| Literature DB >> 16407771 |
Marcel M Daadi1, Phillip Pivirotto, John Bringas, Janet Cunningham, John Forsayeth, Jamie Eberling, Krys S Bankiewicz.
Abstract
The present report describes for the first time, the stability of recombinant adeno-associated virus serotype 2 (AAV2) human aromatic L-amino acid decarboxylase (hAADC) gene transfer after 3-year survival time in a non-human primate model of Parkinson's disease. 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine-lesioned monkeys were treated with six injections of 30 microl/site of AAV2-hAADC at a concentration of 2 x 10(12) vg/ml into the caudate and putamen. Stereological analysis revealed a 46.6% increase in the total number of AAV2-hAADC-transduced cells in the striatum between 8 weeks and 3 years after gene transfer survival time. In the 8-week animals, the distribution of the AADC+ cells was dispersed and heterogeneous, whereas in the 3-year animals it was widespread and homogenous. Confocal analysis demonstrated that approximately 85% of the AADC+ cells were neuronal nuclei immunoreactive.Entities:
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Year: 2006 PMID: 16407771 DOI: 10.1097/01.wnr.0000198952.38563.05
Source DB: PubMed Journal: Neuroreport ISSN: 0959-4965 Impact factor: 1.837