Jn. Zuckerman et al., Evaluation of a new hepatitis B triple-antigen vaccine in inadequate responders to current vaccines, HEPATOLOGY, 34(4), 2001, pp. 798-802
In this double-blind, randomized, controlled study, healthcare professional
s with a history of inadequate response to currently available single-antig
en hepatitis B vaccines confirmed by measuring hepatitis B surface antibody
titer before entry to the study were revaccinated with a 20-mug dose eithe
r of a novel triple-antigen (S, pre-S1, and pre-S2) recombinant vaccine or
of a present single-antigen (S only) vaccine. Hepatitis B surface antibody
titers were measured 8 weeks' post revaccination. A total of 925 individual
s were randomized and vaccinated, of whom 915 (98.9%) completed the study a
nd were included in the efficacy analysis. A single dose of the new triple-
antigen hepatitis B vaccine (Hepacare) produced a successful response in ov
er three quarters of these subjects who had not mounted an adequate respons
e to current vaccines. The antibody response was statistically significantl
y superior (P = .002) to that after a single dose of current vaccines. An e
valuation of the overall response showed that only the triple-antigen vacci
ne was able to raise the average antibody response (geometric mean titer [G
MT]) to over 100 IU/L. The superior effect of the new vaccine was most pron
ounced in subjects who were previously complete nonresponders to currently
available hepatitis B vaccines. Both vaccines were well tolerated and had s
imilar safety profiles. This study demonstrated that in healthcare workers
who had responded inadequately to at least a full course of immunization (m
edian, 5 doses), a single 20-mug dose of a new triple-antigen vaccine induc
ed protective antibody level in more vaccinees (P = .002) and increased the
average antibody titer (GMT) in those protected successfully to a greater
degree (P < .001) than a further attempt with a current vaccine (Engerix-B)
.