Novel insights into IL-37: an anti-inflammatory cytokine with emerging roles in anti-cancer process

Front Immunol. 2023 Oct 20:14:1278521. doi: 10.3389/fimmu.2023.1278521. eCollection 2023.

Abstract

Interleukin-37 (IL-37) is a newly discovered member of IL-1 family. The cytokine was proved to have extensive protective effects in infectious diseases, allergic diseases, metabolic diseases, autoimmune diseases and tumors since its discovery. IL-37 was mainly produced by immune and some non-immune cells in response to inflammatory stimulus. The IL-37 precursors can convert into the mature forms after caspase-1 cleavage and activation intracellularly, and then bind to Smad-3 and transfer to the nucleus to inhibit the production and functions of proinflammatory cytokines; extracellularly, IL-37 binds to cell surface receptors to form IL-37/IL-18Rα/IL-1R8 complex to exert immunosuppressive function via inhibiting/activating multiple signal pathways. In addition, IL-37 can attenuate the pro-inflammatory effect of IL-18 through directly or forming an IL-37/IL-18BP/IL-18Rβ complex. Therefore, IL-37 has the ability to suppress innate and acquired immunity of the host, and effectively control inflammatory stimulation, which was considered as a new hallmark of cancer. Specifically, it is concluded that IL-37 can inhibit the growth and migration of tumor cells, prohibit angiogenesis and mediate the immunoregulation in tumor microenvironment, so as to exert effective anti-tumor effects. Importantly, latest studies also showed that IL-37 may be a novel therapeutic target for cancer monitoring. In this review, we summarize the immunoregulation roles and mechanisms of IL-37 in anti-tumor process, and discuss its progress so far and potential as tumor immunotherapy.

Keywords: IL-37; anti-tumor; immunomodulation; immunotherapy; inflammation inhibition.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adaptive Immunity
  • Cytokines* / immunology
  • Humans
  • Interleukin-1* / immunology
  • Neoplasms* / metabolism
  • Neoplasms* / therapy
  • Signal Transduction
  • Tumor Microenvironment

Substances

  • Cytokines
  • IL37 protein, human
  • Interleukin-1

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by grants from the National Natural Science Foundation of China (82272401, 82202610), Jiangsu Province Capability Improvement Project through Science and Technology and Education (ZDXK202239) and the Priority Academic Program Development of Jiangsu Higher Education Institutions.