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Fetoplacental transmission and placental response to SARS-CoV-2: Evidence from the literature

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a dreadful novel coronavirus with global health concerns among pregnant women. To date, the vertical transmission of SARS-CoV-2 during pregnancy remains controversial. We briefly report recent findings of placental response to SARS-CoV-...

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Autores principales: Ezechukwu, Henry C., Shi, Jiahua, Fowora, Muinah A., Diya, Cornelius A., Elfaki, Faiz, Adegboye, Oyelola A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9426356/
https://www.ncbi.nlm.nih.gov/pubmed/36052328
http://dx.doi.org/10.3389/fmed.2022.962937
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author Ezechukwu, Henry C.
Shi, Jiahua
Fowora, Muinah A.
Diya, Cornelius A.
Elfaki, Faiz
Adegboye, Oyelola A.
author_facet Ezechukwu, Henry C.
Shi, Jiahua
Fowora, Muinah A.
Diya, Cornelius A.
Elfaki, Faiz
Adegboye, Oyelola A.
author_sort Ezechukwu, Henry C.
collection PubMed
description Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a dreadful novel coronavirus with global health concerns among pregnant women. To date, the vertical transmission of SARS-CoV-2 during pregnancy remains controversial. We briefly report recent findings of placental response to SARS-CoV-2 infection and updates on vertical transmission. We systematically searched PubMed and Google Scholar databases according to PRISMA guidelines for studies reporting the effects of SARS-CoV-2 infection on the placenta and possibility of vertical transmission. We identified 45 studies reporting 1,280 human placentas that were analyzed by molecular pathology methods and 11,112 placenta-derived cells from a publicly available database that was analyzed using bioinformatics tools. The main finding of this study is that the SARS-CoV-2 canonical entry receptors (ACE2 and TMPRSS2) are abundantly expressed on the placenta during the first trimester, and this expression diminishes across gestational age. Out of 45 eligible studies identified, 24 (53.34%) showed no evidence of vertical transmission, 15 (33.33%) supported the hypothesis of very rare, low possibility of vertical transmission and 6 (13.33%) were indecisive and had no comment on vertical transmission. Furthermore, 433 placentas from 12 studies were also identified for placental pathology investigation. There was evidence of at least one form of maternal vascular malperfusion (MVM), 57/433 (13.1%), fetal vascular malperfusion (FVM), 81/433 (18.7%) and placental inflammation with excessive infiltration of CD3+ CD8+ lymphocytes, CD68+ macrophages and CD20+ lymphocytes in most of the eligible studies. Decidual vasculopathy (3.2%), infarction (3.2%), chronic histiocytic intervillositis (6.0%), thrombi vasculopathy (5.1%) were also observed in most of the MVM and FVM reported cases. The results indicated that SARS-CoV-2 induces placenta inflammation, and placenta susceptibility to SARS-CoV-2 decreases across the pregnancy window. Thus, SARS-CoV-2 infection in early pregnancy may adversely affect the developing fetus.
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spelling pubmed-94263562022-08-31 Fetoplacental transmission and placental response to SARS-CoV-2: Evidence from the literature Ezechukwu, Henry C. Shi, Jiahua Fowora, Muinah A. Diya, Cornelius A. Elfaki, Faiz Adegboye, Oyelola A. Front Med (Lausanne) Medicine Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a dreadful novel coronavirus with global health concerns among pregnant women. To date, the vertical transmission of SARS-CoV-2 during pregnancy remains controversial. We briefly report recent findings of placental response to SARS-CoV-2 infection and updates on vertical transmission. We systematically searched PubMed and Google Scholar databases according to PRISMA guidelines for studies reporting the effects of SARS-CoV-2 infection on the placenta and possibility of vertical transmission. We identified 45 studies reporting 1,280 human placentas that were analyzed by molecular pathology methods and 11,112 placenta-derived cells from a publicly available database that was analyzed using bioinformatics tools. The main finding of this study is that the SARS-CoV-2 canonical entry receptors (ACE2 and TMPRSS2) are abundantly expressed on the placenta during the first trimester, and this expression diminishes across gestational age. Out of 45 eligible studies identified, 24 (53.34%) showed no evidence of vertical transmission, 15 (33.33%) supported the hypothesis of very rare, low possibility of vertical transmission and 6 (13.33%) were indecisive and had no comment on vertical transmission. Furthermore, 433 placentas from 12 studies were also identified for placental pathology investigation. There was evidence of at least one form of maternal vascular malperfusion (MVM), 57/433 (13.1%), fetal vascular malperfusion (FVM), 81/433 (18.7%) and placental inflammation with excessive infiltration of CD3+ CD8+ lymphocytes, CD68+ macrophages and CD20+ lymphocytes in most of the eligible studies. Decidual vasculopathy (3.2%), infarction (3.2%), chronic histiocytic intervillositis (6.0%), thrombi vasculopathy (5.1%) were also observed in most of the MVM and FVM reported cases. The results indicated that SARS-CoV-2 induces placenta inflammation, and placenta susceptibility to SARS-CoV-2 decreases across the pregnancy window. Thus, SARS-CoV-2 infection in early pregnancy may adversely affect the developing fetus. Frontiers Media S.A. 2022-08-16 /pmc/articles/PMC9426356/ /pubmed/36052328 http://dx.doi.org/10.3389/fmed.2022.962937 Text en Copyright © 2022 Ezechukwu, Shi, Fowora, Diya, Elfaki and Adegboye. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Ezechukwu, Henry C.
Shi, Jiahua
Fowora, Muinah A.
Diya, Cornelius A.
Elfaki, Faiz
Adegboye, Oyelola A.
Fetoplacental transmission and placental response to SARS-CoV-2: Evidence from the literature
title Fetoplacental transmission and placental response to SARS-CoV-2: Evidence from the literature
title_full Fetoplacental transmission and placental response to SARS-CoV-2: Evidence from the literature
title_fullStr Fetoplacental transmission and placental response to SARS-CoV-2: Evidence from the literature
title_full_unstemmed Fetoplacental transmission and placental response to SARS-CoV-2: Evidence from the literature
title_short Fetoplacental transmission and placental response to SARS-CoV-2: Evidence from the literature
title_sort fetoplacental transmission and placental response to sars-cov-2: evidence from the literature
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9426356/
https://www.ncbi.nlm.nih.gov/pubmed/36052328
http://dx.doi.org/10.3389/fmed.2022.962937
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