Wingett D, Forcier K, Nielson C P
Immunopharmacology Research, Veterans Affairs Medical Center, Boise, ID 83702, USA.
FEBS Lett. 1996 Dec 2;398(2-3):308-11. doi: 10.1016/s0014-5793(96)01238-0.
The chemokine RANTES has been implicated in the pathogenesis of allergic inflammatory diseases including asthma and rhinitis which are frequently treated with glucocorticoids. We observed that dexamethasone dramatically inhibited RANTES mRNA expression dose dependently in anti-CD3 activated Hut-78 T cells and human PBMCs. Inhibition of RANTES expression did not appear to be secondary to IL-2 inhibition and required binding to the intracellular glucocorticoid receptor. The down-regulation of RANTES expression by glucocorticoids in T cells may directly contribute to the efficacy of these agents in suppressing cellular infiltration and to their anti-inflammatory properties.
趋化因子RANTES与包括哮喘和鼻炎在内的过敏性炎症性疾病的发病机制有关,这些疾病常用糖皮质激素治疗。我们观察到,地塞米松在抗CD3激活的Hut-78 T细胞和人外周血单核细胞中剂量依赖性地显著抑制RANTES mRNA表达。RANTES表达的抑制似乎不是IL-2抑制的继发结果,且需要与细胞内糖皮质激素受体结合。糖皮质激素在T细胞中对RANTES表达的下调可能直接有助于这些药物在抑制细胞浸润方面的疗效及其抗炎特性。