TY - JOUR
T1 - Management of chronic rejection after lung transplantation
AU - Bedair, Bahaa
AU - Hachem, Ramsey R.
N1 - Funding Information:
Conflicts of Interest: Both authors have completed the ICMJE uniform disclosure form (available at: http://dx.doi. org/10.21037/jtd-2021-19). The series “Lung Transplantation: Past, Present, and Future” was commissioned by the editorial office without any funding or sponsorship. RRH reports personal fees from Transmedics, grants from Bristol Myers Squibb, personal fees from CareDx, personal fees from Theravance, personal fees from Vectura, outside the submitted work. Both authors have no other conflicts of interest to declare.
Publisher Copyright:
© 2021 AME Publishing Company. All rights reserved.
PY - 2021/11
Y1 - 2021/11
N2 - Outcomes after lung transplantation are limited by chronic lung allograft dysfunction (CLAD). The incidence of CLAD is high, and its clinical course tends to be progressive over time, culminating in graft failure and death. Indeed, CLAD is the leading cause of death beyond the first year after lung transplantation. Therapy for CLAD has been limited by a lack of high-quality studies to guide management. In this review, we will discuss the diagnosis of CLAD in light of the recent changes to definitions and will discuss the current clinical evidence available for treatment. Recently, the diagnosis of CLAD has been subdivided into bronchiolitis obliterans syndrome (BOS) and restrictive allograft syndrome (RAS). The current evidence for treatment of CLAD mainly revolves around treatment of BOS with more limited data existing for RAS. The best supported treatment to date for CLAD is the macrolide antibiotic azithromycin which has been associated with a small improvement in lung function in a minority of patients. Other therapies that have more limited data include switching immunosuppression from cyclosporine to tacrolimus, fundoplication for gastroesophageal reflux, montelukast, extracorporeal photopheresis (ECP), aerosolized cyclosporine, cytolytic anti-lymphocyte therapies, total lymphoid irradiation (TLI) and the antifibrotic agent pirfenidone. Most of these treatments are supported by case series and observational studies. Finally, we will discuss the role of retransplantation for CLAD.
AB - Outcomes after lung transplantation are limited by chronic lung allograft dysfunction (CLAD). The incidence of CLAD is high, and its clinical course tends to be progressive over time, culminating in graft failure and death. Indeed, CLAD is the leading cause of death beyond the first year after lung transplantation. Therapy for CLAD has been limited by a lack of high-quality studies to guide management. In this review, we will discuss the diagnosis of CLAD in light of the recent changes to definitions and will discuss the current clinical evidence available for treatment. Recently, the diagnosis of CLAD has been subdivided into bronchiolitis obliterans syndrome (BOS) and restrictive allograft syndrome (RAS). The current evidence for treatment of CLAD mainly revolves around treatment of BOS with more limited data existing for RAS. The best supported treatment to date for CLAD is the macrolide antibiotic azithromycin which has been associated with a small improvement in lung function in a minority of patients. Other therapies that have more limited data include switching immunosuppression from cyclosporine to tacrolimus, fundoplication for gastroesophageal reflux, montelukast, extracorporeal photopheresis (ECP), aerosolized cyclosporine, cytolytic anti-lymphocyte therapies, total lymphoid irradiation (TLI) and the antifibrotic agent pirfenidone. Most of these treatments are supported by case series and observational studies. Finally, we will discuss the role of retransplantation for CLAD.
KW - Bronchiolitis obliterans syndrome
KW - Chronic lung allograft dysfunction
KW - Chronic rejection
KW - Restrictive allograft syndrome
UR - http://www.scopus.com/inward/record.url?scp=85120431255&partnerID=8YFLogxK
U2 - 10.21037/jtd-2021-19
DO - 10.21037/jtd-2021-19
M3 - Review article
C2 - 34992842
AN - SCOPUS:85120431255
SN - 2072-1439
VL - 13
SP - 6645
EP - 6653
JO - Journal of Thoracic Disease
JF - Journal of Thoracic Disease
IS - 11
ER -