TY - JOUR
T1 - Malignant cutaneous T-cell lymphoma cells express IL-17 utilizing the Jak3/Stat3 signaling pathway
AU - Krejsgaard, Thorbjørn Frej
AU - Ralfkiaer, Ulrik
AU - Clasen-Linde, Erik
AU - Eriksen, Karsten Wessel Kam
AU - Kopp, Katharina Luise Maria
AU - Bonefeld, Charlotte Menné
AU - Geisler, Carsten
AU - Dabelsteen, Sally Anne Malene
AU - Wasik, Mariusz A
AU - Ralfkiaer, Elisabeth
AU - Woetmann, Anders
AU - Odum, Niels
PY - 2011
Y1 - 2011
N2 - 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.
AB - 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.
KW - Cell Line, Tumor
KW - Humans
KW - Interleukin-17
KW - Janus Kinase 3
KW - Lymphoma, T-Cell, Cutaneous
KW - STAT3 Transcription Factor
KW - Signal Transduction
KW - Skin Neoplasms
KW - T-Lymphocytes
UR - https://www.scopus.com/pages/publications/79956003644
U2 - 10.1038/jid.2011.27
DO - 10.1038/jid.2011.27
M3 - Journal article
C2 - 21346774
SN - 0022-202X
VL - 131
SP - 1331
EP - 1338
JO - Journal of Investigative Dermatology
JF - Journal of Investigative Dermatology
IS - 6
ER -