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Thymoglobulin and ischemia reperfusion injury in kidney and liver transplantation
Since the beginning of organ transplantation, graft preservation has been one of the most important concerns. Ischemia reperfusion injury (IRI), which plays an important role in the quality and function of the graft, is a major cause for increased length of hospitalization and decreased long term gr...
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Published in: | Nephrology, dialysis, transplantation dialysis, transplantation, 2007-09, Vol.22 (suppl-8), p.viii54-viii60 |
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creator | Mehrabi, A. Mood, Zh. A. Sadeghi, M. Schmied, B. M. Müller, S. A. Welsch, Th Kuttymuratov, G. Wente, M. N. Weitz, J. Zeier, M. Morath, Ch Riediger, C. Schemmer, P. Encke, J. Büchler, M. W. Schmidt, J. |
description | Since the beginning of organ transplantation, graft preservation has been one of the most important concerns. Ischemia reperfusion injury (IRI), which plays an important role in the quality and function of the graft, is a major cause for increased length of hospitalization and decreased long term graft survival. Among numerous attempts which have been made to minimize graft damage associated with IRI, the use of Thymoglobulin (TG) seems to offer potential benefits. TG is a polyclonal antibody which blocks multiple antigens related to IRI, in addition to its better known T cell depleting effects. This review will focus on the use of TG in preventing IRI in kidney transplantation (KTx) and liver transplantation (LTx). Different studies in experimental and clinical transplantation have shown that TG protects renal and liver grafts from IRI. Improvement in early graft function and decreased delayed graft function (DGF) rates are some of the clinical benefits of TG. Additionally, it is used in patients with hepatorenal syndrome to support the recovery of kidney function after LTx, by allowing reduced exposure to nephrotoxic calcineurin inhibitors as well as improving liver graft function by minimizing IRI. TG can reduce acute rejection rates in kidney and liver transplant recipients, decrease the length of hospital stay, and hence reduce transplantation costs. TG can play an important role in expanding the donor pool in both KTx and LTx by improving long-term graft and patient survival rates which increases the possibility of using marginal donors. Although controversial, the development of post-transplant lymphoproliferative disorder is a potential side effect of TG. No single optimal immunosuppressive regimen has given consistent results in decreasing the graft damage following IRI; however, TG usage in KTx and LTx appears to have some benefits in reducing IRI. |
doi_str_mv | 10.1093/ndt/gfm651 |
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A. ; Sadeghi, M. ; Schmied, B. M. ; Müller, S. A. ; Welsch, Th ; Kuttymuratov, G. ; Wente, M. N. ; Weitz, J. ; Zeier, M. ; Morath, Ch ; Riediger, C. ; Schemmer, P. ; Encke, J. ; Büchler, M. W. ; Schmidt, J.</creator><creatorcontrib>Mehrabi, A. ; Mood, Zh. A. ; Sadeghi, M. ; Schmied, B. M. ; Müller, S. A. ; Welsch, Th ; Kuttymuratov, G. ; Wente, M. N. ; Weitz, J. ; Zeier, M. ; Morath, Ch ; Riediger, C. ; Schemmer, P. ; Encke, J. ; Büchler, M. W. ; Schmidt, J.</creatorcontrib><description>Since the beginning of organ transplantation, graft preservation has been one of the most important concerns. Ischemia reperfusion injury (IRI), which plays an important role in the quality and function of the graft, is a major cause for increased length of hospitalization and decreased long term graft survival. Among numerous attempts which have been made to minimize graft damage associated with IRI, the use of Thymoglobulin (TG) seems to offer potential benefits. TG is a polyclonal antibody which blocks multiple antigens related to IRI, in addition to its better known T cell depleting effects. This review will focus on the use of TG in preventing IRI in kidney transplantation (KTx) and liver transplantation (LTx). Different studies in experimental and clinical transplantation have shown that TG protects renal and liver grafts from IRI. Improvement in early graft function and decreased delayed graft function (DGF) rates are some of the clinical benefits of TG. Additionally, it is used in patients with hepatorenal syndrome to support the recovery of kidney function after LTx, by allowing reduced exposure to nephrotoxic calcineurin inhibitors as well as improving liver graft function by minimizing IRI. TG can reduce acute rejection rates in kidney and liver transplant recipients, decrease the length of hospital stay, and hence reduce transplantation costs. TG can play an important role in expanding the donor pool in both KTx and LTx by improving long-term graft and patient survival rates which increases the possibility of using marginal donors. Although controversial, the development of post-transplant lymphoproliferative disorder is a potential side effect of TG. No single optimal immunosuppressive regimen has given consistent results in decreasing the graft damage following IRI; however, TG usage in KTx and LTx appears to have some benefits in reducing IRI.</description><identifier>ISSN: 0931-0509</identifier><identifier>EISSN: 1460-2385</identifier><identifier>DOI: 10.1093/ndt/gfm651</identifier><identifier>PMID: 17890265</identifier><identifier>CODEN: NDTREA</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Antibodies, Monoclonal - chemistry ; Antibodies, Monoclonal - therapeutic use ; Antilymphocyte Serum ; Biological and medical sciences ; Clinical Trials as Topic ; Emergency and intensive care: renal failure. Dialysis management ; Graft Rejection ; Graft Survival ; Humans ; Immunosuppressive Agents - therapeutic use ; Intensive care medicine ; ischemia reperfusion injury ; kidney transplantation ; Kidney Transplantation - methods ; liver transplantation ; Liver Transplantation - methods ; Liver, biliary tract, pancreas, portal circulation, spleen ; Medical sciences ; Reperfusion Injury - therapy ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Surgery of the digestive system ; Surgery of the urinary system ; thymoglobulin ; Transplantation, Homologous ; Treatment Outcome</subject><ispartof>Nephrology, dialysis, transplantation, 2007-09, Vol.22 (suppl-8), p.viii54-viii60</ispartof><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-986c0ec7cbd642f36e0a26dcae69a9b69377bdfd9cd66051b26a246b99c1d61a3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19225343$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17890265$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mehrabi, A.</creatorcontrib><creatorcontrib>Mood, Zh. A.</creatorcontrib><creatorcontrib>Sadeghi, M.</creatorcontrib><creatorcontrib>Schmied, B. M.</creatorcontrib><creatorcontrib>Müller, S. A.</creatorcontrib><creatorcontrib>Welsch, Th</creatorcontrib><creatorcontrib>Kuttymuratov, G.</creatorcontrib><creatorcontrib>Wente, M. N.</creatorcontrib><creatorcontrib>Weitz, J.</creatorcontrib><creatorcontrib>Zeier, M.</creatorcontrib><creatorcontrib>Morath, Ch</creatorcontrib><creatorcontrib>Riediger, C.</creatorcontrib><creatorcontrib>Schemmer, P.</creatorcontrib><creatorcontrib>Encke, J.</creatorcontrib><creatorcontrib>Büchler, M. W.</creatorcontrib><creatorcontrib>Schmidt, J.</creatorcontrib><title>Thymoglobulin and ischemia reperfusion injury in kidney and liver transplantation</title><title>Nephrology, dialysis, transplantation</title><addtitle>Nephrol Dial Transplant</addtitle><description>Since the beginning of organ transplantation, graft preservation has been one of the most important concerns. Ischemia reperfusion injury (IRI), which plays an important role in the quality and function of the graft, is a major cause for increased length of hospitalization and decreased long term graft survival. Among numerous attempts which have been made to minimize graft damage associated with IRI, the use of Thymoglobulin (TG) seems to offer potential benefits. TG is a polyclonal antibody which blocks multiple antigens related to IRI, in addition to its better known T cell depleting effects. This review will focus on the use of TG in preventing IRI in kidney transplantation (KTx) and liver transplantation (LTx). Different studies in experimental and clinical transplantation have shown that TG protects renal and liver grafts from IRI. Improvement in early graft function and decreased delayed graft function (DGF) rates are some of the clinical benefits of TG. Additionally, it is used in patients with hepatorenal syndrome to support the recovery of kidney function after LTx, by allowing reduced exposure to nephrotoxic calcineurin inhibitors as well as improving liver graft function by minimizing IRI. TG can reduce acute rejection rates in kidney and liver transplant recipients, decrease the length of hospital stay, and hence reduce transplantation costs. TG can play an important role in expanding the donor pool in both KTx and LTx by improving long-term graft and patient survival rates which increases the possibility of using marginal donors. Although controversial, the development of post-transplant lymphoproliferative disorder is a potential side effect of TG. No single optimal immunosuppressive regimen has given consistent results in decreasing the graft damage following IRI; however, TG usage in KTx and LTx appears to have some benefits in reducing IRI.</description><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Antibodies, Monoclonal - chemistry</subject><subject>Antibodies, Monoclonal - therapeutic use</subject><subject>Antilymphocyte Serum</subject><subject>Biological and medical sciences</subject><subject>Clinical Trials as Topic</subject><subject>Emergency and intensive care: renal failure. Dialysis management</subject><subject>Graft Rejection</subject><subject>Graft Survival</subject><subject>Humans</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Intensive care medicine</subject><subject>ischemia reperfusion injury</subject><subject>kidney transplantation</subject><subject>Kidney Transplantation - methods</subject><subject>liver transplantation</subject><subject>Liver Transplantation - methods</subject><subject>Liver, biliary tract, pancreas, portal circulation, spleen</subject><subject>Medical sciences</subject><subject>Reperfusion Injury - therapy</subject><subject>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</subject><subject>Surgery of the digestive system</subject><subject>Surgery of the urinary system</subject><subject>thymoglobulin</subject><subject>Transplantation, Homologous</subject><subject>Treatment Outcome</subject><issn>0931-0509</issn><issn>1460-2385</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNpF0MtKAzEUBuAgiq3VjQ8gs9GFMDaXmUyzlKJWLYilSnETMkmmTTs3kxmxb2-0g12dxfn4OecH4BzBGwQZGZaqGS6zgsboAPRRRGGIySg-BH2_RCGMIeuBE-fWEEKGk-QY9FAyYhDTuA9e56ttUS3zKm1zUwaiVIFxcqULIwKra22z1pmqDEy5bu3Wj2BjVKm3fzI3X9oGjRWlq3NRNqLx9BQcZSJ3-qybA_B2fzcfT8Lpy8Pj-HYaygjDJmQjKqGWiUwVjXBGqIYCUyWFpkywlDKSJKnKFJOKUhijFFOBI5oyJpGiSJABuNrl1rb6bLVreOEv17k_RFet4xhGFEPGPLzeQWkr56zOeG1NIeyWI8h_C-S-QL4r0OOLLrVNC632tGvMg8sOCCdFnvnnpXF7xzCOSUS8C3fOuEZ__--F3XCakCTmk8UHn0WL6ez5acbfyQ8CHoru</recordid><startdate>20070901</startdate><enddate>20070901</enddate><creator>Mehrabi, A.</creator><creator>Mood, Zh. A.</creator><creator>Sadeghi, M.</creator><creator>Schmied, B. M.</creator><creator>Müller, S. A.</creator><creator>Welsch, Th</creator><creator>Kuttymuratov, G.</creator><creator>Wente, M. N.</creator><creator>Weitz, J.</creator><creator>Zeier, M.</creator><creator>Morath, Ch</creator><creator>Riediger, C.</creator><creator>Schemmer, P.</creator><creator>Encke, J.</creator><creator>Büchler, M. W.</creator><creator>Schmidt, J.</creator><general>Oxford University Press</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope></search><sort><creationdate>20070901</creationdate><title>Thymoglobulin and ischemia reperfusion injury in kidney and liver transplantation</title><author>Mehrabi, A. ; Mood, Zh. A. ; Sadeghi, M. ; Schmied, B. M. ; Müller, S. A. ; Welsch, Th ; Kuttymuratov, G. ; Wente, M. 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Dialysis management</topic><topic>Graft Rejection</topic><topic>Graft Survival</topic><topic>Humans</topic><topic>Immunosuppressive Agents - therapeutic use</topic><topic>Intensive care medicine</topic><topic>ischemia reperfusion injury</topic><topic>kidney transplantation</topic><topic>Kidney Transplantation - methods</topic><topic>liver transplantation</topic><topic>Liver Transplantation - methods</topic><topic>Liver, biliary tract, pancreas, portal circulation, spleen</topic><topic>Medical sciences</topic><topic>Reperfusion Injury - therapy</topic><topic>Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases</topic><topic>Surgery of the digestive system</topic><topic>Surgery of the urinary system</topic><topic>thymoglobulin</topic><topic>Transplantation, Homologous</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mehrabi, A.</creatorcontrib><creatorcontrib>Mood, Zh. 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W.</creatorcontrib><creatorcontrib>Schmidt, J.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Nephrology, dialysis, transplantation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mehrabi, A.</au><au>Mood, Zh. A.</au><au>Sadeghi, M.</au><au>Schmied, B. M.</au><au>Müller, S. A.</au><au>Welsch, Th</au><au>Kuttymuratov, G.</au><au>Wente, M. N.</au><au>Weitz, J.</au><au>Zeier, M.</au><au>Morath, Ch</au><au>Riediger, C.</au><au>Schemmer, P.</au><au>Encke, J.</au><au>Büchler, M. W.</au><au>Schmidt, J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Thymoglobulin and ischemia reperfusion injury in kidney and liver transplantation</atitle><jtitle>Nephrology, dialysis, transplantation</jtitle><addtitle>Nephrol Dial Transplant</addtitle><date>2007-09-01</date><risdate>2007</risdate><volume>22</volume><issue>suppl-8</issue><spage>viii54</spage><epage>viii60</epage><pages>viii54-viii60</pages><issn>0931-0509</issn><eissn>1460-2385</eissn><coden>NDTREA</coden><abstract>Since the beginning of organ transplantation, graft preservation has been one of the most important concerns. Ischemia reperfusion injury (IRI), which plays an important role in the quality and function of the graft, is a major cause for increased length of hospitalization and decreased long term graft survival. Among numerous attempts which have been made to minimize graft damage associated with IRI, the use of Thymoglobulin (TG) seems to offer potential benefits. TG is a polyclonal antibody which blocks multiple antigens related to IRI, in addition to its better known T cell depleting effects. This review will focus on the use of TG in preventing IRI in kidney transplantation (KTx) and liver transplantation (LTx). Different studies in experimental and clinical transplantation have shown that TG protects renal and liver grafts from IRI. Improvement in early graft function and decreased delayed graft function (DGF) rates are some of the clinical benefits of TG. Additionally, it is used in patients with hepatorenal syndrome to support the recovery of kidney function after LTx, by allowing reduced exposure to nephrotoxic calcineurin inhibitors as well as improving liver graft function by minimizing IRI. TG can reduce acute rejection rates in kidney and liver transplant recipients, decrease the length of hospital stay, and hence reduce transplantation costs. TG can play an important role in expanding the donor pool in both KTx and LTx by improving long-term graft and patient survival rates which increases the possibility of using marginal donors. Although controversial, the development of post-transplant lymphoproliferative disorder is a potential side effect of TG. No single optimal immunosuppressive regimen has given consistent results in decreasing the graft damage following IRI; however, TG usage in KTx and LTx appears to have some benefits in reducing IRI.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>17890265</pmid><doi>10.1093/ndt/gfm651</doi><oa>free_for_read</oa></addata></record> |
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subjects | Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Antibodies, Monoclonal - chemistry Antibodies, Monoclonal - therapeutic use Antilymphocyte Serum Biological and medical sciences Clinical Trials as Topic Emergency and intensive care: renal failure. Dialysis management Graft Rejection Graft Survival Humans Immunosuppressive Agents - therapeutic use Intensive care medicine ischemia reperfusion injury kidney transplantation Kidney Transplantation - methods liver transplantation Liver Transplantation - methods Liver, biliary tract, pancreas, portal circulation, spleen Medical sciences Reperfusion Injury - therapy Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases Surgery of the digestive system Surgery of the urinary system thymoglobulin Transplantation, Homologous Treatment Outcome |
title | Thymoglobulin and ischemia reperfusion injury in kidney and liver transplantation |
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