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Malignant Cutaneous T-Cell Lymphoma Cells Express IL-17 Utilizing the Jak3/Stat3 Signaling Pathway
被引:93
作者:

Krejsgaard, Thorbjorn
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Univ Copenhagen, Dept Int Hlth Immunol & Microbiol, DK-2200 Copenhagen N, Denmark
Univ Copenhagen, Dept Biol, DK-2200 Copenhagen N, Denmark Univ Copenhagen, Dept Int Hlth Immunol & Microbiol, DK-2200 Copenhagen N, Denmark

Ralfkiaer, Ulrik
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Univ Copenhagen Hosp, Dept Pathol, DK-2100 Copenhagen, Denmark Univ Copenhagen, Dept Int Hlth Immunol & Microbiol, DK-2200 Copenhagen N, Denmark

Clasen-Linde, Erik
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h-index: 0
机构:
Univ Copenhagen Hosp, Dept Pathol, DK-2100 Copenhagen, Denmark Univ Copenhagen, Dept Int Hlth Immunol & Microbiol, DK-2200 Copenhagen N, Denmark

Eriksen, Karsten W.
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机构:
Univ Copenhagen, Dept Int Hlth Immunol & Microbiol, DK-2200 Copenhagen N, Denmark Univ Copenhagen, Dept Int Hlth Immunol & Microbiol, DK-2200 Copenhagen N, Denmark

Kopp, Katharina L.
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h-index: 0
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Univ Copenhagen, Dept Int Hlth Immunol & Microbiol, DK-2200 Copenhagen N, Denmark
Univ Copenhagen, Dept Biol, DK-2200 Copenhagen N, Denmark Univ Copenhagen, Dept Int Hlth Immunol & Microbiol, DK-2200 Copenhagen N, Denmark

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Dabelsteen, Sally
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机构:
Univ Copenhagen, Sch Dent, Dept Oral Med Pathol & Anat, DK-2200 Copenhagen N, Denmark Univ Copenhagen, Dept Int Hlth Immunol & Microbiol, DK-2200 Copenhagen N, Denmark

Wasik, Mariusz A.
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Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA Univ Copenhagen, Dept Int Hlth Immunol & Microbiol, DK-2200 Copenhagen N, Denmark

Ralfkiaer, Elisabeth
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Univ Copenhagen Hosp, Dept Pathol, DK-2100 Copenhagen, Denmark Univ Copenhagen, Dept Int Hlth Immunol & Microbiol, DK-2200 Copenhagen N, Denmark

Woetmann, Anders
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h-index: 0
机构:
Univ Copenhagen, Dept Int Hlth Immunol & Microbiol, DK-2200 Copenhagen N, Denmark
Univ Copenhagen, Dept Biol, DK-2200 Copenhagen N, Denmark Univ Copenhagen, Dept Int Hlth Immunol & Microbiol, DK-2200 Copenhagen N, Denmark

Odum, Niels
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h-index: 0
机构:
Univ Copenhagen, Dept Int Hlth Immunol & Microbiol, DK-2200 Copenhagen N, Denmark
Univ Copenhagen, Dept Biol, DK-2200 Copenhagen N, Denmark Univ Copenhagen, Dept Int Hlth Immunol & Microbiol, DK-2200 Copenhagen N, Denmark
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.
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页码:1331 / 1338
页数:8
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