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34 - Status of neural repair clinical trials in brain diseases

from Section B4 - Translational research: application to human neural injury

Published online by Cambridge University Press:  05 March 2012

Olle Lindvall
Affiliation:
Section of Restorative Neurology, Wallenberg Neuroscience Center, University Hospital
Peter Hagell
Affiliation:
Section of Restorative Neurology, Wallenberg Neuroscience Center, University Hospital and Department of Nursing, Lund University, Lund, Sweden
Michael Selzer
Affiliation:
University of Pennsylvania
Stephanie Clarke
Affiliation:
Université de Lausanne, Switzerland
Leonardo Cohen
Affiliation:
National Institute of Mental Health, Bethesda, Maryland
Pamela Duncan
Affiliation:
University of Florida
Fred Gage
Affiliation:
Salk Institute for Biological Studies, San Diego
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Summary

Introduction

The interest in neuronal replacement therapies for human brain disorders dates back to the late 1970s when it was demonstrated that intrastriatal grafts of embryonic mesencephalic tissue, rich in dopamine (DA) neurons, induced functional recovery in rats with neurotoxin-induced lesions of the nigrostriatal dopaminergic system (for references see, e.g., Brundin et al., 1994). These observations provided the first evidence that neurons implanted into the adult brain could reverse behavioral deficits in an animal model of a human neurological disorder, Parkinson's disease (PD). Based on a bulk of experimental data in rodents and non-human primates (Annett, 1994; Brundin et al., 1994), the first clinical trials with neural transplantation in PD were initiated in 1987. Successful studies in animal models of Huntington's disease (HD) (for references see, e.g., Dunnett et al., 2000) lead to the first attempts with embryonic striatal grafts implanted into the striatum of HD patients in the 1990s. In addition, neural transplantation has been applied, with varying degree of scientific foundation, also in patients with other disorders such as stroke and epilepsy. Although the clinical studies with primary embryonic tissue seem to provide proof-of-principle for the cell replacement strategy, at least in PD (see Volume II, Chapter 6), it is obvious that other sources of cells are needed if cell-based approaches should become clinically competitive.

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Publisher: Cambridge University Press
Print publication year: 2006

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