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Updated: Jul 3, 2026

Ex vivo Culture of Human Placental Explants for the Study of Viral Transmission Across the Maternal-Fetal Interface
Published on: December 30, 2025
Effect of first, second, and third trimester placental factors on CD4, CCR5, and CXCR4 expression in human peripheral
Li-Ping Li1, Jia-Li Kang, Wei Xia
1Department of Gynecology and Obstetrics, Guangzhou First Municipal Peopleos Hospital, Guangzhou 510180, China. selinalee@tom.com
Insights
Placental factors (PF) from all trimesters reduce CCR5 expression on immune cells, potentially preventing HIV entry. First-trimester PF showed the highest efficacy in reducing CCR5, suggesting a role in preventing vertical HIV transmission.
Area of Science:
- Immunology
- Virology
- Obstetrics
Background:
- Human immunodeficiency virus (HIV) vertical transmission remains a significant concern.
- Understanding the role of placental factors (PF) in modulating immune responses is crucial for preventing mother-to-child transmission.
- CD4, CCR5, and CXCR4 are key receptors involved in HIV entry into host cells.
Purpose of the Study:
- To investigate the effect of first, second, and third trimester placental factors (PF) on CD4, CCR5, and CXCR4 expression in human peripheral blood lymphocytes (PBLs).
- To explore the influence of these placental factors on the vertical transmission of human immunodeficiency virus (HIV).
Main Methods:
- Human peripheral blood mononuclear cells (PBMCs) were exposed to first, second, and third trimester PF (25% concentration) for 24 hours.
- Flow cytometry was employed to determine the expression of CD4, CCR5, and CXCR4 in PBLs.
- The percentages of CCR5(+), CXCR4(+), and CCR5(+)CXCR4(+) cells within peripheral blood CD4(+) lymphocytes were quantified.
Main Results:
- All trimester PFs significantly reduced CCR5 expression in PBLs, with first-trimester PF demonstrating higher efficacy.
- A significant decrease in the percentage of CCR5(+) and CCR5(+)CXCR4(+) cells in peripheral blood CD4(+) lymphocytes was observed in PF-treated groups compared to controls.
- The first-trimester PF group showed a more pronounced reduction in CCR5(+) and CCR5(+)CXCR4(+) cells compared to the second and third trimester groups.
Conclusions:
- Placental factors can effectively reduce CCR5 expression on human PBLs and CD4(+) lymphocytes.
- This reduction in CCR5 suggests that PF may inhibit R5-tropic HIV entry, thereby playing a vital role in preventing intrauterine HIV infection.
- The findings highlight the potential of placental factors in mitigating vertical HIV transmission.
Objective:
To investigate effect of first, second, and third trimester placental factors (PF) on CD4, CCR5, and CXCR4 expression in human peripheral blood lymphocytes (PBLs), and to explore their influence on human immunodeficiency virus (HIV) vertical transmission.
Methods:
Human peripheral blood mononuclear cells (PBMCs) were treated with first, second, and third trimester PF (concentration 25%) respectively for 24 hours. The expression of CD4, CCR5, and CXCR4 in PBLs, and the percentages of CCR5(+), CXCR4(+)ìand CCR5(+)CXCR4(+) cells in peripheral blood CD4(+) lymphocytes were determined with flow cytometry.
Results:
All trimester PFs reduced CCR5 expression in PBLs. The efficiency of the first trimester PF was higher than that of the second and third trimester PF. The percentage of CCR5(+) cells in peripheral blood CD4(+) lymphocytes of PF groups was significantly lower than that of the control group, and the percentage of CCR5(+) cells in peripheral blood CD4(+) lymphocytes of the first trimester PF group was significantly lower than that of the second and third trimester group. The percentages of CCR5(+)CXCR4(+) cells in peripheral blood CD4(+) lymphocytes of PF groups were significantly decreased as compared with the control group, and the percentage of CCR5(+)CXCR4(+) cells in peripheral blood CD4(+) lymphocytes of the first trimester PF group was significantly lower than that of the third trimester PF group.
Conclusion:
PF can reduce the expression of CCR5 in human PBLs and peripheral blood CD4(+) lymphocytes, indicating that PF might reduce R5 virus infection via preventing HIV entry, and might play an important role in reducing R5 virus intrauterine infection.

