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Correlation of peripheral blood and endometrial immunophenotyping in ART: is peripheral blood sampling useful?
Kevin Marron1, Conor Harrity2,3
1Sims IVF Clinic, Clonskeagh Road, Clonskeagh, Dublin 14, Ireland. drkevinmarron@gmail.com.
Insights
Peripheral blood analysis offers a less invasive method to assess the uterine immune environment. While distinct, endometrial and blood immune cells show correlations, suggesting peripheral blood evaluation
Area of Science:
- Reproductive immunology
- Flow cytometry
- Immunophenotyping
Background:
- Endometrial immunophenotype is crucial for assessing the peri-implantation environment.
- Current methods for endometrial assessment are invasive.
Purpose of the Study:
- To compare mid-luteal immunophenotypes from peripheral blood and endometrium.
- To determine if peripheral blood evaluation is a viable alternative to endometrial biopsy for assessing the reproductive immune status.
Main Methods:
- Simultaneous collection of peripheral blood and endometrial biopsy samples from 55 patients.
- Comprehensive multi-parameter flow cytometric analysis of lymphocyte subpopulations in both sample types.
- Comparison of cellular proportions and correlations between compartments.
Main Results:
- Distinct lymphocyte proportions were observed between peripheral blood and endometrial compartments.
- The ratio of CD4+ to CD8+ T cells and Th1/Th2 ratios differed significantly between the two sites.
- Positive correlations were found for CD57+ NK cells, CD3+ NK-T cells, and CD4+ Th1 cells in both compartments.
Conclusions:
- Flow cytometry provides rapid and objective immunophenotyping.
- While endometrial biopsies are the gold standard, peripheral blood evaluation may offer valuable insights.
- Peripheral blood lymphocyte subset analysis can indicate potential uterine immune alterations non-invasively.
Purpose:
Using a comprehensive flow cytometric panel, simultaneously obtained mid-luteal immunophenotypes from peripheral blood and endometrium were compared and values correlated. Is a peripheral blood evaluation of reproductive immunophenotype status meritorious relative to local endometrial evaluation to directly assess the peri-implantation environment?
Methods:
Fifty-five patients had a mid-luteal biopsy to assess the local endometrial immunophenotype, while simultaneously providing a peripheral blood sample for analysis. Both samples were immediately assessed using a comprehensive multi-parameter panel, and lymphocyte subpopulations were described and compared.
Results:
Distinct lymphocyte proportions and percentage differences were noted across the two compartments, confirming the hypothesis that they are distinct environments. The ratio of CD4 + to CD8 + T cells were reversed between the two compartments, as were Th1 and Th2-type CD4 + T cell ratios. Despite these differences, some direct relationships were noted. Positive Pearson correlations were found between the levels of CD57 + expressing natural killer cells, CD3 + NK-T cells and CD4 + Th1 cells in both compartments.
Conclusions:
Flow cytometric evaluation provides a rapid and objective analysis of lymphocyte subpopulations. Endometrial biopsies have become the gold standard technique to assess the uterine immunophenotype in adverse reproductive outcome, but there may still a place for peripheral blood evaluation in this context. The findings demonstrate significant variations in cellular proportions across the two regions, but some positive correlations are present. Immunological assessment of these specific peripheral blood lymphocyte subtypes may provide insight into patients with potential alterations of the uterine immune environment, without the risks and inconveniences associated with an invasive procedure.
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