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Updated: Mar 13, 2026

A Murine Model of Fetal Exposure to Maternal Inflammation to Study the Effects of Acute Chorioamnionitis on Newborn Intestinal Development
Published on: June 24, 2020
Clinical chorioamnionitis at term VII: the amniotic fluid cellular immune response
Alicia Martinez-Varea1, Roberto Romero1, Yi Xu1
1, NICHD/NIH/DHHS, Bethesda, MD, USA.
Insights
Chorioamnionitis involves increased neutrophils and monocytes in amniotic fluid, with distinct cytokine profiles. This study characterizes these immune cells and their inflammatory cytokine production in intra-amniotic infections.
Area of Science:
- Obstetrics and Gynecology
- Immunology
- Perinatology
Background:
- Clinical chorioamnionitis is a pregnancy complication often linked to intra-amniotic infection.
- Understanding the immune response within the amniotic fluid is crucial for managing this condition.
Purpose of the Study:
- To analyze the cellular composition of amniotic fluid in term patients with clinical chorioamnionitis.
- To characterize cytokine production by amniotic fluid white blood cells using flow cytometry.
Main Methods:
- Amniotic fluid samples from 20 women with clinical chorioamnionitis were analyzed.
- Cultivation techniques identified microorganisms; flow cytometry assessed leukocyte immunophenotyping and cytokine expression.
Main Results:
- Neutrophils and monocytes were the predominant leukocytes in amniotic fluid.
- Higher neutrophil and monocyte counts were observed in patients with detectable microorganisms.
- Differential cytokine production was noted: neutrophils produced TNF-α and MIP-1β, while monocytes produced IL-1β and IL-1α.
Conclusions:
- Neutrophils and monocytes are key immune cells in the amniotic fluid during intra-amniotic infection associated with chorioamnionitis.
- This study provides the first characterization of differential cytokine expression by these cells in this pregnancy complication.
Objectives:
1) To characterize the cellular composition of the amniotic fluid of patients diagnosed with clinical chorioamnionitis at term, as a function of the presence or absence of microorganisms determined by cultivation techniques, and 2) to characterize the cytokine production by white blood cells present in the amniotic fluid using flow cytometry-based techniques.
Materials And Methods:
Amniotic fluid samples from 20 women who had the diagnosis of clinical chorioamnionitis at term were analyzed using cultivation techniques (for aerobic and anaerobic bacteria as well as genital Mycoplasmas). Amniotic fluid IL-6 concentrations were determined by an enzyme-linked immunosorbent assay. Amniotic fluid leukocytes were visualized by using hematoxylin and eosin staining and immunofluorescence. Immunophenotyping of surface markers and cytokines was performed in amniotic fluid leukocytes using flow cytometry.
Results:
1) Neutrophils (CD45+CD15+ cells) were the most common leukocyte subset found in the amniotic fluid, followed by monocytes (CD45+CD14+ cells); other white blood cells (such as lymphocytes and natural killer cells) were scarce in the amniotic fluid; 2) the absolute counts of neutrophils and monocytes were significantly higher in patients with microorganisms found in the amniotic fluid than in those without detectable microorganisms, using cultivation techniques; 3) there was a significant correlation between the absolute counts of neutrophils and monocytes determined by flow cytometry (Spearman's correlation=0.97; P<0.001); 4) there was a significant correlation between the absolute white blood cell count determined with a hemocytometer chamber and by flow cytometric analysis (Spearman's correlation=0.88; P<0.001); and 5) the profile of cytokine expression differed between monocytes and neutrophils; while neutrophils predominantly produced TNF-α and MIP-1β, monocytes expressed higher levels of IL-1β and IL-1α.
Conclusion:
Flow cytometry analysis of the amniotic fluid of patients with intra-amniotic infection and clinical chorioamnionitis at term demonstrated that neutrophils and monocytes are the most common cells participating in the inflammatory process. We have characterized, for the first time, the differential cytokine expression by these cells in this important complication of pregnancy.
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