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Rituximab Administered for Recurrent Membranous Nephropathy in a Kidney Transplant Recipient Did Not Eliminate Donor-Specific Antibodies

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Autore
Giannopoulou M., Tarassi K., Tsouka G., Christodoulidou C., Stefanidis I., Eleftheriadis T.
Data
2022
Language
en
DOI
10.6002/ect.2022.0146
Soggetto
antibody
basiliximab
creatinine
donor specific antibody
HLA antigen
HLA antigen class 1
HLA antigen class 2
HLA DQ4 antibody
HLA DQ5 antibody
HLA DQ6 antibody
HLA DQA1 antibody
HLA DR51 antibody
methylprednisolone
mycophenolic acid
phospholipase A2 receptor
rituximab
tacrolimus
unclassified drug
antibody
immunosuppressive agent
rituximab
adult
antibody detection
antibody mediated rejection
Article
case report
clinical article
creatinine blood level
end stage renal disease
graft recipient
hemodialysis
histology
human
human tissue
immunosuppressive treatment
kidney biopsy
kidney donor
kidney transplantation
living donor
male
membranous glomerulonephritis
proteinuria
wife
adverse event
graft rejection
membranous glomerulonephritis
pathology
treatment outcome
Antibodies
Glomerulonephritis, Membranous
Graft Rejection
Humans
Immunosuppressive Agents
Kidney Transplantation
Male
Rituximab
Treatment Outcome
Baskent University
Mostra tutti i dati dell'item
Abstract
Chronic active antibody-mediated rejection is the leading cause of kidney transplant failure. Although various immunosuppressive agents have been tested, rituximab included, presently there is no effective treatment. There are reports about the beneficial role of certain immunosuppressive protocols that include rituximab to reduce donor-specific antibodies, the cause of chronic active antibody-mediated rejection. If an immunosuppressive agent reduces donor-specific antibodies, its administration before the occurrence of chronic active antibody-mediated rejection may be beneficial. We describe a case of a renal transplant recipient with recurrent membranous nephropathy and recent development of donor-specific antibodies but without histological evidence of active antibody-mediated rejection. The patient received 3 weekly doses of rituximab for recurrent membranous nephropathy, and complete remission was achieved. One year after, he has preserved an excellent renal function without proteinuria. However, repeated measurements of donor-specific antibodies revealed that rituximab only modestly reduced donor-specific antibodies. Donor-specific antibody levels remained considerably higher than the laboratory reference value. Thus, rituximab alone may not have a role to prevent chronic active antibody-mediated rejection in patients with donor-specific antibodies. © Başkent University 2022 Printed in Turkey. All Rights Reserved.
URI
http://hdl.handle.net/11615/72338
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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