“…38 Atherosclerosis is typically characterized by systemic inflammation, cytokine dysregulation, and invasion of inflammatory cells as well, contributing in the development of atherosclerotic plaques. 26 Furthermore, T helper 1 and 17, regulatory T cells and natural killer T cells have been implicated in the pathogenetic pathways of both diseases. [39][40][41] Among other inflammatory molecules, interleukins 2,6,7,8,12,15,17,18,20, and 23; tumor necrosis factor a; and interferon g participate in the expression of other chemokines and growth factors resulting in stimulation of inflammatory cells, endothelial dysfunction, and vascular smooth muscle proliferation that are all implicated in the pathophysiology of both psoriasis and atherosclerosis.…”