VIVEbiotech Adds EvoLVcell to Its Catalogue of LVV-Manufacturing Products

VIVEbiotech, a lentiviral vector (LVV) Contract Development and Manufacturing Organization (CDMO), has added EvoLVcell, a stable producer cell line (SCL) generation platform to its catalogue of LVV-manufacturing products, representing a cost-effective, transfection-free alternative to its existing transient transfection process.

The thoroughly characterized, inducible, monoclonal lentiviral packaging cell line (PCL) derisks stable producer cell line (SCL) generation by incorporating the therapeutic transgene that typically would be transfected together with the helper plasmids. This SCL platform generation enables VIVEbiotech to get a prototype cell line in three months.

EvoLVcell is designed to reduce batch‑to‑batch variability, improve vector quality, and provide a more predictable long‑term production strategy for LVVs. The fully integrated platform requires only the addition of a developer’s transgenic element to the fully characterized monoclonal PCL, avoiding transfection – simplifying the manufacturing workflow, improving long-term predictability, and reducing reliance on plasmid and transfection reagent supply chains.

“Achieving cost efficiency and high reproducibility is essential for the scalable production of lentiviral vectors and for expanding patient access. Stable producer cell lines provide a reliable and scalable manufacturing platform to support this goal,” said Andrés Lamsfus-Calle, PhD, Product Development Manager at VIVEbiotech. “EvoLVcell provides a powerful alternative to transient transfection — one that de‑risks production, improves quality, and supports long‑term scalability for our partners.”

The EvoLVcell platform is initially available for VSV‑G pseudotyped lentiviral vectors, the most widely used LVV envelope. EvoLVcell will complement VIVEbiotech’s established transient transfection, offering developers more flexibility depending on program needs.

Other features include:

• Helper genes remain fully silent during cell expansion, limiting potential toxicity and cell instability.
• Expression activated with low concentrations of doxycycline, minimizing risk of residual inducer in the final product.
• Demonstrates strong repression when off and high titers when on, important to maintain cell stability and transgene integrity.
• No requirement of plasmids and transfection agents, reducing considerably COGs.
• Manufacturing flexibility. Adaptable to adherent or suspension platforms.
• Improvement in vector quality, decreasing total amount of contaminants associated with the manufacturing process.