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Recombinant hepatitis B lentiviral vector is an investigational gene therapy designed to treat chronic hepatitis B virus (HBV) infection. This therapy uses a replication-deficient lentiviral vector engineered to deliver genetic material targeting HBV, with the aim of inhibiting viral replication in hepatocytes. Lentiviral vectors are commonly used in gene therapy due to their ability to stably integrate therapeutic genes into host cell genomes, enabling long-term expression. The approach leverages RNA interference or other genetic mechanisms delivered by the vector to suppress HBV activity within infected liver cells[4][5][2]. Early-phase clinical trials have been initiated to evaluate its safety, tolerability, and initial efficacy in patients with chronic HBV infection[2].
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