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Therapeutic approaches to modulate the immune microenvironment in gliomas
Andreas Sarantopoulos1, Chibawanye Ene2, Elisa Aquilanti3
1School of Medicine, European University of Cyprus, Nicosia, Cyprus.
Abstract:
Immunomodulatory therapies, including immune checkpoint inhibitors, have drastically changed outcomes for certain cancer types over the last decade. Gliomas are among the cancers that have seem limited benefit from these agents, with most trials yielding negative results. The unique composition of the glioma immune microenvironment is among the culprits for this lack of efficacy. In recent years, several efforts have been made to improve understanding of the glioma immune microenvironment, aiming to pave the way for novel therapeutic interventions. In this review, we discuss some of the main components of the glioma immune microenvironment, including macrophages, myeloid-derived suppressor cells, neutrophils and microglial cells, as well as lymphocytes. We then provide a comprehensive overview of novel immunomodulatory agents that are currently in clinical development, namely oncolytic viruses, vaccines, cell-based therapies such as CAR-T cells and CAR-NK cells as well as antibodies and peptides.
Insights
Immunomodulatory therapies show promise in cancer treatment but have limited efficacy in gliomas due to their unique immune microenvironment. This review explores glioma immunology and novel immunotherapies in development.
Area of Science:
- Neuro-oncology
- Immunology
- Cancer Therapy
Background:
- Immunomodulatory therapies, like immune checkpoint inhibitors, have revolutionized cancer treatment for many types.
- Gliomas have shown limited benefit from current immunotherapies, largely due to their complex immune microenvironment.
- Understanding the glioma immune microenvironment is crucial for developing effective treatments.
Purpose of the Study:
- To review the key cellular components of the glioma immune microenvironment.
- To provide a comprehensive overview of novel immunomodulatory agents in clinical development for glioma treatment.
Main Methods:
- Literature review of the glioma immune microenvironment.
- Survey of emerging immunotherapeutic strategies for gliomas.
Main Results:
- Key glioma immune cells include macrophages, myeloid-derived suppressor cells, neutrophils, microglial cells, and lymphocytes.
- Novel agents under investigation include oncolytic viruses, vaccines, CAR-T/NK cells, antibodies, and peptides.
Conclusions:
- The unique glioma immune microenvironment presents challenges for immunotherapy efficacy.
- Emerging immunotherapies offer potential new avenues for treating gliomas.
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