Immune checkpoint pathways in glioblastoma: a diverse and evolving landscape

被引:0
|
作者
Inocencio, Julio F. [1 ]
Mitrasinovic, Stefan [1 ]
Asad, Mohammad [1 ]
Parney, Ian F. [2 ,3 ]
Zang, Xingxing [4 ,5 ]
Himes, Benjamin T. [1 ,4 ]
机构
[1] Albert Einstein Coll Med, Montefiore Med Ctr, Dept Neurol Surg, Bronx, NY 10461 USA
[2] Mayo Clin, Dept Neurol Surg, Rochester, MN USA
[3] Mayo Clin, Dept Immunol, Rochester, MN USA
[4] Albert Einstein Coll Med, Dept Microbiol & Immunol, Bronx, NY 10461 USA
[5] Albert Einstein Coll Med, Dept Oncol, Bronx, NY USA
来源
FRONTIERS IN IMMUNOLOGY | 2024年 / 15卷
关键词
immune checkpoints; glioblastoma; immune microenvironment; tumor immunosuppression; immunotherapy; REGULATORY T-CELLS; ENDOTHELIAL GROWTH-FACTOR; TUMOR MUTATIONAL BURDEN; DENDRITIC CELLS; PD-L1; EXPRESSION; MISMATCH-REPAIR; MACROPHAGE ACTIVATION; PROGNOSTIC IMPACT; SUPPRESSOR-CELLS; POOR-PROGNOSIS;
D O I
10.3389/fimmu.2024.1424396
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immune checkpoint (IC) inhibition in glioblastoma (GBM) has not shown promising results in the last decade compared to other solid tumors. Several factors contributing to the lack of immunotherapy response include the profound immunosuppressive nature of GBM, highly redundant signaling pathways underlying immune checkpoints, and the negative immunogenic impact of current standard of care on the tumor microenvironment. In this review, we will discuss various ICs in the context of GBM, their interplay with the tumor immune microenvironment, relevant pre-clinical and clinical studies, and the impact of current treatment modalities on GBM IC blockade therapy. Understanding the molecular mechanisms that drive ICs, and how they contribute to an immunosuppressive tumor microenvironment is critical in advancing IC inhibition therapy in GBM. Furthermore, revisiting current treatment modalities and their impact on the immune landscape is instrumental in designing future combinatorial therapies that may overcome treatment resistance.
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页数:21
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