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J Clin Immunol. 2009 May;29(3):247-56. doi: 10.1007/s10875-009-9278-8. Epub 2009 Feb 28.

Cytokine-producing dendritic cells in the pathogenesis of inflammatory skin diseases.

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1
Laboratory for Investigative Dermatology, The Rockefeller University, 1230 York Ave., New York, NY 10065, USA.

Abstract

INTRODUCTION:

Inflammatory skin diseases can be examined from many viewpoints. In this review, we consider three distinct cutaneous inflammatory diseases from the point of view of their major lesional dendritic cell (DC) subpopulations. The DC populations considered are Langerhans cells, myeloid DCs, and plasmacytoid DCs (pDCs), with specific attention to the presence and role of the inflammatory counterparts of these cells. From such a "dendritic cell-centric" focus, psoriasis, atopic dermatitis (AD), and cutaneous lupus erythematosus (CLE) are explored.

DISCUSSION:

In psoriasis, there is a specific population of myeloid "inflammatory" DCs that appears to play an important pathogenic role, while pDCs have been recently implicated in the initiation of psoriatic lesions. In AD, Langerhans cells may be important during initiation, while "inflammatory dendritic epidermal cells" (IDECs) appear to be abundant in lesional epidermis and dermis and contribute to maintenance of AD. These IDECs may actually be analogous to the myeloid inflammatory DCs found in the epidermal and dermal compartments of the skin in psoriasis, although they express distinct surface markers and induce different T cell polarities as a result of different cytokine milieu in which they develop. CLE has been recently characterized as a type I IFN-mediated disease, and pDCs are integral to the pathogenesis of this disease.

CONCLUSION:

Thus, these DC subpopulations and their products will be reviewed in the context of these three cutaneous diseases to provide clinico-pathophysiological correlations between the lesional DCs, their products, and the skin diseases.

PMID:
19252974
PMCID:
PMC2874976
DOI:
10.1007/s10875-009-9278-8
[Indexed for MEDLINE]
Free PMC Article
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