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Fox-P3-positive regulatory T cells are present in the skin of generalized atopic eczema patients and are not particularly affected by medium-dose UVA1 therapy
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作者:

Schnopp, Christina
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机构: Tech Univ Munich, Klin & Poliklin Dermatol & Allergol, D-80802 Munich, Germany

Rad, Roland
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机构: Tech Univ Munich, Klin & Poliklin Dermatol & Allergol, D-80802 Munich, Germany

Weidinger, Anke
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机构: Tech Univ Munich, Klin & Poliklin Dermatol & Allergol, D-80802 Munich, Germany

Weidinger, Stefan
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机构: Tech Univ Munich, Klin & Poliklin Dermatol & Allergol, D-80802 Munich, Germany

Ring, Johannes
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机构: Tech Univ Munich, Klin & Poliklin Dermatol & Allergol, D-80802 Munich, Germany

Eberlein, Bernadette
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机构: Tech Univ Munich, Klin & Poliklin Dermatol & Allergol, D-80802 Munich, Germany

Ollert, Markus
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机构: Tech Univ Munich, Klin & Poliklin Dermatol & Allergol, D-80802 Munich, Germany

Mempel, Martin
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机构: Tech Univ Munich, Klin & Poliklin Dermatol & Allergol, D-80802 Munich, Germany
机构:
[1] Tech Univ Munich, Klin & Poliklin Dermatol & Allergol, D-80802 Munich, Germany
[2] Tech Univ Munich, Dept Gastroenterol, D-80802 Munich, Germany
[3] Tech Univ Munich, Div Environm Dermatol & Allergy, GSF, Natl Res Ctr Environm & Hlth, D-80802 Munich, Germany
[4] Tech Univ Munich, Clin Res Div Mol & Clin Allergotoxicol, D-80802 Munich, Germany
关键词:
D O I:
10.1111/j.1600-0781.2007.00284.x
中图分类号:
R75 [皮肤病学与性病学];
学科分类号:
100206 ;
摘要:
Background. Regulatory T cells (T-reg cells) have been described as an important cell population in the UV treatment of inflammatory skin diseases. Methods: We have treated five patients with generalized atopic eczema (AE) using medium-dose (15 cycles of 50 J/cm(2), total dose of 750 j/cm(2)) UVA1 therapy and have analyzed the skin-infiltrating T-cellular subsets before and after therapy. Skin biopsies were split for immunohistochemistry and Real-time PCR and analyzed for CD4, Fox-P3, GATA-3, and IL-10 transcription as well as for CD3, CD4, CD152, Fox-P3, and GITR staining. Results: In all the investigated patients, we observed a good clinical response to UVA1. As described previously, the number of epidermal T cells slightly declined after irradiation. However, we did not observe a general decrease in T cell numbers. Within the population of T cells, no specific difference in the kinetics of Fox-P3-positive cells and Fox-P3-specific mRNA was noted as compared with GATA-3 positive T cells. These results were paralleled by RT-PCR for IL-10 and staining for CD152, a surface molecule that has been described for T-reg cells. Conclusion: In our hands, the clinical benefit of UVA1 treatment in AE patients does not seem to be due to a preferential survival/proliferation of T-reg cells.
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页码:81 / 85
页数:5
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