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IL-18 Induces PD-1–Dependent Immunosuppression in Cancer

Authors: Mélanie Desbois; Guido Kroemer; Bernhard Ryffel; Joachim L. Schultze; Nicolas F. Delahaye; Magali Terme; Sophie Viaud; +10 Authors

IL-18 Induces PD-1–Dependent Immunosuppression in Cancer

Abstract

AbstractImmunosuppressive cytokines subvert innate and adaptive immune responses during cancer progression. The inflammatory cytokine interleukin-18 (IL-18) is known to accumulate in cancer patients, but its pathophysiological role remains unclear. In this study, we show that low levels of circulating IL-18, either exogenous or tumor derived, act to suppress the NK cell arm of tumor immunosurveillance. IL-18 produced by tumor cells promotes the development of NK-controlled metastases in a PD-1–dependent manner. Accordingly, PD-1 is expressed by activated mature NK cells in lymphoid organs of tumor bearers and is upregulated by IL-18. RNAi-mediated knockdown of IL-18 in tumors, or its systemic depletion by IL-18–binding protein, are sufficient to stimulate NK cell-dependent immunosurveillance in various tumor models. Together, these results define IL-18 as an immunosuppressive cytokine in cancer. Our findings suggest novel clinical implementations of anti-PD-1 antibodies in human malignancies that produce IL-18. Cancer Res; 71(16); 5393–9. ©2011 AACR.

Keywords

Mice, Inbred BALB C, Programmed Cell Death 1 Receptor, Interleukin-18, Melanoma, Experimental, Enzyme-Linked Immunosorbent Assay, Killer Cells, Natural, Mice, Inbred C57BL, Mice, Antigens, Surface, Immune Tolerance, Animals, Female, Neoplasm Metastasis, Apoptosis Regulatory Proteins, Autoantibodies

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
301
Top 1%
Top 1%
Top 1%
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