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他卡西醇长期治疗对银屑病表皮的影响。流式细胞术分析。

The effect of long-term treatment with tacalcitol on the psoriatic epidermis. A flow cytometric analysis.

作者信息

Mommers J M, Castelijns F A, Seegers B A, Van Rossum M M, Van Hooijdonk C A, Van Erp P E, Van De Kerkhof P C

机构信息

Department of Dermatology, University Hospital Nijmegen, PO Box 9101, 6500 HB Nijmegen, The Netherlands.

出版信息

Br J Dermatol. 1998 Sep;139(3):468-71. doi: 10.1046/j.1365-2133.1998.02411.x.

Abstract

During the last decade, novel analogues of 1alpha,25-dihydroxy vitamin D3 have been developed for the treatment of psoriasis. Recently, the efficacy of short-term treatment with the novel derivative tacalcitol (1alpha,24-dihydroxy vitamin D3) has been documented. However, data on the long-term effect of tacalcitol on psoriatic skin are sparse. In this study, we assessed the cell characteristics of the psoriatic epidermis after treatment with tacalcitol for up to 24 weeks. We investigated how long-term treatment with tacalcitol modulates the percentages of differentiated keratinocytes, inflammation cells and basal keratinocytes, and the percentage of cells in the SG2M phase in the basal cell population. From 11 patients who were treated with tacalcitol for up to 18 months, we obtained single-cell suspensions of a representative psoriatic lesion after 0, 8, 12, 18 and 24 weeks of treatment. A Psoriasis Area and Severity Index was performed at each visit as well. Cell suspensions were stained with markers for inflammation (Vim3B4), differentiation (RKSE60) and proliferation (TO-PRO-3 iodide) and analysed flow cytometrically. Clinically, patients improved significantly after 8 weeks of treatment. This clinical effect was preserved for the rest of the period of treatment with no further significant improvement. Proliferative activity also decreased significantly after 8 weeks of treatment. Proliferation did not show further significant decreases or habituation after 12, 18 and 24 weeks. For inflammation, no statistically reliable trends could be seen. Differentiation improved significantly after 8 weeks of treatment, but decreased again significantly after 12 weeks. In the period from 12 to 24 weeks, no further significant change was observed. We conclude that tacalcitol is an effective antipsoriatic drug. Prolonged treatment with tacalcitol will generally maintain improvement at the level reached after 8 weeks. Owing to the beneficial effect on both clinical state and proliferation, tacalcitol is likely to be an adequate maintenance therapy.

摘要

在过去十年中,已开发出1α,25 - 二羟基维生素D3的新型类似物用于治疗银屑病。最近,新型衍生物他卡西醇(1α,24 - 二羟基维生素D3)短期治疗的疗效已有文献记载。然而,关于他卡西醇对银屑病皮肤长期影响的数据却很少。在本研究中,我们评估了他卡西醇治疗长达24周后银屑病表皮的细胞特征。我们研究了他卡西醇长期治疗如何调节分化角质形成细胞、炎症细胞和基底角质形成细胞的百分比,以及基底细胞群中处于SG2M期的细胞百分比。从11例接受他卡西醇治疗长达18个月的患者中,我们在治疗0、8、12、18和24周后获得了代表性银屑病皮损的单细胞悬液。每次就诊时还进行了银屑病面积和严重程度指数评估。细胞悬液用炎症标志物(Vim3B4)、分化标志物(RKSE60)和增殖标志物(碘化丙锭)染色,并进行流式细胞术分析。临床上,患者在治疗8周后有显著改善。这种临床效果在治疗的剩余时间内得以维持,没有进一步的显著改善。治疗8周后增殖活性也显著降低。在12、18和24周后,增殖没有进一步显著下降或出现适应性变化。对于炎症,未观察到统计学上可靠的趋势。治疗8周后分化显著改善,但在12周后再次显著下降。在12至24周期间,未观察到进一步的显著变化。我们得出结论,他卡西醇是一种有效的抗银屑病药物。他卡西醇的长期治疗通常会将改善维持在8周后达到的水平。由于对临床状态和增殖均有有益作用,他卡西醇可能是一种合适的维持治疗药物。

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