Abstract 2560: Radiotherapy shapes memory T cell dynamics and region-specific PD-1 expression in the glioblastoma microenvironment

Abstract Glioblastoma (GBM) is the most common and aggressive malignant brain tumor in adults, where radiation therapy (RT) remains standard care. However, the precise immunomodulatory effects of RT-specifically on T cell checkpoint receptor profiles and memory T cells dynamics -within the tumor microenvironment are not fully elucidated. In this translational study, we utilized an orthotopic patient-derived xenograft (PDX) model, CRT361, engineered with a Luc+ reporter. This system was supported by an HLA-matched peripheral blood mononuclear cell (PBMC) humanization platform, providing a clinically relevant context for immune analysis. CRT361 cells were implanted intracranially into the right hemisphere, and tumors progression was monitored via multimodal imaging, bioluminescence imaging (BLI) and magnetic resonance imaging (MRI). Following successful PBMC engraftment and a single-dose focal irradiation (2 Gy), T cells were harvested from both peripheral blood and distinct brain hemispheres for profiling via spectral flow cytometry. Our results demonstrate that focal irradiation increased the frequency of both CD8+ and CD4+ central memory T cells (TCM) in both blood and brain. Furthermore, irradiation led to elevated programmed cell death protein 1 (PD-1) expression on both CD8+ and CD4+ TCM and naïve T cells in peripheral blood. Crucially, we observed an inverse response in the central nervous system: CD8+ TCM within the brain exhibited lowerPD-1 expression levels exclusively in the irradiated right hemisphere.These novel findings provide critical insight into the capacity of radiotherapy to dynamically influence T cell phenotypes and checkpoint receptor landscapes in a tissue-, region-, and cell type-specific manner within the GBM microenvironment. This study design and results establish a robust foundation for the rationale design and optimization of combinatorial strategies leveraging both radiation and emerging immunotherapies. Citation Format: Hsin-Yu Sherry Liu, Sanghee Lee, Itzel Gutierrez, Jasmine Borroel, Paris Offor, Emily Eastwood, Javier Rodriguez, Kristen Buck, Derrick Gorospe, Elizabeth Valencia, Catherine Elix, Bridget Corcoran, Manuel Reyes, Samantha Lin, Raffaella Pippa. Radiotherapy shapes memory T cell dynamics and region-specific PD-1 expression in the glioblastoma microenvironment [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2560.

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Publication Details

Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-2560
Primary Topic
Glioma Diagnosis and Treatment
Type
article
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article

Abstract 2560: Radiotherapy shapes memory T cell dynamics and region-specific PD-1 expression in the glioblastoma microenvironment

Jasmine Borroel, Catherine Elix, S. Lee, Kristen Buck et al.
Cancer Research
Glioma Diagnosis and Treatment
article

Abstract 2560: Radiotherapy shapes memory T cell dynamics and region-specific PD-1 expression in the glioblastoma microenvironment

Jasmine Borroel, Catherine Elix, S. Lee, Kristen Buck, Bridget Corcoran, Raffaella Pippa, Paris Offor, Emily Eastwood, Samantha Lin, Manuel Reyes, Derrick Gorospe, Elizabeth Valencia, Itzel Gutierrez, Hsin-Yu Sherry Liu, Javier Rodriguez
article en

Abstract

Abstract Glioblastoma (GBM) is the most common and aggressive malignant brain tumor in adults, where radiation therapy (RT) remains standard care. However, the precise immunomodulatory effects of RT-specifically on T cell checkpoint receptor profiles and memory T cells dynamics -within the tumor microenvironment are not fully elucidated. In this translational study, we utilized an orthotopic patient-derived xenograft (PDX) model, CRT361, engineered with a Luc+ reporter. This system was supported by an HLA-matched peripheral blood mononuclear cell (PBMC) humanization platform, providing a clinically relevant context for immune analysis. CRT361 cells were implanted intracranially into the right hemisphere, and tumors progression was monitored via multimodal imaging, bioluminescence imaging (BLI) and magnetic resonance imaging (MRI). Following successful PBMC engraftment and a single-dose focal irradiation (2 Gy), T cells were harvested from both peripheral blood and distinct brain hemispheres for profiling via spectral flow cytometry. Our results demonstrate that focal irradiation increased the frequency of both CD8+ and CD4+ central memory T cells (TCM) in both blood and brain. Furthermore, irradiation led to elevated programmed cell death protein 1 (PD-1) expression on both CD8+ and CD4+ TCM and naïve T cells in peripheral blood. Crucially, we observed an inverse response in the central nervous system: CD8+ TCM within the brain exhibited lowerPD-1 expression levels exclusively in the irradiated right hemisphere.These novel findings provide critical insight into the capacity of radiotherapy to dynamically influence T cell phenotypes and checkpoint receptor landscapes in a tissue-, region-, and cell type-specific manner within the GBM microenvironment. This study design and results establish a robust foundation for the rationale design and optimization of combinatorial strategies leveraging both radiation and emerging immunotherapies. Citation Format: Hsin-Yu Sherry Liu, Sanghee Lee, Itzel Gutierrez, Jasmine Borroel, Paris Offor, Emily Eastwood, Javier Rodriguez, Kristen Buck, Derrick Gorospe, Elizabeth Valencia, Catherine Elix, Bridget Corcoran, Manuel Reyes, Samantha Lin, Raffaella Pippa. Radiotherapy shapes memory T cell dynamics and region-specific PD-1 expression in the glioblastoma microenvironment [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2560.

Cancer ResearchVol. 86(7_Supplement)
Good health and well-being
Openalex Percentile: Top 26%
Glioma Diagnosis and Treatment
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