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dc.creatorGiannopoulou M., Tarassi K., Tsouka G., Christodoulidou C., Stefanidis I., Eleftheriadis T.en
dc.date.accessioned2023-01-31T07:42:01Z
dc.date.available2023-01-31T07:42:01Z
dc.date.issued2022
dc.identifier10.6002/ect.2022.0146
dc.identifier.issn13040855
dc.identifier.urihttp://hdl.handle.net/11615/72338
dc.description.abstractChronic 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.en
dc.language.isoenen
dc.sourceExperimental and Clinical Transplantationen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85135501013&doi=10.6002%2fect.2022.0146&partnerID=40&md5=e0430dadee1e2e77aa34cbec206842ba
dc.subjectantibodyen
dc.subjectbasiliximaben
dc.subjectcreatinineen
dc.subjectdonor specific antibodyen
dc.subjectHLA antigenen
dc.subjectHLA antigen class 1en
dc.subjectHLA antigen class 2en
dc.subjectHLA DQ4 antibodyen
dc.subjectHLA DQ5 antibodyen
dc.subjectHLA DQ6 antibodyen
dc.subjectHLA DQA1 antibodyen
dc.subjectHLA DR51 antibodyen
dc.subjectmethylprednisoloneen
dc.subjectmycophenolic aciden
dc.subjectphospholipase A2 receptoren
dc.subjectrituximaben
dc.subjecttacrolimusen
dc.subjectunclassified drugen
dc.subjectantibodyen
dc.subjectimmunosuppressive agenten
dc.subjectrituximaben
dc.subjectadulten
dc.subjectantibody detectionen
dc.subjectantibody mediated rejectionen
dc.subjectArticleen
dc.subjectcase reporten
dc.subjectclinical articleen
dc.subjectcreatinine blood levelen
dc.subjectend stage renal diseaseen
dc.subjectgraft recipienten
dc.subjecthemodialysisen
dc.subjecthistologyen
dc.subjecthumanen
dc.subjecthuman tissueen
dc.subjectimmunosuppressive treatmenten
dc.subjectkidney biopsyen
dc.subjectkidney donoren
dc.subjectkidney transplantationen
dc.subjectliving donoren
dc.subjectmaleen
dc.subjectmembranous glomerulonephritisen
dc.subjectproteinuriaen
dc.subjectwifeen
dc.subjectadverse eventen
dc.subjectgraft rejectionen
dc.subjectmembranous glomerulonephritisen
dc.subjectpathologyen
dc.subjecttreatment outcomeen
dc.subjectAntibodiesen
dc.subjectGlomerulonephritis, Membranousen
dc.subjectGraft Rejectionen
dc.subjectHumansen
dc.subjectImmunosuppressive Agentsen
dc.subjectKidney Transplantationen
dc.subjectMaleen
dc.subjectRituximaben
dc.subjectTreatment Outcomeen
dc.subjectBaskent Universityen
dc.titleRituximab Administered for Recurrent Membranous Nephropathy in a Kidney Transplant Recipient Did Not Eliminate Donor-Specific Antibodiesen
dc.typejournalArticleen


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