Skin-Infiltrating CD8 super(+) T Cells Initiate Atopic Dermatitis Lesions

Skin lesions in the allergic form of atopic dermatitis (AD) are induced by allergen-specific T cells that infiltrate the skin at the site of allergen exposure. Although Th2-type CD4 super(+) T cells appear to be crucial in AD pathophysiology, little is known about the contribution of CD8 super(+) T cells in the development of the allergic skin inflammation. In the present study, we have analyzed the respective role of CD8 super(+) and CD4 super(+) T cells in the development of AD skin lesions in a mouse model of allergen-induced AD. In sensitized mice, CD8 super(+) T cells are rapidly and transiently recruited to the allergen-exposed site and initiate the inflammatory process leading to skin infiltration with eosinophils and Th1/Th2-producing cells. CD8 super(+) T cell-depleted mice show no inflammation, demonstrating that these cells are mandatory for the development of AD. In contrast, CD4 super(+) T cell-depleted mice develop a severe form of eczema. Furthermore, adoptive transfer of CD8 super(+) T cells from sensitized mice into naive recipient mice leads to skin inflammation soon after allergen exposure. These data indicate that allergen-primed CD8 super(+) T cells are required for the development of AD-like lesions in mice.