Targeting a specific DNA sequence to the desired tissues is an important st
ep in gene therapy. The hepatitis B virus (HBV) is the only DNA virus that
has hepatocyte specificity. We attempted to construct an HBV-based vector f
or targeting the liver. me observed the replication and secretion of virus
particles in an HBV construct that lacks X gene and carries an extra 63 bp
DNA fragment in vitro. Replication was observed in the cell line HuH-7 but
not HepG2. From this construct, we designed an HBV-based vector that could
carry foreign DNA. HBV based vectors provide for the possibilities of gener
ating therapeutic agents for individual patients. Our host vector system ma
y be used to clear out the HBV from the HBV carrier or chronic hepatitis B
patients by introducing a genetically engineered HBV into these patients. (
C) 1999 Academic Press.