A pilot programme of hepatitis B vaccination was set up in three priso
ns to assess the feasibility and results of this method of reaching a
high-risk population. Hepatitis B vaccine was offered to all inmates w
ho lacked serological markers for hepatitis B virus. The antibody resp
onse was assessed in those who received two or three doses of vaccine.
Candidates for vaccination were 41% of 1755 imprisoned men (20% of in
travenous drug users (IVDU) and 63% of non-IVDU), but complete vaccina
tion could be given to only 33 % of candidates. A further 29% received
two doses. Seroconversion to anti-HBs (titres > 10 IU l-1) occurred i
n 33% of vaccinees after two doses and in 76% after three doses. The o
verall rate of susceptible inmates who became protected for hepatitis
B was 34%. The seroconversion rate was higher when the interval betwee
n the first two doses was shorter than 3 weeks (91%), than in cases wi
th an interval of 3-6 weeks (79%) or longer than 6 weeks (33%). Age gr
eater than 35 years and history of IVDU were associated with a lower r
esponse to the vaccine, while anti-HIV seropositivity did not influenc
e the response. In conclusion, vaccination of prisoners susceptible to
HBV may achieve protection in at least a third of cases. Shortening i
ntervals between the priming doses of vaccine may improve compliance a
nd increases the response.