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Circulating Tumor Reactive KIR+CD8+ T cells Suppress Anti-Tumor Immunity in Patients with Melanoma.

David A HaflerBenjamin Y LuLiliana LuccaWesley LewisJiping WangCatarina NogeuiraSebastian HeerPierre-Paul AxisaNicholas Buitrago-PocasangreGiang PhamMina KojimaWei WeiLilach AizenbudAntonietta BacchiocchiLin ZhangJoseph WalewskiVeronica ChiangKelly OlinoJames CluneRuth HalabanYuval KlugerAnthony CoyleJan KisielowFranz-Josef ObermairHarriet Kluger
Published in: Research square (2024)
Effective anti-tumor immunity is largely driven by cytotoxic CD8 + T cells that can specifically recognize tumor antigens. However, the factors which ultimately dictate successful tumor rejection remain poorly understood. Here we identify a subpopulation of CD8 + T cells which are tumor antigen-specific in patients with melanoma but resemble KIR + CD8 + T cells with a regulatory function (Tregs). These tumor antigen-specific KIR + CD8 + T cells are detectable in both the tumor and the blood, and higher levels of this population are associated with worse overall survival. Our findings therefore suggest that KIR + CD8 + Tregs are tumor antigen-specific but uniquely suppress anti-tumor immunity in patients with melanoma.
Keyphrases
  • transcription factor
  • circulating tumor
  • circulating tumor cells
  • cell free
  • skin cancer
  • nk cells