Long-term impact of 10-valent pneumococcal conjugate vaccination on invasive pneumococcal disease among children in Finland

被引:54
作者
Rinta-Kokko, Hanna [1 ]
Palmu, Arto A. [2 ]
Auranen, Kari [3 ]
Nuorti, J. Pekka [4 ,5 ]
Toropainen, Maija [4 ]
Siira, Lotta [4 ]
Virtanen, Mikko J. [4 ]
Nohynek, Hanna [4 ]
Jokinen, Jukka [1 ]
机构
[1] Natl Inst Hlth & Welf, Dept Publ Hlth Solut, POB 30, FI-00271 Helsinki, Finland
[2] Natl Inst Hlth & Welf, Dept Publ Hlth Solut, Biokatu 10, FI-33520 Tampere, Finland
[3] Univ Turku, Dept Math & Stat, Turku 20014, Finland
[4] Natl Inst Hlth & Welf, Dept Hlth Secur, POB 30, FI-00271 Helsinki, Finland
[5] Univ Tampere, Sch Hlth Sci, Dept Epidemiol, Kalevantie 4, FI-33014 Tampere, Finland
关键词
Pneumococcal conjugate vaccines; Invasive pneumococcal disease; National vaccination programme; Register study; Vaccine impact; STREPTOCOCCUS-PNEUMONIAE; UNITED-STATES; ANTIMICROBIAL RESISTANCE; SEROTYPES; CARRIAGE; VACCINES; ENGLAND; PROGRAM; QUEBEC; WALES;
D O I
10.1016/j.vaccine.2018.03.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: The ten-valent pneumococcal conjugate vaccine (PCV10) was introduced into the Finnish National Vaccination Programme (NVP) in September 2010. The impact of PCV10 vaccination against invasive pneumococcal disease (IPD) in vaccine-eligible children has been high. We evaluated the long-term impact of PCV10 vaccination against IPD in vaccine-eligible and older, unvaccinated children six years after PCV10 introduction with a special focus on cross-protection against PCV10-related serotypes (serotypes in the same serogroups as the PCV10 types). Methods: We used data on IPD from the national, population-based surveillance. A target cohort of vaccine-eligible children (born June 2010 or later) was followed from 3 months of age until the end of 2016. For the indirect effect, another cohort of older PCV10-ineligible children was followed from 2012 through 2016. IPD rates were compared with those of season- and age-matched reference cohorts before NVP introduction. Results: Among vaccine-eligible children, the incidence of all IPD decreased by 79% (95% CI 74-83%). There was a statistically significant reduction in the incidence of 6A IPD, but for 19A, the reduction was non-significant and the incidence of 19A increased towards the end of the study period in the older vaccine-eligible children. The increase in non-PCV10 related serotypes was non-significant. Results: In the unvaccinated older children, the incidence of all IPD decreased by 33% (95% CI 8-52%) compared to the reference cohort, and there was no impact on serotype 6A or 19A IPD. Conclusion: Overall, the impact of PCV10 vaccination on IPD was high in vaccine-eligible children, with a major reduction in vaccine-type disease, and without notable replacement by other serotype groups. Our data suggest that PCV10 results in long-lasting direct cross-protection against 6A IPD. For 19A, no net reduction was observed six years after NVP introduction in the vaccine-eligible cohort. The indirect impact on IPD in unvaccinated children sustained. (C) 2018 Published by Elsevier Ltd.
引用
收藏
页码:1934 / 1940
页数:7
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