HLA‐matched kidney transplantation in the era of modern immunosuppressive therapy

BACKGROUND The effect of HLA match on renal graft survival has become controversial as has the policy of mandatory sharing of kidneys. METHOD We performed a retrospective analysis of HLA matched (M) and mismatched (MM) kidney transplants in our center. Tacrolimus, mycophenolic acid, and steroids wer...

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Veröffentlicht in:Dialysis & transplantation 2010-05, Vol.39 (5), p.193-198
Hauptverfasser: Amatya, Arun, Florman, Sandy, Paramesh, Anil, Amatya, Anup, McGee, Jennifer, Killackey, Mary, Ren, Quing, Alper, Brent, Heneghan, Jean, Simon, Eric, Sullivan, Karen, Slakey, Douglas, Zhang, Rubin
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container_end_page 198
container_issue 5
container_start_page 193
container_title Dialysis & transplantation
container_volume 39
creator Amatya, Arun
Florman, Sandy
Paramesh, Anil
Amatya, Anup
McGee, Jennifer
Killackey, Mary
Ren, Quing
Alper, Brent
Heneghan, Jean
Simon, Eric
Sullivan, Karen
Slakey, Douglas
Zhang, Rubin
description BACKGROUND The effect of HLA match on renal graft survival has become controversial as has the policy of mandatory sharing of kidneys. METHOD We performed a retrospective analysis of HLA matched (M) and mismatched (MM) kidney transplants in our center. Tacrolimus, mycophenolic acid, and steroids were used as maintenance therapy and basiliximab induction was added for high‐risk patients. RESULT A total of 229 kidney transplants were included with median follow‐up of 5.1 years. The 5‐year death‐censored graft survival by Kaplan‐Meier method was significantly higher in the M group than in the MM group for deceased‐donor kidney transplants (log‐rank, p = .018). This graft survival advantage was detected in patients with a peak panel reactive antibody (PRA) greater than 20% (p = .023), but not in those with a PRA level of less than 20% (p = .32). The graft survival was not statistically different for live donor kidney transplants (p = .077). A mismatched kidney was an independent risk for graft loss (hazard ratio: 2.27, 95% confidence interval: 1.009–5.09, p = .047) and acute rejection was a significant cause of graft loss in mismatched deceased‐donor transplants (p = .035). CONCLUSION Acute rejection remains a significant cause of graft loss in HLA‐6‐antigen mismatched deceased‐donor kidney transplants. Our data support mandatory sharing of HLA‐matched kidneys in sensitized patients with a PRA level greater than 20%.
doi_str_mv 10.1002/dat.20439
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METHOD We performed a retrospective analysis of HLA matched (M) and mismatched (MM) kidney transplants in our center. Tacrolimus, mycophenolic acid, and steroids were used as maintenance therapy and basiliximab induction was added for high‐risk patients. RESULT A total of 229 kidney transplants were included with median follow‐up of 5.1 years. The 5‐year death‐censored graft survival by Kaplan‐Meier method was significantly higher in the M group than in the MM group for deceased‐donor kidney transplants (log‐rank, p = .018). This graft survival advantage was detected in patients with a peak panel reactive antibody (PRA) greater than 20% (p = .023), but not in those with a PRA level of less than 20% (p = .32). The graft survival was not statistically different for live donor kidney transplants (p = .077). A mismatched kidney was an independent risk for graft loss (hazard ratio: 2.27, 95% confidence interval: 1.009–5.09, p = .047) and acute rejection was a significant cause of graft loss in mismatched deceased‐donor transplants (p = .035). CONCLUSION Acute rejection remains a significant cause of graft loss in HLA‐6‐antigen mismatched deceased‐donor kidney transplants. Our data support mandatory sharing of HLA‐matched kidneys in sensitized patients with a PRA level greater than 20%.</description><identifier>ISSN: 0090-2934</identifier><identifier>ISSN: 1932-6920</identifier><identifier>EISSN: 1932-6920</identifier><identifier>DOI: 10.1002/dat.20439</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Antibodies ; Data processing ; Donors ; Graft rejection ; Histocompatibility antigen HLA ; Immunosuppressive agents ; Kidney transplantation ; Mycophenolic acid ; Risk factors ; Risk groups ; Steroid hormones ; Survival ; Tacrolimus</subject><ispartof>Dialysis &amp; transplantation, 2010-05, Vol.39 (5), p.193-198</ispartof><rights>Copyright © 2010 Wiley Periodicals, Inc.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3029-c59cee013f3edfe30985e82ccb0f5f60d30ffcde4a3f88dc421d7950daba9b053</citedby><cites>FETCH-LOGICAL-c3029-c59cee013f3edfe30985e82ccb0f5f60d30ffcde4a3f88dc421d7950daba9b053</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fdat.20439$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fdat.20439$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Amatya, Arun</creatorcontrib><creatorcontrib>Florman, Sandy</creatorcontrib><creatorcontrib>Paramesh, Anil</creatorcontrib><creatorcontrib>Amatya, Anup</creatorcontrib><creatorcontrib>McGee, Jennifer</creatorcontrib><creatorcontrib>Killackey, Mary</creatorcontrib><creatorcontrib>Ren, Quing</creatorcontrib><creatorcontrib>Alper, Brent</creatorcontrib><creatorcontrib>Heneghan, Jean</creatorcontrib><creatorcontrib>Simon, Eric</creatorcontrib><creatorcontrib>Sullivan, Karen</creatorcontrib><creatorcontrib>Slakey, Douglas</creatorcontrib><creatorcontrib>Zhang, Rubin</creatorcontrib><title>HLA‐matched kidney transplantation in the era of modern immunosuppressive therapy</title><title>Dialysis &amp; transplantation</title><description>BACKGROUND The effect of HLA match on renal graft survival has become controversial as has the policy of mandatory sharing of kidneys. METHOD We performed a retrospective analysis of HLA matched (M) and mismatched (MM) kidney transplants in our center. Tacrolimus, mycophenolic acid, and steroids were used as maintenance therapy and basiliximab induction was added for high‐risk patients. RESULT A total of 229 kidney transplants were included with median follow‐up of 5.1 years. The 5‐year death‐censored graft survival by Kaplan‐Meier method was significantly higher in the M group than in the MM group for deceased‐donor kidney transplants (log‐rank, p = .018). This graft survival advantage was detected in patients with a peak panel reactive antibody (PRA) greater than 20% (p = .023), but not in those with a PRA level of less than 20% (p = .32). The graft survival was not statistically different for live donor kidney transplants (p = .077). A mismatched kidney was an independent risk for graft loss (hazard ratio: 2.27, 95% confidence interval: 1.009–5.09, p = .047) and acute rejection was a significant cause of graft loss in mismatched deceased‐donor transplants (p = .035). CONCLUSION Acute rejection remains a significant cause of graft loss in HLA‐6‐antigen mismatched deceased‐donor kidney transplants. 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A mismatched kidney was an independent risk for graft loss (hazard ratio: 2.27, 95% confidence interval: 1.009–5.09, p = .047) and acute rejection was a significant cause of graft loss in mismatched deceased‐donor transplants (p = .035). CONCLUSION Acute rejection remains a significant cause of graft loss in HLA‐6‐antigen mismatched deceased‐donor kidney transplants. Our data support mandatory sharing of HLA‐matched kidneys in sensitized patients with a PRA level greater than 20%.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><doi>10.1002/dat.20439</doi><tpages>6</tpages></addata></record>
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subjects Antibodies
Data processing
Donors
Graft rejection
Histocompatibility antigen HLA
Immunosuppressive agents
Kidney transplantation
Mycophenolic acid
Risk factors
Risk groups
Steroid hormones
Survival
Tacrolimus
title HLA‐matched kidney transplantation in the era of modern immunosuppressive therapy
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