评估 COVID-19 疫苗在孕妇中的免疫原性和反应原性。

Evaluation of immunogenicity and reactogenicity of COVID-19 vaccines in pregnant women.

机构信息

Fetal Medicine Unit, St George's University Hospitals NHS Foundation Trust, University of London, London, UK.

Immunisation and Vaccine Preventable Diseases Division, UK Health Security Agency, London, UK.

出版信息

Ultrasound Obstet Gynecol. 2022 Nov;60(5):673-680. doi: 10.1002/uog.26050.

Abstract

OBJECTIVE

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in pregnancy is associated with increased risk of adverse maternal and perinatal outcomes. Vaccines are highly effective at preventing severe coronavirus disease 2019 (COVID-19), but there are limited data on COVID-19 vaccines in pregnancy. This study aimed to investigate the reactogenicity and immunogenicity of COVID-19 vaccines in pregnant women when administered according to the 12-week-interval dosing schedule recommended in the UK.

METHODS

This was a cohort study of pregnant women receiving COVID-19 vaccination between April and September 2021. The outcomes were immunogenicity and reactogenicity after COVID-19 vaccination. Pregnant women were recruited by phone, e-mail and/or text and were vaccinated according to vaccine availability at their local vaccination center. For immunogenicity assessment, blood samples were taken at specific timepoints after each dose to evaluate nucleocapsid protein (N) and spike protein (S) antibody titers. The comparator group comprised non-pregnant female healthcare workers in the same age group who were vaccinated as part of the national immunization program in a contemporaneous longitudinal cohort study. Longitudinal changes in serum antibody titers and association with pregnancy status were assessed using a two-step regression approach. Reactogenicity assessment in pregnant women was undertaken using an online questionnaire. The comparator group comprised non-pregnant women aged 18-49 years who had received two vaccine doses in primary care. The association of pregnancy status with reactogenicity was assessed using logistic regression analysis.

RESULTS

Overall, 67 pregnant women, of whom 66 had received a mRNA vaccine, and 79 non-pregnant women, of whom 50 had received a mRNA vaccine, were included in the immunogenicity study. Most (61.2%) pregnant women received their first vaccine dose in the third trimester, while 3.0% received it in the first trimester and 35.8% in the second trimester. SARS-CoV-2 S-antibody geometric mean concentrations after mRNA vaccination were not significantly different at 2-6 weeks after the first dose but were significantly lower at 2-6 weeks after the second dose in infection-naïve pregnant compared with non-pregnant women. In pregnant women, prior infection was associated with higher antibody levels at 2-6 weeks after the second vaccine dose. Reactogenicity analysis included 108 pregnant women and 116 non-pregnant women. After the first dose, tiredness and chills were reported less commonly in pregnant compared with non-pregnant women (P = 0.043 and P = 0.029, respectively). After the second dose, feeling generally unwell was reported less commonly (P = 0.046) in pregnant compared with non-pregnant women.

CONCLUSIONS

Using an extended 12-week interval between vaccine doses, antibody responses after two doses of mRNA COVID-19 vaccine were found to be lower in pregnant compared with non-pregnant women. Strong antibody responses were achieved after one dose in previously infected women, regardless of pregnancy status. Pregnant women reported fewer adverse events after both the first and second dose of vaccine. These findings should now be addressed in larger controlled studies. © 2022 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.

摘要

目的

严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染与孕妇不良母婴和围产结局风险增加相关。疫苗在预防严重的 2019 年冠状病毒病(COVID-19)方面非常有效,但关于孕妇 COVID-19 疫苗的数据有限。本研究旨在调查按照英国推荐的 12 周间隔剂量方案接种 COVID-19 疫苗时孕妇的疫苗反应原性和免疫原性。

方法

这是一项在 2021 年 4 月至 9 月期间接受 COVID-19 疫苗接种的孕妇队列研究。结局为 COVID-19 疫苗接种后的免疫原性和疫苗反应原性。通过电话、电子邮件和/或短信招募孕妇,并根据当地疫苗接种中心的疫苗供应情况进行接种。为了评估免疫原性,在每次接种后特定时间点采集血样,以评估核衣壳蛋白(N)和刺突蛋白(S)抗体滴度。对照组为同期纵向队列研究中年龄组相同的非妊娠女性医护人员,他们作为国家免疫计划的一部分接种了疫苗。使用两步回归方法评估血清抗体滴度的纵向变化及其与妊娠状态的关系。使用在线问卷评估孕妇的疫苗反应原性。对照组为年龄在 18-49 岁之间接受两剂疫苗接种的非妊娠女性,她们在初级保健机构接种疫苗。使用逻辑回归分析评估妊娠状态与疫苗反应原性的关系。

结果

共有 67 名孕妇(其中 66 名接受了 mRNA 疫苗)和 79 名非孕妇(其中 50 名接受了 mRNA 疫苗)纳入了免疫原性研究。大多数(61.2%)孕妇在妊娠晚期接受了第一剂疫苗,而 3.0%在妊娠早期接受,35.8%在妊娠中期接受。与非妊娠女性相比,mRNA 疫苗接种后第 2-6 周 SARS-CoV-2 S 抗体几何平均浓度在第一剂后无显著差异,但在第二剂后显著降低。在感染前孕妇中,在接种第二剂疫苗后 2-6 周时,抗体水平更高。反应原性分析包括 108 名孕妇和 116 名非孕妇。与非妊娠女性相比,在接种第一剂后,疲倦和寒战在妊娠女性中报告的频率较低(P=0.043 和 P=0.029)。与非妊娠女性相比,在接种第二剂后,感觉不适的频率较低(P=0.046)。

结论

使用延长的 12 周疫苗接种间隔,与非妊娠女性相比,接受两剂 mRNA COVID-19 疫苗后,抗体反应较低。先前感染的女性在接种一剂后即可产生强烈的抗体反应,而与妊娠状态无关。孕妇在接种第一剂和第二剂疫苗后报告的不良事件较少。这些发现现在应该在更大的对照研究中得到解决。

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