Endothelial STING-JAK1 interaction promotes tumor vasculature normalization and antitumor immunity

J Clin Invest. 2025 Jan 16;135(2):e180622. doi: 10.1172/JCI180622.

Abstract

Stimulator of interferon genes (STING) agonists have been developed and tested in clinical trials for their antitumor activity. However, the specific cell population(s) responsible for such STING activation-induced antitumor immunity have not been completely understood. In this study, we demonstrated that endothelial STING expression was critical for STING agonist-induced antitumor activity. STING activation in endothelium promoted vessel normalization and CD8+ T cell infiltration - which required type I IFN (IFN-I) signaling- but not IFN-γ or CD4+ T cells. Rather than an upstream adaptor for inducing IFN-I signaling, STING acted downstream of interferon-α/β receptor (IFNAR) in endothelium for the JAK1-STAT signaling activation. Mechanistically, IFN-I stimulation induced JAK1-STING interaction and promoted JAK1 phosphorylation, which involved STING palmitoylation at the Cysteine 91 site but not its C-terminal tail (CTT) domain. Endothelial STING and JAK1 expression was significantly associated with immune cell infiltration in patients with cancer, and STING palmitoylation level correlated positively with CD8+ T cell infiltration around STING-positive blood vessels in tumor tissues from patients with melanoma. In summary, our findings uncover a previously unrecognized function of STING in regulating JAK1/STAT activation downstream of IFN-I stimulation and provide a new insight for future design and clinical application of STING agonists for cancer therapy.

Keywords: Cancer immunotherapy; Immunology; Oncology.

MeSH terms

  • Animals
  • CD8-Positive T-Lymphocytes* / immunology
  • Endothelial Cells / immunology
  • Endothelial Cells / metabolism
  • Endothelial Cells / pathology
  • Humans
  • Janus Kinase 1* / genetics
  • Janus Kinase 1* / immunology
  • Janus Kinase 1* / metabolism
  • Melanoma / genetics
  • Melanoma / immunology
  • Melanoma / metabolism
  • Melanoma / pathology
  • Melanoma, Experimental / blood supply
  • Melanoma, Experimental / immunology
  • Melanoma, Experimental / pathology
  • Membrane Proteins* / genetics
  • Membrane Proteins* / immunology
  • Membrane Proteins* / metabolism
  • Mice
  • Neovascularization, Pathologic / immunology
  • Signal Transduction

Substances

  • Janus Kinase 1
  • Membrane Proteins
  • JAK1 protein, human
  • STING1 protein, human
  • Sting1 protein, mouse
  • Jak1 protein, mouse