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Updated: Oct 2, 2025

Author Spotlight: Advancing Reproductive Immunology with a Protocol for the Quantitative Evaluation of Endometrial Immune Cells
Published on: October 13, 2023
Programmed Cell Death Ligand-1 (PDL-1) Correlates With Tumor Infiltration by Immune Cells and Represents a Promising
Thomas Hecking1, Thore Thiesler2, Janina Halbe1
1Department of Gynecology and Gynecological Oncology, Center for Integrated Oncology, University of Bonn, Bonn, Germany.
Background/Aim:
Endometrial carcinoma (EC) is one of the most common gynecological cancers in the Western Hemisphere. Nevertheless, there are not enough appropriate treatment options, especially for advanced stages. The immune checkpoint blockade represents a promising alternative to established cancer therapies by suppressing the immune-inhibitory activity of the immune checkpoint factors programmed cell death-1 (PD-1) and programmed cell death ligand-1 (PD-L1). In the present study, we characterized the clinical relevance of the biomarker PD-L1 expression in terms of its prognostic capabilities in EC.
Patients And Methods:
Tumor tissue samples from 87 EC patients were retrospectively analyzed by immunohistochemistry (PD-L1, p16, estrogen receptor, progesterone receptor, HER2/neu, Ki-67, CD3, CD20, CD68).
Results:
A total of 17.3% of EC patients were PD-L1 positive. PD-L1 status did not represent a suitable prognostic marker in EC, but correlated with T3/T4stage, positive lymph node status, p16 expression, and absence of estrogen and progesterone receptor. PD-L1 positive tissues showed increased infiltration with lymphocytes, monocytes, and macrophages, although not statistically significant in every case.
Conclusion:
In EC, PD-L1 expression has no prognostic significance, but correlates with other oncogenic factors and indicates increased infiltration of the tumor with immune cells. Thus, PD-1/PD-L1 immunecheckpoint blockade seems to be very promising, at least in a subset of EC patients.
Insights
Programmed cell death ligand-1 (PD-L1) expression is not a prognostic marker in endometrial carcinoma (EC). However, PD-L1 correlates with advanced stages and increased immune cell infiltration, suggesting potential benefit from PD-1/PD-L1 blockade therapy in a subset of EC patients.
Area of Science:
- Gynecologic Oncology
- Immunohistochemistry
- Cancer Biomarkers
Background:
- Endometrial carcinoma (EC) is a prevalent gynecological malignancy with limited treatment options for advanced stages.
- Immune checkpoint inhibitors targeting programmed cell death-1 (PD-1) and programmed cell death ligand-1 (PD-L1) offer a promising therapeutic avenue.
- Assessing the prognostic value of PD-L1 expression is crucial for optimizing EC treatment strategies.
Purpose of the Study:
- To investigate the clinical relevance and prognostic significance of PD-L1 expression in endometrial carcinoma.
- To explore the correlation between PD-L1 expression and clinicopathological features in EC.
- To evaluate the potential of PD-L1 as a biomarker for immune cell infiltration in EC.
Main Methods:
- Retrospective analysis of tumor tissue samples from 87 EC patients.
- Immunohistochemical assessment of PD-L1 expression and other markers including p16, hormone receptors, HER2/neu, Ki-67, and immune cell markers (CD3, CD20, CD68).
Main Results:
- PD-L1 expression was observed in 17.3% of EC patients.
- PD-L1 status did not show prognostic value but correlated with advanced tumor stage (T3/T4), lymph node positivity, p16 expression, and absence of estrogen/progesterone receptors.
- PD-L1 positive tumors exhibited a trend towards increased infiltration of lymphocytes, monocytes, and macrophages.
Conclusions:
- PD-L1 expression lacks prognostic significance in endometrial carcinoma.
- PD-L1 correlates with specific oncogenic factors and suggests enhanced immune cell infiltration in the tumor microenvironment.
- The findings support the potential efficacy of PD-1/PD-L1 immune checkpoint blockade therapy in a subset of EC patients.
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