Yale Institute for Global Health, New Haven, CT, USA; Department of Internal Medicine (Infectious Diseases), Yale School of Medicine, New Haven, CT, USA; Yale School of Nursing, New Haven, CT, USA; Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT, USA.
Department of Epidemiology, Emory University Rollins School of Public Health, Atlanta, GA, USA.
Lancet Respir Med. 2020 Jun;8(6):597-608. doi: 10.1016/S2213-2600(19)30479-5.
Maternal influenza immunisation can reduce morbidity and mortality associated with influenza infection in pregnant women and young infants. We aimed to determine the vaccine efficacy of maternal influenza immunisation against maternal and infant PCR-confirmed influenza, duration of protection, and the effect of gestational age at vaccination on vaccine efficacy, birth outcomes, and infant growth up to 6 months of age.
We did a pooled analysis of three randomised controlled trials done in Nepal (2011-2014), Mali (2011-2014), and South Africa (2011-2013). Pregnant women, gestational age 17-34 weeks in Nepal, 28 weeks or more in Mali, and 20-36 weeks in South Africa, were enrolled. Women were randomly assigned 1:1 to a study group, in which they received trivalent inactivated influenza vaccine (IIV) in all three trials, or a control group, in which they received saline placebo in Nepal and South Africa or quadrivalent meningococcal conjugate vaccine in Mali. Enrolment at all sites was complete by April 24, 2013. Infants and women were assessed for respiratory illness, and samples from those that met the case definition were tested for influenza by PCR testing. Growth measurements, including length and weight, were obtained at birth at all sites, at 24 weeks in South Africa, and at 6 months in Nepal and Mali. The three trials are registered with ClinicalTrials.gov, numbers NCT01430689, NCT01034254, and NCT02465190.
10 002 women and 9800 liveborn infants were included. Pooled efficacy of maternal vaccination to prevent infant PCR-confirmed influenza up to 6 months of age was 35% (95% CI 19 to 47). The pooled estimate was 56% (28 to 73) within the first 2 months of life, 39% (11 to 58) between 2 and 4 months, and 19% (-9 to 40) between 4 and 6 months. In women, from enrolment during pregnancy to the end of follow-up at 6 months postpartum, the vaccine was 50% (95% CI 32-63) efficacious against PCR-confirmed influenza. Efficacy was 42% (12 to 61) during pregnancy and 60% (36 to 75) postpartum. In women vaccinated before 29 weeks gestational age, the estimated efficacy was 30% (-2 to 52), and in women vaccinated at or after 29 weeks, efficacy was 71% (50 to 83). Efficacy was similar in infants born to mothers vaccinated before or after 29 weeks gestation (34% [95% CI 12 to 51] vs 35% [11 to 52]). There was no overall association between maternal vaccination and low birthweight, stillbirth, preterm birth, and small for gestational age. At 6 months of age, the intervention and control groups were similar in terms of underweight (weight-for-age), stunted (length-for-age), and wasted (weight-for-length). Median centile change from birth to 6 months of age was similar between the intervention and the control groups for both weight and length.
The assessment of efficacy for women vaccinated before 29 weeks gestational age might have been underpowered, because the point estimate suggests that there might be efficacy despite wide CIs. Estimates of efficacy against PCR-confirmed influenza and safety in terms of adverse birth outcomes should be incorporated into any further consideration of maternal influenza immunisation recommendations.
Bill & Melinda Gates Foundation.
母体流感免疫接种可以降低孕妇和婴儿因流感感染而导致的发病率和死亡率。我们旨在确定母体流感免疫接种对母婴 PCR 确诊流感的疫苗效力、保护持续时间,以及妊娠年龄对疫苗效力、出生结局和婴儿生长至 6 个月的影响。
我们对在尼泊尔(2011-2014 年)、马里(2011-2014 年)和南非(2011-2013 年)进行的三项随机对照试验进行了汇总分析。招募了妊娠 17-34 周的尼泊尔孕妇、28 周或以上的马里孕妇和 20-36 周的南非孕妇。将孕妇以 1:1 的比例随机分配到研究组,在所有三项试验中,她们均接受了三价灭活流感疫苗(IIV),或对照组,在尼泊尔和南非接受生理盐水安慰剂,而在马里则接受四价脑膜炎球菌结合疫苗。所有地点的入组均在 2013 年 4 月 24 日前完成。对婴儿和妇女进行呼吸道疾病评估,对符合病例定义的样本进行 PCR 检测流感。在所有地点,在出生时、南非的 24 周时以及在尼泊尔和马里的 6 个月时,均进行了生长测量,包括长度和体重。这三项试验均在 ClinicalTrials.gov 上注册,编号为 NCT01430689、NCT01034254 和 NCT02465190。
纳入了 10002 名妇女和 9800 名活产婴儿。母婴接种疫苗预防婴儿 6 个月内 PCR 确诊流感的总有效率为 35%(95%CI 19-47)。出生后前 2 个月内的汇总估计值为 56%(28-73),2-4 个月为 39%(11-58),4-6 个月为 19%(-9-40)。在妇女中,从妊娠期间入组到产后 6 个月随访结束,疫苗对 PCR 确诊流感的有效性为 50%(95%CI 32-63)。妊娠期间的有效性为 42%(12-61),产后为 60%(36-75)。在妊娠 29 周前接种疫苗的妇女中,估计的有效性为 30%(-2-52),而在妊娠 29 周或之后接种疫苗的妇女中,有效性为 71%(50-83)。在妊娠 29 周前或后接种疫苗的母亲所生婴儿的有效性相似(34%[95%CI 12-51]vs 35%[11-52])。母体接种疫苗与低出生体重、死胎、早产和小于胎龄儿之间没有总体关联。在 6 个月时,干预组和对照组在体重不足(体重年龄)、发育迟缓(年龄长度)和消瘦(体重长度)方面相似。干预组和对照组的体重和长度中位数从出生到 6 个月的变化相似。
对妊娠 29 周前接种疫苗的妇女进行疫苗效力评估的效能可能不足,因为点估计表明,尽管 CIs 较宽,但可能存在疗效。对 PCR 确诊流感的疫苗效力和不良出生结局的安全性的估计应该纳入母体流感免疫接种建议的进一步考虑。
比尔及梅琳达·盖茨基金会。