Abstract
Gliomas are the most common primary brain tumors in adults. Despite the fact that they are relatively rare, they cause significant morbidity and mortality. High-grade gliomas or glioblastomas are rapidly progressing tumors with a very poor prognosis. The presence of an intrinsic immune system in the central nervous system is now more accepted. During the last decade, there has been no major progress in glioma therapy. The lack of effective treatment for gliomas can be explained by the strategies that cancer cells use to escape the immune system. This being said, immunotherapy, which involves blockade of immune checkpoint inhibitors, has improved patients’ survival in different cancer types. This novel cancer therapy appears to be one of the most promising approaches. In the present study, we will start with a review of the general concept of immune response within the brain and glioma microenvironment. Then, we will try to decipher the role of various immune checkpoint inhibitors within the glioma microenvironment. Finally, we will discuss some promising therapeutic pathways, including immune checkpoint blockade and the body’s effective anti-glioma immune response.
Highlights
The immune system is made up of several cell types, which defend the body against possible pathogens [1].Gliomas or glial tumors are the most common primary brain tumors and they account for 81% of all malignant ones
The present review aims at describing the immune response within the glioma microenvironment, and discussing the involvement of various immune checkpoint inhibitor molecules used by glioma cells in order to escape the immune response
We managed to collect further evidence which demonstrates that the immune system is involved in glioma physiopathology and describes the general concept of immune response within the glioma microenvironment
Summary
The immune system is made up of several cell types, which defend the body against possible pathogens [1]. Glioma cells secrete different types of chemokines, cytokines and growth factors that enhance infiltration of various cells such as astrocytes, pericytes, endothelial cells, circulating progenitor cells, and a range of immune cells including microglia, peripheral macrophages, myeloid-derived suppressor cells (MDSC), CD4+ T cells as well as Treg cells into the tumor [56,57,58,59]. Identification of these factors may facilitate the improvement of glioma immunotherapy as immunomodulatory and immune evasion mechanisms used by glioma cells. Galstyan et al attempted to Frontiers in Immunology | www.frontiersin.org
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.