International audienceGene therapy based on the use of viral vectors is entirely dependent on the use of animal cell lines, mainly of mammalian origin, but also of insect origin. As for any biotechnology product for clinical use, viral -vectors have to be produced with cells derived from an extensively characterized cell bank to maintain the appropriate standard for assuring the lowest risk for the patients to be treated. Although many different cell types and lines have been used for the production of viral vectors, HEK293 cells or their derivatives have been extensively used for production of different vector types: adenovirus, oncorectrovirus, lentivirus, and AAV vectors, because of their easy handling and the possibility to grow them ad...
Lentiviral vectors (LV) represent a key tool for gene and cell therapy applications. The production ...
Gene therapy is the introduction or alteration of genetic material with the intention to treat disea...
Genetically modified adenoviruses (Ads) make attractive vectors for the delivery of exogenous DNA to...
Viruses and viral vectors are extensively used as delivery systems for gene and cell therapies, onco...
The field of gene therapy has changed drastically since the first human gene transfer experiment con...
The emerging number of clinical trials in the gene therapy field poses the challenge to the industry...
Lentiviral vectors (LVs) are promising vectors for gene therapy. Most often, they are used to delive...
A study of the production of adenoviral vectors in suspension 293 cells has been explored. A defined...
The potential of Madine Darby Canine Kidney (MDCK) cells for the production of influenza vaccines ha...
A general introduction on virus vaccine production is given by discussing economical and social aspe...
Abstract: A study of the production of adenoviral vectors in suspension 293 cells has been explored....
Lentiviral vectors (LVs) are promising vectors for gene therapy. Most often, they are used to delive...
The development of gene therapy is hampered by the difficulty of producing large stocks of retrovira...
Lentiviral vectors (LVs) are excellent tools to promote gene transfer and stable gene expression. Th...
Several patients with severe combined immunodeficiency-X1 disease and adenosine deaminase deficiency...
Lentiviral vectors (LV) represent a key tool for gene and cell therapy applications. The production ...
Gene therapy is the introduction or alteration of genetic material with the intention to treat disea...
Genetically modified adenoviruses (Ads) make attractive vectors for the delivery of exogenous DNA to...
Viruses and viral vectors are extensively used as delivery systems for gene and cell therapies, onco...
The field of gene therapy has changed drastically since the first human gene transfer experiment con...
The emerging number of clinical trials in the gene therapy field poses the challenge to the industry...
Lentiviral vectors (LVs) are promising vectors for gene therapy. Most often, they are used to delive...
A study of the production of adenoviral vectors in suspension 293 cells has been explored. A defined...
The potential of Madine Darby Canine Kidney (MDCK) cells for the production of influenza vaccines ha...
A general introduction on virus vaccine production is given by discussing economical and social aspe...
Abstract: A study of the production of adenoviral vectors in suspension 293 cells has been explored....
Lentiviral vectors (LVs) are promising vectors for gene therapy. Most often, they are used to delive...
The development of gene therapy is hampered by the difficulty of producing large stocks of retrovira...
Lentiviral vectors (LVs) are excellent tools to promote gene transfer and stable gene expression. Th...
Several patients with severe combined immunodeficiency-X1 disease and adenosine deaminase deficiency...
Lentiviral vectors (LV) represent a key tool for gene and cell therapy applications. The production ...
Gene therapy is the introduction or alteration of genetic material with the intention to treat disea...
Genetically modified adenoviruses (Ads) make attractive vectors for the delivery of exogenous DNA to...