Gamble Elizabeth, Grootendorst Diana C, Brightling Christopher E, Troy Susannah, Qiu Yusheng, Zhu Jie, Parker Debbie, Matin Dean, Majumdar Swati, Vignola Antonio M, Kroegel Claus, Morell Ferran, Hansel Trevor T, Rennard Stephen I, Compton Christopher, Amit Ohad, Tat Tri, Edelson Jeffrey, Pavord Ian D, Rabe Klaus F, Barnes Neil C, Jeffery Peter K
Department of Pulmonology, Leiden University Medical Centre, Leiden, The Netherlands.
Am J Respir Crit Care Med. 2003 Oct 15;168(8):976-82. doi: 10.1164/rccm.200212-1490OC. Epub 2003 Jun 19.
Cilomilast (Ariflo), a new oral phosphodiesterase-4 selective inhibitor, improves lung function in chronic obstructive pulmonary disease (COPD). We have evaluated its antiinflammatory effects in 59 patients with COPD randomized to receive cilomilast, 15 mg two times a day, or placebo for 12 weeks. Induced sputum differential cell counts were obtained at baseline and at five further visits. Interleukin-8 and neutrophil elastase were measured in sputum supernatant. Bronchial biopsies obtained at baseline and at Week 10 were immunostained and counted for neutrophils, CD8+ and CD4+ T-lymphocyte subsets, and CD68+ macrophages. Cells expressing the genes for interleukin-8 and tumor necrosis factor-alpha were identified by in situ hybridization and quantified. Compared with placebo, analysis of variance (ANOVA) of the change from baseline showed that cilomilast did not alter any sputum endpoint or FEV1. However, bronchial biopsies demonstrated that cilomilast treatment was associated with reductions in CD8+ (p = 0.001; ANOVA) and CD68+ cells (p < 0.05; ANOVA). In addition, by Poisson analysis, comparison of cell counts analyzed as a ratio of active to placebo demonstrated reductions of CD8+ (48% p < 0.01) and CD68+ (47% p = 0.001) cells. This is the first demonstration of reduction by any agent of airway tissue inflammatory cells characteristic of COPD. Phosphodiesterase-4 inhibitors represent a promising new class of substances for use in antiinflammatory treatment of this disease.
西洛司特(Ariflo)是一种新型口服磷酸二酯酶-4选择性抑制剂,可改善慢性阻塞性肺疾病(COPD)患者的肺功能。我们对59例COPD患者进行了评估,这些患者被随机分为两组,一组接受西洛司特治疗,剂量为每日两次,每次15毫克,另一组接受安慰剂治疗,为期12周。在基线期以及另外五次随访时获取诱导痰的细胞分类计数。检测痰上清液中的白细胞介素-8和中性粒细胞弹性蛋白酶。在基线期和第10周获取支气管活检组织,进行免疫染色,并对中性粒细胞、CD8 +和CD4 + T淋巴细胞亚群以及CD68 +巨噬细胞进行计数。通过原位杂交鉴定并定量表达白细胞介素-8和肿瘤坏死因子-α基因的细胞。与安慰剂相比,对基线期变化的方差分析(ANOVA)表明,西洛司特未改变任何痰液指标或第一秒用力呼气容积(FEV1)。然而,支气管活检显示,西洛司特治疗与CD8 +细胞(p = 0.001;ANOVA)和CD68 +细胞减少有关(p < 0.05;ANOVA)。此外,通过泊松分析,将细胞计数作为活性药物与安慰剂的比例进行比较,结果显示CD8 +细胞减少了48%(p < 0.01),CD68 +细胞减少了47%(p = 0.001)。这是首次证明任何药物可减少COPD特征性气道组织炎症细胞。磷酸二酯酶-4抑制剂代表了一类有前景的新型物质,可用于该疾病的抗炎治疗。