Dentener Mieke A, Creutzberg Eva C, Pennings Herman-Jan, Rijkers Ger T, Mercken Evi, Wouters Emiel F M
Nutrition and Toxicology Research Institute Maastricht, Department of Respiratory Medicine, University Hospital Maastricht, Maastricht, The Netherlands.
Respiration. 2008;76(3):275-82. doi: 10.1159/000117386. Epub 2008 Feb 15.
Chronic obstructive pulmonary disease (COPD) with cachexia is characterized by inflammation reflected by increased levels of tumor necrosis factor-alpha (TNF-alpha).
In this study, infliximab, an anti-TNF-alpha antibody, was evaluated for its effects on systemic (plasma) and local (exhaled breath condensate, EBC) inflammation in cachectic patients with COPD. Also, baseline levels of new inflammatory markers were compared to control subjects.
Sixteen cachectic patients with moderate to severe COPD were examined for inflammatory status at baseline and compared to 25 control subjects. Patients were randomized (1:1) to receive infliximab (5 mg/kg) or placebo at weeks 0, 2 and 6. Patients were evaluated at weeks 8 and 12 and followed through week 26.
EBC analysis revealed increased levels of several novel inflammatory markers, including macrophage migration inhibitory factor, IL-12, RANTES and sICAM-1, in patients with COPD compared to controls. EBC levels of inflammatory markers were unchanged in patients receiving infliximab. In addition, systemic levels of acute-phase proteins (C-reactive protein, fibrinogen and lipopolysaccharide-binding protein), IL-6 and soluble TNF receptor (sTNFR) 55 had not changed at weeks 8 or 12. Small increases in circulating levels of sTNFR75, myeloperoxidase and Clara cell protein 16 were seen at week 8, but not at week 12.
In this small study, infliximab did not produce an observable decrease in local inflammation in cachectic patients with COPD and had minor effects on systemic inflammation. The detection of new inflammatory markers in EBC can help to further characterize local inflammatory processes in COPD.
伴有恶病质的慢性阻塞性肺疾病(COPD)的特征是炎症,表现为肿瘤坏死因子-α(TNF-α)水平升高。
在本研究中,评估了抗TNF-α抗体英夫利昔单抗对伴有恶病质的COPD患者全身(血浆)和局部(呼出气冷凝液,EBC)炎症的影响。此外,还将新炎症标志物的基线水平与对照组进行了比较。
对16例伴有恶病质的中重度COPD患者进行基线炎症状态检查,并与25例对照受试者进行比较。患者在第0、2和6周随机(1:1)接受英夫利昔单抗(5 mg/kg)或安慰剂治疗。在第8周和第12周对患者进行评估,并随访至第26周。
EBC分析显示,与对照组相比,COPD患者中几种新的炎症标志物水平升高,包括巨噬细胞迁移抑制因子、IL-12、RANTES和sICAM-1。接受英夫利昔单抗治疗的患者炎症标志物的EBC水平未发生变化。此外,急性期蛋白(C反应蛋白、纤维蛋白原和脂多糖结合蛋白)、IL-6和可溶性TNF受体(sTNFR)55的全身水平在第8周或第12周时未发生变化。第8周时sTNFR75、髓过氧化物酶和克拉拉细胞蛋白16的循环水平略有升高,但在第12周时未升高。
在这项小型研究中,英夫利昔单抗并未使伴有恶病质的COPD患者的局部炎症明显减轻,对全身炎症的影响也较小。在EBC中检测新的炎症标志物有助于进一步明确COPD中的局部炎症过程。