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皮肤肥大细胞减少是局部使用皮质类固醇所致。

Cutaneous mast cell depletion results from topical corticosteroid usage.

作者信息

Lavker R M, Schechter N M

出版信息

J Immunol. 1985 Oct;135(4):2368-73.

PMID:4031494
Abstract

The effect of long-term topical application of corticosteroids on human cutaneous mast cells was examined. Two potent corticosteroids, clobetasol-17-propionate and fluocinonide, produced a greater than 85% decrease in histamine content over a 6-wk treatment period, whereas betamethasone valerate, a less potent corticosteroid, produced a 66% decrease. Electron microscopic examination of the biopsies taken from sites after 6 wk of treatment indicate that the reduced levels of histamine were caused by the depletion of mast cells, as evidenced by: the inability to identify any cells representative of mast cells by detailed electron microscopy of the biopsies; and the marked acellularity around the vasculature where mast cells are certain to be detected. Histamine levels did not begin to decline until after 3 wk of corticosteroid treatment, indicating that corticosteroids are not immediately harmful to mast cells. Electron microscopic examination of biopsies taken at the beginning of treatment and 1 wk later showed normal-appearing mast cells, whereas at 3 wk, a small population of mast cells was detected with features usually associated with degenerating or dying cells. These observations suggest that protracted application of corticosteroids to skin is toxic to mast cells. After discontinuation of treatment, the drug-related atrophy associated with chronic application of potent corticosteroids to skin is rapidly reversed, and skin structure returns to near normal by 14 days. Over this time period, however, histamine levels did not increase and mature mast cells could not be observed by electron microscopy. At 14 days post-steroid treatment, the first signs of cells containing sparse amounts of granules having the characteristics of mast cell granules were seen. We interpret this to represent new mast cells beginning to mature in the skin. By 3 mo, histamine levels returned to normal, demonstrating the reversibility of the steroid-induced mast cell depletion. The studies presented here establish the deleterious effects of long-term topical corticosteroid treatment on cutaneous mast cells, and begin to establish a system in which the development of mast cells in tissue can be investigated.

摘要

研究了长期局部应用皮质类固醇对人皮肤肥大细胞的影响。两种强效皮质类固醇丙酸氯倍他索和氟轻松,在6周的治疗期内使组胺含量降低了85%以上,而效力较弱的皮质类固醇戊酸倍他米松使组胺含量降低了66%。对治疗6周后取材部位的活检组织进行电子显微镜检查表明,组胺水平降低是由于肥大细胞的耗竭所致,证据如下:通过对活检组织进行详细的电子显微镜检查无法识别任何代表肥大细胞的细胞;以及在血管周围明显无细胞,而在该部位肯定能检测到肥大细胞。直到皮质类固醇治疗3周后组胺水平才开始下降,这表明皮质类固醇不会立即对肥大细胞产生有害影响。对治疗开始时和1周后取材的活检组织进行电子显微镜检查显示肥大细胞外观正常,而在3周时,检测到一小部分具有通常与退化或濒死细胞相关特征的肥大细胞。这些观察结果表明,长期将皮质类固醇应用于皮肤对肥大细胞有毒性。停止治疗后,与长期将强效皮质类固醇应用于皮肤相关的药物性萎缩迅速逆转,皮肤结构在14天时恢复到接近正常。然而,在此期间,组胺水平并未升高,通过电子显微镜也未观察到成熟的肥大细胞。在类固醇治疗后14天,首次看到含有少量具有肥大细胞颗粒特征颗粒的细胞迹象。我们认为这代表新的肥大细胞开始在皮肤中成熟。到3个月时,组胺水平恢复正常,表明类固醇诱导的肥大细胞耗竭具有可逆性。本文介绍的研究确定了长期局部应用皮质类固醇治疗对皮肤肥大细胞的有害影响,并开始建立一个可以研究组织中肥大细胞发育的系统。

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