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健康人皮肤和自身免疫性皮肤病中FOXP3 +调节性T细胞的免疫组织化学分析。

Immunohistochemical analysis of FOXP3+ regulatory T cells in healthy human skin and autoimmune dermatoses.

作者信息

Terras Sarah, Gambichler Thilo, Moritz Rose K C, Altmeyer Peter, Lambert Jo

机构信息

Department of Dermatology, Ghent University Hospital, Ghent, Belgium; Department of Dermatology, Ruhr-University Bochum, Bochum, Germany.

出版信息

Int J Dermatol. 2014 Mar;53(3):294-9. doi: 10.1111/j.1365-4632.2012.05808.x. Epub 2013 Aug 22.

DOI:10.1111/j.1365-4632.2012.05808.x
PMID:23968190
Abstract

BACKGROUND

Regulatory T cells (Tregs) play an important role in autoimmune diseases. In skin, the presence of Tregs is thought to be mandatory for suppression of autoreactive T cells. Here, we assess the number of Tregs in skin of healthy subjects and patients with an autoimmune dermatosis.

METHODS

Immunohistochemical stainings for CD3 and FOXP3 on skin biopsies of healthy subjects and subjects with psoriasis, vitiligo, pemphigus vulgaris, bullous pemphigoid, and halo nevus to assess the number of T and regulatory T cells, respectively.

RESULTS

Low numbers of CD3+ and FOXP3+ cells were seen in the skin of healthy controls (median = 0.5%). A significantly higher frequency of Tregs was seen in lesional skin of patients with psoriasis (median = 12.4%) and patients with bullous pemphigoid (median = 10.1%) as compared to controls. In vitiligo (median = 0.0%), pemphigus vulgaris (median = 5.2%), and halo nevi (median = 5.4%), no significant difference in number of FOXP3+ cells was observed when compared to controls.

CONCLUSIONS

As confirmed in the literature, few Tregs were seen in healthy skin. A high number of Tregs were present in lesional skin from patients with psoriasis and bullous pemphigoid. These results support the hypothesis that not a decrease in number but rather a decrease in function of Tregs would be at the basis of autoimmune skin diseases, which could result in unrestrained activation autoreactive T cells in skin of patients with autoimmune dermatoses.

摘要

背景

调节性T细胞(Tregs)在自身免疫性疾病中起重要作用。在皮肤中,Tregs的存在被认为是抑制自身反应性T细胞所必需的。在此,我们评估健康受试者和自身免疫性皮肤病患者皮肤中Tregs的数量。

方法

对健康受试者以及患有银屑病、白癜风、寻常型天疱疮、大疱性类天疱疮和晕痣的受试者的皮肤活检组织进行CD3和FOXP3免疫组织化学染色,分别评估T细胞和调节性T细胞的数量。

结果

在健康对照者的皮肤中可见少量CD3+和FOXP3+细胞(中位数=0.5%)。与对照组相比,银屑病患者(中位数=12.4%)和大疱性类天疱疮患者(中位数=10.1%)的皮损中Tregs频率显著更高。在白癜风(中位数=0.0%)、寻常型天疱疮(中位数=5.2%)和晕痣(中位数=5.4%)中,与对照组相比,FOXP3+细胞数量未观察到显著差异。

结论

正如文献所证实的,健康皮肤中Tregs数量很少。银屑病和大疱性类天疱疮患者的皮损中有大量Tregs。这些结果支持这样的假设,即自身免疫性皮肤病的基础不是Tregs数量的减少,而是其功能的降低,这可能导致自身免疫性皮肤病患者皮肤中自身反应性T细胞不受抑制的激活。

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