Immunological Evasion in Glioblastoma

Author:

Magaña-Maldonado Roxana1,Chávez-Cortez Elda Georgina1,Olascoaga-Arellano Nora Karen1,López-Mejía Mariana1,Maldonado-Leal Fernando Manuel1,Sotelo Julio1,Pineda Benjamín1ORCID

Affiliation:

1. Neuroimmunology and Neurooncology Unit, The National Institute of Neurology and Neurosurgery (NINN), Insurgentes Sur 3877, 14269 Mexico City, DF, Mexico

Abstract

Glioblastoma is the most aggressive tumor in Central Nervous System in adults. Among its features, modulation of immune system stands out. Although immune system is capable of detecting and eliminating tumor cells mainly by cytotoxic T and NK cells, tumor microenvironment suppresses an effective response through recruitment of modulator cells such as regulatory T cells, monocyte-derived suppressor cells, M2 macrophages, and microglia as well as secretion of immunomodulators including IL-6, IL-10, CSF-1, TGF-β, and CCL2. Other mechanisms that induce immunosuppression include enzymes as indolamine 2,3-dioxygenase. For this reason it is important to develop new therapies that avoid this immune evasion to promote an effective response against glioblastoma.

Funder

Consejo Nacional de Ciencia y Tecnología

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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