Boston Combined Residency Program, Boston Children's Hospital, Boston, Massachusetts, USA.
Department of Pediatrics, Boston Medical Center, Boston, Massachusetts, USA.
Am J Reprod Immunol. 2022 Dec;88(6):e13625. doi: 10.1111/aji.13625. Epub 2022 Oct 3.
COVID-19 infection during pregnancy increases maternal and fetal morbidity and mortality. Infection in the second or third trimester leads to changes in the decidual leukocyte populations. However, it is not known whether COVID-19 infection in the first trimester or COVID-19 vaccination during pregnancy alters the decidual immune environment.
We examined decidual biopsies obtained at delivery from women who had COVID-19 in the first trimester (n = 8), were fully vaccinated against COVID-19 during pregnancy (n = 17), or were neither infected nor vaccinated during pregnancy (n = 9). Decidual macrophages, NK cells, and T cells were quantified by immunofluorescence. Decidual IL-6, IL-10, and IP-10 were quantified by ELISA.
There were no differences in decidual macrophages, NK cells, T cells, or cytokines between the first trimester COVID-19 group and the control group. The vaccinated cohort had lower levels of macrophages and NK cells compared to the control group. There were no differences in cytokines between the vaccinated and control groups.
COVID-19 infection in the first trimester did not cause significant decidual leukocyte or cytokine changes at the maternal-fetal interface. Additionally, vaccination was not associated with decidual inflammation, supporting the safety of SARS-CoV-2 vaccination during pregnancy.
COVID-19 感染在妊娠期间增加了母婴发病率和死亡率。妊娠中期或晚期的感染会导致蜕膜白细胞群发生变化。然而,尚不清楚妊娠早期的 COVID-19 感染或妊娠期间的 COVID-19 疫苗接种是否会改变蜕膜免疫环境。
我们检查了分娩时从妊娠早期 COVID-19 感染的女性(n=8)、在妊娠期间完全接种 COVID-19 疫苗的女性(n=17)或妊娠期间既未感染也未接种疫苗的女性(n=9)获得的蜕膜活检。通过免疫荧光定量检测蜕膜巨噬细胞、NK 细胞和 T 细胞。通过 ELISA 定量检测蜕膜 IL-6、IL-10 和 IP-10。
妊娠早期 COVID-19 组与对照组之间的蜕膜巨噬细胞、NK 细胞、T 细胞或细胞因子无差异。接种组的巨噬细胞和 NK 细胞水平低于对照组。接种组和对照组之间细胞因子无差异。
妊娠早期的 COVID-19 感染不会导致母体-胎儿界面蜕膜白细胞或细胞因子发生显著变化。此外,接种疫苗与蜕膜炎症无关,支持在妊娠期间接种 SARS-CoV-2 疫苗的安全性。