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Eur J Immunol. 2010 Dec;40(12):3347-57. doi: 10.1002/eji.201041037.

IL-1β regulates a novel myeloid-derived suppressor cell subset that impairs NK cell development and function.

Author information

1
Innate Immunity Unit, Institut Pasteur, Paris, France.

Abstract

Chronic inflammation is associated with promotion of malignancy and tumor progression. Many tumors enhance the accumulation of myeloid-derived suppressor cells (MDSC), which contribute to tumor progression and growth by suppressing anti-tumor immune responses. Tumor-derived IL-1β secreted into the tumor microenvironment has been shown to induce the accumulation of MDSC possessing an enhanced capacity to suppress T cells. In this study, we found that the enhanced suppressive potential of IL-1β-induced MDSC was due to the activity of a novel subset of MDSC lacking Ly6C expression. This subset was present at low frequency in tumor-bearing mice in the absence of IL-1β-induced inflammation; however, under inflammatory conditions, Ly6C(neg) MDSC were predominant. Ly6C(neg) MDSC impaired NK cell development and functions in vitro and in vivo. These results identify a novel IL-1β-induced subset of MDSC with unique functional properties. Ly6C(neg) MDSC mediating NK cell suppression may thus represent useful targets for therapeutic interventions.

PMID:
21110318
PMCID:
PMC3373225
DOI:
10.1002/eji.201041037
[Indexed for MEDLINE]
Free PMC Article

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