Abstract
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 β 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.
Original language | English |
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Journal | Journal of Investigative Dermatology |
Volume | 131 |
Issue number | 6 |
Pages (from-to) | 1331-8 |
Number of pages | 8 |
ISSN | 0022-202X |
DOIs | |
Publication status | Published - 2011 |
Keywords
- Cell Line, Tumor
- Humans
- Interleukin-17
- Janus Kinase 3
- Lymphoma, T-Cell, Cutaneous
- STAT3 Transcription Factor
- Signal Transduction
- Skin Neoplasms
- T-Lymphocytes