Circulating tumor-reactive KIR+CD8+ T cells suppress anti-tumor immunity in patients with melanoma

Nat Immunol. 2025 Jan;26(1):82-91. doi: 10.1038/s41590-024-02023-4. Epub 2024 Nov 28.

Abstract

Effective anti-tumor immunity is driven by cytotoxic CD8+ T cells with specificity for tumor antigens. However, the factors that control successful tumor rejection are not well understood. Here we identify a subpopulation of CD8+ T cells that are tumor-antigen-specific and can be identified by KIR expression but paradoxically impair anti-tumor immunity in patients with melanoma. These tumor-antigen-specific KIR+CD8+ regulatory T cells target other tumor-antigen-specific CD8+ T cells, can be detected in both the tumor and the blood, have a conserved transcriptional program and are associated with a poor overall survival. These findings broaden our understanding of the transcriptional and functional heterogeneity of human CD8+ T cells and implicate KIR+CD8+ regulatory T cells as a cellular mediator of immune evasion in human cancer.

MeSH terms

  • Antigens, Neoplasm / immunology
  • CD8-Positive T-Lymphocytes* / immunology
  • Female
  • Humans
  • Melanoma* / immunology
  • Receptors, KIR* / immunology
  • Receptors, KIR* / metabolism
  • T-Lymphocytes, Regulatory / immunology
  • Tumor Escape

Substances

  • Receptors, KIR
  • Antigens, Neoplasm