Nüsslein H G, Weber G, Kalden J R
Department of Internal Medicine III, University of Erlangen, Germany.
Allergy. 1994 May;49(5):365-70. doi: 10.1111/j.1398-9995.1994.tb02283.x.
Recently, hydrocortisone (HC) has been shown significantly to enhance interleukin-4 (IL-4)-induced in vitro IgE synthesis. For investigation of possible effects of synthetic corticosteroids but also of effects of other important human hormones, peripheral blood mononuclear cells (PBMC) were incubated with IL-4 and various concentrations of the hormones. IgE secreted in the supernatant was determined after a 14-d culture period. Like HC, all synthetic corticosteroids potentiated IgE secretion. A minor effect was noted for the mineralocorticoid aldosterone. No modulating effect on IL-4-induced IgE formation was observed for adrenocorticotropic hormone (ACTH), somatotropin (STH), thyroid-stimulating hormone (TSH), triiodothyronine, thyroxine, epinephrine, noradrenaline, insulin, and glucagon.
最近研究表明,氢化可的松(HC)能显著增强白细胞介素-4(IL-4)诱导的体外IgE合成。为研究合成皮质类固醇的可能作用以及其他重要人体激素的作用,将外周血单个核细胞(PBMC)与IL-4及不同浓度的激素一起孵育。培养14天后测定上清液中分泌的IgE。与HC一样,所有合成皮质类固醇均增强了IgE分泌。盐皮质激素醛固酮的作用较小。促肾上腺皮质激素(ACTH)、生长激素(STH)、促甲状腺激素(TSH)、三碘甲状腺原氨酸、甲状腺素、肾上腺素、去甲肾上腺素、胰岛素和胰高血糖素对IL-4诱导的IgE形成均无调节作用。