IgM-enriched Human Intravenous Immunoglobulin for Treatment of Early Antibody Mediated Rejection after Heart Transplantation

2018 ◽  
Vol 102 ◽  
pp. S828
Author(s):  
Markus J Barten ◽  
Christian Buchholz ◽  
Alexander Bernhardt ◽  
Meike Rybczynski ◽  
Hanno Grahn ◽  
...  
2021 ◽  
Author(s):  
Michelle M. Kittleson ◽  
Nikhil Patel ◽  
David H. Chang ◽  
Evan P. Kransdorf ◽  
Jon A. Kobashigawa ◽  
...  

2014 ◽  
Vol 98 ◽  
pp. 432 ◽  
Author(s):  
A. Aliabadi ◽  
K. Uyanik-Uenal ◽  
J. Goekler ◽  
S. Wallner ◽  
M. Masseti ◽  
...  

2020 ◽  
Vol 4 (1) ◽  
pp. 1-4
Author(s):  
Bernd Ludwig ◽  
Johanna Schneider ◽  
Daniela Föll ◽  
Qian Zhou

Abstract Background Antibody-mediated rejection (AMR) in cardiac transplantation may manifest early within the first weeks after transplantation but also late after months to years following transplantation resulting in mild heart failure to cardiogenic shock. While patients with early cardiac AMR are less affected and seem to have survival rates comparable to transplant recipients without AMR, late cardiac AMR is frequently associated with graft dysfunction, fulminant forms of cardiac allograft vasculopathy, and a high mortality rate. Nevertheless, AMR of cardiac allografts remains difficult to diagnose and to treat. Case summary We report the case of a 47-year-old male patient with late AMR of the cardiac allograft 3 years after heart transplantation. Antibody-mediated rejection was confirmed by endomyocardial biopsy and the presence of donor-specific antibodies (DSA). The patient was treated with high dose of prednisolone, plasmapheresis, intravenous Gamma Globulin, rituximab, immunoadsorption, and bortezomib. Under this treatment regimen left ventricular ejection fraction and pro B-type natriuretic peptide recovered, and the patient improved to New York Heart Association Class I. Currently, 3 years after the diagnosis of cardiac AMR, graft function continues to be nearly normal, and there is no evidence for transplant vasculopathy. Discussion This case illustrates that AMR can occur at any time after transplantation. Although graft function fully recovered after treatment in our patient, the level of DSA remained high, suggesting that DSA may not be a reliable parameter to determine the intensity and duration of the therapy.


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