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Mild/asymptomatic COVID-19 in unvaccinated pregnant mothers impairs neonatal immune responses

  • Brianna M. Doratt
  • , Suhas Sureshchandra
  • , Heather True
  • , Monica Rincon
  • , Nicole E. Marshall
  • , Ilhem Messaoudi

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

Maternal SARS-CoV-2 infection triggers placental inflammation and alters cord blood immune cell composition. However, most studies focus on outcomes of severe maternal infection. Therefore, we analyzed cord blood and chorionic villi from newborns of unvaccinated mothers who experienced mild/asymptomatic SARS-CoV-2 infection during pregnancy. We investigated immune cell rewiring using flow cytometry, single-cell RNA sequencing, and functional readouts using ex vivo stimulation with TLR agonists and pathogens. Maternal infection was associated with increased frequency of memory T and B cells and nonclassical monocytes in cord blood. Ex vivo T and B cell responses to stimulation were attenuated, suggesting a tolerogenic state. Maladaptive responses were also observed in cord blood monocytes, where antiviral responses were dampened but responses to bacterial TLRs were increased. Maternal infection was also associated with expansion and activation of placental Hofbauer cells, secreting elevated levels of myeloid cell–recruiting chemokines. Moreover, we reported increased activation of maternally derived monocytes/macrophages in the fetal placenta that were transcriptionally primed for antiviral responses. Our data indicate that even in the absence of vertical transmission or symptoms in the neonate, mild/asymptomatic maternal COVID-19 altered the transcriptional and functional state in fetal immune cells in circulation and in the placenta.

Original languageEnglish
Article numbere172658
JournalJCI insight
Volume8
Issue number19
DOIs
StatePublished - Oct 2023

Bibliographical note

Publisher Copyright:
© 2023, Doratt et al.

Funding

We are grateful to all participants in the study. We thank the Maternal Fetal Medicine Research Unit at OHSU for sample collection and Allen Jankeel, Michael Z. Zulu, Gouri Ajith, Isaac Cinco, and Hannah Debray at UCI for assistance with tissue processing. We thank Jennifer Atwood at the University of California, Irvine Institute for Immunology Flow Cytometry Core for assistance with FACS sorting, and imaging flow cytometry, and Melanie Oakes at the University of California, Irvine Genomics Research and Technology Hub for assistance with 10x Genomics library preparation and sequencing. This study was supported by grants from the NIH 1K23HD06952 (to NEM), 1R01AI145910 (to IM), R03AI11280 (to IM), and 1R01AI142841 (to IM).

FundersFunder number
University of California, Irvine Genomics Research and Technology Hub
University of California, Irvine Institute for Immunology
National Institutes of Health (NIH)1K23HD06952, 1R01AI142841, 1R01AI145910, R03AI11280
Oregon Institute of Occupational Health Sciences, Oregon Health and Science University

    ASJC Scopus subject areas

    • General Medicine

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