Gauthier Jason M, Hachem Ramsey R, Kreisel Daniel
Department of Surgery, Washington University in St. Louis, Saint Louis, MO.
Department of Medicine, Washington University in St. Louis, Saint Louis, MO.
Curr Transplant Rep. 2016 Sep;3(3):185-191. doi: 10.1007/s40472-016-0112-y. Epub 2016 Aug 2.
Chronic lung allograft dysfunction (CLAD) encompasses a range of pathologies that cause a transplanted lung to not achieve or maintain normal function. CLAD manifests as airflow restriction and/or obstruction and is predominantly a result of chronic rejection. Three distinct phenotypes of chronic rejection are now recognized: bronchiolitis obliterans, neutrophilic reversible allograft dysfunction, and restrictive allograft syndrome. Recent investigations have revealed that each phenotype has a unique pathology and histopathological findings, suggesting that treatment regimens should be tailored to the underlying etiology. CLAD is poorly responsive to treatment once diagnosed, and therefore the prevention of the factors that predispose a patient to develop CLAD is critically important. Small and large animal models have contributed significantly to our understanding of CLAD and more studies are needed to develop treatment regimens that are effective in humans.
慢性肺移植功能障碍(CLAD)涵盖一系列导致移植肺无法实现或维持正常功能的病理状况。CLAD表现为气流受限和/或阻塞,主要是慢性排斥反应的结果。目前已认识到慢性排斥反应的三种不同表型:闭塞性细支气管炎、嗜中性粒细胞可逆性移植功能障碍和限制性移植综合征。最近的研究表明,每种表型都有独特的病理和组织病理学表现,这表明治疗方案应根据潜在病因进行调整。一旦确诊,CLAD对治疗的反应较差,因此预防使患者易患CLAD的因素至关重要。大小动物模型对我们理解CLAD做出了重大贡献,还需要更多研究来开发对人类有效的治疗方案。