AAV5-miHTT gene therapy demonstrates suppression of mutant huntingtin aggregation and neuronal dysfunction in a rat model of Huntington's disease.

Détails

Ressource 1Télécharger: gt201771a.pdf (2798.69 [Ko])
Etat: Public
Version: Final published version
ID Serval
serval:BIB_4A0A2A0ACFFD
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
AAV5-miHTT gene therapy demonstrates suppression of mutant huntingtin aggregation and neuronal dysfunction in a rat model of Huntington's disease.
Périodique
Gene therapy
Auteur⸱e⸱s
Miniarikova J., Zimmer V., Martier R., Brouwers C.C., Pythoud C., Richetin K., Rey M., Lubelski J., Evers M.M., van Deventer S.J., Petry H., Déglon N., Konstantinova P.
ISSN
1476-5462 (Electronic)
ISSN-L
0969-7128
Statut éditorial
Publié
Date de publication
10/2017
Peer-reviewed
Oui
Volume
24
Numéro
10
Pages
630-639
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: ppublish
Résumé
Huntington's disease (HD) is a fatal progressive neurodegenerative disorder caused by a mutation in the huntingtin (HTT) gene. To date, there is no treatment to halt or reverse the course of HD. Lowering of either total or only the mutant HTT expression is expected to have therapeutic benefit. This can be achieved by engineered micro (mi)RNAs targeting HTT transcripts and delivered by an adeno-associated viral (AAV) vector. We have previously showed a miHTT construct to induce total HTT knock-down in Hu128/21 HD mice, while miSNP50T and miSNP67T constructs induced allele-selective HTT knock-down in vitro. In the current preclinical study, the mechanistic efficacy and gene specificity of these selected constructs delivered by an AAV serotype 5 (AAV5) vector was addressed using an acute HD rat model. Our data demonstrated suppression of mutant HTT messenger RNA, which almost completely prevented mutant HTT aggregate formation, and ultimately resulted in suppression of DARPP-32-associated neuronal dysfunction. The AAV5-miHTT construct was found to be the most efficient, although AAV5-miSNP50T demonstrated the anticipated mutant HTT allele selectivity and no passenger strand expression. Ultimately, AAV5-delivered-miRNA-mediated HTT lowering did not cause activation of microglia or astrocytes suggesting no immune response to the AAV5 vector or therapeutic precursor sequences. These preclinical results suggest that using gene therapy to knock-down HTT may provide important therapeutic benefit for HD patients and raised no safety concerns, which supports our ongoing efforts for the development of an RNA interference-based gene therapy product for HD.

Mots-clé
Animals, Dependovirus/genetics, Genetic Vectors/genetics, Humans, Huntington Disease/genetics, Huntington Disease/therapy, Male, Microglia/metabolism, Mutation, Nerve Tissue Proteins/genetics, Nerve Tissue Proteins/metabolism, Neurons/metabolism, Neurons/pathology, Nuclear Proteins/genetics, Nuclear Proteins/metabolism, RNAi Therapeutics/adverse effects, RNAi Therapeutics/methods, Rats, Rats, Sprague-Dawley
Pubmed
Web of science
Open Access
Oui
Création de la notice
05/09/2017 17:45
Dernière modification de la notice
20/08/2019 14:57
Données d'usage