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糖皮质激素抑制粒细胞-巨噬细胞集落刺激因子-1和白细胞介素-5增强人嗜酸性粒细胞的体外存活。

Glucocorticoids inhibit granulocyte-macrophage colony-stimulating factor-1 and interleukin-5 enhanced in vitro survival of human eosinophils.

作者信息

Hallsworth M P, Litchfield T M, Lee T H

机构信息

Department of Allergy and Allied Respiratory Disorders, U.M.D.S., Guy's Hospital, London, U.K.

出版信息

Immunology. 1992 Feb;75(2):382-5.

Abstract

The effects of three corticosteroids, hydrocortisone, dexamethasone and methylprednisolone, on eosinophil survival enhanced by recombinant human granulocyte-macrophage colony-stimulating factor (rhGM-CSF) and recombinant murine interleukin-5 (rmIL-5) have been studied. Eosinophils were incubated at a concentration of 5 x 10(5) cells/ml in the presence of different concentrations of the three steroids with either rhGM-CSF (1 ng/ml) or rmIL-5 (50 U/ml). The eosinophils were cultured in the presence of the same concentrations of rhGM-CSF and rmIL-5 alone as a positive control and medium alone as a negative control. Viability was assessed after 7 days by trypan blue exclusion. All three steroids inhibited rhGM-CSF-enhanced eosinophil survival in a dose-dependent manner; the dose of these drugs producing 50% inhibition (IC50) was greater than 1.0 x 10(-4) M, 6.5 x 10(-6) M and 1.8 x 10(-6) M for hydrocortisone, dexamethasone and methylprednisolone, respectively. When eosinophils were cultured with the same concentration of rhGM-CSF in the presence of two non-glucocorticoids, beta-oestradiol and testosterone, neither of these steroids inhibited eosinophil survival over the concentration range 1 x 10(-10) M to 1 x 10(-4) M (n = 5). Dexamethasone and methylprednisolone, but not hydrocortisone, also inhibited eosinophil survival induced by rmIL-5 in a dose-dependent manner. These results suggest one mechanism for the efficacy of corticosteroids against eosinophil-related disorders.

摘要

研究了三种皮质类固醇激素氢化可的松、地塞米松和甲泼尼龙对由重组人粒细胞巨噬细胞集落刺激因子(rhGM-CSF)和重组鼠白细胞介素-5(rmIL-5)增强的嗜酸性粒细胞存活的影响。嗜酸性粒细胞在浓度为5×10⁵个细胞/ml的条件下培养,同时存在不同浓度的这三种类固醇激素,以及rhGM-CSF(1 ng/ml)或rmIL-5(50 U/ml)。嗜酸性粒细胞在单独存在相同浓度的rhGM-CSF和rmIL-5时作为阳性对照,单独的培养基作为阴性对照进行培养。7天后通过台盼蓝排斥法评估细胞活力。所有三种类固醇激素均以剂量依赖性方式抑制rhGM-CSF增强的嗜酸性粒细胞存活;产生50%抑制作用(IC50)的这些药物剂量,氢化可的松、地塞米松和甲泼尼龙分别大于1.0×10⁻⁴ M、6.5×10⁻⁶ M和1.8×10⁻⁶ M。当嗜酸性粒细胞在两种非糖皮质激素β-雌二醇和睾酮存在的情况下与相同浓度的rhGM-CSF一起培养时,在1×10⁻¹⁰ M至1×10⁻⁴ M的浓度范围内,这两种类固醇激素均未抑制嗜酸性粒细胞存活(n = 5)。地塞米松和甲泼尼龙,但不是氢化可的松,也以剂量依赖性方式抑制rmIL-5诱导的嗜酸性粒细胞存活。这些结果提示了皮质类固醇激素治疗嗜酸性粒细胞相关疾病疗效的一种机制。

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