SCH527123, a novel CXCR2 antagonist, inhibits ozone-induced neutrophilia in healthy subjects

被引:156
作者
Holz, O. [1 ]
Khalilieh, S. [2 ]
Ludwig-Sengpiel, A. [1 ]
Watz, H. [1 ]
Stryszak, P. [2 ]
Soni, P. [2 ]
Tsai, M. [2 ]
Sadeh, J. [2 ]
Magnussen, H. [1 ]
机构
[1] Hosp Grosshansdorf, Pulm Res Inst, D-22927 Grosshansdorf, Germany
[2] Schering Plough Res Inst, Kenilworth, NJ USA
关键词
Anti-inflammatory; chronic obstructive pulmonary disease; interleukin-8; myeloperoxidase; pharmacodynamics; OBSTRUCTIVE PULMONARY-DISEASE; AIRWAY INFLAMMATION; HISTONE DEACETYLASE; ACTIVATION MARKERS; INDUCED SPUTUM; BONE-MARROW; RECRUITMENT; EXPOSURES; FEV(1); COPD;
D O I
10.1183/09031936.00048509
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
SCH527123 is a novel, selective CXC chemokine receptor 2 antagonist that inhibits neutrophil activation and modulates neutrophil trafficking in animal models, characteristics that may be beneficial in the treatment of conditions with unbalanced pulmonary neutrophilia, such as chronic obstructive pulmonary disease. The purpose of this proof-of-principle study was to determine whether SCH527123 inhibits ozone-induced neutrophil recruitment in healthy humans. In a randomised, double-blind, placebo-controlled, three-way crossover study, oral SCH527123 (50 mg once daily, 4 days), prednisolone (50 mg once), or placebo was alternated with 2-week washouts. 18 healthy ozone responders (>20% increase in sputum neutrophils) underwent ozone challenge tests (250 ppb, 3 h intermittent exercise) 1 h after the last treatment dose. Sputum was induced at 3 h post-challenge. After SCH527123 treatment, the ozone challenge resulted in significantly lower sputum neutrophil counts (0.13 x 10(6).mL(-1)) compared with prednisolone (0.84 x 10(6).mL(-1); p<0.001) or placebo (2.98 x 10(6).mL(-1); p<0.001). Comparable results were obtained for total cell count, percentage of sputum neutrophils, and for interleukin-8 and myeloperoxidase in sputum supernatant. Post-challenge, SCH527123 inhibited neutrophilia in peripheral blood but significantly less than in sputum. All treatments were safe and well tolerated. SCH527123 causes significant attenuation of ozone-induced airway neutrophilia in healthy subjects. Further evaluation in a large trial of patients with pulmonary disorders is warranted.
引用
收藏
页码:564 / 570
页数:7
相关论文
共 30 条
[1]   Chemokines: Leucocyte recruitment and activation cytokines [J].
Adams, DH ;
Lloyd, AR .
LANCET, 1997, 349 (9050) :490-495
[2]   Fluticasone propionate protects against ozone-induced airway inflammation and modified immune cell activation markers in healthy volunteers [J].
Alexis, Neil E. ;
Lay, John C. ;
Haczku, Angela ;
Gong, Henry ;
Linn, William ;
Hazucha, Milan J. ;
Harris, Brad ;
Tal-Singer, Ruth ;
Peden, David B. .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2008, 116 (06) :799-805
[3]   Ozone-induced decrements in FEV(1) and FVC do not correlate with measures of inflammation [J].
Balmes, JR ;
Chen, LL ;
Scannell, C ;
Tager, I ;
Christian, D ;
Hearne, PQ ;
Kelly, T ;
Aris, RM .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 153 (03) :904-909
[4]   Reduced histone deacetylase in COPD - Clinical implications [J].
Barnes, PJ .
CHEST, 2006, 129 (01) :151-155
[5]   A novel, orally active CXCR1/2 receptor antagonist, sch527123, inhibits neutrophil recruitment, mucus production, and goblet cell hyperplasia in animal models of pulmonary inflammation [J].
Chapman, Richard W. ;
Minnicozzi, Michael ;
Celly, Chander S. ;
Phillips, Jonathan E. ;
Kung, Ted T. ;
Hipkin, R. William ;
Fan, Xuedong ;
Rindgen, Diane ;
Deno, Gregory ;
Bond, Richard ;
Gonsiorek, Waldemar ;
Billah, Motasim M. ;
Fine, Jay S. ;
Hey, John A. .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2007, 322 (02) :486-493
[6]  
EVANS E, 2007, EUR RESP J S51, V30, pS775
[7]  
Holz O, 1998, CLIN EXP ALLERGY, V28, P284
[8]   Ozone-induced airway inflammatory changes differ between individuals and are reproducible [J].
Holz, O ;
Jörres, RA ;
Timm, P ;
Mücke, M ;
Richter, K ;
Koschyk, S ;
Magnussen, H .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1999, 159 (03) :776-784
[9]   Validation of the human ozone challenge model as a tool for assessing anti-inflammatory drugs in early development [J].
Holz, O ;
Tal-Singer, R ;
Kanniess, F ;
Simpson, KJ ;
Gibson, A ;
Vessey, RSJ ;
Janicki, S ;
Magnussen, H ;
Jörres, RA ;
Richter, K .
JOURNAL OF CLINICAL PHARMACOLOGY, 2005, 45 (05) :498-503
[10]   Repeated ozone exposures enhance bronchial allergen responses in subjects with rhinitis or asthma [J].
Holz, O ;
Mücke, M ;
Paasch, K ;
Böhme, S ;
Timm, P ;
Richter, K ;
Magnussen, H ;
Jörres, RA .
CLINICAL AND EXPERIMENTAL ALLERGY, 2002, 32 (05) :681-689