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Comparison of expression of heat-shock protein 60, Toll-like receptors 2 and 4, and T-cell receptor gamma delta in plaque and guttate psoriasis

BackgroundPsoriasis is a chronic skin disease that appears to be autoimmune in nature. Recently, it is thought that microbial pathogens of skin can affect the pathogenesis of psoriasis by inducing autoimmunity. Heat-shock proteins (HSPs) are known to play an important role in immune and inflammatory...

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Bibliographic Details
Published in:Journal of cutaneous pathology 2007-12, Vol.34 (12), p.903-911
Main Authors: Seung, Na Reu, Park, Eun Joo, Kim, Chul Woo, Kim, Kwang Ho, Kim, Kwang Joong, Cho, Hee Jin, Park, Hye Rim
Format: Article
Language:English
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Summary:BackgroundPsoriasis is a chronic skin disease that appears to be autoimmune in nature. Recently, it is thought that microbial pathogens of skin can affect the pathogenesis of psoriasis by inducing autoimmunity. Heat-shock proteins (HSPs) are known to play an important role in immune and inflammatory responses of the skin including psoriasis. Recent studies have suggested that Toll-like receptors (TLR) 2, 4 and gamma delta T-cell receptors (TCR- gamma delta ) may recognize HSP60 as a ligand and consequently activate the immune system. MethodsThe biopsy specimens of 12 of guttate psoriasis, 12 of plaque psoriasis and five of normal skin were studied using immunohistochemical staining. The expressions of HSP60, TLR2 and TLR4 were evaluated using an immunostaining-intensity-distribution (IID) index and TCR- gamma delta positive cells were counted. ResultsThe expression of HSP60 was significantly higher in guttate and plaque psoriasis than in normal skin. The expression of TLR4 was higher in guttate psoriasis than in plaque psoriasis and normal skin. The expression of TCR- gamma delta was higher in guttate and plaque psoriasis than in normal skin, but there was no correlation found between the expression of HSP60 and TLRs 2 and 4, or between that of HSP60 and TCR- gamma delta . ConclusionsHSP60 may be related to the pathogenesis of both guttate and plaque psoriasis and TLR4 may be related to the pathogenesis of guttate psoriasis.
ISSN:0303-6987
1600-0560
DOI:10.1111/j.1600-0560.2007.00756.x