Clinical application of stem cell therapy in Parkinson's disease
(2012) In BMC Medicine 10.- Abstract
- Cell replacement therapies in Parkinson's disease (PD) aim to provide long-lasting relief of patients' symptoms. Previous clinical trials using transplantation of human fetal ventral mesencephalic (hfVM) tissue in the striata of PD patients have provided proof-of-principle that such grafts can restore striatal dopaminergic (DA-ergic) function. The transplants survive, reinnervate the striatum, and generate adequate symptomatic relief in some patients for more than a decade following operation. However, the initial clinical trials lacked homogeneity of outcomes and were hindered by the development of troublesome graft-induced dyskinesias in a subgroup of patients. Although recent knowledge has provided insights for overcoming these... (More)
- Cell replacement therapies in Parkinson's disease (PD) aim to provide long-lasting relief of patients' symptoms. Previous clinical trials using transplantation of human fetal ventral mesencephalic (hfVM) tissue in the striata of PD patients have provided proof-of-principle that such grafts can restore striatal dopaminergic (DA-ergic) function. The transplants survive, reinnervate the striatum, and generate adequate symptomatic relief in some patients for more than a decade following operation. However, the initial clinical trials lacked homogeneity of outcomes and were hindered by the development of troublesome graft-induced dyskinesias in a subgroup of patients. Although recent knowledge has provided insights for overcoming these obstacles, it is unlikely that transplantation of hfVM tissue will become routine treatment for PD owing to problems with tissue availability and standardization of the grafts. The main focus now is on producing DA-ergic neuroblasts for transplantation from stem cells (SCs). There is a range of emerging sources of SCs for generating a DA-ergic fate in vitro. However, the translation of these efforts in vivo currently lacks efficacy and sustainability. A successful, clinically competitive SC therapy in PD needs to produce longlasting symptomatic relief without side effects while counteracting PD progression. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/2416045
- author
- Politis, Marios and Lindvall, Olle LU
- organization
- publishing date
- 2012
- type
- Contribution to journal
- publication status
- published
- subject
- in
- BMC Medicine
- volume
- 10
- publisher
- BioMed Central (BMC)
- external identifiers
-
- wos:000300168300001
- scopus:84855291126
- pmid:22216957
- ISSN
- 1741-7015
- DOI
- 10.1186/1741-7015-10-1
- language
- English
- LU publication?
- yes
- id
- b479f93f-b00f-4bbb-9a39-596e57e21431 (old id 2416045)
- date added to LUP
- 2016-04-01 14:40:24
- date last changed
- 2022-05-08 00:10:57
@article{b479f93f-b00f-4bbb-9a39-596e57e21431, abstract = {{Cell replacement therapies in Parkinson's disease (PD) aim to provide long-lasting relief of patients' symptoms. Previous clinical trials using transplantation of human fetal ventral mesencephalic (hfVM) tissue in the striata of PD patients have provided proof-of-principle that such grafts can restore striatal dopaminergic (DA-ergic) function. The transplants survive, reinnervate the striatum, and generate adequate symptomatic relief in some patients for more than a decade following operation. However, the initial clinical trials lacked homogeneity of outcomes and were hindered by the development of troublesome graft-induced dyskinesias in a subgroup of patients. Although recent knowledge has provided insights for overcoming these obstacles, it is unlikely that transplantation of hfVM tissue will become routine treatment for PD owing to problems with tissue availability and standardization of the grafts. The main focus now is on producing DA-ergic neuroblasts for transplantation from stem cells (SCs). There is a range of emerging sources of SCs for generating a DA-ergic fate in vitro. However, the translation of these efforts in vivo currently lacks efficacy and sustainability. A successful, clinically competitive SC therapy in PD needs to produce longlasting symptomatic relief without side effects while counteracting PD progression.}}, author = {{Politis, Marios and Lindvall, Olle}}, issn = {{1741-7015}}, language = {{eng}}, publisher = {{BioMed Central (BMC)}}, series = {{BMC Medicine}}, title = {{Clinical application of stem cell therapy in Parkinson's disease}}, url = {{https://lup.lub.lu.se/search/files/4102554/2835984.pdf}}, doi = {{10.1186/1741-7015-10-1}}, volume = {{10}}, year = {{2012}}, }