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Recurrent Pregnancy Loss (1) is a common pregnancy complication that can have a negative impact on both the physical and mental health of pregnant women. Despite various associations, the precise etiology of RPL remains unclear, necessitating further research. Immune cells are recognized to play a pivotal role in successful pregnancy. This article focuses on the role of macrophages, the second most abundant leukocyte population in the decidua. Decidual macrophages are instrumental in promoting embryo implantation and maintaining immune homeostasis. Macrophages are traditionally categorized into activated M1 and alternatively activated M2 states, each serving distinct immunological roles, but in fact this classification is no longer applicable. In this review, we discussed the classification of decidual macrophages and their impact on embryo implantation and development, including their regulation of trophoblasts and decidual stromal cells, and explore their potential association with RPL. Macrophages play a role in regulating both trophoblasts invasion and apoptosis processes. We also discuss how trophoblasts and decidual stromal cells influence macrophages. Additionally, we explored the interplay between macrophages and immune cells, such as T cells, NKs and DCs, to uncover the potential link between macrophage-related immune regulation and RPL. While substantial knowledge exists regarding the role of macrophages in pregnancy regulation, many aspects remain obscure. Thus, this review aims to discuss the interaction between decidual macrophages and other cells at the maternal-fetal interface, exploring their connection to RPL.
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http://dx.doi.org/10.1016/j.placenta.2025.05.025 | DOI Listing |
The placenta is a complex organ with multiple immune and non-immune cell types that promote fetal tolerance and facilitate the transfer of nutrients and oxygen. The nonhuman primate (NHP) is a key experimental model for studying human pregnancy complications, in part due to similarities in placental structure, which makes it essential to understand how single-cell populations compare across the human and NHP maternal-fetal interface. We constructed a single-cell RNA-Seq (scRNA-Seq) atlas of the placenta from the pigtail macaque ( ) in the third trimester, comprising three different tissues at the maternal-fetal interface: the chorionic villi (placental disc), chorioamniotic membranes, and the maternal decidua.
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August 2025
Medical Center for Human Reproduction, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, People's Republic of China.
Complex intercellular interactions occur at the maternal-fetal interface during pregnancy. Human uterine decidual epithelial cells play a crucial role in maternal immune tolerance and placental development. Macrophages are major cells at the maternal-fetal interface regulating tissue remodeling and immune response.
View Article and Find Full Text PDFAdv Sci (Weinh)
August 2025
Reproductive Medical Center, Department of Obstetrics and Gynecology, West China Second University Hospital, Sichuan University, Chengdu, 610041, China.
Obstetric antiphospholipid syndrome (OAPS) is an autoimmune disorder characterized by pathologic pregnancies and the presence of antiphospholipid antibodies (aPLs). Despite significant infiltration of decidual macrophages observed in OAPS patients, the underlying connections between decidual and peripheral immune cells remain unclear. In this study, an integrated single-cell atlas is constructed of the decidua and peripheral blood mononuclear cells (PBMCs) from OAPS patients and HCs.
View Article and Find Full Text PDFbioRxiv
July 2025
Department of Microbiology, Immunology, and Molecular Genetics, College of Medicine, University of Kentucky; Lexington, KY 40536, USA.
Maternal opioid use disorder (OUD) poses significant risks to maternal and fetal health. Adverse outcomes associated with maternal OUD are believed to be mediated, in part, by changes in placenta structure and function; however, few studies have addressed this question. Here, we utilized a combination of flow cytometry, histology, spatial and single-cell transcriptomics to uncover the impact of OUD on placental tissues.
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August 2025
Department of Obstetrics and Gynecology, Beijing Friendship Hospital, Capital Medical University, 100050 Beijing, China. Electronic address:
Hypertensive disorders of pregnancy (HDP), including gestational hypertension, preeclampsia, and eclampsia, represent significant causes of maternal and perinatal morbidity and mortality. The core pathogenesis of HDP involves an imbalance in the immune microenvironment at the maternal-fetal interface, manifested by aberrant interactions among trophoblast cells, decidual immune cells, and systemic inflammatory responses. Trophoblast dysfunction and inadequate spiral artery remodeling result in placental ischemia and hypoxia, which in turn trigger the release of anti-angiogenic factors (such as sFlt-1 and sEng) and damage-associated molecular patterns (DAMPs), leading to systemic inflammation and endothelial injury.
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