Hohlfeld Jens M, Schoenfeld Kerstin, Lavae-Mokhtari Mehyar, Schaumann Frank, Mueller Meike, Bredenbroeker Dirk, Krug Norbert, Hermann Robert
Department of Clinical Airway Research, Fraunhofer Institute of Toxicology and Experimental Medicine (ITEM), Nikolai-Fuchs-Street 1A, D-30625 Hannover, Germany.
Pulm Pharmacol Ther. 2008 Aug;21(4):616-23. doi: 10.1016/j.pupt.2008.02.002. Epub 2008 Feb 21.
Roflumilast, an investigational, targeted phosphodiesterase 4 inhibitor, reduces the in vitro and in vivo inflammatory activity of cells such as neutrophils, eosinophils, macrophages, and monocytes.
The aim of this study was to explore the anti-inflammatory properties of roflumilast in a human model of segmental bronchial endotoxin challenge.
In a randomized, placebo-controlled, double-blind, single-center parallel-group study, 37 healthy subjects of either sex were treated for 28 days with either oral roflumilast 500 microg once daily or placebo. At day 29, a baseline bronchoalveolar lavage was performed, followed by segmental endotoxin challenge (4 ng/kg) and saline control challenge. After 24h, bronchoalveolar lavage fluid was sampled from the challenged segments and cells were counted and differentiated.
After endotoxin challenge, influx of total cells (difference from baseline) in bronchoalveolar lavage of roflumilast-treated subjects was 36% lower than with placebo (p=0.02). Correspondingly, the influx of neutrophils and eosinophils of roflumilast-treated subjects was 39% (p=0.02) and 74% (p=0.01) lower than with placebo, respectively. In contrast, endotoxin-induced influx of monocytes was not different between roflumilast- and placebo-treated subjects. No significant differences existed between the groups pertaining to endotoxin-induced influx of macrophages and lymphocytes. Roflumilast was well tolerated. No unexpected or serious treatment-emergent signs and symptoms were observed.
Roflumilast attenuated the endotoxin-induced influx of neutrophils and eosinophils into the airways. This study demonstrates the anti-inflammatory properties of roflumilast on bronchoalveolar granulocytes in endotoxin-induced airway inflammation in healthy subjects.
罗氟司特是一种处于研究阶段的靶向磷酸二酯酶4抑制剂,可降低中性粒细胞、嗜酸性粒细胞、巨噬细胞和单核细胞等细胞的体外和体内炎症活性。
本研究旨在探讨罗氟司特在节段性支气管内毒素激发的人体模型中的抗炎特性。
在一项随机、安慰剂对照、双盲、单中心平行组研究中,37名健康受试者(男女不限)接受为期28天的治疗,其中一组每天口服一次500微克罗氟司特,另一组口服安慰剂。在第29天,进行基线支气管肺泡灌洗,随后进行节段性内毒素激发(4纳克/千克)和生理盐水对照激发。24小时后,从激发节段采集支气管肺泡灌洗液,对细胞进行计数和分类。
内毒素激发后,罗氟司特治疗组受试者支气管肺泡灌洗中总细胞流入量(与基线相比的差异)比安慰剂组低36%(p = 0.02)。相应地,罗氟司特治疗组受试者中性粒细胞和嗜酸性粒细胞的流入量分别比安慰剂组低39%(p = 0.02)和74%(p = 0.01)。相比之下,罗氟司特治疗组和安慰剂治疗组受试者之间内毒素诱导的单核细胞流入量没有差异。在与内毒素诱导的巨噬细胞和淋巴细胞流入量相关的组间未观察到显著差异。罗氟司特耐受性良好。未观察到意外或严重的治疗突发体征和症状。
罗氟司特减轻了内毒素诱导的中性粒细胞和嗜酸性粒细胞向气道的流入。本研究证明了罗氟司特在健康受试者内毒素诱导的气道炎症中对支气管肺泡粒细胞的抗炎特性。