University Hospital Basel, Basel.
Eur Respir J. 2014 Jan;43(1):221-32. doi: 10.1183/09031936.00199312. Epub 2013 May 3.
Bronchiolitis obliterans is a complication after allogeneic haematopoietic stem cell transplantation (HSCT). Management of bronchiolitis obliterans comprises intensive immunosuppression, but treatment response is poor. We investigated the effect of cyclosporine A (CsA), tacrolimus (FK506), methylprednisolone (mPRED), mycophenolate mofetil (MMF) and everolimus on the proliferation of primary lung myofibroblasts from HSCT patients with bronchiolitis obliterans syndrome (BOS). Cells were isolated from surgical lung biopsies of eight HSCT patients with BOS. Proliferation was assessed by [(3)H]-thymidine incorporation. Biopsies revealed constrictive bronchiolitis obliterans in three patients and lymphocytic bronchiolitis in five patients. CsA and FK506 significantly induced proliferation of myofibroblasts. mPRED and MMF caused a significant inhibition of proliferation, whereas everolimus had no effect. Costimulation with FK506, mPRED and MMF significantly inhibited proliferation. Serial pulmonary function tests over 12 months after lung biopsy and under triple therapy demonstrated that patients with lymphocytic bronchiolitis had a significant improvement in forced expiratory volume in 1 s (FEV1), whereas FEV1 of patients with bronchiolitis obliterans was unchanged. Our data demonstrate a pro-proliferative effect of calcineurin inhibitors on primary human lung myofibroblasts obtained from patients with BOS after HSCT. In contrast, based on the observed antiproliferative capacity of MMF in vitro, MMF-based calcineurin inhibitor-free treatment strategies should be further evaluated in patients with bronchiolitis obliterans after HSCT.
闭塞性细支气管炎是异基因造血干细胞移植(HSCT)后的一种并发症。闭塞性细支气管炎的治疗包括强化免疫抑制,但治疗反应较差。我们研究了环孢素 A(CsA)、他克莫司(FK506)、甲基强的松龙(mPRED)、霉酚酸酯(MMF)和依维莫司对 HSCT 后闭塞性细支气管炎综合征(BOS)患者原代肺成纤维细胞增殖的影响。细胞从 8 例 BOS 患者的手术肺活检中分离出来。通过[(3)H]胸苷掺入评估增殖。活检显示 3 例患者为缩窄性闭塞性细支气管炎,5 例患者为淋巴细胞性闭塞性细支气管炎。CsA 和 FK506 显著诱导成纤维细胞增殖。mPRED 和 MMF 显著抑制增殖,而依维莫司则没有作用。FK506、mPRED 和 MMF 的共刺激显著抑制增殖。肺活检后 12 个月的连续肺功能测试和三联治疗显示,淋巴细胞性细支气管炎患者的 1 秒用力呼气量(FEV1)显著改善,而闭塞性细支气管炎患者的 FEV1 则没有变化。我们的数据表明,钙调神经磷酸酶抑制剂对 HSCT 后 BOS 患者的原代人肺成纤维细胞具有促增殖作用。相比之下,根据 MMF 在体外观察到的抗增殖能力,应进一步评估 MMF 为基础的钙调神经磷酸酶抑制剂免疗策略在 HSCT 后闭塞性细支气管炎患者中的应用。