Despite the availability of an effective vaccine, there are still 400
million people, worldwide who are chronically infected with hepatitis B
virus (HBV). For them, the vaccine, as currently applied, has no value.
Given the possible consequences of HBV infection, the number of those
chronically infected with HBV presents an enormous public health
challenge. For example, the major etiology of hepatocellular carcinoma
(HCC) is chronic infection with HBV. Although fifth in cancer incidence,
worldwide, HCC/liver cancer is the third leading cause of cancer death.
The high mortality as- ciated with HCC arises because the disease is
often detected late and is unresponsive to treatment. The number of
deaths caused by PHCC is expected to rise over the next 20 years. Those
chronically infected with HBV have a life risk of death to HCC of
between 10 and 25%. Even the limited efficacy of drugs for the treatment
of chronic HBV helps underscore the point that this disease is
responsive to therapy. Drugs that target the polymerase (e. g., hepsera
and lamivudine) and interferon alpha represent two distinct strategies
and show that both conventional antiviral and immunothe- peutic
approaches can be used in management. However, the current inventory of
therapeutics is inadequate. Interferon alpha is of limited value, only
parenterally ava- able, and fraught with adverse reactions.