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Updated: Sep 20, 2026

Isolation of Dendritic Cells from the Human Female Reproductive Tract for Phenotypical and Functional Studies
Published on: March 13, 2018
Blood myeloid and lymphoid dendritic cells are stable during the menstrual cycle but deficient during mid-gestation
D Darmochwal-Kolarz1, J Rolinski, J Tabarkiewicz
1Department of Obstetrics and Perinatology, University School of Medicine, 20-950 Lublin, Poland. dorotak@mp.pl
Insights
Peripheral blood dendritic cell populations (CD1c(+), BDCA-2(+), BDCA-4(+)) and their ratios vary during the ovarian cycle and pregnancy. A lower CD1c(+):BDCA-2(+) ratio occurs in the luteal phase, and dendritic cell numbers decrease in the second trimester of pregnancy.
Area of Science:
- Immunology
- Reproductive Biology
- Cell Biology
Background:
- Dendritic cells (DCs) are crucial immune regulators.
- Peripheral blood myeloid and lymphoid DCs play roles in immune surveillance.
- Changes in DC populations during the ovarian cycle and pregnancy are not fully understood.
Purpose of the Study:
- To quantify peripheral blood myeloid and lymphoid dendritic cells (CD1c(+), BDCA-2(+), BDCA-4(+)) and the CD1c(+):BDCA-2(+) ratio.
- To analyze these populations during different phases of the ovarian cycle and in normal pregnancy.
- To investigate the influence of hormonal changes on DC populations.
Main Methods:
- Peripheral blood samples were collected from non-pregnant and pregnant women.
- Dendritic cells were isolated and stained with monoclonal antibodies against BDCA-1, BDCA-2, and BDCA-4.
- Flow cytometry was used to estimate the percentages and ratios of specific DC populations.
Main Results:
- CD1c(+), BDCA-2(+), and BDCA-4(+) DCs were present throughout the ovarian cycle and pregnancy.
- The CD1c(+):BDCA-2(+) ratio was significantly lower in the luteal phase compared to the follicular phase.
- DC numbers were lowest in the second trimester of pregnancy, with a higher CD1c(+):BDCA-2(+) ratio.
Conclusions:
- Peripheral blood myeloid and lymphoid DCs appear unaffected by steroid hormones during the menstrual cycle.
- The decrease in peripheral blood DCs during the second trimester of pregnancy may be due to uterine migration.
- These findings contribute to understanding immune adaptations during pregnancy.
Abstract:
The aim of this study was to estimate the populations of peripheral blood myeloid and lymphoid dendritic cells (CD1c(+), BDCA-2(+), BDCA-4(+)) and the CD1c(+):BDCA-2(+) ratio in phases of the ovarian cycle and in normal pregnant patients. 18 non-pregnant women and 17 normal pregnant women were included. Dendritic cells were isolated from peripheral blood, stained with monoclonal antibodies (mAbs) against blood dendritic cell antigens (anti-BDCA-1, BDCA-2, BDCA-4) and estimated using flow cytometry. CD1c(+), BDCA-2(+) and BDCA-4(+) dendritic cells were present in the follicular and luteal phases of the ovarian cycle and in all trimesters of normal pregnancy. The percentages of CD1c(+) dendritic cells did not differ between the follicular and luteal phases of the ovarian cycle. The percentage of BDCA-2(+) dendritic cells was lower in the luteal phase of the ovarian cycle compared with the follicular phase, but the differences were not statistically significant. The CD1c(+):BDCA-2(+) cell ratio was significantly lower in the luteal phase compared with the follicular phase of the ovarian cycle. The numbers of dendritic cells were significantly lower in the second trimester when compared with the first and third trimesters of normal pregnancy. Furthermore, in the second trimester, the CD1c(+):BDCA-2(+) ratio was higher than in the other trimesters of normal pregnancy. All populations of dendritic cells and the CD1c(+):BDCA-2(+) ratio did not differ in the first and third trimesters of physiological pregnancy. Our results suggest that myeloid and lymphoid dendritic cells are not affected by steroid hormones during the menstrual cycle. The deficiency of peripheral blood dendritic cells observed during the second trimester of normal pregnancy can be associated with their migration to the uterus during the second physiological invasion by cytotrophoblast.
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