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PD-L1/PD-1 Axis in Glioblastoma Multiforme
Jakub Litak1,2, Marek Mazurek3, Cezary Grochowski4,5
1Department of Immunology, Medical University of Lublin, Jaczewskiego 8, 20-954 Lublin, Poland. jakub.litak@gmail.com.
International Journal of Molecular Sciences
|October 31, 2019
Summary
Glioblastoma (GBM) is an aggressive brain cancer with poor survival. Targeting the programmed cell death-1 (PD-1) and programmed cell death ligand (PD-L1) pathway shows promise in preclinical models for treating GBM.
Area of Science:
- Neuro-oncology
- Immunology
- Cancer Biology
Background:
- Glioblastoma (GBM) is an aggressive primary brain cancer with a median survival of 14-17 months.
- The programmed cell death-1 (PD-1) and programmed cell death ligand (PD-L1) pathway plays a crucial role in GBM invasion and immune evasion.
- PD-L1 expression on GBM cells can suppress T cell responses by activating PD-1 receptors on microglia.
Purpose of the Study:
- To investigate the role of the PD-1/PD-L1 axis in glioblastoma multiforme (GBM) pathogenesis.
- To evaluate the therapeutic potential of targeting the PD-1/PD-L1 pathway in preclinical GBM models.
Main Methods:
- Analysis of PD-1/PD-L1 interactions in GBM.
- Assessment of PD-L1 expression as a potential tumor biomarker.
- Evaluation of monoclonal antibodies targeting the PD-1/PD-L1 axis in preclinical GBM mouse models.
Main Results:
- The PD-1/PD-L1 axis promotes GBM invasion and immune suppression.
- PD-L1 expression correlates with glioma WHO grading.
- Monoclonal antibodies targeting PD-1/PD-L1 demonstrated safety and efficacy in preclinical GBM models, leading to tumor regression and prolonged survival.
Conclusions:
- Targeting the PD-1/PD-L1 pathway represents a promising therapeutic strategy for GBM.
- Further clinical trials are warranted to assess the efficacy of PD-1/PD-L1 inhibitors in patients with recurrent glioblastoma.

