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Single-cell immunophenotyping of the fetal immune response to maternal SARS-CoV-2 infection in late gestation
by
Matute, Juan D
, Edlow, Andrea G
, Villani Alexandra-Chloe
, Finander Benjamin
, Li, Jonathan Z
, Kalish, Brian T
, Ai Xingbin
, Pepin, David
, Smith, Neal P
, Lerou Paul H
in
Coronaviruses
/ COVID-19
/ Gene expression
/ Immune response
/ Immune system
/ Infections
/ Severe acute respiratory syndrome coronavirus 2
/ T cell receptors
/ Well being
2022
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Single-cell immunophenotyping of the fetal immune response to maternal SARS-CoV-2 infection in late gestation
by
Matute, Juan D
, Edlow, Andrea G
, Villani Alexandra-Chloe
, Finander Benjamin
, Li, Jonathan Z
, Kalish, Brian T
, Ai Xingbin
, Pepin, David
, Smith, Neal P
, Lerou Paul H
in
Coronaviruses
/ COVID-19
/ Gene expression
/ Immune response
/ Immune system
/ Infections
/ Severe acute respiratory syndrome coronavirus 2
/ T cell receptors
/ Well being
2022
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
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Single-cell immunophenotyping of the fetal immune response to maternal SARS-CoV-2 infection in late gestation
by
Matute, Juan D
, Edlow, Andrea G
, Villani Alexandra-Chloe
, Finander Benjamin
, Li, Jonathan Z
, Kalish, Brian T
, Ai Xingbin
, Pepin, David
, Smith, Neal P
, Lerou Paul H
in
Coronaviruses
/ COVID-19
/ Gene expression
/ Immune response
/ Immune system
/ Infections
/ Severe acute respiratory syndrome coronavirus 2
/ T cell receptors
/ Well being
2022
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Single-cell immunophenotyping of the fetal immune response to maternal SARS-CoV-2 infection in late gestation
Journal Article
Single-cell immunophenotyping of the fetal immune response to maternal SARS-CoV-2 infection in late gestation
2022
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Overview
BackgroundDuring the COVID-19 pandemic, thousands of pregnant women have been infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The implications of maternal SARS-CoV-2 infection on fetal and childhood well-being need to be characterized. We aimed to characterize the fetal immune response to maternal SARS-CoV-2 infection.MethodsWe performed single-cell RNA-sequencing and T cell receptor sequencing on cord blood mononuclear cells (CBMCs) from newborns of mothers infected with SARS-CoV-2 in the third trimester (cases) or without SARS-CoV-2 infection (controls).ResultsWe identified widespread gene expression changes in CBMCs from cases, including upregulation of interferon-stimulated genes and major histocompatibility complex genes in CD14+ monocytes, transcriptional changes suggestive of activation of plasmacytoid dendritic cells, and activation and exhaustion of natural killer cells. Lastly, we observed fetal T cell clonal expansion in cases compared to controls.ConclusionsAs none of the infants were infected with SARS-CoV-2, our results suggest that maternal SARS-CoV-2 infection might modulate the fetal immune system in the absence of vertical transmission.ImpactThe implications of maternal SARS-CoV-2 infection in the absence of vertical transmission on fetal and childhood well-being are poorly understood.Maternal SARS-CoV-2 infection might modulate the fetal immune system in the absence of vertical transmission.This study raises important questions about the untoward effects of maternal SARS-CoV-2 on the fetus, even in the absence of vertical transmission.
Publisher
Nature Publishing Group
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