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From mice to women: the conundrum of immunity to infection during pregnancy
Resistance to infection is the ability of the host to evoke a strong immune response sufficient to eliminate the infectious agent. In contrast, maternal tolerance to the fetus necessitates careful regulation of immune responses. Successful pregnancy requires the maternal host to effectively balance...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier Ireland Ltd.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3748615/ https://www.ncbi.nlm.nih.gov/pubmed/23432873 http://dx.doi.org/10.1016/j.jri.2012.10.015 |
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author | Krishnan, Lakshmi Nguyen, Tina McComb, Scott |
author_facet | Krishnan, Lakshmi Nguyen, Tina McComb, Scott |
author_sort | Krishnan, Lakshmi |
collection | PubMed |
description | Resistance to infection is the ability of the host to evoke a strong immune response sufficient to eliminate the infectious agent. In contrast, maternal tolerance to the fetus necessitates careful regulation of immune responses. Successful pregnancy requires the maternal host to effectively balance the opposing processes of maternal immune reactivity and tolerance to the fetus. However, this balance can be perturbed by infections which are recognized as the major cause of adverse pregnancy outcome including pre-term labor. Select pathogens also pose a serious threat of severe maternal illness. These include intracellular and chronic pathogens that have evolved immune evasive strategies. Murine models of intracellular bacteria and parasites that mimic pathogenesis of infection in humans have been developed. While human epidemiological studies provide insight into maternal immunity to infection, experimental infection in pregnant mice is a vital tool to unravel the complex molecular mechanisms of placental infection, congenital transmission and maternal illness. We will provide a comprehensive review of the pathogenesis of several infection models in pregnant mice and their clinical relevance. These models have revealed the immunological function of the placenta in responding to, and resisting infection. Murine feto-placental infection provides an effective way to evaluate new intervention strategies for managing infections during pregnancy, adverse fetal outcome and long-term effects on the offspring and mother. |
format | Online Article Text |
id | pubmed-3748615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Published by Elsevier Ireland Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-37486152013-09-01 From mice to women: the conundrum of immunity to infection during pregnancy Krishnan, Lakshmi Nguyen, Tina McComb, Scott J Reprod Immunol Article Resistance to infection is the ability of the host to evoke a strong immune response sufficient to eliminate the infectious agent. In contrast, maternal tolerance to the fetus necessitates careful regulation of immune responses. Successful pregnancy requires the maternal host to effectively balance the opposing processes of maternal immune reactivity and tolerance to the fetus. However, this balance can be perturbed by infections which are recognized as the major cause of adverse pregnancy outcome including pre-term labor. Select pathogens also pose a serious threat of severe maternal illness. These include intracellular and chronic pathogens that have evolved immune evasive strategies. Murine models of intracellular bacteria and parasites that mimic pathogenesis of infection in humans have been developed. While human epidemiological studies provide insight into maternal immunity to infection, experimental infection in pregnant mice is a vital tool to unravel the complex molecular mechanisms of placental infection, congenital transmission and maternal illness. We will provide a comprehensive review of the pathogenesis of several infection models in pregnant mice and their clinical relevance. These models have revealed the immunological function of the placenta in responding to, and resisting infection. Murine feto-placental infection provides an effective way to evaluate new intervention strategies for managing infections during pregnancy, adverse fetal outcome and long-term effects on the offspring and mother. Published by Elsevier Ireland Ltd. 2013-03 2013-02-20 /pmc/articles/PMC3748615/ /pubmed/23432873 http://dx.doi.org/10.1016/j.jri.2012.10.015 Text en Crown copyright © 2012 Published by Elsevier Ireland Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Krishnan, Lakshmi Nguyen, Tina McComb, Scott From mice to women: the conundrum of immunity to infection during pregnancy |
title | From mice to women: the conundrum of immunity to infection during pregnancy |
title_full | From mice to women: the conundrum of immunity to infection during pregnancy |
title_fullStr | From mice to women: the conundrum of immunity to infection during pregnancy |
title_full_unstemmed | From mice to women: the conundrum of immunity to infection during pregnancy |
title_short | From mice to women: the conundrum of immunity to infection during pregnancy |
title_sort | from mice to women: the conundrum of immunity to infection during pregnancy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3748615/ https://www.ncbi.nlm.nih.gov/pubmed/23432873 http://dx.doi.org/10.1016/j.jri.2012.10.015 |
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