Antibody-response to three recombinant hepatitis B vaccines: comparative evaluation of multicenter travel-clinic based experience

被引:82
作者
Rendi-Wagner, P
Kundi, M
Stemberger, H
Wiedermann, G
Holzmann, H
Hofer, M
Wiesinger, K
Kollaritsch, H
机构
[1] Univ Vienna, Inst Pathophysiol, Dept Specif Prophylaxis & Trop Med, A-1095 Vienna, Austria
[2] Univ Vienna, Inst Environm Hlth, A-1095 Vienna, Austria
[3] Inst Travel & Trop Med, A-1080 Vienna, Austria
[4] Univ Vienna, Inst Virol, A-1095 Vienna, Austria
关键词
hepatitis B vaccines; combined vaccine; immunogenicity; adults;
D O I
10.1016/S0264-410X(00)00410-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The immunogenicity of three currently used hepatitis B vaccines was compared in an unselected study population in an every day travel clinical setting. Five hundred and eighteen vaccinees received Engerix(TM)-B (EB), 990 received Twinrix(TM) (TWX), and 366 were immunised with Gen-HB-Vax(TM) (GHB). Overall, 88.6% of the vaccinees, tested within the first 6 months after completion of the vaccination series, developed protective levels of anti-HBs ( greater than or equal to 10 mIU/ml). However, GHB recipients showed significantly lower seroprotection rates (SPR) than EB and TWX recipients (79.3%, vs. 87.7% vs. 92.3%. P < 0.000001). GMTs for anti-HBs, tested within 6 months after the third vaccination, showed the lowest results in the GHB group, followed by EB and TWX (142 vs. 523 vs. 1008 mIU/ml, P < 0.000001). TWX vaccinees. however, showing a higher antibody decline rate than EB recipients within the first years after completion of the full immunisation course (30% vs. 25%; P = 0.0538). This study confirms an overall good immune response to the 20 mug-dose vaccine, in the course of a regular clinical setting. The significant difference in SPRs and GMTs to the 10 Gig-dose vaccine, however, may influence future immunisation practices for the elderly. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2055 / 2060
页数:6
相关论文
共 44 条
[1]  
*ACIP, 1985, MMWR-MORBID MORTAL W, V34, P313
[2]  
*ACIP, 1997, MMWR-MORBID MORTAL W, V36, P353
[3]   A hepatitis B vaccine formulated with a novel adjuvant system [J].
Ambrosch, F ;
Wiedermann, G ;
Kundi, M ;
Leroux-Roels, G ;
Desombere, I ;
Garcon, N ;
Thiriart, C ;
Slaoui, M ;
Thoelen, S .
VACCINE, 2000, 18 (20) :2095-2101
[4]  
AMBROSCH F, 1987, POSTGRAD MED J, V63, P129
[5]  
Banatvala J, 2000, LANCET, V355, P561, DOI 10.1016/S0140-6736(99)07239-6
[6]  
Carman WF, 1997, HEPATOLOGY, V26, P1658, DOI 10.1002/hep.510260640
[7]  
CARMAN WF, 1998, VIRAL HEPATITIS, P141
[8]   Seroepidemiology of hepatitis B virus infection in children - Ten years of mass vaccination in Taiwan [J].
Chen, HL ;
Chang, MH ;
Ni, YH ;
Hsu, HY ;
Lee, PI ;
Lee, CY ;
Chen, DS .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1996, 276 (11) :906-908
[9]   RESPONSE TO AN EXTRA DOSE OF HEPATITIS-B VACCINE AND SPECIFIC ANTIBODY PERSISTENCE IN NONRESPONDERS TO PRIMARY IMMUNIZATION [J].
CHIARAMONTE, M ;
NGATCHU, T ;
MAJORI, S ;
BALDO, V ;
MOSCHEN, ME ;
RENZULLI, G ;
TRIVELLO, R .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1995, 30 (06) :601-603
[10]   Two different dosages of yeast derived recombinant hepatitis B vaccines: A comparison of immunogenicity [J].
Chiaramonte, M ;
Majori, S ;
Ngatchu, T ;
Moschen, ME ;
Baldo, V ;
Renzulli, G ;
Simoncello, I ;
Rocco, S ;
Bertin, T ;
Naccarato, R ;
Trivello, R .
VACCINE, 1996, 14 (02) :135-137