Groetzner Jan, Wittwer Thorsten, Kaczmarek Ingo, Ueberfuhr Peter, Strauch Justus, Nagib Ragi, Meiser Bruno, Franke Ulrich, Reichart Bruno, Wahlers Thorsten
Department of Cardiothoracic and Vascular Surgery, Friedrich Schiller University Hospital, Jena, Germany.
Transplantation. 2006 Feb 15;81(3):355-60. doi: 10.1097/01.tp.0000195781.02268.5e.
Bronchiolitis obliterans syndrome (BOS) is the major problem after lung and heart-lung transplantation (LTx/HLTx). Sirolimus (Sir) and Mycophenolate (MMF) showed a promising efficacy in the treatment of BOS in animal models. The first clinical experience in converting LTx/HLTx-recipients with BOS from calcineurin inhibitor-(CNI)-based immunosuppression to a Sir-MMF based immunosuppression is reported herein.
Six LTx- and five HLTx-recipients (eight men; 0.9 to 8 years after transplantation) with CNI-based immunosuppression (plus MMF) in whom BOS was diagnosed were included in the study. Mean patient age was 37+/-13 years (range 17-62 years). Sir was started with 6 mg and continued adjusted to according target trough levels (8-14 ng/ml). Subsequently, the CNIs were tapered down and finally stopped. Follow up included self determined pulmonary function tests, microbiological screening, chest radiographs, and laboratory studies
Two acute rejection episodes occurred during the study period. The incidence of infection was 2.2+/-1.3 infections/patient-year after conversion. Mean FEV1 decreased after a mean follow up of 14.8+/-1.4 months: from 2.1+/-0.7 l prior conversion to 1.3+/-0.6l after conversion (P=0.03). However, graft function remained stable in three patients and progression of BOS slowed down in three patients. Overall, 2 of 10 patients died due to ongoing BOS while awaiting retransplantation
After BOS was diagnosed, conversion to MMF and Sir stabilized graft function only in some of the converted patients. Therefore, earlier administration of Sir-based immunosuppression might be a more promising approach. Whether conversion to CNI-free immunosuppression can actually ameliorate the extent or progression of BOS has to be investigated in randomized trials.
闭塞性细支气管炎综合征(BOS)是肺移植和心肺移植(LTx/HLTx)后的主要问题。西罗莫司(Sir)和霉酚酸酯(MMF)在动物模型中治疗BOS显示出有前景的疗效。本文报道了将基于钙调神经磷酸酶抑制剂(CNI)免疫抑制的LTx/HLTx合并BOS受者转换为基于Sir-MMF免疫抑制的首例临床经验。
研究纳入6例肺移植受者和5例心肺移植受者(8例男性;移植后0.9至8年),这些受者接受基于CNI的免疫抑制(加MMF)且被诊断为BOS。患者平均年龄为37±13岁(范围17 - 62岁)。Sir起始剂量为6mg,并根据目标谷浓度(8 - 14ng/ml)持续调整。随后,逐渐减少CNI剂量并最终停用。随访包括自行测定的肺功能测试、微生物筛查、胸部X线片和实验室检查。
研究期间发生了2次急性排斥反应。转换后感染发生率为2.2±1.3次感染/患者年。平均随访14.8±1.4个月后,平均第一秒用力呼气容积(FEV1)下降:从转换前的2.1±0.7L降至转换后的1.3±0.6L(P = 0.03)。然而,3例患者的移植物功能保持稳定,3例患者的BOS进展减缓。总体而言,10例患者中有2例在等待再次移植期间因持续的BOS死亡。
诊断为BOS后,转换为MMF和Sir仅使部分转换患者的移植物功能稳定。因此,更早给予基于Sir的免疫抑制可能是更有前景的方法。转换为无CNI免疫抑制是否真能改善BOS的程度或进展,必须在随机试验中进行研究。