Glioblastoma cells potentiate the induction of the Th1-like profile in phosphoantigen-stimulated γδ T lymphocytes
Autor: | Juan Iturrizaga, Irene Angélica Keitelman, Fernando D. Gómez, David Antonio Rosso, Nazareno González, Carolina Maiumi Shiromizu, Alejandra T. Rabadán, Micaela Rosato, Gabriela Salamone, Carolina Jancic, Juan Valentin Coronel, María Marta Amaral |
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Rok vydání: | 2021 |
Předmět: |
Cancer Research
Tumor microenvironment medicine.diagnostic_test biology T cell CD69 medicine.medical_treatment Immunotherapy Flow cytometry Transcriptome 03 medical and health sciences 0302 clinical medicine medicine.anatomical_structure Neurology Oncology Perforin Antigen 030220 oncology & carcinogenesis medicine biology.protein Cancer research Neurology (clinical) 030217 neurology & neurosurgery |
Zdroj: | Journal of Neuro-Oncology. 153:403-415 |
ISSN: | 1573-7373 0167-594X |
DOI: | 10.1007/s11060-021-03787-7 |
Popis: | γδ T lymphocytes are non-conventional T cells that participate in protective immunity and tumor surveillance. In healthy humans, the main subset of circulating γδ T cells express the TCRVγ9Vδ2. This subset responds to non-peptide prenyl-pyrophosphate antigens such as (E)-4-hydroxy-3-methyl-but-enyl pyrophosphate (HMBPP). This unique feature of Vγ9Vδ2 T cells makes them a candidate for anti-tumor immunotherapy. In this study, we investigated the response of HMBPP-activated Vγ9Vδ2 T lymphocytes to glioblastoma multiforme (GBM) cells. Human purified γδ T cells were stimulated with HMBPP (1 µM) and incubated with GBM cells (U251, U373 and primary GBM cultures) or their conditioned medium. After overnight incubation, expression of CD69 and perforin was evaluated by flow cytometry and cytokines production by ELISA. As well, we performed a meta-analysis of transcriptomic data obtained from The Cancer Genome Atlas. HMBPP-stimulated γδ T cells cultured with GBM or its conditioned medium increased CD69, intracellular perforin, IFN-γ, and TNF-α production. A meta-analysis of transcriptomic data showed that GBM patients display better overall survival when mRNA TRGV9, the Vγ9 chain-encoding gene, was expressed in high levels. Moreover, its expression was higher in low-grade GBM compared to GBM. Interestingly, there was an association between γδ T cell infiltrates and TNF-α expression in the tumor microenvironment. GBM cells enhanced Th1-like profile differentiation in phosphoantigen-stimulated γδ T cells. Our results reinforce data that have demonstrated the implication of Vγ9Vδ2 T cells in the control of GBM, and this knowledge is fundamental to the development of immunotherapeutic protocols to treat GBM based on γδ T cells. |
Databáze: | OpenAIRE |
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