Department of Obstetrics & Gynecology, Carmel Medical Center, Haifa, Israel; Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
Department of Obstetrics & Gynecology, Carmel Medical Center, Haifa, Israel; Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
Eur J Obstet Gynecol Reprod Biol. 2022 Jul;274:148-154. doi: 10.1016/j.ejogrb.2022.05.029. Epub 2022 May 30.
BNT162b2 messenger RNA (mRNA) COVID-19 vaccine administered during pregnancy was found to produce a strong maternal immunoglobulin (IgG) response which crosses the placenta to the newborn. Our aim was to evaluate maternal and neonatal SARS-CoV-2 IgG antibody levels at birth, following a COVID-19 booster vaccine during the third trimester.
A prospective cohort study including women admitted to delivery ward at least 7 days after their BNT162b2 (Pfizer/BioNTech) booster vaccination without a prior clinical COVID-19 infection. SARS-CoV-2 IgG antibodies levels were measured in maternal blood upon admission to delivery and in the umbilical blood within 30 min following delivery. The correlation between antibody titers, feto-maternal characteristics, maternal side effects following vaccination, and time interval from vaccination to delivery were analyzed.
Between September to November 2021, high antibody levels were measured in all 102 women and 93 neonatal blood samples, at a mean ± standard deviation duration of 7.0 ± 2.9 weeks after the third vaccine. We found positive correlation between maternal and neonatal antibodies (r = 0.73, 95% confidence interval [CI] 0.61 to 0.81, p < 0.001), with neonatal titers approximately 1.4 times higher compared to maternal titers. In the multivariable analysis maternal antibody levels dropped by -7.2% (95% CI -12.0 to -2.3%, p = 0.005) for each week that passed since the receipt of the third vaccine dose. In contrary, systemic side effects after the third vaccine were associated with higher maternal antibody levels of 52.0% (95% CI 4.7 to 120.8%, p = 0.028). Also, for each 1 unit increase in maternal body mass index, maternal antibody levels increased by 3.6% (95% CI 0.4 to 6.9%, p = 0.025).
BNT162b2 mRNA COVID-19 booster dose during the third trimester of pregnancy was associated with strong maternal and neonatal responses as reflected by maternal and neonatal SARS-CoV-2 IgG antibody levels measured at birth. These findings support the administration of the COVID-19 booster to pregnant women to restore maternal and neonatal protection during the ongoing pandemic.
在怀孕期间接种 BNT162b2 信使 RNA(mRNA)COVID-19 疫苗,发现可产生强烈的母体免疫球蛋白(IgG)反应,该反应可穿过胎盘到达新生儿。我们的目的是评估在第三孕期 COVID-19 加强疫苗接种后出生时的母体和新生儿 SARS-CoV-2 IgG 抗体水平。
这是一项前瞻性队列研究,包括至少在接受 BNT162b2(辉瑞/生物技术)加强疫苗接种后 7 天入住分娩病房且无先前临床 COVID-19 感染的女性。在分娩时入院时测量母体血液中的 SARS-CoV-2 IgG 抗体水平,并在分娩后 30 分钟内测量脐带血中的 SARS-CoV-2 IgG 抗体水平。分析了抗体滴度、母婴特征、接种后母体副作用以及从接种到分娩的时间间隔之间的相关性。
在 2021 年 9 月至 11 月期间,在接种第三剂疫苗后平均 7.0±2.9 周时,我们在 102 名女性和 93 名新生儿的血液样本中均检测到高抗体水平。我们发现母体和新生儿抗体之间存在正相关(r=0.73,95%置信区间 [CI]0.61 至 0.81,p<0.001),新生儿滴度比母体滴度高约 1.4 倍。在多变量分析中,自接种第三剂疫苗以来,每过去一周,母体抗体水平下降 7.2%(95%CI-12.0 至-2.3%,p=0.005)。相反,接种第三剂疫苗后的全身副作用与母体抗体水平升高 52.0%(95%CI4.7 至 120.8%,p=0.028)相关。此外,母体体重指数每增加 1 个单位,母体抗体水平增加 3.6%(95%CI0.4 至 6.9%,p=0.025)。
在妊娠晚期接种 BNT162b2 mRNA COVID-19 加强疫苗与出生时测量的母体和新生儿 SARS-CoV-2 IgG 抗体水平所反映的强烈母体和新生儿反应相关。这些发现支持在当前大流行期间为孕妇接种 COVID-19 加强疫苗,以恢复母体和新生儿的保护。