Evaluation of strain coverage of the multicomponent meningococcal serogroup B vaccine (4CMenB) administered in infants according to different immunisation schedules

被引:13
作者
Biolchi, Alessia [1 ]
Tomei, Sara [1 ]
Santini, Laura [1 ]
Welsch, Jo Anne [2 ]
Toneatto, Daniela [1 ]
Gaitatzis, Nikolaos [3 ]
Bai, Xilian [4 ]
Borrow, Ray [4 ]
Giuliani, Marzia Monica [1 ]
Mori, Elena [1 ]
Pizza, Mariagrazia [1 ]
机构
[1] GSK, Via Fiorentina 1, I-53100 Siena, SI, Italy
[2] PATH, San Francisco, CA USA
[3] GSK, Marburg, Germany
[4] Publ Hlth England, Meningococcal Reference Unit, Manchester, Lancs, England
关键词
meningococcal serogroup B; 4CMenB vaccine; strain coverage; serum bactericidal antibody assay; pooled sera; infant immunisation schedule; DISEASE;
D O I
10.1080/21645515.2018.1537756
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The 4-component vaccine 4CMenB, developed against invasive disease caused by meningococcal serogroup B, is approved for use in infants in several countries worldwide. 4CMenB is mostly used as 3 + 1 schedule, except for the UK, where a 2 + 1 schedule is used, and where the vaccine showed an effectiveness of 82.9%. Here we compared the coverage of two 4CMenB vaccination schedules (3 + 1 [2.5, 3.5, 5, 11 months] versus 2 + 1 [3.5, 5, 11 months of age]) against 40 serogroup B strains, representative of epidemiologically-relevant isolates circulating in England and Wales in 2007-2008, using sera from a previous phase 3b clinical trial. The strains were tested using hSBA on pooled sera of infants, collected at one month post-primary and booster vaccination. 4CMenB coverage was defined as the percentage of strains with positive killing (hSBA titres >= 4 after immunisation and negative baseline hSBA titres < 2). Coverage of 4CMenB was 40.0% (95% confidence interval [CI]: 24.9-56.7) and 87.5% (95%CI: 73.2-95.8) at one month post-primary and booster vaccination, respectively, regardless of immunisation schedule. Using a more conservative threshold (post-immunisation hSBA titres >= 8; baseline <= 2), at one month post-booster dose, strain coverages were 80% (3 + 1) and 70% (2 + 1). We used a linear regression model to assess correlation between post-immunisation hSBA data for each strain in the two groups; Pearson's correlation coefficients were 0.93 and 0.99 at one month post-primary and booster vaccination. Overall, there is no evidence for a difference in strain coverage when 4CMenB is administered according to a 3 + 1 or 2 + 1 infant vaccination schedule.
引用
收藏
页码:725 / 731
页数:7
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