Foetal Cell Transplantation for Parkinson’s Disease: Focus on Graft-Induced Dyskinesia

Transplantation of dopamine- (DA-) rich foetal ventral mesencephalic cells emerged as a promising therapy for Parkinson’s disease (PD), as it allowed significant improvement of motor symptoms in several PD patients in open-label studies. However, double-blind clinical trials have been largely disapp...

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Main Authors: Elisabetta Tronci, Camino Fidalgo, Manolo Carta
Format: Article
Language:English
Published: Hindawi Limited 2015-01-01
Series:Parkinson's Disease
Online Access:http://dx.doi.org/10.1155/2015/563820
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spelling doaj-113d41db1bd74b67942fd48698bd98b82020-11-25T00:19:58ZengHindawi LimitedParkinson's Disease2090-80832042-00802015-01-01201510.1155/2015/563820563820Foetal Cell Transplantation for Parkinson’s Disease: Focus on Graft-Induced DyskinesiaElisabetta Tronci0Camino Fidalgo1Manolo Carta2Department of Biomedical Sciences, Section of Physiology, Cagliari University, SS 554, km 4.500, 09042 Monserrato, ItalyDepartment of Biomedical Sciences, Section of Physiology, Cagliari University, SS 554, km 4.500, 09042 Monserrato, ItalyDepartment of Biomedical Sciences, Section of Physiology, Cagliari University, SS 554, km 4.500, 09042 Monserrato, ItalyTransplantation of dopamine- (DA-) rich foetal ventral mesencephalic cells emerged as a promising therapy for Parkinson’s disease (PD), as it allowed significant improvement of motor symptoms in several PD patients in open-label studies. However, double-blind clinical trials have been largely disappointing. The general agreement in the field is that the lack of standardization of tissue collection and preparation, together with the absence of postsurgical immunosuppression, played a key role in the failure of these studies. Moreover, a further complication that emerged in previous studies is the appearance of the so-called graft-induced dyskinesia (GID), in a subset of grafted patients, which resembles dyskinesia induced by L-DOPA but in the absence of medication. Preclinical evidence pointed to the serotonin neurons as possible players in the appearance of GID. In agreement, clinical investigations have shown that grafted tissue may contain a large number of serotonin neurons, in the order of half of the DA cells; moreover, the serotonin 5-HT1A receptor agonist buspirone has been found to produce significant dampening of GID in grafted patients. In this paper, we will review the recent preclinical and clinical studies focusing on cell transplantation for PD and on the mechanisms underlying GID.http://dx.doi.org/10.1155/2015/563820
collection DOAJ
language English
format Article
sources DOAJ
author Elisabetta Tronci
Camino Fidalgo
Manolo Carta
spellingShingle Elisabetta Tronci
Camino Fidalgo
Manolo Carta
Foetal Cell Transplantation for Parkinson’s Disease: Focus on Graft-Induced Dyskinesia
Parkinson's Disease
author_facet Elisabetta Tronci
Camino Fidalgo
Manolo Carta
author_sort Elisabetta Tronci
title Foetal Cell Transplantation for Parkinson’s Disease: Focus on Graft-Induced Dyskinesia
title_short Foetal Cell Transplantation for Parkinson’s Disease: Focus on Graft-Induced Dyskinesia
title_full Foetal Cell Transplantation for Parkinson’s Disease: Focus on Graft-Induced Dyskinesia
title_fullStr Foetal Cell Transplantation for Parkinson’s Disease: Focus on Graft-Induced Dyskinesia
title_full_unstemmed Foetal Cell Transplantation for Parkinson’s Disease: Focus on Graft-Induced Dyskinesia
title_sort foetal cell transplantation for parkinson’s disease: focus on graft-induced dyskinesia
publisher Hindawi Limited
series Parkinson's Disease
issn 2090-8083
2042-0080
publishDate 2015-01-01
description Transplantation of dopamine- (DA-) rich foetal ventral mesencephalic cells emerged as a promising therapy for Parkinson’s disease (PD), as it allowed significant improvement of motor symptoms in several PD patients in open-label studies. However, double-blind clinical trials have been largely disappointing. The general agreement in the field is that the lack of standardization of tissue collection and preparation, together with the absence of postsurgical immunosuppression, played a key role in the failure of these studies. Moreover, a further complication that emerged in previous studies is the appearance of the so-called graft-induced dyskinesia (GID), in a subset of grafted patients, which resembles dyskinesia induced by L-DOPA but in the absence of medication. Preclinical evidence pointed to the serotonin neurons as possible players in the appearance of GID. In agreement, clinical investigations have shown that grafted tissue may contain a large number of serotonin neurons, in the order of half of the DA cells; moreover, the serotonin 5-HT1A receptor agonist buspirone has been found to produce significant dampening of GID in grafted patients. In this paper, we will review the recent preclinical and clinical studies focusing on cell transplantation for PD and on the mechanisms underlying GID.
url http://dx.doi.org/10.1155/2015/563820
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