Binks Michael J, Moberley Sarah A, Balloch Anne, Leach Amanda J, Nelson Sandra, Hare Kim M, Wilson Cate, Morris Peter S, Nelson Jane, Chatfield Mark D, Tang Mimi L K, Torzillo Paul, Carapetis Jonathan R, Mulholland E Kim, Andrews Ross M
Menzies School of Health Research, Charles Darwin University, Darwin, NT, Australia.
Menzies School of Health Research, Charles Darwin University, Darwin, NT, Australia.
Vaccine. 2015 Nov 27;33(48):6579-87. doi: 10.1016/j.vaccine.2015.10.101. Epub 2015 Oct 31.
We assessed maternal 23-valent pneumococcal polysaccharide (23vPPV) vaccine efficacy (VE) against middle ear disease and pneumococcal carriage amongst Australian Indigenous infants.
In an open label, allocation concealed, outcome-assessor blinded, community stratified, randomised controlled trial, healthy pregnant Indigenous women aged 17-39 years in the Northern Territory of Australia received the 23vPPV (1:1:1) at: 30-36 weeks gestation, birth, or were unvaccinated (ClinicalTrials.gov NCT00714064). Co-primary outcomes were the point prevalences of infant middle ear disease and 23vPPV-type carriage at age 7 months.
The consent rate was 50% (313/632). Among 227 eligible participants randomised, retention rates were 86% (66/77) controls; 89% (67/75) pregnancy vaccinees; 88% (66/75) birth vaccinees. At infant age 7 months, ear disease prevalence was: 71% (47/66) controls, 63% (42/67) pregnancy vaccinees, 76% (50/66) birth vaccinees; and 23vPPV-type carriage was: 26% (17/66) controls, 18% (12/67) pregnancy vaccinees, 18% (12/66) birth vaccinees. For pregnancy vaccinees, VE was 12% (95% CI -12% to 31%) against infant ear disease and 30% (95% CI -34% to 64%) against 23vPPV-type carriage. In a post-hoc analysis, VE against infant ear disease concurrent with carriage of 23vPPV or related types was 51% (95% CI -2% to 76%). There were no serious adverse effects following receipt of the 23vPPV in pregnancy or at birth.
In a high risk population, our study was unable to demonstrate efficacy of 23vPPV in pregnancy against the co-primary outcomes of either all-cause infant ear disease or 23vPPV-type nasopharyngeal carriage at age 7 months. Efficacy against ear disease concurrent with carriage of vaccine-related serotypes (a more specific outcome) suggests 23vPPV in pregnancy may complement childhood pneumococcal vaccination programs.
我们评估了澳大利亚原住民婴儿中母亲接种23价肺炎球菌多糖(23vPPV)疫苗预防中耳疾病和肺炎球菌携带的效果。
在一项开放标签、分配隐藏、结果评估者盲法、社区分层的随机对照试验中,澳大利亚北领地17 - 39岁的健康怀孕原住民妇女按1:1:1比例在以下时间接种23vPPV:妊娠30 - 36周、分娩时,或不接种(ClinicalTrials.gov NCT00714064)。共同主要结局是婴儿7个月大时中耳疾病和23vPPV型携带的点患病率。
同意率为50%(313/632)。在227名随机分组的符合条件参与者中,保留率分别为:对照组86%(66/77);妊娠接种组89%(67/75);分娩接种组88%(66/75)。婴儿7个月大时,耳部疾病患病率分别为:对照组71%(47/66),妊娠接种组63%(42/67),分娩接种组76%(50/66);23vPPV型携带率分别为:对照组26%(17/66),妊娠接种组18%(12/67),分娩接种组18%(12/66)。对于妊娠接种组,预防婴儿耳部疾病的疫苗效力为12%(95%CI -12%至31%),预防23vPPV型携带的疫苗效力为30%(95%CI -34%至64%)。在一项事后分析中,预防与23vPPV或相关类型携带同时发生的婴儿耳部疾病的疫苗效力为51%(95%CI -2%至76%)。妊娠或分娩时接种23vPPV后未出现严重不良反应。
在高危人群中,我们的研究未能证明妊娠期间接种23vPPV对7个月大婴儿全因性耳部疾病或23vPPV型鼻咽部携带这两个共同主要结局的有效性。对与疫苗相关血清型携带同时发生的耳部疾病的有效性(一个更具体的结局)表明,妊娠期间接种23vPPV可能补充儿童肺炎球菌疫苗接种计划。