» Articles » PMID: 37304294

Harnessing Type I Interferon-mediated Immunity to Target Malignant Brain Tumors

Overview
Journal Front Immunol
Date 2023 Jun 12
PMID 37304294
Authors
Affiliations
Soon will be listed here.
Abstract

Type I interferons have long been appreciated as a cytokine family that regulates antiviral immunity. Recently, their role in eliciting antitumor immune responses has gained increasing attention. Within the immunosuppressive tumor microenvironment (TME), interferons stimulate tumor-infiltrating lymphocytes to promote immune clearance and essentially reshape a "cold" TME into an immune-activating "hot" TME. In this review, we focus on gliomas, with an emphasis on malignant glioblastoma, as these brain tumors possess a highly invasive and heterogenous brain TME. We address how type I interferons regulate antitumor immune responses against malignant gliomas and reshape the overall immune landscape of the brain TME. Furthermore, we discuss how these findings can translate into future immunotherapies targeting brain tumors in general.

Citing Articles

Impact of developmental state, p53 status, and interferon signaling on glioblastoma cell response to radiation and temozolomide treatment.

Berezovsky A, Nuga O, Datta I, Bergman K, Sabedot T, Gurdziel K PLoS One. 2025; 20(2):e0315171.

PMID: 39919036 PMC: 11805374. DOI: 10.1371/journal.pone.0315171.


Combined PARP14 inhibition and PD-1 blockade promotes cytotoxic T cell quiescence and modulates macrophage polarization in relapsed melanoma.

Leshem R, Sefton K, Wong C, Lin I, Isaac D, Niepel M J Immunother Cancer. 2025; 13(1).

PMID: 39870492 PMC: 11772928. DOI: 10.1136/jitc-2024-010683.


An Update on the Clinical Status, Challenges, and Future Directions of Oncolytic Virotherapy for Malignant Gliomas.

Stergiopoulos G, Concilio S, Galanis E Curr Treat Options Oncol. 2024; 25(7):952-991.

PMID: 38896326 PMC: 11878440. DOI: 10.1007/s11864-024-01211-6.


Pan-cancer spatially resolved single-cell analysis reveals the crosstalk between cancer-associated fibroblasts and tumor microenvironment.

Ma C, Yang C, Peng A, Sun T, Ji X, Mi J Mol Cancer. 2023; 22(1):170.

PMID: 37833788 PMC: 10571470. DOI: 10.1186/s12943-023-01876-x.

References
1.
Tay R, Richardson E, Toh H . Revisiting the role of CD4 T cells in cancer immunotherapy-new insights into old paradigms. Cancer Gene Ther. 2020; 28(1-2):5-17. PMC: 7886651. DOI: 10.1038/s41417-020-0183-x. View

2.
Zemek R, Chin W, Fear V, Wylie B, Casey T, Forbes C . Temporally restricted activation of IFNβ signaling underlies response to immune checkpoint therapy in mice. Nat Commun. 2022; 13(1):4895. PMC: 9390963. DOI: 10.1038/s41467-022-32567-8. View

3.
de Palma M, Mazzieri R, Politi L, Pucci F, Zonari E, Sitia G . Tumor-targeted interferon-alpha delivery by Tie2-expressing monocytes inhibits tumor growth and metastasis. Cancer Cell. 2008; 14(4):299-311. DOI: 10.1016/j.ccr.2008.09.004. View

4.
Kwart D, He J, Srivatsan S, Lett C, Golubov J, Oswald E . Cancer cell-derived type I interferons instruct tumor monocyte polarization. Cell Rep. 2022; 41(10):111769. DOI: 10.1016/j.celrep.2022.111769. View

5.
Katlinski K, Gui J, Katlinskaya Y, Ortiz A, Chakraborty R, Bhattacharya S . Inactivation of Interferon Receptor Promotes the Establishment of Immune Privileged Tumor Microenvironment. Cancer Cell. 2017; 31(2):194-207. PMC: 5313042. DOI: 10.1016/j.ccell.2017.01.004. View