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Review
. 2022 Feb;23(1):1-11.
doi: 10.1038/s41435-021-00161-5. Epub 2022 Jan 19.

Immunogenic cell death and its therapeutic or prognostic potential in high-grade glioma

Affiliations
Review

Immunogenic cell death and its therapeutic or prognostic potential in high-grade glioma

Brecht Decraene et al. Genes Immun. 2022 Feb.

Erratum in

Abstract

Immunogenic cell death (ICD) has emerged as a key component of therapy-induced anti-tumor immunity. Over the past few years, ICD was found to play a pivotal role in a wide variety of novel and existing treatment modalities. The clinical application of these techniques in cancer treatment is still in its infancy. Glioblastoma (GBM) is the most lethal primary brain tumor with a dismal prognosis despite maximal therapy. The development of new therapies in this aggressive type of tumors remains highly challenging partially due to the cold tumor immune environment. GBM could therefore benefit from ICD-based therapies stimulating the anti-tumor immune response. In what follows, we will describe the mechanisms behind ICD and the ICD-based (pre)clinical advances in anticancer therapies focusing on GBM.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1. Clinical setting of ICD-based GBM vaccination.
After GBM resection, ICD will be induced using GBM cells from resected tumor tissue. Next, DC vaccine are prepared ex vivo by exposing autologous DCs to GBM cells dying through ICD. The vaccine contains GBM cells, which are avitalized after ICD induction, and DAMPs, which are either exposed, secreted or released. After applying to the patient, with tumor antigen presented by DCs, effective and GBM-specific T-cell response will be triggered and augmented. Remaining GBM cells will then be targeted to suppress GBM growth and regression. As a result, prolonged survival of the patient might occur.

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