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Evaluation of a new hepatitis B triple‐antigen vaccine in inadequate responders to current vaccines
Author(s) -
Zuckerman Jane N.,
Zuckerman Arie J.,
Symington Ian,
Du Wei,
Williams Anthony,
Dickson Brian,
Young Michael D.
Publication year - 2001
Publication title -
hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.488
H-Index - 361
eISSN - 1527-3350
pISSN - 0270-9139
DOI - 10.1053/jhep.2001.27564
Subject(s) - medicine , hepatitis b vaccine , antigen , vaccination , immunology , immunization , hepatitis b , titer , antibody , antibody titer , antibody response , virology , hepatitis b virus , hbsag , virus
In this double‐blind, randomized, controlled study, healthcare professionals with a history of inadequate response to currently available single‐antigen hepatitis B vaccines confirmed by measuring hepatitis B surface antibody titer before entry to the study were revaccinated with a 20‐μg dose either 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 individuals were randomized and vaccinated, of whom 915 (98.9%) completed the study and were included in the efficacy analysis. A single dose of the new triple‐antigen hepatitis B vaccine (Hepacare) produced a successful response in over three quarters of these subjects who had not mounted an adequate response to current vaccines. The antibody response was statistically significantly superior ( P = .002) to that after a single dose of current vaccines. An evaluation of the overall response showed that only the triple‐antigen vaccine was able to raise the average antibody response (geometric mean titer [GMT]) to over 100 IU/L. The superior effect of the new vaccine was most pronounced in subjects who were previously complete nonresponders to currently available hepatitis B vaccines. Both vaccines were well tolerated and had similar safety profiles. This study demonstrated that in healthcare workers who had responded inadequately to at least a full course of immunization (median, 5 doses), a single 20‐μg dose of a new triple‐antigen vaccine induced 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).