SARS-COV-2 IgG antibody response in pregnant women at delivery.


Journal

Journal of gynecology obstetrics and human reproduction
ISSN: 2468-7847
Titre abrégé: J Gynecol Obstet Hum Reprod
Pays: France
ID NLM: 101701588

Informations de publication

Date de publication:
Sep 2021
Historique:
received: 24 10 2020
revised: 04 12 2020
accepted: 07 12 2020
pubmed: 15 12 2020
medline: 26 8 2021
entrez: 14 12 2020
Statut: ppublish

Résumé

The prevalence of COVID-19 infection during pregnancy is not known. COVIPREG is a prospective French multicenter study to assess the seroprevalence at the time of delivery and the maternal and neonatal impact of COVID-19 infection during pregnancy. In order to study factors associated with poor outcomes after COVID-19 Infection during pregnancy and adapt the sample size of the study, a preliminary assessment of the prevalence of SARS-CoV-2 IgG was planned after 500 inclusions in a one perinatal center of Paris area. To assess the prevalence of SARS-CoV-2 IgG antibody response in pregnant women at the time of delivery during the COVID-19 pandemia. A prospective observational study at Cochin hospital (Level III maternity). Patients admitted for delivery were offered to participate to the study. Each patient participating to the study was tested for anti-SARS-CoV-2-IgG antibodies using a commercially available ELISA. Among the 529 patients included in the COVIPREG study between April 29 and June 26, 529 were assessed for SARS-CoV-2 IgG antibody response and 25 had a positive test, ie 4.7 % with a confidence interval at 95 % [3.0 %-6.9 %]). Four months after the beginning of the infection in Paris, the seroprevalence of SARS-CoV-2 IgG in pregnant women at the time of delivery is low. Studies evaluating the impact of COVID-19 infection during pregnancy should take this information in account in order to adapt the sample size.

Sections du résumé

BACKGROUND BACKGROUND
The prevalence of COVID-19 infection during pregnancy is not known. COVIPREG is a prospective French multicenter study to assess the seroprevalence at the time of delivery and the maternal and neonatal impact of COVID-19 infection during pregnancy. In order to study factors associated with poor outcomes after COVID-19 Infection during pregnancy and adapt the sample size of the study, a preliminary assessment of the prevalence of SARS-CoV-2 IgG was planned after 500 inclusions in a one perinatal center of Paris area.
OBJECTIVES OBJECTIVE
To assess the prevalence of SARS-CoV-2 IgG antibody response in pregnant women at the time of delivery during the COVID-19 pandemia.
STUDY DESIGN METHODS
A prospective observational study at Cochin hospital (Level III maternity). Patients admitted for delivery were offered to participate to the study. Each patient participating to the study was tested for anti-SARS-CoV-2-IgG antibodies using a commercially available ELISA.
RESULTS RESULTS
Among the 529 patients included in the COVIPREG study between April 29 and June 26, 529 were assessed for SARS-CoV-2 IgG antibody response and 25 had a positive test, ie 4.7 % with a confidence interval at 95 % [3.0 %-6.9 %]).
CONCLUSIONS CONCLUSIONS
Four months after the beginning of the infection in Paris, the seroprevalence of SARS-CoV-2 IgG in pregnant women at the time of delivery is low. Studies evaluating the impact of COVID-19 infection during pregnancy should take this information in account in order to adapt the sample size.

Identifiants

pubmed: 33310133
pii: S2468-7847(20)30417-7
doi: 10.1016/j.jogoh.2020.102041
pmc: PMC7831450
pii:
doi:

Substances chimiques

Antibodies, Viral 0
Immunoglobulin G 0

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

102041

Informations de copyright

Copyright © 2020 Elsevier Masson SAS. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest CVF has obtained a grand from Ferring pharmaceutics for the COVIPREG study.

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Auteurs

Vassilis Tsatsaris (V)

Université de Paris, F-75006 Paris, France; Maternité Port-Royal, AP-HP, FHU PREMA, Hôpital Cochin, F-75014 Paris, France. Electronic address: vassilis.tsatsaris@aphp.fr.

Alice-Andrée Mariaggi (AA)

Université de Paris, F-75006 Paris, France; Laboratoire de Virologie, AP-HP, Hôpital Cochin, F-75014 Paris, France.

Odile Launay (O)

Université de Paris, F-75006 Paris, France; CIC vaccinologie, AP-HP, FHU PREMA, Hôpital Cochin, F-75014 Paris, France.

Camille Couffignal (C)

Université de Paris, F-75006 Paris, France; Unité de recherche clinique PNVS, AP-HP, Hôpital Bichat, F-75018 Paris, France.

Jessica Rousseau (J)

Unité de recherche clinique, CIC-Mère enfant, AP-HP, FHU PREMA, Hôpital Cochin, F-75014 Paris, France.

Pierre Yves Ancel (PY)

Université de Paris, F-75006 Paris, France; Unité de recherche clinique, CIC-Mère enfant, AP-HP, FHU PREMA, Hôpital Cochin, F-75014 Paris, France.

Estelle Marcault (E)

Université de Paris, F-75006 Paris, France; Unité de recherche clinique PNVS, AP-HP, Hôpital Bichat, F-75018 Paris, France.

Yves Ville (Y)

Université de Paris, F-75006 Paris, France; Maternité, AP-HP, Hôpital Necker, F-75007 Paris, France.

Anne-Gaël Cordier (AG)

Maternité, AP-HP, Hôpital Bicêtre, F-94270 Le Kremlin-Bicêtre, France.

Alexandre Vivanti (A)

Université Paris-Saclay, 94804 Villejuif, France; Maternité, AP-HP, Hôpital Antoine Béclère, F-92140 Clamart, France.

Julie Carrara (J)

Maternité, AP-HP, Hôpital Antoine Béclère, F-92140 Clamart, France.

Dominique Luton (D)

Université de Paris, F-75006 Paris, France; Maternité, AP-HP, Hôpital Bichat, F-75018 Paris, France; Groupe de Recherche sur les Infections pendant la Grossesse (GRIG), France.

Marc Dommergues (M)

Sorbonne Université, F-75006 Paris, France; Maternité, AP-HP, Hôpital Pitié-Salpêtrière, F-75013 Paris, France.

Constance Borie (C)

Université de Paris, F-75006 Paris, France; Maternité, AP-HP, Hôpital Robert Debré, F-75019 Paris, France.

Gilles Kayem (G)

Sorbonne Université, F-75006 Paris, France; Maternité, AP-HP, Hôpital Trousseau, F-75012 Paris, France.

Vivien Alessandrini (V)

Université de Paris, F-75006 Paris, France; Maternité Port-Royal, AP-HP, FHU PREMA, Hôpital Cochin, F-75014 Paris, France.

Laurence Lecomte (L)

Unité de recherche clinique, CIC-Mère enfant, AP-HP, FHU PREMA, Hôpital Cochin, F-75014 Paris, France.

Jean François Meritet (JF)

Maternité Port-Royal, AP-HP, FHU PREMA, Hôpital Cochin, F-75014 Paris, France.

Marianne Leruez-Ville (M)

Laboratoire de Virologie, AP-HP, Hôpital Necker, F-75007 Paris, France.

François Goffinet (F)

Université de Paris, F-75006 Paris, France; Maternité Port-Royal, AP-HP, FHU PREMA, Hôpital Cochin, F-75014 Paris, France.

Claire Dubois (C)

Université de Paris, F-75006 Paris, France; Laboratoire de Virologie, AP-HP, Hôpital Paul-Brousse, F-94804 Villejuif, France.

Olivier Picone (O)

Université de Paris, F-75006 Paris, France; Maternité, AP-HP, Hôpital Louis Mourier, F-75007 Paris, France.

Christelle Vauloup Fellous (C)

Université Paris-Saclay, 94804 Villejuif, France; Laboratoire de Virologie, AP-HP, Hôpital Paul-Brousse, F-94804 Villejuif, France.

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