Lentiviral vectors (LVV), derived from the Human Immunodeficiency Virus (HIV), are engineered RNA-based viral vectors. The key advantage of lentiviral vectors lies in their ability to integrate the exogenous genes into the host genome, ensuring long-term, stable gene expression. This feature renders them particularly useful for the generation of stable cell lines and is also a cornerstone in the realm of clinical immunocyte therapies.
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