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Updated: Nov 5, 2025

Multiplexed Fluorescent Immunohistochemical Staining of Four Endometrial Immune Cell Types in Recurrent Miscarriage
Published on: August 4, 2021
Decreased level of Eomes+dCD8+ T cells with altered function might be associated with miscarriage
Lanting Chen1, Fengrun Sun1, Mengdie Li1
1Laboratory for Reproductive Immunology, Key Laboratory of Reproduction Regulation of NPFPC, SIPPR, IRD, Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases, Hospital of Obstetrics and Gynecology, Shanghai Medical College, Fudan University, Shanghai, China.
Eomesodermin (Eomes) expression on CD8+ T cells is higher in normal early pregnancy but decreases during miscarriage. Eomes may be an early target for preventing pregnancy loss and ensuring reproductive safety.
Area of Science:
- Immunology
- Reproductive Biology
- Cell Biology
Background:
- Eomesodermin (Eomes) is crucial for CD8+ T cell homeostasis and function.
- Its role in regulating CD8+ T cells during pregnancy is not well understood.
Purpose of the Study:
- To investigate the functional regulation of Eomes in CD8+ T cells during normal early pregnancy and miscarriage.
- To explore Eomes as a potential therapeutic target for pregnancy complications.
Main Methods:
- Analysis of Eomes expression in dCD8+ T cells from pregnant individuals and miscarriage cases.
- In vitro studies using primary trophoblasts and HTR8/SVneo cell lines to assess Eomes modulation.
Main Results:
- Elevated Eomes expression in dCD8+ T cells during normal early pregnancy.
- Decreased Eomes+dCD8+ T cells and a shift towards a pro-inflammatory phenotype in miscarriage.
- Trophoblast cells increased Eomes expression in dCD8+ T cells from both normal and miscarriage groups.
Conclusions:
- Eomes+dCD8+ T cells may serve as early warning indicators for miscarriage.
- Modulating Eomes offers a potential therapeutic strategy for promoting maternal-fetal tolerance and preventing pregnancy loss.
- Reproductive safety must be considered when manipulating Eomes in CD8+ T cells to avoid T cell exhaustion.
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