Infectious Disease Section, Department of Pediatrics, Baylor College of Medicine, Houston, Texas.
Department of Obstetrics and Gynecology, Baylor College of Medicine, Houston, Texas.
JAMA. 2018 Oct 9;320(14):1464-1470. doi: 10.1001/jama.2018.14298.
Immunization with tetanus, diphtheria, and acellular pertussis (Tdap) vaccine is recommended in the United States during weeks 27 through 36 of pregnancy to prevent life-threatening infant pertussis. The optimal gestation for immunization to maximize concentrations of neonatal pertussis toxin antibodies is unknown.
To determine pertussis toxin antibody concentrations in cord blood from neonates born to women immunized and unimmunized with Tdap vaccine in pregnancy and optimal gestational age for immunization to maximize concentrations of neonatal antibodies.
DESIGN, SETTING, AND PARTICIPANTS: Prospective, observational, cohort study of term neonates in Houston, Texas (December 2013-March 2014).
Tdap immunization during weeks 27 through 36 of pregnancy or no Tdap immunization.
Primary outcome was geometric mean concentrations (GMCs) of pertussis toxin antibodies in cord blood of Tdap-exposed and Tdap-unexposed neonates and proportions of Tdap-exposed and Tdap-unexposed neonates with pertussis toxin antibody concentrations of 15 IU/mL or higher, 30 IU/mL or higher, and 40 IU/mL or higher, cutoffs representing quantifiable antibodies or levels that may be protective until the infant immunization series begins. Secondary outcome was the optimal gestation for immunization to achieve maximum pertussis toxin antibodies.
Six hundred twenty-six pregnancies (mean maternal age, 29.7 years; 41% white, 27% Hispanic, 26% black, 5% Asian, 1% other; mean gestation, 39.4 weeks) were included. Three hundred twelve women received Tdap vaccine at a mean gestation of 31.2 weeks (range, 27.3-36.4); 314 were unimmunized. GMC of neonatal cord pertussis toxin antibodies from the Tdap-exposed group was 47.3 IU/mL (95% CI, 42.1-53.2) compared with 12.9 IU/mL (95% CI, 11.7-14.3) in the Tdap-unexposed group, for a GMC ratio of 3.6 (95% CI, 3.1-4.2; P < .001). More Tdap-exposed than Tdap-unexposed neonates had pertussis toxin antibody concentrations of 15 IU/mL or higher (86% vs 37%; difference, 49% [95% CI, 42%-55%]), 30 IU/mL or higher (72% vs 17%; difference, 55% [95% CI, 49%-61%]), and 40 IU/mL or higher (59% vs 12%; difference, 47% [95% CI, 41%-54%]); P < .001 for each analysis. GMCs of pertussis toxin antibodies were highest when Tdap vaccine was administered during weeks 27 through 30 and declined thereafter, reaching a peak at week 30 (57.3 IU/mL [95% CI, 44.0-74.6]).
Immunization with Tdap vaccine during the third trimester of pregnancy, compared with no immunization, was associated with higher neonatal concentrations of pertussis toxin antibodies. Immunization early in the third trimester was associated with the highest concentrations.
在美国,推荐在妊娠 27 周到 36 周期间为孕妇接种破伤风、白喉和无细胞百日咳(Tdap)疫苗,以预防危及生命的婴儿百日咳。最佳妊娠时间接种疫苗以最大限度地提高新生儿百日咳毒素抗体浓度尚不清楚。
确定孕妇在妊娠期间接种 Tdap 疫苗和未接种 Tdap 疫苗的新生儿脐带血中百日咳毒素抗体浓度,以及为最大限度地提高新生儿抗体浓度而进行免疫接种的最佳妊娠时间。
设计、地点和参与者:前瞻性、观察性队列研究,研究对象为德克萨斯州休斯顿的足月新生儿(2013 年 12 月至 2014 年 3 月)。
妊娠 27 周到 36 周期间接种 Tdap 疫苗或未接种 Tdap 疫苗。
主要结局是 Tdap 暴露和未暴露新生儿脐带血中百日咳毒素抗体的几何平均浓度(GMC),以及 Tdap 暴露和未暴露新生儿中百日咳毒素抗体浓度为 15 IU/mL 或更高、30 IU/mL 或更高、40 IU/mL 或更高的比例,这些截点代表可量化的抗体或可能具有保护作用的水平,直到婴儿开始免疫接种系列。次要结局是为实现最大百日咳毒素抗体而进行免疫接种的最佳妊娠时间。
共纳入 626 例妊娠(平均母亲年龄 29.7 岁;41%为白人,27%为西班牙裔,26%为黑人,5%为亚洲人,1%为其他;平均妊娠周数为 39.4 周)。312 名女性在平均妊娠 31.2 周时(范围 27.3-36.4)接种了 Tdap 疫苗;314 名未接种疫苗。Tdap 暴露组新生儿脐带血中百日咳毒素抗体的 GMC 为 47.3 IU/mL(95%CI,42.1-53.2),而 Tdap 未暴露组为 12.9 IU/mL(95%CI,11.7-14.3),GMC 比值为 3.6(95%CI,3.1-4.2;P < .001)。与 Tdap 未暴露组相比,更多的 Tdap 暴露组新生儿的百日咳毒素抗体浓度为 15 IU/mL 或更高(86%比 37%;差异为 49%[95%CI,42%-55%])、30 IU/mL 或更高(72%比 17%;差异为 55%[95%CI,49%-61%])、40 IU/mL 或更高(59%比 12%;差异为 47%[95%CI,41%-54%]);每项分析的 P < .001。当 Tdap 疫苗在 27 周到 30 周期间接种时,百日咳毒素抗体的 GMC 最高,此后下降,在第 30 周达到峰值(57.3 IU/mL[95%CI,44.0-74.6])。
与未免疫相比,孕妇在妊娠晚期接种 Tdap 疫苗与新生儿百日咳毒素抗体浓度较高有关。在妊娠早期进行免疫接种与最高浓度相关。