More than 300 million people worldwide are chronically infected with h
epatitis B virus (HBV), and are at greatly increased risk of developin
g liver cirrhosis and eventually primary liver carcinoma. While infect
ion can, with relative success, be prevented by vaccination, no genera
lly effective therapy for chronic hepatitis B is available. Hence ther
e is an urgent need for novel antiviral strategies. Recent advances in
our understanding of the mechanisms underlying virus replication and
assembly provide opportunities for the rational design of molecules th
at could specifically interfere with these processes; some of these po
ssibilities are discussed in this review.