期刊
FRONTIERS IN IMMUNOLOGY
卷 12, 期 -, 页码 -出版社
FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2021.718098
关键词
reactive nitrogen species; cytokines; immunosuppression; post-translational modification; tumor microenvironment
类别
资金
- Italian Ministry of Health [2009-GR-2009-1558698]
- Cariparo Fundation Fellowship
Reactive oxygen species, including RNS, play a crucial role in controlling immune cell functions within the tumor microenvironment, and GM-CSF activity is significantly impacted by RNS-induced post-translational modifications. The nitration of a single tryptophan residue in GM-CSF sequence facilitates the expansion of highly immunosuppressive myeloid subsets in tumor-bearing hosts, providing a potential target for remodeling the TME and enhancing protective immunity against cancer.
Reactive oxygen species, including RNS, contribute to the control of multiple immune cell functions within the tumor microenvironment (TME). Tumor-infiltrating myeloid cells (TIMs) represent the archetype of tolerogenic cells that actively contribute to dismantle effective immunity against cancer. TIMs inhibit T cell functions and promote tumor progression by several mechanisms including the amplification of the oxidative/nitrosative stress within the TME. In tumors, TIM expansion and differentiation is regulated by the granulocyte-macrophage colony-stimulating factor (GM-CSF), which is produced by cancer and immune cells. Nevertheless, the role of GM-CSF in tumors has not yet been fully elucidated. In this study, we show that GM-CSF activity is significantly affected by RNS-triggered post-translational modifications. The nitration of a single tryptophan residue in the sequence of GM-CSF nourishes the expansion of highly immunosuppressive myeloid subsets in tumor-bearing hosts. Importantly, tumors from colorectal cancer patients express higher levels of nitrated tryptophan compared to non-neoplastic tissues. Collectively, our data identify a novel and selective target that can be exploited to remodel the TME and foster protective immunity against cancer.
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