Related Experiment Video
Updated: Jul 5, 2025

Isolation and Flow Cytometric Analysis of Glioma-infiltrating Peripheral Blood Mononuclear Cells
Published on: November 28, 2015
Targeting Innate Immunity in Glioma Therapy
Andrew G Gillard1,2, Dong Ho Shin1,2, Lethan A Hampton1
1Department of Neuro-Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Abstract:
Currently, there is a lack of effective therapies for the majority of glioblastomas (GBMs), the most common and malignant primary brain tumor. While immunotherapies have shown promise in treating various types of cancers, they have had limited success in improving the overall survival of GBM patients. Therefore, advancing GBM treatment requires a deeper understanding of the molecular and cellular mechanisms that cause resistance to immunotherapy. Further insights into the innate immune response are crucial for developing more potent treatments for brain tumors. Our review provides a brief overview of innate immunity. In addition, we provide a discussion of current therapies aimed at boosting the innate immunity in gliomas. These approaches encompass strategies to activate Toll-like receptors, induce stress responses, enhance the innate immune response, leverage interferon type-I therapy, therapeutic antibodies, immune checkpoint antibodies, natural killer (NK) cells, and oncolytic virotherapy, and manipulate the microbiome. Both preclinical and clinical studies indicate that a better understanding of the mechanisms governing the innate immune response in GBM could enhance immunotherapy and reinforce the effects of chemotherapy and radiotherapy. Consequently, a more comprehensive understanding of the innate immune response against cancer should lead to better prognoses and increased overall survival for GBM patients.
Insights
Glioblastoma (GBM) immunotherapy faces challenges due to treatment resistance. Understanding innate immunity mechanisms is key to developing effective brain tumor therapies and improving patient survival.
Area of Science:
- Neuro-oncology
- Immunology
- Cancer Biology
Background:
- Glioblastomas (GBMs) are aggressive brain tumors with limited effective therapies.
- Immunotherapy has shown limited success in improving overall survival for GBM patients.
- Understanding immunotherapy resistance mechanisms is crucial for advancing GBM treatment.
Purpose of the Study:
- To review the role of innate immunity in glioblastoma.
- To discuss current and emerging immunotherapies targeting innate immunity in gliomas.
- To highlight the potential of enhancing innate immune responses for improved GBM treatment outcomes.
Main Methods:
- Literature review of preclinical and clinical studies on innate immunity in GBM.
- Discussion of various therapeutic strategies to boost innate immunity.
- Analysis of mechanisms underlying immunotherapy resistance in brain tumors.
Main Results:
- Innate immunity plays a critical role in the tumor microenvironment of GBM.
- Several strategies, including TLR activation, interferon therapy, and NK cell therapy, show promise.
- Manipulating the microbiome may also impact GBM immunotherapy efficacy.
Conclusions:
- A deeper understanding of innate immunity in GBM is essential for overcoming treatment resistance.
- Enhancing innate immune responses can improve the efficacy of immunotherapy, chemotherapy, and radiotherapy.
- Targeting innate immunity offers a promising avenue for improving prognoses and survival in GBM patients.

