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In vitro induced CD8+ regulatory T cells inhibitskin inflammation

机译:体外诱导的CD8 +调节性T细胞抑制皮肤发炎

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摘要

CD8+ regulatory T cells appear impaired in number and/or function in some autoimmune diseases. However, the role of CD8+ regulatory T cells in the pathogenesis of skin inflammation and psoriasis remains unknown. In this study, we set out to analyze the capability of CD8+ regulatory T cells to inhibit skin inflammation in a murine model and to determine the frequency of CD8+ regulatory T cells in patients with psoriasis. We demonstrate that murine fully competent CD8+ regulatory T cells can be induced by stimulating naïve CD8+ T cells in the presence of TGF-β and retinoic acid (RA). Importantly, in vitro induced CD8+ regulatory T cells significantly suppressed skin inflammation in vivo. Furthermore, we found that the frequency of regulatory CD8+CD25+Foxp3+ T cells is decreased in peripheral blood but increased in lesional psoriatic skin of patients with psoriasis. Thus, our study suggests a previously unappreciated role of CD8+CD25+Foxp3+ T cells in skin disorders, and induction of these cells in vitro may be an effective immunotherapy for skin inflammation.
机译:在某些自身免疫性疾病中,CD8 + 调节性T细胞的数量和/或功能似乎受损。然而,CD8 + 调节性T细胞在皮肤炎症和牛皮癣发病机理中的作用仍然未知。在这项研究中,我们着手分析CD8 + 调节性T细胞在鼠模型中抑制皮肤炎症的能力,并确定CD8 + 调节性T细胞的频率在牛皮癣患者中。我们证明,在存在TGF-β和视黄酸(RA)的情况下,通过刺激幼稚的CD8 + T细胞可以诱导鼠完全有能力的CD8 + 调节性T细胞。重要的是,体外诱导的CD8 + 调节性T细胞在体内显着抑制皮肤炎症。此外,我们发现调节性CD8 + CD25 + Foxp3 + T细胞的频率在外周血中减少,而在皮损性牛皮癣皮肤中增加银屑病患者。因此,我们的研究表明,CD8 + CD25 + Foxp3 + T细胞在皮肤疾病中的作用是前所未有的,并且在体外诱导这些细胞可能是一种有效的皮肤炎症免疫疗法。

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