述的是一种由各种特征不明确的疾病组成的实体,这些疾病彼此相似。它们的特点是由各种疾病机制引起的慢性神经元死亡。它们导致运动和相关非运动特征的发作,这两种特征都对个性化药物组合和手术治疗有反应。未满足的需求是有益的病程改变与修复和神经发生。目的是讨论基于细胞分泌组的治疗的价值,包括神经元移植,并建议作为一种替代刺激的内源性可用的方法来修复神经元。慢性神经退行性过程由不同的异质性,但互补的代谢,病理级联序列引起。从实验研究中积累的证据表明,神经元移植、干细胞应用和基于细胞分泌组的治疗是未来有希望的治疗方法,最终目标是治愈。迄今为止,对疾病改善治疗的临床试验主要集中在替代或修复诊断后剩余的多巴胺合成神经元。在诊断时,许多仍然存活和功能,但已经受到影响的神经元已经失去了大部分轴突,并准备细胞死亡。一个更有希望的治疗概念可能是刺激周围和中枢神经系统中现有的内源性修复系统。丰富的蛋白排斥引导分子A阻断修复和神经发生,这两者都是通过新生素受体介导的。抑制排斥性引导分子A的生理作用是慢性神经退行性变的内源性有效修复途径。这种蛋白与抗体的拮抗或对新生素受体的刺激应被视为最初的修复步骤。它是细胞替代、干细胞或相关细胞分泌组概念的替代方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

View Point: Disease Modification and Cell Secretome Based Approaches in Parkinson's Disease: Are We on the Right Track?

View Point: Disease Modification and Cell Secretome Based Approaches in Parkinson's Disease: Are We on the Right Track?

The term idiopathic Parkinson's disease describes an entity of various not well-characterized disorders resembling each other. They are characterized by chronic neuronal dying originating from various disease mechanisms. They result in the onset of motor and related non-motor features, both of which respond to administration of personalized drug combinations and surgical therapies. The unmet need is beneficial disease course modification with repair and neurogenesis. Objectives are to discuss the value of cell secretome based treatments including neuronal graft transplantation and to suggest as an alternative the stimulation of an endogenous available approach for neuronal repair. Chronic neurodegenerative processes result from different heterogeneous, but complementing metabolic, pathological cascade sequences. Accumulated evidence from experimental research suggested neuron transplantation, stem cell application and cell secretome-based therapies as a promising future treatment with cure as an ultimate goal. To date, clinical testing of disease-modifying treatments has focused on substitution or repair of the remaining dopamine synthesizing neurons following diagnosis. At diagnosis, many of the still surviving and functioning, but already affected neurons have lost most of their axons and are primed for cell death. A more promising therapeutic concept may be the stimulation of an existing, endogenous repair system in the peripheral and central nervous systems. The abundant protein repulsive guidance molecule A blocks restoration and neurogenesis, both of which are mediated via the neogenin receptor. Inhibition of the physiological effects of repulsive guidance molecule A is an endogenous available repair pathway in chronic neurodegeneration. Antagonism of this protein with antibodies or stimulation of the neogenin receptor should be considered as an initial repair step. It is an alternative to cell replacement, stem cell or associated cell secretome concepts.

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来源期刊
Biologics : Targets & Therapy
Biologics : Targets & Therapy MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
8.30
自引率
0.00%
发文量
22
审稿时长
16 weeks
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