SARS-CoV-2 replicates in the placenta after maternal infection during pregnancy.

Anda-Petronela Radan, Patricia Renz, Luigi Raio, Anna-Sophie Villiger, Valérie Haesler, Mafalda Trippel, Daniel Surbek
Author Information
  1. Anda-Petronela Radan: Department of Obstetrics and Feto-Maternal Medicine, University Hospital of Bern, University of Bern, Bern, Switzerland.
  2. Patricia Renz: Department of Obstetrics and Feto-Maternal Medicine, University Hospital of Bern, University of Bern, Bern, Switzerland.
  3. Luigi Raio: Department of Obstetrics and Feto-Maternal Medicine, University Hospital of Bern, University of Bern, Bern, Switzerland.
  4. Anna-Sophie Villiger: Department of Obstetrics and Feto-Maternal Medicine, University Hospital of Bern, University of Bern, Bern, Switzerland.
  5. Valérie Haesler: Department of Obstetrics and Feto-Maternal Medicine, University Hospital of Bern, University of Bern, Bern, Switzerland.
  6. Mafalda Trippel: Department of Pathology, University of Bern, Bern, Switzerland.
  7. Daniel Surbek: Department of Obstetrics and Feto-Maternal Medicine, University Hospital of Bern, University of Bern, Bern, Switzerland.

Abstract

Objectives: Pregnant women are at increased risk for severe SARS-CoV-2 infection and adverse neonatal outcome, primarily preterm birth and stillbirth. Our study aimed to investigate to which extent SARS-CoV-2 affects placental tissue and if viral replication within the placenta is evident, thus if there is a correlation between placental damage and adverse pregnancy outcome such as stillbirth.
Methods: We prospectively collected placentas from 61 SARS-CoV-2 infected pregnant women and 10 controls. Histopathological, immunohistochemical, and hybridization studies were performed on all placentas with antibodies for SARS-CoV-2 proteins, ACE2, various immune cells, and inflammatory markers or probes for SARS-CoV-2 genes and an antisense strand.
Results: The measured scores of SARS-CoV-2 glycoprotein, nucleocapsid, and antisense strand indicating replication correlated with both the severity of maternal symptoms and presence of stillbirth. Specifically, 15/61 placentas exhibited replication, while the three cases with stillbirth had high or maximal replication scores. ACE2-H-score was significantly higher in COVID-19 patients, while the expression of various immune cells did not differ statistically. In multivariate analysis, presence of maternal comorbidities correlated with presence of severe COVID-19 infection.
Conclusion: We report evidence of active SARS-CoV-2 replication in the placenta after maternal infection in pregnancy in a case-control setting in a large population. Intensity of placental viral replication as well as viral levels were higher in women with severe or critical COVID-19 disease, supporting the rationale that severity of maternal SARS-CoV-2 infection could correlate with the severity of placentitis. Replication was maximal in cases of stillbirth, which suggests direct placental involvement in the pathophysiology of this dramatic outcome. Continuing to advocate for preventive measures against COVID-19 during pregnancy, including (re)vaccination, as well as appropriately counseling women with diagnosed infection, are of utter importance.

Keywords

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Word Cloud

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