A prospective cohort study of confirmed severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection during pregnancy evaluating SARS-CoV-2 antibodies in maternal and umbilical cord blood and SARS-CoV-2 in vaginal swabs.

cohort studies coronavirus disease 2019 obstetric delivery placental dysfunction pregnancy complications pregnancy outcome prospective studies severe acute respiratory syndrome coronavirus 2 vertical transmission

Journal

Acta obstetricia et gynecologica Scandinavica
ISSN: 1600-0412
Titre abrégé: Acta Obstet Gynecol Scand
Pays: United States
ID NLM: 0370343

Informations de publication

Date de publication:
12 2021
Historique:
revised: 15 09 2021
received: 30 05 2021
accepted: 22 09 2021
pubmed: 2 11 2021
medline: 1 12 2021
entrez: 1 11 2021
Statut: ppublish

Résumé

Evidence about the consequences of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in pregnancy is rapidly increasing; however, data on antibody response and risk of transmission during pregnancy and delivery are still limited. The aim of this study was to evaluate if SARS-CoV-2 is detectable in vaginal swabs and whether antibodies against SARS-CoV-2 are present in maternal and umbilical cord blood of pregnant women with confirmed SARS-CoV-2. A single-unit prospective cohort study in Denmark including pregnant women with SARS-CoV-2 infection confirmed by a pharyngeal swab between August 20, 2020, and March 1, 2021, who gave birth during the same period. All patients admitted to the maternity ward and antepartum clinic were screened for SARS-CoV-2 infection. A maternal blood sample and vaginal swabs were collected at inclusion. If included antepartum, these samples were repeated intrapartum when an umbilical cord blood sample was also collected. Swabs were analyzed for SARS-CoV-2 and blood samples were analyzed for SARS-CoV-2 total antibodies. Placental and neonatal swabs as well as placental histopathological examinations were performed on clinical indications. We included 28 women, of whom four had serious maternal or fetal outcomes including one case of neonatal death. Within the first 8 days after confirmed SARS-CoV-2 infection, SARS-CoV-2 was detectable in two vaginal swabs (2/28) and SARS-CoV-2 antibodies were detected in 1 of 13 women. From 16 days after confirmed infection, antibodies were observed in 19 of 21 of women. Antibodies in cord blood were not detected during the first 16 days after confirmed infection (n = 7). However, from 26 days, antibodies were present in 16 of 17 cord blood samples of seropositive mothers. Placental examination in two cases of severe fetal outcomes preceded by reduced fetal movements revealed SARS-CoV-2 in swabs and severe histopathological abnormalities. SARS-CoV-2 was detected in only 2 of 28 vaginal swabs within 8 days after confirmed infection in pregnant women. Our data suggest that maternal seroconversion occurs between days 8 and 16, whereas antibodies in cord blood of seropositive mothers were present in the majority from 26 days after confirmed infection. Additional data are needed regarding timing of seroconversion for the mother and appearance of antibodies in cord blood.

Identifiants

pubmed: 34719780
doi: 10.1111/aogs.14274
pmc: PMC8653183
doi:

Substances chimiques

Antibodies 0
Antibodies, Viral 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2268-2277

Subventions

Organisme : Ferring
Organisme : The Research Foundation at North Zealand Hospital, Hillerod

Informations de copyright

© 2021 The Authors. Acta Obstetricia et Gynecologica Scandinavica published by John Wiley & Sons Ltd on behalf of Nordic Federation of Societies of Obstetrics and Gynecology (NFOG).

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Auteurs

Julie Milbak (J)

Department of Obstetrics and Gynecology, Copenhagen University Hospital - North Zealand, Hilleroed, Denmark.

Victoria M F Holten (VMF)

Department of Obstetrics and Gynecology, Copenhagen University Hospital - North Zealand, Hilleroed, Denmark.

Paul Bryde Axelsson (PB)

Department of Obstetrics and Gynecology, Copenhagen University Hospital - North Zealand, Hilleroed, Denmark.

Jane Marie Bendix (JM)

Department of Obstetrics and Gynecology, Copenhagen University Hospital - North Zealand, Hilleroed, Denmark.

Anna J M Aabakke (AJM)

Department of Obstetrics and Gynecology, Copenhagen University Hospital-Holbaek, Denmark.
Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.

Lene Nielsen (L)

Department of Clinical Microbiology, Copenhagen University Hospital - Herlev and Gentofte, Herlev, Denmark.

Martin Barfred Friis (MB)

Department of Clinical Microbiology, Copenhagen University Hospital - Herlev and Gentofte, Herlev, Denmark.

Claus A J Jensen (CAJ)

Department of Clinical Biochemistry, Copenhagen University Hospital - North Zealand, Hilleroed, Denmark.

Ellen Christine Leth Løkkegaard (ECL)

Department of Obstetrics and Gynecology, Copenhagen University Hospital - North Zealand, Hilleroed, Denmark.
Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.

Tina Elisabeth Olsen (TE)

Department of Pathology, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.

Line Rode (L)

Department of Clinical Biochemistry, Copenhagen University Hospital - Rigshospitalet, Glostrup, Denmark.

Tine Dalsgaard Clausen (TD)

Department of Obstetrics and Gynecology, Copenhagen University Hospital - North Zealand, Hilleroed, Denmark.
Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.

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