Hepatitis B is a major public health problem. More than 300 million pe
ople are chronically infected by the virus. During infection very larg
e quantities of complete virions and empty envelopes, consisting of sp
herical or filamentous lipoprotein particles, are present in the blood
. DNA genome coding for envelopes is divided into three domains, preS1
, preS2 and S. All available data suggest that the preS1 and preS2 pro
ducts are exposed at the surface of the virions. These proteins are mo
re immunogenic than S in terms of in vivo antibody response and the nu
mber of epitopes identified. The three dimensional mapping of antigeni
c sites of the HBV will provide important strategic information for va
ccine development and identification of targets for immunorecognition
or immunoregulation of the disease.