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异基因造血干细胞移植后迟发性非感染性肺部并发症的临床表现、结局及危险因素

Clinical presentation, outcome and risk factors of late-onset non-infectious pulmonary complications after allogeneic stem cell transplantation.

作者信息

Patriarca Francesca, Poletti Venerino, Costabel Ulrich, Battista Marta Lisa, Sperotto Alessandra, Medeot Marta, Toffoletti Eleonora, Fanin Renato

机构信息

Department of Morphological and Clinical Researches, University Hospital, Udine, Italy.

出版信息

Curr Stem Cell Res Ther. 2009 May;4(2):161-7. doi: 10.2174/157488809788167436.

DOI:10.2174/157488809788167436
PMID:19442201
Abstract

The term late-onset non-infectious pulmonary complications (LONIPCs) has been used to refer to events occurring later than 3 months after allogeneic hematopoietic stem transplant (HSCT), such as bronchiolitis obliterans, bronchiolitis obliterans with organizing pneumonia, and lymphocytic or idiopathic interstitial pneumonia. The incidence of LONIPCs varies widely, ranging between 10% and 26%. Median time for LONIPC development is about 8-12 months after HSCT. Clinical symptoms may be insidious and non specific at the beginning and can be present in different types of infections. The diagnosis is made on the basis of thoracic high-resolution computed tomography and pulmonary function tests (PFT). It usually requires that standard cultures for infective agents on bronchoalveolar lavage are negative and is confirmed by transbronchial or lung biopsy, whenever possible. Total body irradiation and high doses of drugs used in the conditioning regimens, HLA disparity between donor and recipient, and chronic graft-versus-host disease (GVHD) are the main risk factors for LONIPCs. Since patients with LONIPCs have an increased risk of mortality because of infections or respiratory failure, pre- and post-transplant PFTs are strongly recommended in order to timely identify affected patients. The administration of antithymocyte globulin before unrelated donor transplants and slow taper of cyclosporine after transplant have been shown to prevent chronic GVHD and, therefore, the occurrence of LONIPCs.

摘要

迟发性非感染性肺部并发症(LONIPC)这一术语用于指异基因造血干细胞移植(HSCT)后3个月以后发生的事件,如闭塞性细支气管炎、伴有机化性肺炎的闭塞性细支气管炎以及淋巴细胞性或特发性间质性肺炎。LONIPC的发生率差异很大,在10%至26%之间。LONIPC发生的中位时间约为HSCT后8至12个月。临床症状起初可能隐匿且不具特异性,可出现在不同类型的感染中。诊断基于胸部高分辨率计算机断层扫描和肺功能测试(PFT)。通常要求支气管肺泡灌洗的感染病原体标准培养结果为阴性,且尽可能通过经支气管或肺活检来确诊。全身照射、预处理方案中使用的高剂量药物、供体与受体之间的HLA差异以及慢性移植物抗宿主病(GVHD)是LONIPC的主要危险因素。由于LONIPC患者因感染或呼吸衰竭而死亡的风险增加,强烈建议在移植前后进行PFT,以便及时识别受影响的患者。已证明在无关供体移植前给予抗胸腺细胞球蛋白以及移植后缓慢减量环孢素可预防慢性GVHD,从而预防LONIPC的发生。

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