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Maternal-Fetal Immune Responses in Pregnant Women Infected with SARS-CoV-2

Pregnant women are 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. Herein, we report that SARS-CoV-2 infection durin...

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Detalles Bibliográficos
Autores principales: Garcia-Flores, Valeria, Romero, Roberto, Xu, Yi, Theis, Kevin, Arenas-Hernandez, Marcia, Miller, Derek, Peyvandipour, Azam, Galaz, Jose, Levenson, Dustyn, Bhatti, Gaurav, Gershater, Meyer, Pusod, Errile, Kracht, David, Florova, Violetta, Leng, Yaozhu, Tao, Li, Faucett, Megan, Para, Robert, Hsu, Chaur-Dong, Zhang, Gary, Tarca, Adi L., Pique-Regi, Roger, Gomez-Lopez, Nardhy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8020997/
https://www.ncbi.nlm.nih.gov/pubmed/33821263
http://dx.doi.org/10.21203/rs.3.rs-362886/v1
Descripción
Sumario:Pregnant women are 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. Herein, we report that SARS-CoV-2 infection during pregnancy primarily induced specific maternal inflammatory responses in the circulation and at the maternal-fetal interface, the latter being governed by T cells and macrophages. SARS-CoV-2 infection during pregnancy was also associated with a cytokine response in the fetal circulation (i.e. umbilical cord blood) without compromising the cellular immune repertoire. Moreover, SARS-CoV-2 infection neither altered fetal cellular immune responses in the placenta nor induced elevated cord blood levels of IgM. Importantly, SARS-CoV-2 was not detected in the placental tissues, nor was 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 further emphasizes the rarity of placental infection.