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Immune Regulation at Maternal-fetal Interface in Early Pregnancy

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摘要 Decidual immune cells(DICs),including T-cells,regulatory T-cells,macrophages/dendritic cells,natural killer cells,and neutrophils,are resident at the maternal-fetal interface,and play vital roles in regulating trophoblast migration,decidual angiogenesis,immune tolerance,placentation,and decidualization during the early pregnancy.Extensive researches have revealed that these maternal DICs cooperated with each other,or with maternal decidual stromal cells,or with fetal-derived trophoblasts,and further formed a special maternal-fetal cross talk at the maternal-fetal interface,which was essential for the construction and maintenance of physiological pregnancy.Once aberrant cross talk and immune regulation arise,many pregnancy complications will inevitably occur,such as spontaneous abortion,intrauterine growth restriction(IUGR),preeclampsia(PE),and preterm birth.Here,we reviewed how critical immune cells are either enriched or excluded from the decidua,how their function is regulated within the decidua,and how they variously contribute to pregnancy success or failure.
出处 《Reproductive and Developmental Medicine》 CSCD 2017年第1期36-44,共9页 生殖与发育医学(英文版)
基金 supported by the National Basic Research Program of China(2015CB943300) the Major Research Program of the National Natural Science Foundation of China(NSFC)(8149044,81471548,and 31671200) the Oriented Project of Science and Technology Innovation from the Key Laboratory of Reproduction Regulation of NPFPC the Program for Zhuoxue of Fudan University,China.
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