Neuroprotective gene therapy for Huntington's disease, using polymer-encapsulated cells engineered to secrete human ciliary neurotrophic factor: results of a phase I study.

Details

Serval ID
serval:BIB_61875A3FCA13
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Neuroprotective gene therapy for Huntington's disease, using polymer-encapsulated cells engineered to secrete human ciliary neurotrophic factor: results of a phase I study.
Journal
Human Gene Therapy
Author(s)
Bloch J., Bachoud-Lévi A.C., Déglon N., Lefaucheur J.P., Winkel L., Palfi S., Nguyen J.P., Bourdet C., Gaura V., Remy P., Brugières P., Boisse M.F., Baudic S., Cesaro P., Hantraye P., Aebischer P., Peschanski M.
ISSN
1043-0342 (Print)
ISSN-L
1043-0342
Publication state
Published
Issued date
2004
Volume
15
Number
10
Pages
968-975
Language
english
Notes
Publication types: Clinical Trial ; Clinical Trial, Phase I ; Journal Article ; Research Support, Non-U.S. Gov'tPublication Status: ppublish
Abstract
Huntington's disease (HD) is a monogenic neurodegenerative disease that affects the efferent neurons of the striatum. The protracted evolution of the pathology over 15 to 20 years, after clinical onset in adulthood, underscores the potential of therapeutic tools that would aim at protecting striatal neurons. Proteins with neuroprotective effects in the adult brain have been identified, among them ciliary neurotrophic factor (CNTF), which protected striatal neurons in animal models of HD. Accordingly, we have carried out a phase I study evaluating the safety of intracerebral administration of this protein in subjects with HD, using a device formed by a semipermeable membrane encapsulating a BHK cell line engineered to synthesize CNTF. Six subjects with stage 1 or 2 HD had one capsule implanted into the right lateral ventricle; the capsule was retrieved and exchanged for a new one every 6 months, over a total period of 2 years. No sign of CNTF-induced toxicity was observed; however, depression occurred in three subjects after removal of the last capsule, which may have correlated with the lack of any future therapeutic option. All retrieved capsules were intact but contained variable numbers of surviving cells, and CNTF release was low in 13 of 24 cases. Improvements in electrophysiological results were observed, and were correlated with capsules releasing the largest amount of CNTF. This phase I study shows the safety, feasibility, and tolerability of this gene therapy procedure. Heterogeneous cell survival, however, stresses the need for improving the technique.
Keywords
Animals, Brain/metabolism, Cell Line, Cell Survival, Ciliary Neurotrophic Factor/chemistry, Ciliary Neurotrophic Factor/genetics, Codon, Cricetinae, Electrophysiology, Female, Gene Therapy/methods, Gene Transfer Techniques, Humans, Huntington Disease/genetics, Huntington Disease/therapy, Male, Neurons/metabolism, Neuroprotective Agents/pharmacology, Polymers/chemistry, Retroviridae/genetics, Time Factors
Pubmed
Web of science
Create date
13/12/2011 17:32
Last modification date
20/08/2019 15:18
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