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Bronchiolitis Obliterans Syndrome and Chronic Lung Allograft Dysfunction: Evolving Concepts and Nomenclature

机译:闭塞性细支气管炎综合征和慢性肺同种异体移植功能障碍:概念和术语的演变。

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摘要

Bronchiolitis obliterans syndrome (BOS) eventually occurs in the majority of lung transplant recipients who survive beyond 1 year, can greatly impair quality of life, and is, directly or indirectly, the major cause of delayed allograft dysfunction and recipient death. A number of associated events or conditions are strongly associated with the risk for developing BOS; these include acute rejection, gastroesophageal reflux, infections, and autoimmune reactions that can occur in the setting of alloimmune responses to the lung allograft as recipients are given intense immunosuppression to prevent allograft rejection. The term chronic lung allograft dysfunction (CLAD) is being increasingly used to refer to recipients with late allograft dysfunction that meets the spirometric criteria for the diagnosis of BOS, but clinicians should recognize that such dysfunction can occur for a variety of reasons other than BOS. The recently identified entity of restrictive allograft syndrome, which is now recognized as a relatively distinct phenotype of CLAD, has features that differentiate it from classic obstructive BOS. A number of other entities that can also significantly affect allograft function must also be considered when significant allograft dysfunction is encountered following lung transplantation.
机译:闭塞性细支气管炎综合征(BOS)最终会在大多数存活超过1年的肺移植接受者中发生,会严重损害生活质量,并且直接或间接地成为同种异体移植功能障碍和接受者死亡延迟的主要原因。许多相关事件或状况与发生BOS的风险密切相关;这些包括急性排斥反应,胃食管反流,感染以及对肺同种异体移植的同种免疫反应中可能发生的自身免疫反应,因为接受者被给予强烈的免疫抑制以防止同种异体移植排斥。术语慢性肺同种异体移植功能障碍(CLAD)越来越多地用于指代满足肺活量测定标准以诊断BOS的晚期同种异体移植功能障碍的接受者,但临床医生应认识到,除了BOS以外,其他各种原因都可能导致这种功能障碍。最近发现的限制性同种异体移植综合征的实体,现在被认为是一种相对独特的CLAD表型,其特征使其与经典的阻塞性BOS区别开来。当在肺移植后遇到严重的同种异体移植功能障碍时,还必须考虑许多其他也会明显影响同种异体移植功能的实体。

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