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Stem cell-based therapies in Parkinson’s disease: future hope or current treatment option?

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Abstract

Parkinson’s disease (PD) is one of the most frequent neurodegenerative diseases and represents a major therapeutic challenge because of the so far missing therapeutic means to influence the ongoing loss of dopaminergic innervation to the striatum. Cell replacement has raised hope to offer the first restorative treatment option. Clinical trials have provided “proof of principle” that transplantation of dopamine-producing neurons into the striatum of PD patients can achieve symptomatic relief given that the striatum is sufficiently re-innervated. Various cell sources have been tested, including fetal ventral midbrain tissue, embryonic stem cells, fetal and adult neural stem cells and, after a ground-breaking discovery, induced pluripotent stem cells. Although embryonic and induced pluripotent stem cells have emerged as the most promising candidates to overcome most of the obstacles to clinical successful cell replacement, each cell source has its unique drawbacks. This review does not only provide a comprehensive overview of the different cellular candidates, including their assets and drawbacks, but also of the various additional issues that need to be addressed in order to convert cellular replacement therapies from an experimental to a clinically relevant therapeutic alternative.

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Conflict of interest

The research of the authors was supported by the Dresden Medical Faculty Research Program MeDDrive, the Bundesministerium für Bildung und Forschung, the Deutsche Forschungsgemeinschaft (DFG) through the Sonderforschungsbereich 655 “From cells to tissues” and the DFG-Research Center and Cluster of Excellence “Center for Regenerative Therapies Dresden (CRTD)”, the Thyssen-Stiftung, and the Landesstiftung Baden-Württemberg.

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Correspondence to Alexander Storch.

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This article is part of a supplement sponsored by GlaxoSmithKline.

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Loewenbrück, K., Storch, A. Stem cell-based therapies in Parkinson’s disease: future hope or current treatment option?. J Neurol 258 (Suppl 2), 346–353 (2011). https://doi.org/10.1007/s00415-011-5974-4

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