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Updated: Jan 27, 2026

Using 22C3 Anti-PD-L1 Antibody Concentrate on Biopsy and Cytology Samples from Non-small Cell Lung Cancer Patients
Published on: September 25, 2018
An update of knowledge on PD-L1 in head and neck cancers: Physiologic, prognostic and therapeutic perspectives
Daniel Lenouvel1, Miguel Ángel González-Moles1,2, Asmae Talbaoui1
1School of Dentistry, University of Granada, Granada, Spain.
Abstract:
Programmed cell death-ligand 1 (PD-L1) is a transmembrane protein that acts as a co-inhibitory factor in the immune response. Its receptor, programmed cell death protein 1 (PD-1), is found on immune cells, where binding to PD-L1 can reduce the proliferation of PD-1-positive cells, inhibit their cytokine secretion and induce apoptosis. PD-L1 in immune-privileged tissue plays a crucial role in peripheral tolerance. PD-L1 can be overexpressed in various malignancies, including oral squamous cell carcinoma, where it can attenuate the host immune response to tumour cells and has been associated with a worse prognosis. Monoclonal antibody therapies targeting the PD-1:PD-L1 axis have shown initial promise, but further research is needed to identify which patients will benefit. We provide an update of knowledge on PD-L1, including its structure, function and regulation. We also review studies on the overexpression of PD-L1 in cancer, specifically oral squamous cell carcinoma, and explore its potential value as a therapeutic target.
Insights
Programmed cell death-ligand 1 (PD-L1) is a protein that can be overexpressed in cancers like oral squamous cell carcinoma. Understanding PD-L1's role is key for developing targeted immunotherapies.
Area of Science:
- Immunology
- Oncology
- Molecular Biology
Background:
- Programmed cell death-ligand 1 (PD-L1) is a transmembrane protein crucial for immune regulation.
- PD-L1 interacts with its receptor, PD-1 on immune cells, inhibiting immune responses and promoting peripheral tolerance.
- Overexpression of PD-L1 is observed in various cancers, including oral squamous cell carcinoma, often correlating with poor prognosis.
Purpose of the Study:
- To provide an updated review of PD-L1, covering its structure, function, and regulation.
- To examine the overexpression of PD-L1 in cancer, with a specific focus on oral squamous cell carcinoma.
- To explore the therapeutic potential of targeting the PD-1:PD-L1 axis in cancer treatment.
Main Methods:
- Literature review of PD-L1 structure, function, and regulation.
- Review of studies investigating PD-L1 overexpression in malignancies, particularly oral squamous cell carcinoma.
- Analysis of current research on monoclonal antibody therapies targeting the PD-1:PD-L1 pathway.
Main Results:
- PD-L1 acts as a co-inhibitory factor, suppressing T-cell proliferation and cytokine secretion.
- PD-L1 overexpression in oral squamous cell carcinoma can attenuate anti-tumor immune responses.
- Monoclonal antibody therapies targeting PD-1:PD-L1 show promise but require further research for patient selection.
Conclusions:
- PD-L1 plays a significant role in immune evasion in oral squamous cell carcinoma.
- Targeting the PD-1:PD-L1 pathway represents a promising therapeutic strategy for various cancers.
- Further research is essential to identify predictive biomarkers and optimize patient response to PD-1:PD-L1 blockade therapies.
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