Unknown

Dataset Information

0

Glioblastoma Immune Landscape and the Potential of New Immunotherapies.


ABSTRACT: Glioblastoma (GBM) are the most common tumors of the central nervous system and among the deadliest cancers in adults. GBM overall survival has not improved over the last decade despite optimization of therapeutic standard-of-care. While immune checkpoint inhibitors (ICI) have revolutionized cancer care, they unfortunately have little therapeutic success in GBM. Here, we elaborate on normal brain and GBM-associated immune landscapes. We describe the role of microglia and tumor-associated macrophages (TAMs) in immune suppression and highlight the impact of energy metabolism in immune evasion. We also describe the challenges and opportunities of immunotherapies in GBM and discuss new avenues based on harnessing the anti-tumor activity of myeloid cells, vaccines, chimeric antigen receptors (CAR)-T and -NK cells, oncolytic viruses, nanocarriers, and combination therapies.

SUBMITTER: Daubon T 

PROVIDER: S-EPMC7591769 | biostudies-literature | 2020

REPOSITORIES: biostudies-literature

altmetric image

Publications

Glioblastoma Immune Landscape and the Potential of New Immunotherapies.

Daubon Thomas T   Hemadou Audrey A   Romero Garmendia Irati I   Saleh Maya M  

Frontiers in immunology 20201014


Glioblastoma (GBM) are the most common tumors of the central nervous system and among the deadliest cancers in adults. GBM overall survival has not improved over the last decade despite optimization of therapeutic standard-of-care. While immune checkpoint inhibitors (ICI) have revolutionized cancer care, they unfortunately have little therapeutic success in GBM. Here, we elaborate on normal brain and GBM-associated immune landscapes. We describe the role of microglia and tumor-associated macroph  ...[more]

Similar Datasets

| S-EPMC8012774 | biostudies-literature
| S-EPMC4915370 | biostudies-literature
| S-EPMC7594513 | biostudies-literature
| S-EPMC7986847 | biostudies-literature
| S-EPMC8377979 | biostudies-literature
| S-EPMC7794906 | biostudies-literature
| S-EPMC6171107 | biostudies-literature
| S-EPMC6994452 | biostudies-literature
| S-EPMC8507767 | biostudies-literature
| 2166592 | ecrin-mdr-crc