Verleden Geert M, Vanaudenaerde Bart M, Dupont Lieven J, Van Raemdonck Dirk E
Department of Respiratory Diseases, University Hospital Gasthuisberg, Leuven, Belgium.
Am J Respir Crit Care Med. 2006 Sep 1;174(5):566-70. doi: 10.1164/rccm.200601-071OC. Epub 2006 Jun 1.
Bronchiolitis obliterans syndrome (BOS) remains the leading cause of death after lung transplantation. Treatment is difficult, although azithromycin has recently been shown to improve FEV(1). The exact mechanism of action is unclear.
(1) Azithromycin reduces airway neutrophilia and interleukin (IL)-8 and (2) airway neutrophilia predicts the improvement in FEV(1).
Fourteen lung transplant patients with BOS (between BOS 0-p and BOS 3) were treated with azithromycin, in addition to their current immunosuppressive treatment. Before and 3 mo after azithromycin was introduced, bronchoscopy with bronchoalveolar lavage (BAL) was performed for cell differentiation and to measure IL-8 and IL-17 mRNA ratios.
The FEV(1) increased from 2.36 (+/- 0.82 L) to 2.67 L (+/- 0.85 L; p = 0.007), whereas the percentage of BAL neutrophilia decreased from 35.1 (+/- 35.7%) to 5.7% (+/- 6.5%; p = 0.0024). There were six responders to azithromycin (with an FEV(1) increase of > 10%) and eight nonresponders. Using categorical univariate linear regression analysis, the main significant differences in characteristics between responders and nonresponders were the initial BAL neutrophilia (p < 0.0001), IL-8 mRNA ratio (p = 0.0009), and the postoperative day at which azithromycin was started (p = 0.036). There was a significant correlation between the initial percentage of BAL neutrophilia and the changes in FEV(1) after 3 mo (r = 0.79, p = 0.0019).
Azithromycin significantly reduces airway neutrophilia and IL-8 mRNA in patients with BOS. Responders have a significantly higher BAL neutrophilia and IL-8 compared with nonresponders and had commenced treatment earlier after transplantation. BAL neutrophilia can be used as a predictor for the FEV(1) response to azithromycin.
闭塞性细支气管炎综合征(BOS)仍是肺移植后死亡的主要原因。尽管最近有研究表明阿奇霉素可改善第一秒用力呼气容积(FEV₁),但治疗仍很困难。其确切作用机制尚不清楚。
(1)阿奇霉素可减轻气道中性粒细胞增多及白细胞介素(IL)-8水平;(2)气道中性粒细胞增多可预测FEV₁的改善情况。
14例患有BOS(BOS 0-p至BOS 3)的肺移植患者,在接受当前免疫抑制治疗的基础上,加用阿奇霉素治疗。在开始使用阿奇霉素前及用药3个月后,进行支气管镜检查及支气管肺泡灌洗(BAL),以进行细胞分化分析,并测量IL-8和IL-17 mRNA比值。
FEV₁从2.36(±0.82L)升至2.67L(±0.85L;p = 0.007),而BAL中性粒细胞增多百分比从35.1(±35.7%)降至5.7%(±6.5%;p = 0.0024)。有6例患者对阿奇霉素有反应(FEV₁增加> 10%),8例无反应。采用分类单变量线性回归分析,有反应者与无反应者在特征上的主要显著差异为初始BAL中性粒细胞增多情况(p < 0.0001)、IL-8 mRNA比值(p = 0.0009)以及开始使用阿奇霉素的术后天数(p = 0.036)。初始BAL中性粒细胞增多百分比与3个月后FEV₁的变化之间存在显著相关性(r = 0.79,p = 0.0019)。
阿奇霉素可显著降低BOS患者气道中性粒细胞增多及IL-8 mRNA水平。与无反应者相比,有反应者的BAL中性粒细胞增多及IL-8水平显著更高,且在移植后更早开始治疗。BAL中性粒细胞增多可作为预测FEV₁对阿奇霉素反应的指标。