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Infections at the maternal–fetal interface: an overview of pathogenesis and defence

Infections are a major threat to human reproductive health, and infections in pregnancy can cause prematurity or stillbirth, or can be vertically transmitted to the fetus leading to congenital infection and severe disease. The acronym ‘TORCH’ (Toxoplasma gondii, other, rubella virus, cytomegalovirus...

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Autores principales: Megli, Christina J., Coyne, Carolyn B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8386341/
https://www.ncbi.nlm.nih.gov/pubmed/34433930
http://dx.doi.org/10.1038/s41579-021-00610-y
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author Megli, Christina J.
Coyne, Carolyn B.
author_facet Megli, Christina J.
Coyne, Carolyn B.
author_sort Megli, Christina J.
collection PubMed
description Infections are a major threat to human reproductive health, and infections in pregnancy can cause prematurity or stillbirth, or can be vertically transmitted to the fetus leading to congenital infection and severe disease. The acronym ‘TORCH’ (Toxoplasma gondii, other, rubella virus, cytomegalovirus, herpes simplex virus) refers to pathogens directly associated with the development of congenital disease and includes diverse bacteria, viruses and parasites. The placenta restricts vertical transmission during pregnancy and has evolved robust mechanisms of microbial defence. However, microorganisms that cause congenital disease have likely evolved diverse mechanisms to bypass these defences. In this Review, we discuss how TORCH pathogens access the intra-amniotic space and overcome the placental defences that protect against microbial vertical transmission.
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spelling pubmed-83863412021-08-25 Infections at the maternal–fetal interface: an overview of pathogenesis and defence Megli, Christina J. Coyne, Carolyn B. Nat Rev Microbiol Review Article Infections are a major threat to human reproductive health, and infections in pregnancy can cause prematurity or stillbirth, or can be vertically transmitted to the fetus leading to congenital infection and severe disease. The acronym ‘TORCH’ (Toxoplasma gondii, other, rubella virus, cytomegalovirus, herpes simplex virus) refers to pathogens directly associated with the development of congenital disease and includes diverse bacteria, viruses and parasites. The placenta restricts vertical transmission during pregnancy and has evolved robust mechanisms of microbial defence. However, microorganisms that cause congenital disease have likely evolved diverse mechanisms to bypass these defences. In this Review, we discuss how TORCH pathogens access the intra-amniotic space and overcome the placental defences that protect against microbial vertical transmission. Nature Publishing Group UK 2021-08-25 2022 /pmc/articles/PMC8386341/ /pubmed/34433930 http://dx.doi.org/10.1038/s41579-021-00610-y Text en © Springer Nature Limited 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Review Article
Megli, Christina J.
Coyne, Carolyn B.
Infections at the maternal–fetal interface: an overview of pathogenesis and defence
title Infections at the maternal–fetal interface: an overview of pathogenesis and defence
title_full Infections at the maternal–fetal interface: an overview of pathogenesis and defence
title_fullStr Infections at the maternal–fetal interface: an overview of pathogenesis and defence
title_full_unstemmed Infections at the maternal–fetal interface: an overview of pathogenesis and defence
title_short Infections at the maternal–fetal interface: an overview of pathogenesis and defence
title_sort infections at the maternal–fetal interface: an overview of pathogenesis and defence
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8386341/
https://www.ncbi.nlm.nih.gov/pubmed/34433930
http://dx.doi.org/10.1038/s41579-021-00610-y
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