Malignant Cutaneous T-Cell Lymphoma Cells Express IL-17 Utilizing the Jak3/Stat3 Signaling Pathway

被引:93
作者
Krejsgaard, Thorbjorn [1 ,2 ]
Ralfkiaer, Ulrik [3 ]
Clasen-Linde, Erik [3 ]
Eriksen, Karsten W. [1 ]
Kopp, Katharina L. [1 ,2 ]
Bonefeld, Charlotte M. [1 ]
Geisler, Carsten [1 ]
Dabelsteen, Sally [4 ]
Wasik, Mariusz A. [5 ]
Ralfkiaer, Elisabeth [3 ]
Woetmann, Anders [1 ,2 ]
Odum, Niels [1 ,2 ]
机构
[1] Univ Copenhagen, Dept Int Hlth Immunol & Microbiol, DK-2200 Copenhagen N, Denmark
[2] Univ Copenhagen, Dept Biol, DK-2200 Copenhagen N, Denmark
[3] Univ Copenhagen Hosp, Dept Pathol, DK-2100 Copenhagen, Denmark
[4] Univ Copenhagen, Sch Dent, Dept Oral Med Pathol & Anat, DK-2200 Copenhagen N, Denmark
[5] Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
关键词
MYCOSIS-FUNGOIDES; GROWTH-FACTOR; CYTOKINES; INTERLEUKIN-15; ACTIVATION; RECEPTOR; ANGIOGENESIS; LYMPHOCYTES; INDUCTION; PSORIASIS;
D O I
10.1038/jid.2011.27
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
IL-17 is a proinflammatory cytokine that is crucial for the host's protection against a range of extracellular pathogens. However, inappropriately regulated expression of IL-17 is associated with the development of inflammatory diseases and cancer. In cutaneous T-cell lymphoma (CTCL), malignant T cells gradually accumulate in skin lesions characterized by massive chronic inflammation, suggesting that IL-17 could be involved in the pathogenesis. In this study we show that IL-17 protein is present in 10 of 13 examined skin lesions but not in sera from 28 CTCL patients. Importantly, IL-17 expression is primarily observed in atypical lymphocytes with characteristic neoplastic cell morphology. In accordance, malignant T-cell lines from CTCL patients produce IL-17 and the synthesis is selectively increased by IL-2 receptor beta chain cytokines. Small-molecule inhibitors or small interfering RNA against Jak3 and signal transducer and activator of transcription 3 (Stat3) reduce the production of IL-17, showing that the Jak3/Stat3 pathway promotes the expression of the cytokine. In summary, our findings indicate that the malignant T cells in CTCL lesions express IL-17 and that this expression is promoted by the Jak3/Stat3 pathway.
引用
收藏
页码:1331 / 1338
页数:8
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