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Updated: Jun 30, 2025

Isolation of Leukocytes from the Murine Tissues at the Maternal-Fetal Interface
Published on: May 21, 2015
Immune cells at the feto-maternal interface: Comprehensive characterization and insights into term labor
Angela Mosebarger1, Manuel S Vidal2, Giovana Fernanda Cosi Bento3
1Division of Basic and Translational Research, Department of Obstetrics and Gynecology, University of Texas Medical Branch at Galveston, Galveston, TX, USA.
Insights
Immune cells in the decidua, particularly natural killer (NK) and T cells, change during term labor. These shifts suggest immune cell migration and senescence, impacting parturition.
Area of Science:
- Reproductive immunology
- Maternal-fetal interface immunology
Background:
- Immune cells are crucial for pregnancy maintenance and parturition.
- Understanding decidual immune cell roles in labor induction is limited due to study heterogeneity.
Purpose of the Study:
- To comprehensively characterize decidual immune cells at term labor.
- To investigate differences in immune cells between term not in labor (TNL) and term in labor (TL) states.
Main Methods:
- Literature review on decidual immune cell differences.
- Isolation and high-dimensional flow cytometry of decidua parietalis immune cells from TNL and TL samples.
Main Results:
- Decidual cell ratios align with literature, but with a lower NK cell percentage.
- Decreased CD4 expression on CD8- NK cells in TL suggests migration.
- Reduced CD38 expression on CD8+ CD57+ T cells in TL indicates cytotoxic T cell senescence.
Conclusions:
- This study provides a detailed profile of immune cells at the decidua-chorion interface during term labor.
- Observed changes in NK and T cells offer insights into labor mechanisms.
Abstract:
Immune cells at the feto-maternal interface play an important role in pregnancy; starting at implantation, maintenance of pregnancy, and parturition. The role of decidual immune cells in induction of labor still needs to be understood. Published reports on this topic show heterogeneity in methods of cell isolation, assay, analysis and cellular characterization making it difficult to collate available information in order to understand the contribution of immune cells at term leading to parturition. In the present study, available literature was reviewed to study the differences in immune cells between the decidua basalis and decidua parietalis, as well as between immune cells in term and preterm labor. Additionally, immune cells at the decidua parietalis were isolated from term not in labor (TNL) or term in labor (TL) samples and characterized via flow cytometry using a comprehensive, high-dimensional antibody panel. This allowed a full view of immune cell differences without combining multiple studies, which must include variation in isolation and analysis methods, for more conclusive data. The ratio of cells found in decidua parietalis in this study generally matched those reported in the literature, although we report a lower percentage of natural killer (NK) cells at term. We report that CD4 expression on CD8- NK cells decreased in term labor compared to not in labor samples, suggesting that natural killer cells may be migrating to other sites during labor. Also, we report a decrease in CD38 expression on CD8+ CD57+ T cells in labor, indicative of cytotoxic T cell senescence. Our study provides a comprehensive status of immune cells at the decidua-chorion interface at term.
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