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

Author:

Hafler David1ORCID,Lu Benjamin2ORCID,Lucca Liliana2,Lewis Wesley1,Wang Jiping3,Nogeuira Catarina4,Heer Sebastian4,Axisa Pierre-Paul1ORCID,Buitrago-Pocasangre Nicholas5ORCID,Pham Giang2,Kojima Mina6,Wei Wei2,Aizenbud Lilach2,Bacchiocchi Antonietta2,Zhang Lin2,Walewski Joseph2,Chiang Veronica2,Olino Kelly2,Clune James2,Halaban Ruth7ORCID,Kluger Yuval7ORCID,Coyle Anthony4,Kisielow Jan8ORCID,Obermair Franz-Josef8ORCID,Kluger Harriet7

Affiliation:

1. Yale University

2. Yale School of Medicine

3. Yale School of Public Health

4. Repertoire Immune Medicines

5. Yale Medical School

6. Department of Genetics, Yale University

7. Yale University School of Medicine

8. Repertoire Immune Medicine (Switzerland)

Abstract

Abstract 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.

Publisher

Research Square Platform LLC

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