T Cells and T Cell-Derived Cytokines as Pathogenic Factors in the Nonallergic Form of Atopic Dermatitis  Cezmi A. Akdis, Mübeccel Akdis, Dagmar Simon,

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T Cells and T Cell-Derived Cytokines as Pathogenic Factors in the Nonallergic Form of Atopic Dermatitis  Cezmi A. Akdis, Mübeccel Akdis, Dagmar Simon, Birgit Dibbert, Martina Weber, Stephanie Gratzl, Oliver Kreyden, Rainer Disch, Brunello Wüthrich, Kurt Blaser, Hans-Uwe Simon  Journal of Investigative Dermatology  Volume 113, Issue 4, Pages 628-634 (October 1999) DOI: 10.1046/j.1523-1747.1999.00720.x Copyright © 1999 The Society for Investigative Dermatology, Inc Terms and Conditions

Figure 1 Inflammatory cells in lesional skin of AD and NAD patients. The majority of the cells represented CD4+ and CD8+ T cells. Many of the T cells were CLA+. The eosinophil infiltration was much less in comparison with the T cell infiltration. No differences were observed between AD and NAD patients. Data are shown in Table 2. Journal of Investigative Dermatology 1999 113, 628-634DOI: (10.1046/j.1523-1747.1999.00720.x) Copyright © 1999 The Society for Investigative Dermatology, Inc Terms and Conditions

Figure 2 IL-13, but not IL-4, is expressed in lesional skin of AD and NAD patients. The positive control for IL-4 was a bladder cancer tissue expressing IL-4. In average, the expression of IL-13 was less in NAD in comparison with AD patients. All data regarding cytokine expression are shown in Table 2. Journal of Investigative Dermatology 1999 113, 628-634DOI: (10.1046/j.1523-1747.1999.00720.x) Copyright © 1999 The Society for Investigative Dermatology, Inc Terms and Conditions

Figure 3 Intracytoplasmic cytokine content of CD4+ and CD8+ skin T cells following stimulation with anti-CD2, anti-CD3, and anti-CD28 MoAb for 16 h. The results are representative of four independent experiments in each group of patients. The skin T cells of AD patients expressed much more IL-5 and IL-13 compared with NAD patients. IL-4 expressing cells were ≤ 3% in both AD and NAD patients. The expression of IFN-γ was lower in AD in comparison with NAD patients. Journal of Investigative Dermatology 1999 113, 628-634DOI: (10.1046/j.1523-1747.1999.00720.x) Copyright © 1999 The Society for Investigative Dermatology, Inc Terms and Conditions

Figure 4 Superantigen response and cytokine profile of skin T cells in AD and NAD. There was no difference in SEB induced proliferation between skin T cells of AD and NAD patients. IL-5 and IL-13 production following stimulation with anti-CD2, anti-CD3, and anti-CD28 MoAb for 72 h of the skin T cells from AD patients was significantly high compared with NAD patients. The levels of released IFN-γ and IL-4 were low, and no differences were observed between AD and NAD patients. The data are presented as mean ± SD of four independent experiments in each patient group (*p < 0.05). Journal of Investigative Dermatology 1999 113, 628-634DOI: (10.1046/j.1523-1747.1999.00720.x) Copyright © 1999 The Society for Investigative Dermatology, Inc Terms and Conditions

Figure 5 Skin T cells from both AD and NAD patients induce IgE production in T cell-depleted PBMC populations (T Depl. PBMC). Only the skin T cells from AD patients helped B cells to produce very high amounts of IgE. The induced IgE production by T cells from AD patients could be blocked with neutralizing anti-IL-13 MoAb and recombinant IL-4/IL-13 antagonist (Y124D), suggesting that IL-13 may play an important part in the induction of IgE synthesis. Results represent means of triplicate cultures ± SD from four independent experiments in each patient group (*p < 0.05). Journal of Investigative Dermatology 1999 113, 628-634DOI: (10.1046/j.1523-1747.1999.00720.x) Copyright © 1999 The Society for Investigative Dermatology, Inc Terms and Conditions