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Innate Lymphoid Cells at the Maternal-Fetal Interface in Human Pregnancy

Pregnancy constitutes a major challenge to the maternal immune system, which must tolerate fetal alloantigen encoded by paternal genes. In addition to their role in inducing maternal-fetal immune tolerance, accumulating evidence indicates that decidual immune cells are involved in several processes...

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Autores principales: Chang, Rui-Qi, Zhou, Wen-Jie, Li, Da-Jin, Li, Ming-Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7053337/
https://www.ncbi.nlm.nih.gov/pubmed/32140065
http://dx.doi.org/10.7150/ijbs.38264
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author Chang, Rui-Qi
Zhou, Wen-Jie
Li, Da-Jin
Li, Ming-Qing
author_facet Chang, Rui-Qi
Zhou, Wen-Jie
Li, Da-Jin
Li, Ming-Qing
author_sort Chang, Rui-Qi
collection PubMed
description Pregnancy constitutes a major challenge to the maternal immune system, which must tolerate fetal alloantigen encoded by paternal genes. In addition to their role in inducing maternal-fetal immune tolerance, accumulating evidence indicates that decidual immune cells are involved in several processes required for a successful pregnancy, including trophoblast invasion as well as tissue and spiral artery remodeling. Innate lymphoid cells (ILCs), an important branch of the innate immune system, which has expanded rapidly in recent years, are strong actors in mucosal immunity, tissue homeostasis and metabolism regulation. With the recent identification of ILCs in the human decidua, the role of ILCs at the maternal-fetal interface raises concern. Herein, we review the presence and characterization of ILCs in the human decidua, as well as their function in normal pregnancy and pathological pregnancy, including reproductive failure, preeclampsia and others.
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spelling pubmed-70533372020-03-05 Innate Lymphoid Cells at the Maternal-Fetal Interface in Human Pregnancy Chang, Rui-Qi Zhou, Wen-Jie Li, Da-Jin Li, Ming-Qing Int J Biol Sci Review Pregnancy constitutes a major challenge to the maternal immune system, which must tolerate fetal alloantigen encoded by paternal genes. In addition to their role in inducing maternal-fetal immune tolerance, accumulating evidence indicates that decidual immune cells are involved in several processes required for a successful pregnancy, including trophoblast invasion as well as tissue and spiral artery remodeling. Innate lymphoid cells (ILCs), an important branch of the innate immune system, which has expanded rapidly in recent years, are strong actors in mucosal immunity, tissue homeostasis and metabolism regulation. With the recent identification of ILCs in the human decidua, the role of ILCs at the maternal-fetal interface raises concern. Herein, we review the presence and characterization of ILCs in the human decidua, as well as their function in normal pregnancy and pathological pregnancy, including reproductive failure, preeclampsia and others. Ivyspring International Publisher 2020-01-30 /pmc/articles/PMC7053337/ /pubmed/32140065 http://dx.doi.org/10.7150/ijbs.38264 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Review
Chang, Rui-Qi
Zhou, Wen-Jie
Li, Da-Jin
Li, Ming-Qing
Innate Lymphoid Cells at the Maternal-Fetal Interface in Human Pregnancy
title Innate Lymphoid Cells at the Maternal-Fetal Interface in Human Pregnancy
title_full Innate Lymphoid Cells at the Maternal-Fetal Interface in Human Pregnancy
title_fullStr Innate Lymphoid Cells at the Maternal-Fetal Interface in Human Pregnancy
title_full_unstemmed Innate Lymphoid Cells at the Maternal-Fetal Interface in Human Pregnancy
title_short Innate Lymphoid Cells at the Maternal-Fetal Interface in Human Pregnancy
title_sort innate lymphoid cells at the maternal-fetal interface in human pregnancy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7053337/
https://www.ncbi.nlm.nih.gov/pubmed/32140065
http://dx.doi.org/10.7150/ijbs.38264
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