The Role of γδ T-Lymphocytes in Glioblastoma: Current Trends and Future Directions

Author:

Ahmedna Taha1,Khela Harmon12,Weber-Levine Carly3ORCID,Azad Tej D.3,Jackson Christopher M.3,Gabrielson Kathleen4,Bettegowda Chetan3,Rincon-Torroella Jordina3ORCID

Affiliation:

1. Department of Biology, Johns Hopkins University, Baltimore, MD 21287, USA

2. Department of Public Health Studies, Johns Hopkins University, Baltimore, MD 21287, USA

3. Department of Neurosurgery, School of Medicine, Johns Hopkins University, Baltimore, MD 21287, USA

4. Department of Molecular and Comparative Pathobiology and Oncology, School of Medicine, Johns Hopkins University, Baltimore, MD 21287, USA

Abstract

Cell-based immunotherapy for glioblastoma (GBM) encounters major challenges due to the infiltration-resistant and immunosuppressive tumor microenvironment (TME). γδ T cells, unconventional T cells expressing the characteristic γδ T cell receptor, have demonstrated promise in overcoming these challenges, suggesting great immunotherapeutic potential. This review presents the role of γδ T cells in GBM and proposes several research avenues for future studies. Using the PubMed, ScienceDirect, and JSTOR databases, we performed a review of the literature studying the biology of γδ T cells and their role in GBM treatment. We identified 15 studies focused on γδ T cells in human GBM. Infiltrative γδ T cells can incite antitumor immune responses in certain TMEs, though rapid tumor progression and TME hypoxia may impact the extent of tumor suppression. In the studies, available findings have shown both the potential for robust antitumor activity and the risk of protumor activity. While γδ T cells have potential as a therapeutic agent against GBM, the technical challenges of extracting, isolating, and expanding γδ T cells, and the activation of antitumoral versus protumoral cascades, remain barriers to their application. Overcoming these limitations may transform γδ T cells into a promising immunotherapy in GBM.

Funder

NINDS R25

Publisher

MDPI AG

Subject

Cancer Research,Oncology

Reference71 articles.

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