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Outcomes of combination therapy for chronic antibody-mediated rejection in renal transplantation

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dc.contributor.authorKim, Myung-Gyu-
dc.contributor.authorKim, Yoon Jung-
dc.contributor.authorKwon, Hyuk Yong-
dc.contributor.authorPark, Hayne Cho-
dc.contributor.authorKoo, Tai Yeon-
dc.contributor.authorJeong, Jong Cheol-
dc.contributor.authorJeon, Hee Jung-
dc.contributor.authorHan, Miyeun-
dc.contributor.authorAhn, Curie-
dc.contributor.authorYang, Jaeseok-
dc.date.accessioned2021-09-05T18:22:31Z-
dc.date.available2021-09-05T18:22:31Z-
dc.date.created2021-06-15-
dc.date.issued2013-12-
dc.identifier.issn1320-5358-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/101440-
dc.description.abstractAimChronic antibody-mediated rejection (CAMR) in renal transplant patients has poor allograft outcomes. However, treatment strategy has not been established yet. Herein, we present short-term outcomes of combination therapy for CAMR. MethodsWe identified nine patients with CAMR or suspicious CAMR who were treated with antihumoral therapy from 2010 to 2011 and analyzed their medical records retrospectively. ResultsFive patients had CAMR, and four patients had suspicious CAMR. Severe transplant glomerulopathy (TG) was observed in seven patients. The estimated glomerular filtration rate (eGFR) was decreased in all patients before treatment. We used three different treatment regimens: (i) high-dose intravenous immunoglobulin (IVIG) and rituximab; (ii) high-dose IVIG, rituximab, and bortezomib; and (iii) plasmapheresis with low-dose IVIG, rituximab and bortezomib. After treatment with one of these three regimens, graft function improved or stabilized in six patients, whereas three patients showed further deterioration of eGFR. The third regimen suppressed deterioration of renal function in all patients. Most patients showed no progression of proteinuria. Infectious complications due to Pneumocystis jirovecii pneumonia and herpes zoster occurred in two patients. ConclusionCombination therapy for CAMR might be effective, even in patients with relatively late-stage CAMR. Summary at a Glance The short term outcomes of three approaches for chronic antibody mediated rejection, including bortezomib, IVIG and rituximab are presented in this clinical experience.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherWILEY-BLACKWELL-
dc.subjectALLOGRAFT-REJECTION-
dc.subjectKIDNEY-TRANSPLANTATION-
dc.subjectPROTEASOME INHIBITION-
dc.subjectRITUXIMAB THERAPY-
dc.subjectALLOANTIBODY-
dc.subjectDESENSITIZATION-
dc.subjectCLASSIFICATION-
dc.subjectGLOMERULOPATHY-
dc.subjectCAPILLARIES-
dc.subjectRECIPIENTS-
dc.titleOutcomes of combination therapy for chronic antibody-mediated rejection in renal transplantation-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Myung-Gyu-
dc.identifier.doi10.1111/nep.12157-
dc.identifier.scopusid2-s2.0-84888862075-
dc.identifier.wosid000327341600011-
dc.identifier.bibliographicCitationNEPHROLOGY, v.18, no.12, pp.820 - 826-
dc.relation.isPartOfNEPHROLOGY-
dc.citation.titleNEPHROLOGY-
dc.citation.volume18-
dc.citation.number12-
dc.citation.startPage820-
dc.citation.endPage826-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaUrology & Nephrology-
dc.relation.journalWebOfScienceCategoryUrology & Nephrology-
dc.subject.keywordPlusALLOGRAFT-REJECTION-
dc.subject.keywordPlusKIDNEY-TRANSPLANTATION-
dc.subject.keywordPlusPROTEASOME INHIBITION-
dc.subject.keywordPlusRITUXIMAB THERAPY-
dc.subject.keywordPlusALLOANTIBODY-
dc.subject.keywordPlusDESENSITIZATION-
dc.subject.keywordPlusCLASSIFICATION-
dc.subject.keywordPlusGLOMERULOPATHY-
dc.subject.keywordPlusCAPILLARIES-
dc.subject.keywordPlusRECIPIENTS-
dc.subject.keywordAuthorbortezomib-
dc.subject.keywordAuthorchronic antibody-mediated rejection-
dc.subject.keywordAuthorimmunoglobulin-
dc.subject.keywordAuthorplasmapheresis-
dc.subject.keywordAuthorrituximab-
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