The expression of genes encoding for Th1, Th2 and Th17
cytokines has been extensively evaluated in differentiated skin cells of psoriatic patients. The microenvironment exerts a control on the phenotype of resident mesenchymal stem cells (MSCs) into the skin of
psoriasis patients. Aim of the study was to extensively evaluate the relative expression of 43 genes encoding for Th1, Th2 and Th17
cytokines in MSCs isolated from skin of
psoriasis patients. MSCs resident into psoriatic skin were isolated, characterized and profiled by PCR array for the relative expression of genes encoding for
cytokines involved in Th1, Th2 and Th17 pathways. MSCs isolated from the skin of healthy subjects were used as control. The MSCs isolated from skin of
psoriasis patients showed a greater relative expression of the most part of the analyzed genes encoding for Th1 and Th17
cytokines: INF-γ, CCR5, CXCL9, CXCL10,
IL6,
IL8, TNF-α, IL23A, CCL2, CCL20, CXCL2, CXCL5, IL17C, IL17F, IL17RA,
IL21, TLR2 than healthy subjects. On the contrary, the relative expression of genes encoding for Th2
cytokines: CCL1, CCL22, CXCL12,
IL2, IL3,
IL4, IL13B, IL 22, IL 27, TGF-β1, was similar between the MSCs isolated from
psoriasis and healthy subjects. In conclusion, the MSCs isolated from
psoriasis show an imbalance between the Th1-Th17 and Th2 pathways, which reflects the well-known abnormal balance observed in differentiated skin cells. This evidence could strengthen the hypothesis of an early involvement of resident MSCs in the pathogenesis of
psoriasis.