Department of Dermatology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, Shanxi Province, China.
Clin Immunol. 2010 Apr;135(1):108-17. doi: 10.1016/j.clim.2009.11.008. Epub 2009 Dec 16.
Both T-helper 17 cells (Th17) and CD4(+)CD25(+) regulatory T cells (Treg) play important roles in the pathogenesis of psoriasis. However, the relationship between Th17 and Treg cells and their dynamic variations in psoriasis remain unclear. In this study, we found that both Th17 and FoxP3(+) Treg cells were increased in psoriasis patients both in the peripheral circulation and skin tissue lesions and were positively correlated with disease severity. The ratio of Th17 to Treg cells in skin tissue lesions was inversely correlated with PASI scores, while it was positively correlated with PASI scores in the circulation. IL-17 secretion by CD4(+) T cells was not regulated by Treg cells, even though Treg cells exhibited significant inhibition on CD4(+) T cells proliferation and IFN-gamma production. These findings provide new information regarding the association between Th17 and Treg cells, which will further our understanding of the pathogenesis of psoriasis.
辅助性 T 细胞 17(Th17)和 CD4+CD25+调节性 T 细胞(Treg)均在银屑病的发病机制中发挥重要作用。然而,Th17 和 Treg 细胞之间的关系及其在银屑病中的动态变化尚不清楚。本研究发现,银屑病患者外周血循环和皮肤组织损伤中均存在 Th17 和 FoxP3+Treg 细胞增加,且与疾病严重程度呈正相关。皮肤组织损伤中 Th17 与 Treg 细胞的比例与 PASI 评分呈负相关,而在循环中与 PASI 评分呈正相关。Treg 细胞不能调节 CD4+T 细胞分泌 IL-17,尽管 Treg 细胞对 CD4+T 细胞增殖和 IFN-γ产生具有显著抑制作用。这些发现为 Th17 和 Treg 细胞之间的关联提供了新信息,将进一步加深我们对银屑病发病机制的理解。