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Maternal-fetal immune responses in pregnant women infected with SARS-CoV-2.
Garcia-Flores, Valeria; Romero, Roberto; Xu, Yi; Theis, Kevin R; Arenas-Hernandez, Marcia; Miller, Derek; Peyvandipour, Azam; Bhatti, Gaurav; Galaz, Jose; Gershater, Meyer; Levenson, Dustyn; Pusod, Errile; Tao, Li; Kracht, David; Florova, Violetta; Leng, Yaozhu; Motomura, Kenichiro; Para, Robert; Faucett, Megan; Hsu, Chaur-Dong; Zhang, Gary; Tarca, Adi L; Pique-Regi, Roger; Gomez-Lopez, Nardhy.
Affiliation
  • Garcia-Flores V; Perinatology Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, US Department of Health and Human Services (NICHD/NIH/DHHS), Bethesda, MD
  • Romero R; Department of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, 48201, USA.
  • Xu Y; Perinatology Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, US Department of Health and Human Services (NICHD/NIH/DHHS), Bethesda, MD
  • Theis KR; Department of Obstetrics and Gynecology, University of Michigan, Ann Arbor, MI, 48109, USA. prbchiefstaff@med.wayne.edu.
  • Arenas-Hernandez M; Department of Epidemiology and Biostatistics, Michigan State University, East Lansing, MI, 48824, USA. prbchiefstaff@med.wayne.edu.
  • Miller D; Center for Molecular Medicine and Genetics, Wayne State University, Detroit, MI, 48201, USA. prbchiefstaff@med.wayne.edu.
  • Peyvandipour A; Detroit Medical Center, Detroit, MI, 48201, USA. prbchiefstaff@med.wayne.edu.
  • Bhatti G; Perinatology Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, US Department of Health and Human Services (NICHD/NIH/DHHS), Bethesda, MD
  • Galaz J; Department of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, 48201, USA.
  • Gershater M; Perinatology Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, US Department of Health and Human Services (NICHD/NIH/DHHS), Bethesda, MD
  • Levenson D; Department of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, 48201, USA.
  • Pusod E; Department of Biochemistry, Microbiology and Immunology, Wayne State University School of Medicine, Detroit, MI, 48201, USA.
  • Tao L; Perinatology Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, US Department of Health and Human Services (NICHD/NIH/DHHS), Bethesda, MD
  • Kracht D; Department of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, 48201, USA.
  • Florova V; Perinatology Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, US Department of Health and Human Services (NICHD/NIH/DHHS), Bethesda, MD
  • Leng Y; Department of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, 48201, USA.
  • Motomura K; Perinatology Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, US Department of Health and Human Services (NICHD/NIH/DHHS), Bethesda, MD
  • Para R; Department of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, 48201, USA.
  • Faucett M; Center for Molecular Medicine and Genetics, Wayne State University, Detroit, MI, 48201, USA.
  • Hsu CD; Perinatology Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, US Department of Health and Human Services (NICHD/NIH/DHHS), Bethesda, MD
  • Zhang G; Department of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, 48201, USA.
  • Tarca AL; Perinatology Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, US Department of Health and Human Services (NICHD/NIH/DHHS), Bethesda, MD
  • Pique-Regi R; Department of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, MI, 48201, USA.
  • Gomez-Lopez N; Perinatology Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, US Department of Health and Human Services (NICHD/NIH/DHHS), Bethesda, MD
Nat Commun ; 13(1): 320, 2022 01 18.
Article in En | MEDLINE | ID: mdl-35042863
ABSTRACT
Pregnant women represent a high-risk population for severe/critical COVID-19 and mortality. However, the maternal-fetal immune responses initiated by SARS-CoV-2 infection, and whether this virus is detectable in the placenta, are still under investigation. Here we show that SARS-CoV-2 infection during pregnancy primarily induces unique inflammatory responses at the maternal-fetal interface, which are largely governed by maternal T cells and fetal stromal cells. SARS-CoV-2 infection during pregnancy is also associated with humoral and cellular immune responses in the maternal blood, as well as with a mild cytokine response in the neonatal circulation (i.e., umbilical cord blood), without compromising the T-cell repertoire or initiating IgM responses. Importantly, SARS-CoV-2 is not detected in the placental tissues, nor is the sterility of the placenta compromised by maternal viral infection. This study provides insight into the maternal-fetal immune responses triggered by SARS-CoV-2 and emphasizes the rarity of placental infection.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Placenta / Pregnancy Complications, Infectious / Infectious Disease Transmission, Vertical / SARS-CoV-2 / COVID-19 / Immunity Limits: Adult / Female / Humans / Newborn / Pregnancy Language: En Journal: Nat Commun Journal subject: BIOLOGIA / CIENCIA Year: 2022 Document type: Article Affiliation country: Moldova

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Placenta / Pregnancy Complications, Infectious / Infectious Disease Transmission, Vertical / SARS-CoV-2 / COVID-19 / Immunity Limits: Adult / Female / Humans / Newborn / Pregnancy Language: En Journal: Nat Commun Journal subject: BIOLOGIA / CIENCIA Year: 2022 Document type: Article Affiliation country: Moldova