Disease-specific suppressive granulocytes participate in glioma progression

Glioblastoma represents one of the most aggressive cancers, characterized by severely limited therapeutic options. Despite extensive investigations into this brain malignancy, cellular and molecular components governing its immunosuppressive microenvironment remain incompletely understood. Here, we identify a distinct neutrophil subpopulation, termed disease-specific suppressive granulocytes (DSSGs), present in human glioblastoma and lower-grade gliomas. DSSGs exhibit the concurrent expression of multiple immunosuppressive and immunomodulatory signals, and their abundance strongly correlates with glioma grades and poor clinical outcomes. Genetic disruption of neutrophil recruitment in immunocompetent mouse models of gliomas, achieved through Cxcl1 knockout in glioma cells or host-specific Cxcr2 deletion or diphtheria toxin A-mediated neutrophil depletion, can significantly enhance antitumor immunity and prolong survival. Further, we reveal that the skull bone marrow and meninges can be the primary sources of neutrophils and DSSGs in human and mouse glioma tumors. These findings demonstrate a critical mechanism underlying the establishment of the immunosuppressive microenvironment in gliomas.

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Publication Details

Journal
Cell Reports
Published
2024-12-01
DOI
https://doi.org/10.1016/j.celrep.2024.115014
Citations
9
Primary Topic
Immune cells in cancer
Type
article
Field-Weighted Citation Impact
2.16

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article

Disease-specific suppressive granulocytes participate in glioma progression

Jing Yang, Penghui Cao, Chunzhao Li, Ying Cao et al.
9 citations
Cell Reports
Immune cells in cancer
2.16
article

Disease-specific suppressive granulocytes participate in glioma progression

Jing Yang, Penghui Cao, Chunzhao Li, Ying Cao, Jiarui Zhao, Nan Ji, Yingying Huang, Ence Yang, Yang Zhang, Jiaqi Liu, Ying Liu, Mengyuan Li, Wenlong Li, Jian Chen, Di Wu, Yiwen Sun, Shixuan Wu, Weichen Zhao
article en
9 citations

Abstract

Glioblastoma represents one of the most aggressive cancers, characterized by severely limited therapeutic options. Despite extensive investigations into this brain malignancy, cellular and molecular components governing its immunosuppressive microenvironment remain incompletely understood. Here, we identify a distinct neutrophil subpopulation, termed disease-specific suppressive granulocytes (DSSGs), present in human glioblastoma and lower-grade gliomas. DSSGs exhibit the concurrent expression of multiple immunosuppressive and immunomodulatory signals, and their abundance strongly correlates with glioma grades and poor clinical outcomes. Genetic disruption of neutrophil recruitment in immunocompetent mouse models of gliomas, achieved through Cxcl1 knockout in glioma cells or host-specific Cxcr2 deletion or diphtheria toxin A-mediated neutrophil depletion, can significantly enhance antitumor immunity and prolong survival. Further, we reveal that the skull bone marrow and meninges can be the primary sources of neutrophils and DSSGs in human and mouse glioma tumors. These findings demonstrate a critical mechanism underlying the establishment of the immunosuppressive microenvironment in gliomas.

Cell ReportsVol. 43(12)
Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Peking University (CN), Beijing Tian Tan Hospital (CN), Chinese Institute for Brain Research (CN), Center for Life Sciences (CN)
National Natural Science Foundation of China, Natural Science Foundation of Beijing Municipality
Zero hunger
Openalex Percentile: Top 12%
Immune cells in cancer
2.16
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