Adeno-associated virus (AAV) is being used successfully in gene therapy. Different serotypes of AAV target specific organs and tissues with high efficiency. There exists an increasing demand to manufacture various AAV serotypes in large quantities for pre-clinical and clinical trials. A generic and scalable method has been described in this study to efficiently produce AAV serotypes (AAV1-9) by transfection of a fully characterized cGMP HEK293SF cell line grown in suspension and serum-free medium. First, the production parameters were evaluated using AAV2 as a model serotype. Second, all nine AAV serotypes were produced successfully with yields of 1013Vg/L cell culture. Subsequently, AAV2 and AAV6 serotypes were produced in 3-L controlled b...
Adenovirus (AdV) vectors are commonly used in cancer gene therapy trials, evaluated in gene therapy ...
Recent advances in recombinant adeno-associated virus vector production. Adeno-associated virus (AAV...
Abstract Background The ability to deliver a gene of interest into a specific cell type is an essent...
Recombinant adeno-associated virus (rAAV) has become a promising candidate vector for gene therapy. ...
Adeno-associated virus vector manufacturing at scale continues to hinder the application of AAV tech...
Adeno-Associated Virus (AAV) vectors showing safety profile in phase I clinical trials and its abili...
Adeno-associated virus (AAV)-based vectors belong to the most promising gene transfer vectors in cli...
Recombinant adeno-associated viruses (rAAV) represent a promising gene therapy vector that may be us...
Manufacturing practices for recombinant adeno-associated viruses (AAV) have improved in the last dec...
Adeno-associated viruses (AAV) are reported to have a great potential for gene therapy. However, a m...
Adeno-associated virus (AAV) has shown great promise as a gene therapy vector in multiple aspects of...
Application of adeno-associated virus (AAV) vector in large animal studies and clinical trials often...
Recombinant adeno-associated virus (rAAV) is a mammalian virus that has been altered to be used as a...
Here we describe methods for the production of adeno-associated viral (AAV) vectors by transient tra...
Adeno-associated virus vectors (AAV) are reported to have a great potential for gene therapy, howeve...
Adenovirus (AdV) vectors are commonly used in cancer gene therapy trials, evaluated in gene therapy ...
Recent advances in recombinant adeno-associated virus vector production. Adeno-associated virus (AAV...
Abstract Background The ability to deliver a gene of interest into a specific cell type is an essent...
Recombinant adeno-associated virus (rAAV) has become a promising candidate vector for gene therapy. ...
Adeno-associated virus vector manufacturing at scale continues to hinder the application of AAV tech...
Adeno-Associated Virus (AAV) vectors showing safety profile in phase I clinical trials and its abili...
Adeno-associated virus (AAV)-based vectors belong to the most promising gene transfer vectors in cli...
Recombinant adeno-associated viruses (rAAV) represent a promising gene therapy vector that may be us...
Manufacturing practices for recombinant adeno-associated viruses (AAV) have improved in the last dec...
Adeno-associated viruses (AAV) are reported to have a great potential for gene therapy. However, a m...
Adeno-associated virus (AAV) has shown great promise as a gene therapy vector in multiple aspects of...
Application of adeno-associated virus (AAV) vector in large animal studies and clinical trials often...
Recombinant adeno-associated virus (rAAV) is a mammalian virus that has been altered to be used as a...
Here we describe methods for the production of adeno-associated viral (AAV) vectors by transient tra...
Adeno-associated virus vectors (AAV) are reported to have a great potential for gene therapy, howeve...
Adenovirus (AdV) vectors are commonly used in cancer gene therapy trials, evaluated in gene therapy ...
Recent advances in recombinant adeno-associated virus vector production. Adeno-associated virus (AAV...
Abstract Background The ability to deliver a gene of interest into a specific cell type is an essent...