Case Study

Cell Line Development For High-Titer Lentivirus Vector Production

Source: OBiO Tech

By Hairui Yang, Han Gao, Houliang Wei, Qinrui You, Guodong Jia, and Weiran Shen, OBiO Tech

Pipette With Cell Culture Plate iStock-520238063

Lentiviral (LV) vectors hold immense promise for gene therapy due to their ability to deliver genes into a wide range of cells. However, producing sufficient quantities of LV vectors for clinical applications remains a hurdle. This study presents a groundbreaking method to significantly enhance LV vector yield using engineered HEK293T cells, the workhorse for LV vector production.

The traditional approach relies on co-transfecting numerous plasmids into HEK293T cells, resulting in inconsistent yields due to variations in cell populations. We propose a novel solution: creating high-performing, monoclonal HEK293T cell lines. Our approach involves meticulously isolating individual cells with exceptional transfection efficiency and cultivating them into entirely new, productive lines.

This innovative method yielded a remarkable 2-4 fold increase in LV vector production compared to conventional methods. Notably, this technique is adaptable for producing LV vectors carrying various genetic materials, making it a versatile strategy for diverse gene therapy applications. This study paves the way for more efficient and large-scale production of LV vectors, accelerating advancements in gene therapy research and development.

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