Adeno-associated virus vector Genomes persist as episomal chromatin in primate muscle

被引:219
作者
Penaud-Budloo, Magalie [3 ]
Le Guiner, Caroline [3 ]
Nowrouzi, Ali [5 ]
Toromanoff, Alice [3 ]
Cherel, Yan [4 ]
Chenuaud, Pierre [3 ]
Schmidt, Manfred [5 ]
von Kalle, Christof [5 ]
Rolling, Fabienne [3 ]
Moullier, Philippe [1 ,3 ,6 ]
Snyder, Richard O. [1 ,2 ,3 ]
机构
[1] Univ Florida, Dept Mol Genet & Microbiol, Coll Med, Gainesville, FL 32610 USA
[2] Univ Florida, Ctr Excellence Regenerat Hlth Biotechnol, Gainesville, FL 32610 USA
[3] CHU Hotel Dieu, INSERM UMR 649, F-44035 Nantes, France
[4] Ecole Natl Vet, INRA UMR 703, F-44000 Nantes, France
[5] German Canc Res Ctr, Dept Translat Oncol, D-69120 Heidelberg, Germany
[6] Etablissement Francais Sand Pays Loire, F-44000 Nantes, France
关键词
D O I
10.1128/JVI.00649-08
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Recombinant adeno-associated virus (rAAV) vectors are capable of mediating long-term gene expression following administration to skeletal muscle. In rodent muscle, the vector genomes persist in the nucleus in concatemeric episomal forms. Here, we demonstrate with nonhuman primates that rAAV vectors integrate inefficiently into the chromosomes of myocytes and reside predominantly as episomal monomeric and concatemeric circles. The episomal rAAV genomes assimilate into chromatin with a typical nucleosomal pattern. The persistence of the vector genomes and gene expression for years in quiescent tissues suggests that a bona fide chromatin structure is important for episomal maintenance and transgene expression. These findings were obtained from primate muscles transduced with rAAV1 and rAAV8 vectors for up to 22 months after intramuscular delivery of 5 x 10(12) viral genomes/kg. Because of this unique context, our data, which provide important insight into in situ vector biology, are highly relevant from a clinical standpoint.
引用
收藏
页码:7875 / 7885
页数:11
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