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Updated: Jul 9, 2025

Multiplexed Immunofluorescence Analysis and Quantification of Intratumoral PD-1+ Tim-3+ CD8+ T Cells
Published on: February 8, 2018
PROGRAMMED CELL DEATH LIGAND 1 (PD-L1) EXPRESSION IN TRIPLE NEGATIVE BREAST CANCER CASES IN BENIN CITY
D O Owolabi1, A N Olu-Eddo1, V J Ekanem2
1Department of Anatomical Pathology, University of Benin Teaching Hospital, Benin City, Nigeria.
Programmed cell death ligand 1 (PD-L1) expression is low in triple-negative breast cancer (TNBC) in Benin City, occurring in 14.1% of cases. This finding indicates that a subset of TNBC patients may benefit from immune checkpoint inhibitor therapy.
Area of Science:
- Oncology
- Immunology
- Pathology
Background:
- Triple-negative breast cancer (TNBC) presents significant management challenges due to a lack of specific cellular receptors, leading to higher morbidity and mortality.
- The programmed cell death 1/programmed cell death ligand 1 (PD-1/PD-L1) pathway is a key target for immunotherapy, particularly in TNBC.
- Understanding PD-L1 expression patterns is crucial for predicting treatment response in TNBC.
Purpose of the Study:
- To investigate the prevalence and patterns of PD-L1 expression in triple-negative breast cancer (TNBC) cases.
- To assess the potential for immune checkpoint inhibitor therapy in TNBC patients in Benin City.
Main Methods:
- A retrospective study was conducted over three years (2017-2019).
- PD-L1 immunostaining was performed on 92 diagnosed TNBC cases.
- Tumour and immune cell PD-L1 expression was analyzed.
Main Results:
- PD-L1 expression was detected in 14.1% (13 out of 92) of TNBC cases.
- Diffuse tumoral PD-L1 staining was observed in 30.8% of PD-L1 positive cases.
- PD-L1 expression showed a significant association with increasing age up to the fifth decade (p=0.030).
Conclusions:
- PD-L1 expression occurs at a low rate in the studied TNBC population.
- Approximately 14.1% of TNBC patients in this cohort may be candidates for immune checkpoint inhibitor therapy.
- Age is a significant factor associated with PD-L1 expression in TNBC.
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