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Cell & Gene Therapy Insights

Cell & Gene Therapy Insights

Stable AAV producer cell lines: elevating vector manufacturing

Sponsored by:

CEVEC Recombinant adeno-associated virus (rAAV) has shown great promise as a suitable vector for in vivo gene therapies. Consequently, there is a rapidly increasing demand for rAAV production and robust and scalable manufacturing processes.

Currently established rAAV production methods rely on transient transfection of plasmid DNA or transduction of the producing cell with helper viruses.

Using an innovative approach based on its proprietary serum-free suspension cell line, CEVEC has developed a production system that uses rAAV producer cells, which have stably integrated into their genome all the elements required for rAAV assembly as well as the ITR-flanked transgene. For rAAV production, no further transfection steps or helper viruses are required.

The platform can be adapted to various serotypes and transgenes and has been designed for scalable production in stirred tank bioreactors. Data from production runs at different scales will be presented.

Attendees find out how to:



Dr. Silke Wissing, Chief Scientific Officer, CEVEC

Dr. Silke Wissing has wide-ranging experience in the fields of virology, cell biology and cell line development, as well as molecular biology. Before joining CEVEC in 2011, she held a position as a group leader in the Gladstone Institute for Virology and Immunology, San Francisco, where she performed research in the field of HIV-1 biology, stem cell research and cell line development. Dr. Silke Wissing holds a PhD in Biochemistry from the University of Tübingen.

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