Trasplante de células troncales como terapia para la esclerosis lateral amiotrófica. Una mirada crítica

间充质干细胞 肌萎缩侧索硬化 干细胞 医学 干细胞疗法 神经营养因子 免疫学 疾病 癌症研究 生物 病理 细胞生物学 内科学 受体
作者
Bernardita Soler,Ricardo Fadić,Rommy von Bernhardi
出处
期刊:Revista De Neurologia [Viguera Publishers]
卷期号:52 (07): 426-426 被引量:11
标识
DOI:10.33588/rn.5207.2010483
摘要

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease. At present, there are not curative therapies for ALS. Pathogenic and progression mechanisms suggest the existence of oxidative stress, abnormal intracellular protein aggregation, mitochondrial dysfunction, axonal transport impairment, impairment of trophic support, altered glial cell function, and glutamate excitoxicity.To evaluate therapeutic results with adult stem cell for ALS treatment.Stem cells represent a potential therapeutic strategy, because their biological mechanisms could act on several of the pathogenic mechanisms proposed for ALS. Bone marrow mesenchymal stem cells are especially interesting among adult stem cells. Mesenchymal stem cells can differentiate in all central nervous system cells and potentially replace them. Furthermore, they have immunomodulatory effects, secreting, especially in neuroinflammatory environments, neurotrophic and antiinflammatory factors. Studies in murine models of ALS show decrease of inflammation and disease progression, and increase on animal highly heterogeneous, suggest that mesenchymal stem cells transplant in ALS appears to be safe. However, they fail showing clinical improvement of patients.Additional preclinical studies are necessary to refine this therapeutic approach, to assess long term survival and differentiation of mesenchymal stem cells, dosing, biological activity and safety should be conducted before any planning further human testing occurs.

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