Hallmarks of the Tumour Microenvironment of Gliomas and Its Interaction with Emerging Immunotherapy Modalities.
Christian A LinaresAnjana VargheseAruni GhoseSayali D ShindeSola AdelekeElisabet SanchezMatin SheriffCyrus ChargariElie RassyStergios BoussiosPublished in: International journal of molecular sciences (2023)
Gliomas are aggressive, primary central nervous system tumours arising from glial cells. Glioblastomas are the most malignant. They are known for their poor prognosis or median overall survival. The current standard of care is overwhelmed by the heterogeneous, immunosuppressive tumour microenvironment promoting immune evasion and tumour proliferation. The advent of immunotherapy with its various modalities-immune checkpoint inhibitors, cancer vaccines, oncolytic viruses and chimeric antigen receptor T cells and NK cells-has shown promise. Clinical trials incorporating combination immunotherapies have overcome the microenvironment resistance and yielded promising survival and prognostic benefits. Rolling these new therapies out in the real-world scenario in a low-cost, high-throughput manner is the unmet need of the hour. These will have practice-changing implications to the glioma treatment landscape. Here, we review the immunobiological hallmarks of the TME of gliomas, how the TME evades immunotherapies and the work that is being conducted to overcome this interplay.
Keyphrases
- poor prognosis
- high grade
- low cost
- stem cells
- high throughput
- nk cells
- long non coding rna
- clinical trial
- healthcare
- induced apoptosis
- single cell
- primary care
- quality improvement
- papillary thyroid
- palliative care
- signaling pathway
- free survival
- cell cycle arrest
- blood pressure
- neuropathic pain
- pain management
- squamous cell
- machine learning
- combination therapy
- oxidative stress
- cell death
- spinal cord
- artificial intelligence
- health insurance
- phase ii
- childhood cancer
- open label