Immune Netw.  2002 Dec;2(4):189-194. 10.4110/in.2002.2.4.189.

Psoriasis as a T-cell-mediated Immunologic Disease

Affiliations
  • 1Department of Dermatology and Cutaneous Biology Research Institute, Yonsei University College of Medicine, Seoul, Korea. wlewderm@yumc.yonsei.ac.kr

Abstract

Although the exact mechanism responsible for the pathogenesis of psoriasis is unclear, interferon-gamma producing type 1 T cells have been reported to play a significant role. Infiltrating activated type 1 T cells in the lesions are believed to be responsible for stimulating keratinocytes, which produce many cytokines and growth factors. The hyperproliferative epidermis is understood to be the result of either the cytokines produced by the intraepidermal T cells or the reactive phenomenon after keratinocyte damage. The microenvironment in psoriatic lesions deviates toward the type 1 status, because of the increased type 1 cytokines and either the decreased or unchanged type 2 cytokines observed in psoriatic lesions. Therefore, this review focused on a T-cell-mediated immunological basis for the current hypothesis of the psoriasis pathogenesis.

Keyword

Psoriasis; type 1 T cells; pathogenesis

MeSH Terms

Cytokines
Epidermis
Immune System Diseases*
Intercellular Signaling Peptides and Proteins
Interferon-gamma
Keratinocytes
Psoriasis*
T-Lymphocytes
Cytokines
Intercellular Signaling Peptides and Proteins
Interferon-gamma
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