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外用皮质类固醇疗法对人皮肤中朗格汉斯细胞抗原呈递功能的影响。

Effects of topical corticosteroid therapy on Langerhans cell antigen presenting function in human skin.

作者信息

Ashworth J, Booker J, Breathnach S M

机构信息

Department of Medicine (Dermatology), Charing Cross and Westminster Medical School, London, U.K.

出版信息

Br J Dermatol. 1988 Apr;118(4):457-69. doi: 10.1111/j.1365-2133.1988.tb02453.x.

Abstract

We have investigated the mechanisms by which topical corticosteroids modulate cutaneous immune reactions in man. Volunteers applied clobetasone butyrate 0.05% (Eumovate; EV), betamethasone valerate 0.1% (Betnovate; BV), clobetasol propionate 0.05% (Dermovate; DV), and control vehicles twice daily to forearm skin for 7 days. Steroid therapy significantly decreased the number of HLA-DR/T6 (CD1a) positive Langerhans cells (LCs) per mm2 in suction blister-derived epidermal sheets, expressed as a mean percentage of controls, as follows: EV 69.2%; BV 67.3%; DV 37.8%. LC antigen presenting capacity was determined in the allogeneic and autologous epidermal cell-lymphocyte reactions. The LC-dependent allostimulatory capacity of epidermal cells, expressed as a mean percentage of controls, was also significantly reduced by steroid therapy: EV 45.1%; BV 41.9%; DV 23.4%. Following therapy with clobetasol propionate 0.05%, the capacity of epidermal cells to present tetanus toxoid to, and to augment concanavalin A mediated lymphocyte stimulation of, autologous lymphocytes was reduced to 33.6% and 19.7% respectively of controls. Depression of epidermal cell allostimulatory capacity was not the result of a steroid-induced decrease in the production of epidermal cell-derived thymocyte activating factor (ETAF)/interleukin 1 by keratinocytes, since it could not be reversed by addition of exogenous interleukin 1. Indomethacin, added to block any potential prostaglandin synthesis during the culture period, did not restore the allostimulatory capacity of epidermal cells from steroid-treated sites. Addition of epidermal cells from DV-treated sites depressed the capacity of control epidermal cells to stimulate lymphocytes in the allogeneic epidermal-lymphocyte reaction. Our results demonstrate that the anti-inflammatory action of topical corticosteroids in man is associated not only with a reduction in the number of HLA-DR/T6 positive LCs, but also with a marked decrease in Langerhans cell-dependent T lymphocyte activation. The effects of the different steroids on both of these parameters correlated with their potency as determined in the standard occlusive vasoconstrictor assay. Topical corticosteroids are widely used for the treatment of inflammatory skin disorders, and inhibit not only the elicitation phase, but also the induction phase, of allergic contact dermatitis reactions.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

我们研究了外用皮质类固醇调节人体皮肤免疫反应的机制。志愿者每天两次将0.05%丁酸氯倍他松(优力肤;EV)、0.1%戊酸倍他米松(倍他米松戊酸酯;BV)、0.05%丙酸氯倍他索(得肤宝;DV)以及对照赋形剂涂抹于前臂皮肤,持续7天。类固醇治疗显著降低了每平方毫米吸疱来源的表皮片中HLA - DR/T6(CD1a)阳性朗格汉斯细胞(LCs)的数量,以相对于对照的平均百分比表示如下:EV为69.2%;BV为67.3%;DV为37.8%。在同种异体和自体表皮细胞 - 淋巴细胞反应中测定了LC的抗原呈递能力。表皮细胞依赖LC的同种异体刺激能力,以相对于对照的平均百分比表示,也因类固醇治疗而显著降低:EV为45.1%;BV为41.9%;DV为23.4%。在用0.05%丙酸氯倍他索治疗后,表皮细胞将破伤风类毒素呈递给自体淋巴细胞以及增强刀豆球蛋白A介导的淋巴细胞刺激的能力分别降至对照的33.6%和19.7%。表皮细胞同种异体刺激能力的降低并非类固醇诱导角质形成细胞产生表皮细胞衍生的胸腺细胞活化因子(ETAF)/白细胞介素1减少的结果,因为添加外源性白细胞介素1无法逆转这种降低。在培养期间添加吲哚美辛以阻断任何潜在的前列腺素合成,并未恢复来自类固醇治疗部位的表皮细胞的同种异体刺激能力。添加来自DV治疗部位的表皮细胞会降低对照表皮细胞在同种异体表皮 - 淋巴细胞反应中刺激淋巴细胞的能力。我们的结果表明,外用皮质类固醇在人体中的抗炎作用不仅与HLA - DR/T6阳性LCs数量的减少有关,还与朗格汉斯细胞依赖的T淋巴细胞活化的显著降低有关。不同类固醇对这两个参数的影响与其在标准封闭性血管收缩试验中测定的效力相关。外用皮质类固醇广泛用于治疗炎症性皮肤病,并且不仅抑制过敏性接触性皮炎反应的激发阶段,还抑制其诱导阶段。(摘要截短至400字)

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