Abstract

Use of lentiviral vectors in clinical trials has increased through the last decade. Lentivirus based products have entered later trial phases, and cell and gene therapy products utilizing lentiviral vectors ex vivo have already been accepted on market by FDA and EMA. Thus, it is no wonder that there is a demand for commercial-scale lentiviral vector production. During the last ten years, large progress has fortunately occurred in both adherent and suspension production enabling manufacturing of large quantities of lentiviral vectors in relatively non-laborious manner. In this review, different scale-up options for lentiviral vector manufacturing are described, and aspects that should be taken into account while scaling up the process are covered.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.