Leuven Lung Transplant Unit, KU Leuven and UZ Gasthuisberg, 3000 Leuven, Belgium.
Transplantation. 2013 May 15;95(9):1167-72. doi: 10.1097/TP.0b013e318286e076.
Chronic rejection is the major problem hampering long-term survival after lung transplantation. Recently, it became clear that patients may develop an obstructive (bronchiolitis obliterans syndrome [BOS]) or a restrictive lung function defect (restrictive allograft syndrome [RAS]), for which specific risk factors are unknown.
A retrospective analysis of our lung transplantation cohort was performed (n=380). Patients with an irreversible decline in forced expiratory volume in 1 second were identified and classified as BOS or RAS. Patient characteristics, bronchoalveolar lavage (BAL) cellularity, rates of respiratory tract infection, colonization, acute rejection, and lymphocytic bronchiolitis were compared between BOS, RAS, and stable patients.
There were 103 patients suffering from chronic rejection, of which 79 had BOS and 24 were diagnosed with RAS. There were more patients with infection and pseudomonal colonizations in BOS and RAS compared with control (P=0.0090 and P=0.0034, respectively). More patients ever experienced acute and severe acute rejections (A≥2; both P<0.0001) and lymphocytic bronchiolitis (P=0.0006) in BOS and RAS versus control. There were more patients experiencing severe lymphocytic bronchiolitis in RAS compared with BOS (P=0.031). BAL neutrophilia in BOS and RAS were elevated at days 360, 540, and 720 versus control. BOS, but especially RAS patients, experienced more frequent episodes of increased BAL eosinophilia (≥2%; P<0.0001).
Acute rejection, lymphocytic bronchiolitis, colonization with pseudomonas, infection, and BAL eosinophilia and neutrophilia are risk factors for the later development not only of RAS but also of BOS.
慢性排斥反应是肺移植后长期生存的主要问题。最近,人们清楚地认识到,患者可能会出现阻塞性(细支气管炎闭塞综合征[BOS])或限制性肺功能缺陷(限制性移植物综合征[RAS]),但具体的危险因素尚不清楚。
对我们的肺移植队列进行了回顾性分析(n=380)。确定了用力呼气量在 1 秒内不可逆下降的患者,并将其分类为 BOS 或 RAS。比较 BOS、RAS 和稳定患者的患者特征、支气管肺泡灌洗液(BAL)细胞计数、呼吸道感染率、定植、急性排斥反应和淋巴细胞性细支气管炎。
有 103 例患者患有慢性排斥反应,其中 79 例患有 BOS,24 例诊断为 RAS。BOS 和 RAS 患者的感染和假单胞菌定植率均高于对照组(P=0.0090 和 P=0.0034)。BOS 和 RAS 患者比对照组更常见急性和严重急性排斥反应(A≥2;均 P<0.0001)和淋巴细胞性细支气管炎(P=0.0006)。与 BOS 相比,RAS 患者发生严重淋巴细胞性细支气管炎的频率更高(P=0.031)。BOS 和 RAS 在第 360、540 和 720 天的 BAL 中性粒细胞增多均高于对照组。BOS 患者,但特别是 RAS 患者,BAL 嗜酸性粒细胞增多(≥2%;P<0.0001)的发作更为频繁。
急性排斥反应、淋巴细胞性细支气管炎、假单胞菌定植、感染以及 BAL 嗜酸性粒细胞和中性粒细胞增多是不仅 RAS 而且 BOS 后期发展的危险因素。