TY - JOUR
T1 - Evolving experience of treating antibody-mediated rejection following lung transplantation
AU - Otani, Shinji
AU - Davis, Amanda K.
AU - Cantwell, Linda
AU - Ivulich, Steven
AU - Pham, Alan
AU - Paraskeva, Miranda A.
AU - Snell, Greg I.
AU - Westall, Glen P.
N1 - Funding Information:
The authors wish to thank the Margaret Pratt Foundation for their support.
PY - 2014/8
Y1 - 2014/8
N2 - Background: The importance of antibody-mediated rejection (AMR) following lung transplantation remains contentious. In particular, the diagnostic criteria suggested to define AMR, namely the presence of donor-specific antibodies (DSA), C4d immunoreactivity, histological features and allograft dysfunction are not always readily applicable or confirmatory in lung transplantation. Methods: In a retrospective single-center study of 255 lung transplant recipients (LTR), we identified 9 patients in whom a clinical diagnosis of AMR was made within 12. months of transplant, and define the immunological, histological, clinical features, as well as the therapeutic response of this cohort. Results: Nine LTR with AMR underwent combination therapy with high-dose intravenous corticosteroid, intravenous immunoglobulin, plasmapheresis and rituximab. Following therapy, while the total number of the original DSA dropped by 17%, and the median value of the mean fluorescence intensity (mfi) of the originally observed DSA decreased from 5292 (IQR 1319-12,754) to 2409 (IQR 920-6825) (p. <. 0.001), clinical outcomes were variable with a number of patients progressing to either chronic lung allograft dysfunction or death within 12. month. Conclusion: AMR in lung transplantation remains both a diagnostic and therapeutic challenge, but when clinically suspected is associated with a variable response to therapy and poor long-term outcomes.
AB - Background: The importance of antibody-mediated rejection (AMR) following lung transplantation remains contentious. In particular, the diagnostic criteria suggested to define AMR, namely the presence of donor-specific antibodies (DSA), C4d immunoreactivity, histological features and allograft dysfunction are not always readily applicable or confirmatory in lung transplantation. Methods: In a retrospective single-center study of 255 lung transplant recipients (LTR), we identified 9 patients in whom a clinical diagnosis of AMR was made within 12. months of transplant, and define the immunological, histological, clinical features, as well as the therapeutic response of this cohort. Results: Nine LTR with AMR underwent combination therapy with high-dose intravenous corticosteroid, intravenous immunoglobulin, plasmapheresis and rituximab. Following therapy, while the total number of the original DSA dropped by 17%, and the median value of the mean fluorescence intensity (mfi) of the originally observed DSA decreased from 5292 (IQR 1319-12,754) to 2409 (IQR 920-6825) (p. <. 0.001), clinical outcomes were variable with a number of patients progressing to either chronic lung allograft dysfunction or death within 12. month. Conclusion: AMR in lung transplantation remains both a diagnostic and therapeutic challenge, but when clinically suspected is associated with a variable response to therapy and poor long-term outcomes.
KW - Antibody-mediated rejection
KW - Bronchiolitis obliterans syndrome
KW - Chronic lung allograft syndrome
KW - Lung transplantation
KW - Plasmapheresis
KW - Rituximab
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U2 - 10.1016/j.trim.2014.06.004
DO - 10.1016/j.trim.2014.06.004
M3 - Article
C2 - 25004453
AN - SCOPUS:84906047960
SN - 0966-3274
VL - 31
SP - 75
EP - 80
JO - Transplant Immunology
JF - Transplant Immunology
IS - 2
ER -