Nature Communications · 2022 · 225 citations · 87 references
Life SciencesImmunologyInfectious DiseasesImmunology Of Infectious DiseasesInflammationInnate ImmunityMaternal-fetal Immune InteractionsNeonatal ImmunityPlacental ImmunologyPlacental PhysiologyPregnancy ImmunologyCellular Inflammatory ResponsesImmune Response In PregnancyInflammatory Response In PregnancyInflammatory T Cell ResponsesMaternal-fetal ImmunologyMaternal-fetal Interface InflammationPlacental CellsSars-cov-2 Infection
Pregnant women represent a high-risk population for severe/critical COVID-19 and mortality. However, the maternal-fetal immune responses initiated by SARS-CoV-2 infection, and whether this virus is detectable in the placenta, are still under investigation. Here we show that SARS-CoV-2 infection during pregnancy primarily induces unique inflammatory responses at the maternal-fetal interface, which are largely governed by maternal T cells and fetal stromal cells. SARS-CoV-2 infection during pregnancy is also associated with humoral and cellular immune responses in the maternal blood, as well as with a mild cytokine response in the neonatal circulation (i.e., umbilical cord blood), without compromising the T-cell repertoire or initiating IgM responses. Importantly, SARS-CoV-2 is not detected in the placental tissues, nor is the sterility of the placenta compromised by maternal viral infection. This study provides insight into the maternal-fetal immune responses triggered by SARS-CoV-2 and emphasizes the rarity of placental infection.
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