Abstract Adeno-associated virus (AAV) differs from most other viruses, as it requires the simultaneous presence of a helper virus for an active infection. Up to 80% of the human population is seropositive for AAV antibodies. AAV has been known to be a non-pathogenic virus and an inhibitor of carcinogenesis caused by coinfecting viruses. However, the recent reports associating AAV infection with hepatocellular carcinoma development and the mysterious cases of acute severe hepatitis in children have challenged the idea that AAV is a harmless virus. Herein, we explore the usefulness of AAV in gene therapy and the importance of AAV as a protector or perpetrator in human carcinogenesis, ultimately reflecting on the dual role of AAV in human heal...
Recombinant AAV efficacy has been demonstrated in numerous gene therapy preclinical studies. As this...
Abstract Background Engineered versions of adeno-associated virus (AAV) are commonly used in gene th...
To examine the potential of AAV as a vector for gene transfer in glial cells, an established astrocy...
International audienceOBJECTIVE:Adeno-associated virus (AAV) is a defective mono-stranded DNA virus,...
The adeno-associated virus (AAV) has rapidly gained popularity in gene therapy since the establishme...
Infection with the helper virus-dependent human parvovirus adeno-associated virus (AAV) is known to ...
Adeno-associated virus (AAV) is a ubiquitous human helper-dependent parvovirus which may interact wi...
International audienceIn recent years, the number of clinical trials in which adeno-associated virus...
Simple Summary Gene therapy is a novel approach to treat diseases by introducing corrective genetic ...
In a recent Nature Genetics letter, entitled “Recurrent AAV2-related insertional mutagenesis in huma...
Adeno-associated viruses (AAV) have emerged as the lead vector in clinical trials and form the basis...
The adeno-associated virus (AAV) vector system has emerged as one of the most attractive methods of ...
Adeno-associated virus (AAV) was first characterized as small “defective” contaminant particles in a...
AbstractAdeno-associated virus (AAV), a common genital virus, may have a “protective” role against h...
International audienceGene therapy with adeno-associated virus (AAV) vectors has demonstrated safety...
Recombinant AAV efficacy has been demonstrated in numerous gene therapy preclinical studies. As this...
Abstract Background Engineered versions of adeno-associated virus (AAV) are commonly used in gene th...
To examine the potential of AAV as a vector for gene transfer in glial cells, an established astrocy...
International audienceOBJECTIVE:Adeno-associated virus (AAV) is a defective mono-stranded DNA virus,...
The adeno-associated virus (AAV) has rapidly gained popularity in gene therapy since the establishme...
Infection with the helper virus-dependent human parvovirus adeno-associated virus (AAV) is known to ...
Adeno-associated virus (AAV) is a ubiquitous human helper-dependent parvovirus which may interact wi...
International audienceIn recent years, the number of clinical trials in which adeno-associated virus...
Simple Summary Gene therapy is a novel approach to treat diseases by introducing corrective genetic ...
In a recent Nature Genetics letter, entitled “Recurrent AAV2-related insertional mutagenesis in huma...
Adeno-associated viruses (AAV) have emerged as the lead vector in clinical trials and form the basis...
The adeno-associated virus (AAV) vector system has emerged as one of the most attractive methods of ...
Adeno-associated virus (AAV) was first characterized as small “defective” contaminant particles in a...
AbstractAdeno-associated virus (AAV), a common genital virus, may have a “protective” role against h...
International audienceGene therapy with adeno-associated virus (AAV) vectors has demonstrated safety...
Recombinant AAV efficacy has been demonstrated in numerous gene therapy preclinical studies. As this...
Abstract Background Engineered versions of adeno-associated virus (AAV) are commonly used in gene th...
To examine the potential of AAV as a vector for gene transfer in glial cells, an established astrocy...