Epidermal Langerhans cells in actinic prurigo: a comparison between lesional and non-lesional skin

Actinic Prurigo (AP) is a chronic pruritic dermatosis of unknown cause affecting sun exposed skin in defined ethnic groups with characteristic MHC alleles. However, the cutaneous dendritic cells have not been assessed. To assess in situ the epidermal Langerhans Cell (LC) status in Actinic Prurigo. F...

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Published in:Journal of the European Academy of Dermatology and Venereology Vol. 23; no. 4; pp. 438 - 440
Main Authors: Calderón-Amador, J, Flores-Langarica, A, Silva-Sánchez, A, Donis-Maturano, L, Granados, J, Vega-Memije, E, Lacy-Niebla, RM, Hojyo-Tomoka, T, Dominguez-Soto, L, Flores-Romo, L
Format: Journal Article
Language:English
Published: Oxford, UK Blackwell Publishing Ltd 01-04-2009
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Summary:Actinic Prurigo (AP) is a chronic pruritic dermatosis of unknown cause affecting sun exposed skin in defined ethnic groups with characteristic MHC alleles. However, the cutaneous dendritic cells have not been assessed. To assess in situ the epidermal Langerhans Cell (LC) status in Actinic Prurigo. Fresh skin samples from three AP patients were used to evaluate in situ the epidermal LC, comparing lesional and non-lesional sites in each subject. AP patients attending the Dermatology Department at the Hospital M. Gea-Gonzalez in Mexico city. Lesional and non-lesional skin samples were taken from each subject to prepare both epidermal sheets and conventional tissue sections. Three markers restricted to LC in epidermis (CD1a, ATPase, MHC-II) were used to quantify the LC per area in epidermal sheets. Compared to non-lesional skin from the same subject, a significant reduction in the number of LC per area of epidermis was found in lesional skin; with any of the three markers evaluated. The frequency of epidermal LC decreases importantly in lesional skin from AP patients.
Bibliography:istex:36E1043BFEAC5ACE9FDCECB510AE99DA01A70CDA
ark:/67375/WNG-3R4V3MDH-4
ArticleID:JDV3060
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0926-9959
1468-3083
DOI:10.1111/j.1468-3083.2008.03060.x