医学
肺移植
肺
肺纤维化
造血干细胞移植
重症监护医学
呼吸道疾病
移植
疾病
肺动脉高压
移植物抗宿主病
呼吸系统
内科学
作者
Saskia Bos,Hanne Beeckmans,Arno Vanstapel,Annelore Sacreas,Vincent Geudens,W. Gardner Lynn,Ine Schreurs,Bart Vanaudenaerde,Hélène Schoemans,Robin Vos
标识
DOI:10.1016/s2213-2600(22)00001-7
摘要
Allogeneic haematopoietic stem-cell transplantation (HSCT) and lung transplantation are both established life-saving treatment options for carefully selected patients with various haematological disorders or end-stage lung diseases, respectively. However, long-term survival after allogeneic HSCT is severely limited by chronic graft-versus-host disease (cGVHD)—of which pulmonary cGVHD in particular has a very poor prognosis—and long-term survival after lung transplantation is hampered by chronic lung allograft dysfunction (CLAD). Both pulmonary cGVHD and CLAD are characterised by similar underlying immunopathology, which results in transplant-related pulmonary fibrosis and structural lung remodelling, leading to respiratory dysfunction. Accurate clinical identification and appropriate management is of utmost importance to allow for timely diagnosis, to further optimise current preventive and treatment strategies of pulmonary cGVHD and CLAD, and to ameliorate quality of life and long-term outcomes after allogeneic HSCT and lung transplantation. In this Review, we provide a unique state-of-the-art perspective of both entities for respiratory care practitioners.
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