IL-36α inhibits melanoma by inducing pro-inflammatory polarization of macrophages

Cancer Immunol Immunother. 2023 Sep;72(9):3045-3061. doi: 10.1007/s00262-023-03477-5. Epub 2023 Jun 15.

Abstract

Interleukin-36α (IL-36α) is essential for various inflammatory conditions, such as psoriasis and rheumatoid arthritis, whereas its role in tumor immunity is unclear. In this study, it was demonstrated that IL-36α could activate the NF-κB and MAPK signaling pathways in macrophages, leading to the expression of IL-1β, IL-6, TNF-α, CXCL1, CXCL2, CXCL3, CXCL5 and iNOS. Importantly, IL-36α has significant antitumor effects, altering the tumor microenvironment and promoting the infiltration of MHC IIhigh macrophages and CD8+ T cells while decreasing the levels of monocyte myeloid-derived suppressor cells, CD4+ T cells and regulatory T cells. This ultimately results in the inhibition of tumor growth and migration. Furthermore, IL-36α synergized with the PD-L1 antibody increased the immune cells infiltration and enhanced the anti-tumor effect of the PD-L1 antibody on melanoma. Collectively, this study reveals a new role for IL-36α in promoting anti-tumor immune responses in macrophages and suggests its potential for cancer immunotherapy.

Keywords: IL-36α; MAPK pathway; Macrophages; Melanoma; NF-κB pathway; PD-L1 antibody.

MeSH terms

  • B7-H1 Antigen* / metabolism
  • CD8-Positive T-Lymphocytes
  • Humans
  • Interleukins / metabolism
  • Macrophages
  • Melanoma* / metabolism
  • Tumor Microenvironment

Substances

  • B7-H1 Antigen
  • Interleukins