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Mechanisms of Key Innate Immune Cells in Early- and Late-Onset Preeclampsia
Preeclampsia is a complex cardiovascular disorder of pregnancy with underlying multifactorial pathogeneses; however, its etiology is not fully understood. It is characterized by the new onset of maternal hypertension after 20 weeks of gestation, accompanied by proteinuria, maternal organ damage, and...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7462000/ https://www.ncbi.nlm.nih.gov/pubmed/33013837 http://dx.doi.org/10.3389/fimmu.2020.01864 |
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author | Aneman, Ingrid Pienaar, Dillan Suvakov, Sonja Simic, Tatjana P. Garovic, Vesna D. McClements, Lana |
author_facet | Aneman, Ingrid Pienaar, Dillan Suvakov, Sonja Simic, Tatjana P. Garovic, Vesna D. McClements, Lana |
author_sort | Aneman, Ingrid |
collection | PubMed |
description | Preeclampsia is a complex cardiovascular disorder of pregnancy with underlying multifactorial pathogeneses; however, its etiology is not fully understood. It is characterized by the new onset of maternal hypertension after 20 weeks of gestation, accompanied by proteinuria, maternal organ damage, and/or uteroplacental dysfunction. Preeclampsia can be subdivided into early- and late-onset phenotypes (EOPE and LOPE), diagnosed before 34 weeks or from 34 weeks of gestation, respectively. Impaired placental development in early pregnancy and subsequent growth restriction is often associated with EOPE, while LOPE is associated with maternal endothelial dysfunction. The innate immune system plays an essential role in normal progression of physiological pregnancy and fetal development. However, inappropriate or excessive activation of this system can lead to placental dysfunction or poor maternal vascular adaptation and contribute to the development of preeclampsia. This review aims to comprehensively outline the mechanisms of key innate immune cells including macrophages, neutrophils, natural killer (NK) cells, and innate B1 cells, in normal physiological pregnancy, EOPE and LOPE. The roles of the complement system, syncytiotrophoblast extracellular vesicles and mesenchymal stem cells (MSCs) are also discussed in the context of innate immune system regulation and preeclampsia. The outlined molecular mechanisms, which represent potential therapeutic targets, and associated emerging treatments, are evaluated as treatments for preeclampsia. Therefore, by addressing the current understanding of innate immunity in the pathogenesis of EOPE and LOPE, this review will contribute to the body of research that could lead to the development of better diagnosis, prevention, and treatment strategies. Importantly, it will delineate the differences in the mechanisms of the innate immune system in two different types of preeclampsia, which is necessary for a more personalized approach to the monitoring and treatment of affected women. |
format | Online Article Text |
id | pubmed-7462000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74620002020-10-01 Mechanisms of Key Innate Immune Cells in Early- and Late-Onset Preeclampsia Aneman, Ingrid Pienaar, Dillan Suvakov, Sonja Simic, Tatjana P. Garovic, Vesna D. McClements, Lana Front Immunol Immunology Preeclampsia is a complex cardiovascular disorder of pregnancy with underlying multifactorial pathogeneses; however, its etiology is not fully understood. It is characterized by the new onset of maternal hypertension after 20 weeks of gestation, accompanied by proteinuria, maternal organ damage, and/or uteroplacental dysfunction. Preeclampsia can be subdivided into early- and late-onset phenotypes (EOPE and LOPE), diagnosed before 34 weeks or from 34 weeks of gestation, respectively. Impaired placental development in early pregnancy and subsequent growth restriction is often associated with EOPE, while LOPE is associated with maternal endothelial dysfunction. The innate immune system plays an essential role in normal progression of physiological pregnancy and fetal development. However, inappropriate or excessive activation of this system can lead to placental dysfunction or poor maternal vascular adaptation and contribute to the development of preeclampsia. This review aims to comprehensively outline the mechanisms of key innate immune cells including macrophages, neutrophils, natural killer (NK) cells, and innate B1 cells, in normal physiological pregnancy, EOPE and LOPE. The roles of the complement system, syncytiotrophoblast extracellular vesicles and mesenchymal stem cells (MSCs) are also discussed in the context of innate immune system regulation and preeclampsia. The outlined molecular mechanisms, which represent potential therapeutic targets, and associated emerging treatments, are evaluated as treatments for preeclampsia. Therefore, by addressing the current understanding of innate immunity in the pathogenesis of EOPE and LOPE, this review will contribute to the body of research that could lead to the development of better diagnosis, prevention, and treatment strategies. Importantly, it will delineate the differences in the mechanisms of the innate immune system in two different types of preeclampsia, which is necessary for a more personalized approach to the monitoring and treatment of affected women. Frontiers Media S.A. 2020-08-18 /pmc/articles/PMC7462000/ /pubmed/33013837 http://dx.doi.org/10.3389/fimmu.2020.01864 Text en Copyright © 2020 Aneman, Pienaar, Suvakov, Simic, Garovic and McClements. http://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 | Immunology Aneman, Ingrid Pienaar, Dillan Suvakov, Sonja Simic, Tatjana P. Garovic, Vesna D. McClements, Lana Mechanisms of Key Innate Immune Cells in Early- and Late-Onset Preeclampsia |
title | Mechanisms of Key Innate Immune Cells in Early- and Late-Onset Preeclampsia |
title_full | Mechanisms of Key Innate Immune Cells in Early- and Late-Onset Preeclampsia |
title_fullStr | Mechanisms of Key Innate Immune Cells in Early- and Late-Onset Preeclampsia |
title_full_unstemmed | Mechanisms of Key Innate Immune Cells in Early- and Late-Onset Preeclampsia |
title_short | Mechanisms of Key Innate Immune Cells in Early- and Late-Onset Preeclampsia |
title_sort | mechanisms of key innate immune cells in early- and late-onset preeclampsia |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7462000/ https://www.ncbi.nlm.nih.gov/pubmed/33013837 http://dx.doi.org/10.3389/fimmu.2020.01864 |
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