Dendritic Cell-Derived IL-32α: A Novel Inhibitory Cytokine of NK Cell Function

被引:20
|
作者
Gorvel, Laurent [1 ]
Korenfeld, Daniel [1 ]
Tung, Thomas [2 ]
Klechevsky, Eynav [1 ]
机构
[1] Washington Univ, Sch Med, Dept Pathol & Immunol, Div Immunobiol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Surg, Div Plast & Reconstruct Surg, St Louis, MO 63110 USA
来源
JOURNAL OF IMMUNOLOGY | 2017年 / 199卷 / 04期
关键词
NATURAL-KILLER-CELLS; CD8(+) T-CELLS; HUMAN LANGERHANS CELLS; INTERLEUKIN; 32; CUTTING EDGE; TNF-ALPHA; IL-32; IL-15; EXPRESSION; CANCER;
D O I
10.4049/jimmunol.1601477
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Cytokines produced by dendritic cells (DCs) can largely determine the direction of immunity. Transcriptional analysis revealed that besides IL-15, IL-32 was the only other cytokine expressed by human Langerhans cells. IL-32 is a human cytokine that exists in four main isoforms. Currently, little is known about the regulation and function of the various IL-32 isoforms. In this study, we found that IL-15 is a potent inducer of IL-32 alpha in DCs. Because IL-15 promotes NK cell activation, we investigated the interplay between IL-32 and IL-15 and their role in NK cell activity. We show that IL-32 alpha acts on NK cells to inhibit IL-15-mediated STAT5 phosphorylation and to suppress their IL-15-induced effector molecule expression and cytolytic capacity. IL-32 alpha also acted on DCs by downregulating IL-15-induced IL-18 production, an important cytokine in NK cell activity. Blocking IL-32 alpha during DC: NK cell coculture enhanced NK cell effector molecule expression as well as their cytolytic capacity. Taken together, our findings suggest a feedback inhibition of IL-15-mediated NK cell activity by IL-32 alpha.
引用
收藏
页码:1290 / 1300
页数:11
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