Chronic lung allograft dysfunction: evolving practice

被引:29
作者
Vos, Robin [1 ]
Verleden, Stijn E.
Verleden, Geert M.
机构
[1] UZ Leuven, B-3000 Leuven, Belgium
关键词
acute fibrinoid-organizing pneumonia; azithromycin responsive allograft dysfunction; bronchiolitis obliterans syndrome; chronic lung allograft dysfunction; restrictive allograft syndrome; BRONCHIOLITIS-OBLITERANS-SYNDROME; PRIMARY GRAFT DYSFUNCTION; RANDOMIZED CONTROLLED-TRIAL; TOTAL LYMPHOID IRRADIATION; EXTRACORPOREAL PHOTOPHERESIS; TRANSPLANT RECIPIENTS; CHRONIC REJECTION; GENETIC-VARIATION; AIR-POLLUTION; LYMPHOCYTIC BRONCHIOLITIS;
D O I
10.1097/MOT.0000000000000236
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Purpose of review Chronic lung allograft dysfunction (CLAD) was recently introduced as an overarching term covering different phenotypes of chronic allograft dysfunction, including obstructive CLAD (bronchiolitis obliterans syndrome), restrictive CLAD (restrictive allograft syndrome) and graft dysfunction due to causes not related to chronic rejection. In the present review, we will highlight the latest insights and current controversies regarding the new CLAD terminology, underlying pathophysiologic mechanisms, diagnostic approach and possible treatment options. Recent findings Different pathophysiological mechanisms are clearly involved in clinically distinct phenotypes of chronic rejection, as is reflected by differences in histology, allograft function and imaging. Therefore, not all CLAD patients may equally benefit from specific therapies. Summary The recent introduction of CLAD importantly changed the clinical practice in lung transplant recipients. Given the relative low accuracy of the current diagnostic tools, future research should focus on specific biomarkers, more sensitive pulmonary function parameters and imaging techniques for timely CLAD diagnosis and phenotyping. Personalized or targeted therapeutic options for adequate prevention and treatment of CLAD are required.
引用
收藏
页码:483 / 491
页数:9
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