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DOI 10.1016/j.humimm.2014.12.008

Медицинская библиотека · Human immunology · 2014

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

Zhou Yan, Hou Weikun, Xu Ke, Han Dan, Jiang Congshan, Mou Kuanhou, Li Yue, Meng Liesu, Lu Shemin

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

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.

Для цитирования: Zhou Yan, Hou Weikun, Xu Ke, Han Dan, Jiang Congshan, Mou Kuanhou, Li Yue, Meng Liesu, Lu Shemin. The elevated expression of Th17-related cytokines and receptors is associated with skin lesion severity in early systemic sclerosis.. Human immunology. 2014. DOI: 10.1016/j.humimm.2014.12.008.

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