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Multiplexed Immunofluorescence Analysis and Quantification of Intratumoral PD-1+ Tim-3+ CD8+ T Cells
Published on: February 8, 2018
PD-L1 expression and CD8 positive lymphocytes in human neoplasms: A tissue microarray study on 11,838 tumor samples
Katharina Möller1, Madeleine Knöll1, Elena Bady1
1Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Programmed death ligand 1 (PD-L1) is expressed in many cancer types. PD-L1 positivity correlates with CD8+ lymphocytes, suggesting immune responses may drive PD-L1 expression in tumors.
Area of Science:
- Oncology
- Immunology
- Pathology
Background:
- Programmed death ligand 1 (PD-L1) is a key target for immune checkpoint inhibitor therapies.
- Understanding PD-L1 expression across diverse cancer types is crucial for effective treatment strategies.
- Current data on PD-L1 expression patterns in human cancers is not uniform.
Purpose of the Study:
- To comprehensively analyze PD-L1 expression in a large cohort of human tumor types.
- To investigate the relationship between PD-L1 expression and tumor-infiltrating CD8+ lymphocytes.
- To identify specific cancer types with high PD-L1 expression.
Main Methods:
- Immunohistochemical analysis of PD-L1 expression was performed on 11,838 samples.
- The study encompassed 118 distinct human tumor types.
- Statistical analysis examined the correlation between PD-L1 expression and CD8+ lymphocyte infiltration.
Main Results:
- PD-L1 positivity in tumor cells (≥10% cutoff) was observed in 72% of 118 tumor types.
- High PD-L1 expression was noted in thymoma (100%), Hodgkin's lymphoma (93%), and anaplastic thyroid carcinoma (76%).
- PD-L1 was detected in immune cells in 87% of tumor types, with high prevalence in hematopoietic and lymphoid tissues (75-100%).
- PD-L1 positivity significantly correlated with intratumoral CD8+ lymphocytes across numerous cancer types (p<0.0001).
Conclusions:
- PD-L1 expression is prevalent in both tumor and inflammatory cells across a broad spectrum of human cancers.
- The strong correlation between PD-L1 and CD8+ lymphocytes suggests that antitumor immune responses may induce PD-L1 expression.
- These findings have implications for the broader application of PD-L1 targeted immunotherapies.
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