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Curr Rheumatol Rep. 2007 Dec;9(6):461-7.

Pathophysiology of psoriasis: recent advances on IL-23 and Th17 cytokines.

Author information

1
Dermatology Service, Veterans Affairs Medical Center, 3710 Southwest US Veterans Hospital Road, Mail Code R&D 55, Portland, OR 97239, USA.

Abstract

T helper (Th) 17 cells, a novel T-cell subset, have been implicated in the pathogenesis of psoriasis and other autoimmune inflammatory diseases. Interleukin (IL)-23 stimulates survival and proliferation of Th17 cells, and thus serves as a key master cytokine regulator for these diseases. In psoriasis, IL-23 is overproduced by dendritic cells and keratinocytes, and this cytokine stimulates Th17 cells within dermis to make IL-17A and IL-22. IL-22, in particular, drives keratinocyte hyperproliferation in psoriasis. Future targeting of these key cytokines is likely to lead to dramatic clinical improvement in patients with psoriasis. This review focuses on the numerous recent studies on the roles of IL-23 and Th17 cells in the pathogenesis of psoriasis.

PMID:
18177599
PMCID:
PMC2893221
[Indexed for MEDLINE]
Free PMC Article

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