Hepatitis B vaccines:: Assessment of the seroprotective efficacy of two recombinant DNA vaccines

被引:126
作者
Coates, T
Wilson, R
Patrick, G
André, F
Watson, V
机构
[1] Omnicare Clin Res United Kingdom, Dept Clin Writing, Chippenham, Wilts, England
[2] Omnicare Clin Res United Kingdom, Dept Med Affairs, Chippenham, Wilts, England
[3] Omnicare Clin Res United Kingdom, Dept Biometr, Chippenham, Wilts, England
[4] Queen Elizabeth Hosp, Woodville, SA 5011, Australia
[5] GlaxoSmithKlin Biol SA, B-1330 Rixensart, Belgium
关键词
hepatitis B vaccine; clinical study review; vaccination program; seroprotection or seroprotective response rates; standards; analysis;
D O I
10.1016/S0149-2918(01)80044-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: In universal vaccination programs, when there is no postvaccination serologic assessment of response, there must be confidence that the vaccines used provide a high degree of seroprotection. Objective: This parallel analysis of 2 recombinant hepatitis B vaccines (Engerix B (R) and Recombivax (R) /HB-Vax II (R)) was conducted to review the seroprotective efficacy of each vaccine in defined populations. Methods: Clinical studies of the 2 vaccines published as manuscripts or conference abstracts in the public domain between January 1986 and April 1999 were identified retrospectively by unrestricted screening of journals through BIOSIS (R), MEDLINE (R), and EMBASE (R) and the Internet. Unpublished or internal company data were excluded to maintain impartiality. The studies were reviewed and analyzed. The studies were not assessed for quality other than a judgment of their eligibility for inclusion in the analysis. The primary outcome measure was the proportion of subjects in defined populations who showed an early seroprotective response to currently licensed vaccination schedules. Summary statistical analyses of seroprotective response rates and 95% CIs were calculated for each vaccine for each population. Seroprotective response was defined by an anti-hepatitis B surface antigen titer greater than or equal to 10 IU/L measured between I and 3 months after the final vaccination. Because the study was designed specifically to review published immunogenicity data, safety data were not assessed. The study was not designed to demonstrate superiority of one vaccine over the other. Results: A total of 181 clinical studies representing 32,904 vaccinated subjects were reviewed and analyzed, of whom 24,277 had been vaccinated with Engerix B and 8627 vaccinated with Recombivax/ MB-Var II. Seroprotection was achieved in 20,060 subjects (95.8%) with Engerix B and in 7774 subjects (94.3%) with Recombivax/HB-Vax II in the normal population vaccinated according to currently licensed 3-dose schedules. In a subgroup analysis, response rates in health care workers were 6492 subjects (94.5%) for Engerix B and 3245 subjects (92.2%) for Recombivax/HB-Vax II. Children and adolescents(1-19 years) showed the highest response rates to vaccination (4612 [98.6%], Engerix B: 2292 [98.9%], Recombivax/HB-Vax II). A total of 2875 infants (<1 year) (95.8%) achieved seroprotection with Engerix B. 701 (88.5%) achieved seroprotection with Recombivax/ MB-Var II. Conclusions: Hepatitis B vaccination programs using either Engerix B or Recombivax/HB-Vax II can achieve high seroprotective response rates, particularly in childhood and adolescence. Ideally, younger populations should be a primary target in current universal vaccination programs.
引用
收藏
页码:392 / 403
页数:12
相关论文
共 33 条
  • [1] Prediction of response to hepatitis B vaccine in health care workers: Whose titers of antibody to hepatitis B surface antigen should be determined after a three-dose series, and what are the implications in terms of cost-effectiveness?
    Alimonos, K
    Nafziger, AN
    Murray, J
    Bertino, JS
    [J]. CLINICAL INFECTIOUS DISEASES, 1998, 26 (03) : 566 - 571
  • [2] [Anonymous], 1996, EXP PROGR IMM HEP B
  • [3] Over a decade of experience with a yeast recombinant hepatitis B vaccine
    Assad, S
    Francis, A
    [J]. VACCINE, 1999, 18 (1-2) : 57 - 67
  • [4] Banatvala J, 2000, LANCET, V355, P561, DOI 10.1016/S0140-6736(99)07239-6
  • [5] EFFECTS OF DIFFERENT DOSE LEVELS AND VACCINATION SCHEDULES ON IMMUNE-RESPONSE TO A RECOMBINANT DNA HEPATITIS-B VACCINE IN HEMODIALYSIS-PATIENTS
    BRUGUERA, M
    RODICIO, JL
    ALCAZAR, JM
    OLIVER, A
    DELRIO, G
    ESTEBANMUR, R
    [J]. VACCINE, 1990, 8 : S47 - S49
  • [6] CADRANEL S, 1990, PEDIAT RES, V27, P535
  • [7] Universal hepatitis B vaccination in Taiwan and the incidence of hepatocellular carcinoma in children
    Chang, MH
    Chen, CJ
    Lai, MS
    Hsu, HM
    Wu, TC
    Kong, MS
    Liang, DC
    Shau, WY
    Chen, DS
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (26) : 1855 - 1859
  • [8] SHOULD UNPUBLISHED DATA BE INCLUDED IN METAANALYSES - CURRENT CONVICTIONS AND CONTROVERSIES
    COOK, DJ
    GUYATT, GH
    RYAN, G
    CLIFTON, J
    BUCKINGHAM, L
    WILLAN, A
    MCLLROY, W
    OXMAN, AD
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1993, 269 (21): : 2749 - 2753
  • [9] HEPATITIS-B VACCINATION IN THE ELDERLY
    DENIS, F
    MOUNIER, M
    HESSEL, L
    MICHEL, JP
    GUALDE, N
    DUBOIS, F
    BARIN, F
    GOUDEAU, A
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1984, 149 (06) : 1019 - 1019
  • [10] IMMUNOGENICITY OF STANDARD AND LOW-DOSE VACCINATION USING YEAST-DERIVED RECOMBINANT HEPATITIS-B SURFACE-ANTIGEN IN ELDERLY VOLUNTEERS
    DERAVE, S
    HEIJTINK, RA
    BAKKERBENDIK, M
    BOOT, J
    SCHALM, SW
    [J]. VACCINE, 1994, 12 (06) : 532 - 534