Division of Respiratory Disease and Tuberculosis, Department of Internal Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
J Allergy Clin Immunol. 2010 Oct;126(4):754-762.e1. doi: 10.1016/j.jaci.2010.08.005.
We have previously shown that inhaled corticosteroids activate indoleamine 2, 3-dioxygenase (IDO) activity through increased IL-10 secretion. Statins might enhance the anti-inflammatory effects of corticosteroids.
In a double-blind study we added simvastatin to patients with mild asthma receiving a low dose of inhaled budesonide and evaluated sputum eosinophil counts, IL-10 secretion, and IDO activity, as well as their putative signaling pathways.
After a 2-week run-in period without treatment, 50 asthmatic patients were treated with 200 μg of budesonide and randomly assigned to either 10 mg of simvastatin or matched placebo for 8 weeks. Inflammation was evaluated through eosinophil counts, secretory signaling molecules, and immunocytochemistry of macrophages in sputum.
Sputum eosinophil percentages were reduced significantly by the combined therapy with budesonide and simvastatin compared with budesonide alone (P = .02). Corticosteroids activated glucocorticoid-induced TNF receptor ligand, which induces activation of p52 through the noncanonical nuclear factor κB pathway, leading to the increased transcription and activation of IDO. Simvastatin enhanced corticosteroid-activated noncanonical nuclear factor κB-dependent induction of IDO by activating type I interferons and also enhanced the effect of corticosteroid on IL-10 release.
A statin enhances the anti-inflammatory effect of an inhaled corticosteroid in asthma, and this was mediated through the alteration of IDO activity in macrophages.
我们之前的研究表明,吸入性皮质类固醇通过增加白细胞介素 10(IL-10)的分泌来激活吲哚胺 2,3-双加氧酶(IDO)活性。他汀类药物可能会增强皮质类固醇的抗炎作用。
在一项双盲研究中,我们在接受低剂量吸入布地奈德治疗的轻度哮喘患者中添加辛伐他汀,并评估痰中嗜酸性粒细胞计数、IL-10 分泌和 IDO 活性及其潜在的信号通路。
在无治疗的 2 周导入期后,50 例哮喘患者接受 200μg 布地奈德治疗,并随机分为辛伐他汀 10mg 或匹配的安慰剂组,治疗 8 周。通过痰中嗜酸性粒细胞计数、分泌信号分子和巨噬细胞免疫细胞化学评估炎症。
与单独使用布地奈德相比,布地奈德和辛伐他汀联合治疗可显著降低痰中嗜酸性粒细胞百分比(P=0.02)。皮质类固醇激活糖皮质激素诱导的肿瘤坏死因子受体配体,通过非经典核因子 κB 途径诱导 p52 的激活,从而增加 IDO 的转录和激活。辛伐他汀通过激活 I 型干扰素增强了皮质类固醇对非经典核因子 κB 依赖性 IDO 诱导的激活,并增强了皮质类固醇对 IL-10 释放的作用。
他汀类药物增强了哮喘患者吸入性皮质类固醇的抗炎作用,这是通过改变巨噬细胞中 IDO 活性介导的。