SARS-CoV-2 infection in pregnancy is associated with robust inflammatory response at the maternal-fetal interface.
Journal
medRxiv : the preprint server for health sciences
Titre abrégé: medRxiv
Pays: United States
ID NLM: 101767986
Informations de publication
Date de publication:
26 Jan 2021
26 Jan 2021
Historique:
pubmed:
4
2
2021
medline:
4
2
2021
entrez:
3
2
2021
Statut:
epublish
Résumé
Pregnant women appear to be at increased risk for severe outcomes associated with COVID-19, but the pathophysiology underlying this increased morbidity and its potential impact on the developing fetus is not well understood. In this study of pregnant women with and without COVID-19, we assessed viral and immune dynamics at the placenta during maternal SARS-CoV-2 infection. Amongst uninfected women, ACE2 was detected by immunohistochemistry in syncytiotrophoblast cells of the normal placenta during early pregnancy but was rarely seen in healthy placentas at full term. Term placentas from women infected with SARS-CoV-2, however, displayed a significant increase in ACE2 levels. Using immortalized cell lines and primary isolated placental cells, we determined the vulnerability of various placental cell types to direct infection by SARS-CoV-2
Identifiants
pubmed: 33532791
doi: 10.1101/2021.01.25.21250452
pmc: PMC7852242
pii:
doi:
Types de publication
Preprint
Langues
eng
Subventions
Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA047904
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI157488
Pays : United States
Organisme : NIMH NIH HHS
ID : K23 MH118999
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM007205
Pays : United States
Organisme : NIDA NIH HHS
ID : U01 DA040588
Pays : United States
Organisme : NICHD NIH HHS
ID : F30 HD093350
Pays : United States
Commentaires et corrections
Type : UpdateIn