Immune rebalancing at the maternal-fetal interface of maternal SARS-CoV-2 infection during early pregnancy.
Chenxiang XiZihui YanDandan BaiYalin ZhangBeiying WangXiaoxiao HanLi WuXiaohui ShiZhiyi HuMing TangZhongqu SuYingdong LiuBinya LiuJiqing YinHong WangXiaocui LiYanping ZhangShao-Rong GaoWenqiang LiuPublished in: Protein & cell (2024)
The current coronavirus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus (SARS-CoV-2) remains a threat to pregnant women. However, the impact of early pregnancy SARS-CoV-2 infection on the maternal-fetal interface remains poorly understood. Here, we present a comprehensive analysis of single-cell transcriptomics and metabolomics in placental samples infected with SARS-CoV-2 during early pregnancy. Compared to control placentas, SARS-CoV-2 infection elicited immune responses at the maternal-fetal interface and induced metabolic alterations in amino acid and phospholipid profiles during the initial weeks post-infection. However, subsequent immune cell activation and heightened immune tolerance in trophoblast cells established a novel dynamic equilibrium that mitigated the impact on the maternal-fetal interface. Notably, the immune response and metabolic alterations at the maternal-fetal interface exhibited a gradual decline during the second trimester. Our study underscores the adaptive immune tolerance mechanisms and establishment of immunological balance during the first two trimesters following maternal SARS-CoV-2 infection.
Keyphrases
- respiratory syndrome coronavirus
- sars cov
- pregnancy outcomes
- coronavirus disease
- birth weight
- immune response
- pregnant women
- single cell
- gestational age
- mass spectrometry
- weight gain
- amino acid
- induced apoptosis
- rna seq
- preterm birth
- high throughput
- molecular dynamics
- body mass index
- cell death
- cell cycle arrest
- oxidative stress
- endoplasmic reticulum stress
- high glucose