The elevated expression of Th17-related cytokines and receptors is associated with skin lesion severity in early systemic sclerosis

Abstract Objective The objective was to survey the expression and localization of Th17-related cytokines and their correlation with skin lesion severity in early systemic sclerosis (SSc). Methods The mRNA expression was detected by real-time quantitative polymerase chain reaction (RT-qPCR) from 21 S...

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Veröffentlicht in:Human immunology 2015-01, Vol.76 (1), p.22-29
Hauptverfasser: Zhou, Yan, Hou, Weikun, Xu, Ke, Han, Dan, Jiang, Congshan, Mou, Kuanhou, Li, Yue, Meng, Liesu, Lu, Shemin
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Sprache:eng
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Zusammenfassung:Abstract Objective The objective was to survey the expression and localization of Th17-related cytokines and their correlation with skin lesion severity in early systemic sclerosis (SSc). Methods The mRNA expression was detected by real-time quantitative polymerase chain reaction (RT-qPCR) from 21 SSc patients and 12 healthy controls (HC). The protein expression was examined by immunohistochemistry (IHC) and Western blotting. Results The RT-qPCR analysis showed a significantly higher expression of IL-17A, IL-21, IL-22, IL-26, IL-17RA, IL-21R, and IL-22R1 mRNA; consistently, the IHC analysis showed an over-expression of IL-17RA, IL-21R and IL-22R1 and the Western blotting analysis showed an over-expression of IL-17A, IL-21, IL-21R and IL-22R1 in early SSc skin lesions. The mRNA levels of IL-21 were higher in diffuse cutaneous than limited cutaneous SSc lesions. The mRNA expression of IL-26, IL-22, IL-22R1, mRNA and protein expression of IL-17A, IL-21, IL-21R were positively correlated with the modified Rodnan skin score of SSc. In addition, the mRNA levels of ICAM-1 were positively correlated with IL-17A/IL-17RA, and VEGFA and IL-4 were both positively correlated with IL-21/IL-21R, while TGF-β were moderately negatively correlated with IL-22/IL-22R1. Conclusions Th17 cytokines contribute to progression in early SSc skin lesions. IL-21/IL-21R could act as potential biomarkers presenting early SSc skin lesions severity.
ISSN:0198-8859
1879-1166
DOI:10.1016/j.humimm.2014.12.008