Infection with hepatitis B virus has become a vaccine-preventable disease.
The recombinant hepatitis B vaccines available today are safe and immunogen
ic. In order for these vaccines to eradicate HBV a universal vaccination of
neonates and/or children needs to be implemented. Major obstacles on the r
oad to global hepatitis B vaccination are poverty and scarcity of human res
ources in those parts of the world who are most badly in need of these vacc
ines.
Despite their proven immunogenicity hepatitis B vaccines are unable to indu
ce an adequate immune response in 5-10% of healthy adults. The non-responsi
veness of these subjects is a selective phenomenon and not the expression o
f a general immune deficiency. Studies that correlated the HLA haplotype of
vaccine recipients with their anti-HBs response patterns has led to the id
entificiation of markers of good and non/poor response.
Universal vaccination of neonates and children has elicited questions about
the durability of antibody persistence and the need for booster doses late
r in life. The European Consensus Group on Hepatitis B Immunity has propose
d a series of recommendations that are summarized in this review.