Living donor kidney transplantation in crossmatch-positive patients enabled by peritransplant immunoadsorption and anti-CD20 therapy

Summary Living donor kidney transplantation in crossmatch‐positive patients is a challenge that requires specific measures. Ten patients with positive crossmatch results (n = 9) or negative crossmatch results but strong donor‐specific antibodies (DSA; n = 1) were desensitized using immunoadsorption...

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Veröffentlicht in:Transplant international 2012-05, Vol.25 (5), p.506-517
Hauptverfasser: Morath, Christian, Beimler, Jörg, Opelz, Gerhard, Scherer, Sabine, Schmidt, Jan, Macher-Goeppinger, Stephan, Klein, Katrin, Sommerer, Claudia, Schwenger, Vedat, Zeier, Martin, Süsal, Caner
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container_end_page 517
container_issue 5
container_start_page 506
container_title Transplant international
container_volume 25
creator Morath, Christian
Beimler, Jörg
Opelz, Gerhard
Scherer, Sabine
Schmidt, Jan
Macher-Goeppinger, Stephan
Klein, Katrin
Sommerer, Claudia
Schwenger, Vedat
Zeier, Martin
Süsal, Caner
description Summary Living donor kidney transplantation in crossmatch‐positive patients is a challenge that requires specific measures. Ten patients with positive crossmatch results (n = 9) or negative crossmatch results but strong donor‐specific antibodies (DSA; n = 1) were desensitized using immunoadsorption (IA) and anti‐CD20 antibody induction. IA was continued after transplantation and accompanied by HLA antibody monitoring and protocol biopsies. After a median of 10 IA treatments, all patients were desensitized successfully and transplanted. Median levels of mean fluorescence intensity (MFI) of Luminex‐DSA before desensitization were 6203 and decreased after desensitization and immediately before transplantation to 891. Patients received a median of seven post‐transplant IA treatments. At last visit, after a median follow‐up of 19 months, 9 of 10 patients had a functioning allograft and a median Luminex‐DSA of 149 MFI; serum creatinine was 1.6 mg/dl, and protein to creatinine ratio 0.1. Reversible acute antibody‐mediated rejection was diagnosed in three patients. One allograft was lost after the second post‐transplant year in a patient with catastrophic antiphospholipid syndrome. We describe a treatment algorithm for desensitization of living donor kidney transplant recipients that allows the rapid elimination of DSA with a low rate of side effects and results in good graft outcome.
doi_str_mv 10.1111/j.1432-2277.2012.01447.x
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Ten patients with positive crossmatch results (n = 9) or negative crossmatch results but strong donor‐specific antibodies (DSA; n = 1) were desensitized using immunoadsorption (IA) and anti‐CD20 antibody induction. IA was continued after transplantation and accompanied by HLA antibody monitoring and protocol biopsies. After a median of 10 IA treatments, all patients were desensitized successfully and transplanted. Median levels of mean fluorescence intensity (MFI) of Luminex‐DSA before desensitization were 6203 and decreased after desensitization and immediately before transplantation to 891. Patients received a median of seven post‐transplant IA treatments. At last visit, after a median follow‐up of 19 months, 9 of 10 patients had a functioning allograft and a median Luminex‐DSA of 149 MFI; serum creatinine was 1.6 mg/dl, and protein to creatinine ratio 0.1. Reversible acute antibody‐mediated rejection was diagnosed in three patients. One allograft was lost after the second post‐transplant year in a patient with catastrophic antiphospholipid syndrome. We describe a treatment algorithm for desensitization of living donor kidney transplant recipients that allows the rapid elimination of DSA with a low rate of side effects and results in good graft outcome.</description><identifier>ISSN: 0934-0874</identifier><identifier>EISSN: 1432-2277</identifier><identifier>DOI: 10.1111/j.1432-2277.2012.01447.x</identifier><identifier>PMID: 22372718</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adult ; Algorithms ; Antibodies, Monoclonal, Murine-Derived - therapeutic use ; antibody-mediated rejection ; Blood Component Removal - methods ; Desensitization, Immunologic - methods ; Female ; Graft Rejection - diagnosis ; Graft Survival ; Histocompatibility Testing ; Humans ; immunoadsorption ; Immunosorbent Techniques ; Immunosuppression - methods ; kidney transplantation ; Kidney Transplantation - adverse effects ; Kidney Transplantation - immunology ; Kidney Transplantation - methods ; living donor ; Living Donors ; Male ; Middle Aged ; positive crossmatch ; Rituximab ; Transplants &amp; implants ; Treatment Outcome</subject><ispartof>Transplant international, 2012-05, Vol.25 (5), p.506-517</ispartof><rights>2012 The Authors. 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Transplant International © 2012 European Society for Organ Transplantation.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3857-df1a6ed27403fe343ac6d68b3319303f3b0e7bd0ef54a9e165334472063250e63</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1432-2277.2012.01447.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1432-2277.2012.01447.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22372718$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Morath, Christian</creatorcontrib><creatorcontrib>Beimler, Jörg</creatorcontrib><creatorcontrib>Opelz, Gerhard</creatorcontrib><creatorcontrib>Scherer, Sabine</creatorcontrib><creatorcontrib>Schmidt, Jan</creatorcontrib><creatorcontrib>Macher-Goeppinger, Stephan</creatorcontrib><creatorcontrib>Klein, Katrin</creatorcontrib><creatorcontrib>Sommerer, Claudia</creatorcontrib><creatorcontrib>Schwenger, Vedat</creatorcontrib><creatorcontrib>Zeier, Martin</creatorcontrib><creatorcontrib>Süsal, Caner</creatorcontrib><title>Living donor kidney transplantation in crossmatch-positive patients enabled by peritransplant immunoadsorption and anti-CD20 therapy</title><title>Transplant international</title><addtitle>Transpl Int</addtitle><description>Summary Living donor kidney transplantation in crossmatch‐positive patients is a challenge that requires specific measures. Ten patients with positive crossmatch results (n = 9) or negative crossmatch results but strong donor‐specific antibodies (DSA; n = 1) were desensitized using immunoadsorption (IA) and anti‐CD20 antibody induction. IA was continued after transplantation and accompanied by HLA antibody monitoring and protocol biopsies. After a median of 10 IA treatments, all patients were desensitized successfully and transplanted. Median levels of mean fluorescence intensity (MFI) of Luminex‐DSA before desensitization were 6203 and decreased after desensitization and immediately before transplantation to 891. Patients received a median of seven post‐transplant IA treatments. At last visit, after a median follow‐up of 19 months, 9 of 10 patients had a functioning allograft and a median Luminex‐DSA of 149 MFI; serum creatinine was 1.6 mg/dl, and protein to creatinine ratio 0.1. Reversible acute antibody‐mediated rejection was diagnosed in three patients. One allograft was lost after the second post‐transplant year in a patient with catastrophic antiphospholipid syndrome. 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Ten patients with positive crossmatch results (n = 9) or negative crossmatch results but strong donor‐specific antibodies (DSA; n = 1) were desensitized using immunoadsorption (IA) and anti‐CD20 antibody induction. IA was continued after transplantation and accompanied by HLA antibody monitoring and protocol biopsies. After a median of 10 IA treatments, all patients were desensitized successfully and transplanted. Median levels of mean fluorescence intensity (MFI) of Luminex‐DSA before desensitization were 6203 and decreased after desensitization and immediately before transplantation to 891. Patients received a median of seven post‐transplant IA treatments. At last visit, after a median follow‐up of 19 months, 9 of 10 patients had a functioning allograft and a median Luminex‐DSA of 149 MFI; serum creatinine was 1.6 mg/dl, and protein to creatinine ratio 0.1. Reversible acute antibody‐mediated rejection was diagnosed in three patients. One allograft was lost after the second post‐transplant year in a patient with catastrophic antiphospholipid syndrome. We describe a treatment algorithm for desensitization of living donor kidney transplant recipients that allows the rapid elimination of DSA with a low rate of side effects and results in good graft outcome.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>22372718</pmid><doi>10.1111/j.1432-2277.2012.01447.x</doi><tpages>12</tpages></addata></record>
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source MEDLINE; EZB Electronic Journals Library; Wiley Blackwell Journals
subjects Adult
Algorithms
Antibodies, Monoclonal, Murine-Derived - therapeutic use
antibody-mediated rejection
Blood Component Removal - methods
Desensitization, Immunologic - methods
Female
Graft Rejection - diagnosis
Graft Survival
Histocompatibility Testing
Humans
immunoadsorption
Immunosorbent Techniques
Immunosuppression - methods
kidney transplantation
Kidney Transplantation - adverse effects
Kidney Transplantation - immunology
Kidney Transplantation - methods
living donor
Living Donors
Male
Middle Aged
positive crossmatch
Rituximab
Transplants & implants
Treatment Outcome
title Living donor kidney transplantation in crossmatch-positive patients enabled by peritransplant immunoadsorption and anti-CD20 therapy
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