Systematic literature review comparing rapid 3-dose administration of the GSK tick-borne encephalitis vaccine with other primary immunization schedules

被引:15
作者
Galgani, Ilaria [1 ]
Bunge, Eveline M. [2 ]
Hendriks, Lisa [2 ]
Schludermann, Christopher [3 ]
Marano, Cinzia [4 ]
De Moerlooze, Laurence [4 ]
机构
[1] GSK, Via Fiorentina 1, I-53100 Siena, Italy
[2] Pallas Hlth Res & Consultancy, Rotterdam, Netherlands
[3] GSK, Vienna, Austria
[4] GSK, Wavre, Belgium
关键词
Adults; children; primary immunization schedules; rapid administration; tick-borne encephalitis; vaccine; TBE BOOSTER IMMUNIZATION; LONG-TERM PERSISTENCE; 5-YEAR FOLLOW-UP; ANTIBODY PERSISTENCE; CHILDREN; IMMUNOGENICITY; EPIDEMIOLOGY; SAFETY; ADULTS; FSME-IMMUN(R);
D O I
10.1080/14760584.2017.1358620
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction: Tick-borne encephalitis (TBE), which is endemic across large regions of Europe and Asia, is most effectively prevented through vaccination. Three-dose primary TBE vaccination schedules are either rapid (0,7,21-days) or conventional (0,28-84-days, 9-12-months). The second dose can also be administered at 14days for faster priming and sero-protection). Areas covered: We used a three-step selection process to identify 21 publications comparing the immunogenicity and/or safety of different schedules. Expert commentary: Priming with two or three TBE vaccine doses was highly immunogenic. After conventional priming (0-28days), 95% adults and 95% children had neutralization test (NT) titers 10 at 14days post-dose-2 compared with 92% adults and 99% children at 21days post-dose-3 (rapid schedule). Most subjects retained NT titers 10 at day 300. A single booster dose induced a strong immune response in all subjects irrespective of primary vaccination schedule or elapsed time since priming. GMT peaked at 42days post-dose-1 (i.e., 21days post-dose 3 [rapid-schedule], or 14-28days post-dose-2 [conventional-schedule]), and declined thereafter. Adverse events were generally rare and declined with increasing doses. In the absence of data to recommend one particular schedule, the regimen choice will remain at the physician's discretion, based on patient constraints and availability.
引用
收藏
页码:919 / 932
页数:14
相关论文
共 49 条
  • [1] Tick related diseases in Switzerland, 2008 to 2011
    Altpeter, Ekkehardt
    Zimmermann, Hanspeter
    Oberreich, Juergen
    Peter, Olivier
    Dvorak, Charles
    [J]. SWISS MEDICAL WEEKLY, 2013, 143
  • [2] Epidemiology of tick-borne encephalitis (TBE) in Europe and its prevention by available vaccines
    Amicizia, Daniela
    Domnich, Alexander
    Panatto, Donatella
    Lai, Piero Luigi
    Cristina, Maria Luisa
    Avio, Ulderico
    Gasparini, Roberto
    [J]. HUMAN VACCINES & IMMUNOTHERAPEUTICS, 2013, 9 (05) : 1163 - 1171
  • [3] [Anonymous], CRIT APPR NOT CHECKL
  • [4] [Anonymous], VACCINES TICK BORNE
  • [5] [Anonymous], EP SIT TICK BORN ENC
  • [6] [Anonymous], CHIEF CTR DIS CONTRO
  • [7] [Anonymous], 2013, PRZEGL EPIDEMIOL
  • [8] Long-term immunity after vaccination against tick-borne encephalitis with Encepur® using the rapid vaccination schedule
    Beran, J
    Douda, P
    Gniel, D
    Zent, O
    [J]. INTERNATIONAL JOURNAL OF MEDICAL MICROBIOLOGY, 2004, 293 : 130 - 133
  • [9] Five year follow-up after a first booster vaccination against tick-borne encephalitis following different primary vaccination schedules demonstrates long-term antibody persistence and safety
    Beran, Jiri
    Xie, Fang
    Zent, Olaf
    [J]. VACCINE, 2014, 32 (34) : 4275 - 4280
  • [10] Sudden increase in tick-borne encephalitis cases in the Czech Republic, 2006
    Daniel, Milan
    Kriz, Bohumir
    Danielova, Vlasta
    Benes, Cestmir
    [J]. INTERNATIONAL JOURNAL OF MEDICAL MICROBIOLOGY, 2008, 298 : 81 - 87