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...
Vectors based on adenovirus (Ad) are one of the most commonly utilized platforms for gene delivery t...
International audienceLegitimate uses of gene transfer technology can benefit from sensitive detecti...
Recentstudies have shown that wild-type and recombinant adeno-associated virus (AAV and rAAV) genome...
International audienceRecombinant adeno-associated virus (rAAV) vectors are capable of mediating lon...
Recombinant adeno-associated viral (rAAV) vectors can support long-term transgene expression in quie...
Profiles of recombinant adeno-associated virus (rAAV)-mediated transduction show interspecies differ...
Recombinant adeno-associated virus (rAAV) vectors have been shown to be useful for efficient gene de...
The liver is a major off-target organ in gene therapy approaches for cardiac and musculoskeletal dis...
Adeno- associated virus (AAV) vectors are one of the most frequently applied gene transfer systems i...
Mesenchymal stromal cells (MSCs) show great promise for ex vivo gene and cell-mediated therapies. Th...
Muscle-directed gene transfer is being considered for the treatment of several metabolic diseases, i...
Previously we showed that recombinant adenoviral helper-dependent (HD) vectors result in long-term t...
International audiencePreclinical gene therapy strategies using recombinant adeno-associated virus (...
AbstractWe demonstrated the presence of two adeno-associated viruses (AAVs), designated AAV10 and AA...
Preclinical gene therapy strategies using recombinant adeno-associated virus (AAV) vectors in animal...
Vectors based on adenovirus (Ad) are one of the most commonly utilized platforms for gene delivery t...
International audienceLegitimate uses of gene transfer technology can benefit from sensitive detecti...
Recentstudies have shown that wild-type and recombinant adeno-associated virus (AAV and rAAV) genome...
International audienceRecombinant adeno-associated virus (rAAV) vectors are capable of mediating lon...
Recombinant adeno-associated viral (rAAV) vectors can support long-term transgene expression in quie...
Profiles of recombinant adeno-associated virus (rAAV)-mediated transduction show interspecies differ...
Recombinant adeno-associated virus (rAAV) vectors have been shown to be useful for efficient gene de...
The liver is a major off-target organ in gene therapy approaches for cardiac and musculoskeletal dis...
Adeno- associated virus (AAV) vectors are one of the most frequently applied gene transfer systems i...
Mesenchymal stromal cells (MSCs) show great promise for ex vivo gene and cell-mediated therapies. Th...
Muscle-directed gene transfer is being considered for the treatment of several metabolic diseases, i...
Previously we showed that recombinant adenoviral helper-dependent (HD) vectors result in long-term t...
International audiencePreclinical gene therapy strategies using recombinant adeno-associated virus (...
AbstractWe demonstrated the presence of two adeno-associated viruses (AAVs), designated AAV10 and AA...
Preclinical gene therapy strategies using recombinant adeno-associated virus (AAV) vectors in animal...
Vectors based on adenovirus (Ad) are one of the most commonly utilized platforms for gene delivery t...
International audienceLegitimate uses of gene transfer technology can benefit from sensitive detecti...
Recentstudies have shown that wild-type and recombinant adeno-associated virus (AAV and rAAV) genome...