Gray Kathryn J, Bordt Evan A, Atyeo Caroline, Deriso Elizabeth, Akinwunmi Babatunde, Young Nicola, Baez Aranxta Medina, Shook Lydia L, Cvrk Dana, James Kaitlyn, De Guzman Rose, Brigida Sara, Diouf Khady, Goldfarb Ilona, Bebell Lisa M, Yonker Lael M, Fasano Alessio, Rabi S Alireza, Elovitz Michal A, Alter Galit, Edlow Andrea G
Department of Obstetrics and Gynecology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA.
Lurie Center for Autism, Department of Pediatrics, Massachusetts General Hospital, Harvard Medical School, Boston, MA.
Am J Obstet Gynecol. 2021 Sep;225(3):303.e1-303.e17. doi: 10.1016/j.ajog.2021.03.023. Epub 2021 Mar 26.
Pregnant and lactating women were excluded from initial coronavirus disease 2019 vaccine trials; thus, data to guide vaccine decision making are lacking.
This study aimed to evaluate the immunogenicity and reactogenicity of coronavirus disease 2019 messenger RNA vaccination in pregnant and lactating women compared with: (1) nonpregnant controls and (2) natural coronavirus disease 2019 infection in pregnancy.
A total of 131 reproductive-age vaccine recipients (84 pregnant, 31 lactating, and 16 nonpregnant women) were enrolled in a prospective cohort study at 2 academic medical centers. Titers of severe acute respiratory syndrome coronavirus 2 spike and receptor-binding domain immunoglobulin G, immunoglobulin A, and immunoglobulin M were quantified in participant sera (n=131) and breastmilk (n=31) at baseline, at the second vaccine dose, at 2 to 6 weeks after the second vaccine, and at delivery by Luminex. Umbilical cord sera (n=10) titers were assessed at delivery. Titers were compared with those of pregnant women 4 to 12 weeks from the natural infection (n=37) by enzyme-linked immunosorbent assay. A pseudovirus neutralization assay was used to quantify neutralizing antibody titers for the subset of women who delivered during the study period. Postvaccination symptoms were assessed via questionnaire. Kruskal-Wallis tests and a mixed-effects model, with correction for multiple comparisons, were used to assess differences among groups.
Vaccine-induced antibody titers were equivalent in pregnant and lactating compared with nonpregnant women (pregnant, median, 5.59; interquartile range, 4.68-5.89; lactating, median, 5.74; interquartile range, 5.06-6.22; nonpregnant, median, 5.62; interquartile range, 4.77-5.98, P=.24). All titers were significantly higher than those induced by severe acute respiratory syndrome coronavirus 2 infection during pregnancy (P<.0001). Vaccine-generated antibodies were present in all umbilical cord blood and breastmilk samples. Neutralizing antibody titers were lower in umbilical cord than maternal sera, although this finding did not achieve statistical significance (maternal sera, median, 104.7; interquartile range, 61.2-188.2; cord sera, median, 52.3; interquartile range, 11.7-69.6; P=.05). The second vaccine dose (boost dose) increased severe acute respiratory syndrome coronavirus 2-specific immunoglobulin G, but not immunoglobulin A, in maternal blood and breastmilk. No differences were noted in reactogenicity across the groups.
Coronavirus disease 2019 messenger RNA vaccines generated robust humoral immunity in pregnant and lactating women, with immunogenicity and reactogenicity similar to that observed in nonpregnant women. Vaccine-induced immune responses were statistically significantly greater than the response to natural infection. Immune transfer to neonates occurred via placenta and breastmilk.
2019冠状病毒病疫苗的初始试验将孕妇和哺乳期妇女排除在外;因此,缺乏指导疫苗决策的数据。
本研究旨在评估2019冠状病毒病信使核糖核酸疫苗在孕妇和哺乳期妇女中的免疫原性和反应原性,并与以下情况进行比较:(1)非孕妇对照;(2)孕期自然感染2019冠状病毒病。
在2个学术医疗中心进行一项前瞻性队列研究,共纳入131名育龄疫苗接种者(84名孕妇、31名哺乳期妇女和16名非孕妇)。在基线、第二剂疫苗接种时、第二剂疫苗接种后2至6周以及分娩时,通过Luminex法对参与者血清(n = 131)和母乳(n = 31)中的严重急性呼吸综合征冠状病毒2刺突蛋白和受体结合域免疫球蛋白G、免疫球蛋白A和免疫球蛋白M滴度进行定量。在分娩时评估脐带血清(n = 10)滴度。通过酶联免疫吸附测定法将滴度与自然感染后4至12周的孕妇(n = 37)的滴度进行比较。使用假病毒中和试验对研究期间分娩的妇女亚组的中和抗体滴度进行定量。通过问卷调查评估接种疫苗后的症状。使用Kruskal-Wallis检验和混合效应模型,并对多重比较进行校正,以评估组间差异。
与非孕妇相比,孕妇和哺乳期妇女疫苗诱导的抗体滴度相当(孕妇,中位数为5.59;四分位间距为4.68 - 5.89;哺乳期妇女,中位数为5.74;四分位间距为5.06 - 6.22;非孕妇,中位数为5.62;四分位间距为4.77 - 5.98,P = 0.24)。所有滴度均显著高于孕期严重急性呼吸综合征冠状病毒2感染诱导的滴度(P < 0.0001)。所有脐带血和母乳样本中均存在疫苗产生的抗体。脐带血中的中和抗体滴度低于母体血清,尽管这一发现未达到统计学显著性(母体血清,中位数为104.7;四分位间距为61.2 - 188.2;脐带血清,中位数为52.3;四分位间距为11.7 - 69.6;P = 0.05)。第二剂疫苗(加强剂量)增加了母体血液和母乳中严重急性呼吸综合征冠状病毒2特异性免疫球蛋白G,但未增加免疫球蛋白A。各组间在反应原性方面未观察到差异。
2019冠状病毒病信使核糖核酸疫苗在孕妇和哺乳期妇女中产生了强大的体液免疫,其免疫原性和反应原性与非孕妇相似。疫苗诱导的免疫反应在统计学上显著大于对自然感染的反应。免疫通过胎盘和母乳传递给新生儿。