Management of sensitized pediatric patients prior to renal transplantation
Background Data on renal allograft outcome in sensitized children are scarce. We report the clinical courses of four children who received desensitization therapy prior to renal transplantation in our institution. Methods Between 2009 and 2011, four pediatric patients with stage 5 chronic kidney dis...
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Veröffentlicht in: | Pediatric nephrology (Berlin, West) West), 2016-10, Vol.31 (10), p.1691-1698 |
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creator | Pirojsakul, Kwanchai Desai, Dev Lacelle, Chantale Seikaly, Mouin G. |
description | Background
Data on renal allograft outcome in sensitized children are scarce. We report the clinical courses of four children who received desensitization therapy prior to renal transplantation in our institution.
Methods
Between 2009 and 2011, four pediatric patients with stage 5 chronic kidney disease received desensitization therapy due to: (1) positive donor-specific antibodies (DSA) and/or crossmatches with potential living donors, (2) more than three positive crossmatches with deceased donors or (3) high calculated panel-reactive antibody of >80 %. Desensitization with rituximab, intravenous immunoglobulin and bortezomib was performed in all patients. Induction therapy included combinations of plasmapheresis and/or alemtuzumab or anti-thymocyte globulin. Standard post-transplant medications included tacrolimus, mycophenolate mofetil and prednisolone.
Results
Post-transplant screening revealed DSA in three patients. Biopsy showed no evidence of rejection at 1 month in two patients, one of whom developed chronic active antibody-mediated rejection 4.5 years later. One patient developed borderline acute cellular rejection at 1 month, but the serum creatinine level was stable and DSA disappeared without treatment 1 month later, with stable long-term allograft function at 3 years. Estimated or measured glomerular filtration rate of the patients ranged between 30 and 75 ml/min/1.73 m
2
after 1 to 4.5 years.
Conclusions
The four sensitized patients reported here who received desensitization therapy had successful renal transplants with a low risk of immediate post-transplant rejection. Overall, long-term allograft functions and complications from immunosuppression were encouraging. |
doi_str_mv | 10.1007/s00467-015-3295-z |
format | Article |
fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_1819140506</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A470430897</galeid><sourcerecordid>A470430897</sourcerecordid><originalsourceid>FETCH-LOGICAL-c541t-27d08d2ff87aae27de8462fbdfb7cc2f289fa61b6a5f512b0c18e49d8e0568c93</originalsourceid><addsrcrecordid>eNqNkkFvFSEUhYmxsc_qD3BjJjExbqZeGGaGWTaNVpsaN5p0Rxjm8kozAyMwi75fL6-v1bZ5JoYFgfudCxwOIW8oHFOA9mME4E1bAq3LinV1uXlGVpRXrKSduHxOVtBVtAROLw_JyxivAUDUonlBDlkjgHacr8j5N-XUGid0qfCmiOiiTXaDQzHjYFUKVhezSjbXYzEH60ORfBHQqbFIQbk4j8qlDHj3ihwYNUZ8fTcfkZ-fP_04_VJefD_7enpyUeqa01SydgAxMGNEqxTmFQreMNMPpm-1ZoaJzqiG9o2qTU1ZD5oK5N0gEOpG6K46Ih92fefgfy0Yk5xs1Djmi6BfoqSCdpRDDc3_oDwbJiqW0XdP0Gu_hPzMW6rKRzcM_lJrNaK0zvhsgt42lSe8BV6B6NpMlXuoNToMavQOjc3bj_jjPXweA05W7xW8fyC4QjWmq-jHZfsN8TFId6AOPsaARuY_nFS4kRTkNkNylyGZMyS3GZKbrHl758TSTzj8UdyHJgNsB8RccmsMD6z6Z9ffAEzPgQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1813568620</pqid></control><display><type>article</type><title>Management of sensitized pediatric patients prior to renal transplantation</title><source>MEDLINE</source><source>SpringerLink Journals</source><creator>Pirojsakul, Kwanchai ; Desai, Dev ; Lacelle, Chantale ; Seikaly, Mouin G.</creator><creatorcontrib>Pirojsakul, Kwanchai ; Desai, Dev ; Lacelle, Chantale ; Seikaly, Mouin G.</creatorcontrib><description>Background
Data on renal allograft outcome in sensitized children are scarce. We report the clinical courses of four children who received desensitization therapy prior to renal transplantation in our institution.
Methods
Between 2009 and 2011, four pediatric patients with stage 5 chronic kidney disease received desensitization therapy due to: (1) positive donor-specific antibodies (DSA) and/or crossmatches with potential living donors, (2) more than three positive crossmatches with deceased donors or (3) high calculated panel-reactive antibody of >80 %. Desensitization with rituximab, intravenous immunoglobulin and bortezomib was performed in all patients. Induction therapy included combinations of plasmapheresis and/or alemtuzumab or anti-thymocyte globulin. Standard post-transplant medications included tacrolimus, mycophenolate mofetil and prednisolone.
Results
Post-transplant screening revealed DSA in three patients. Biopsy showed no evidence of rejection at 1 month in two patients, one of whom developed chronic active antibody-mediated rejection 4.5 years later. One patient developed borderline acute cellular rejection at 1 month, but the serum creatinine level was stable and DSA disappeared without treatment 1 month later, with stable long-term allograft function at 3 years. Estimated or measured glomerular filtration rate of the patients ranged between 30 and 75 ml/min/1.73 m
2
after 1 to 4.5 years.
Conclusions
The four sensitized patients reported here who received desensitization therapy had successful renal transplants with a low risk of immediate post-transplant rejection. Overall, long-term allograft functions and complications from immunosuppression were encouraging.</description><identifier>ISSN: 0931-041X</identifier><identifier>EISSN: 1432-198X</identifier><identifier>DOI: 10.1007/s00467-015-3295-z</identifier><identifier>PMID: 26801944</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Adolescent ; Antibodies ; Apheresis ; Bortezomib - therapeutic use ; Care and treatment ; Child ; Child, Preschool ; Chronic kidney failure ; Desensitization, Immunologic - methods ; Female ; Genetic aspects ; Glomerular Filtration Rate ; Graft Rejection - drug therapy ; Graft Rejection - pathology ; Graft Rejection - prevention & control ; Histocompatibility Testing ; HLA antigens ; HLA Antigens - immunology ; Humans ; Immunoglobulins ; Immunoglobulins, Intravenous - therapeutic use ; Immunosuppressive Agents - therapeutic use ; Infant ; Kidney diseases ; Kidney transplantation ; Kidney Transplantation - methods ; Kidney transplants ; Male ; Medicine ; Medicine & Public Health ; Methods ; Nephrology ; Original Article ; Patients ; Pediatrics ; Physiological aspects ; Plasmapheresis ; Renal Insufficiency, Chronic - immunology ; Renal Insufficiency, Chronic - surgery ; Rituximab - therapeutic use ; Tacrolimus - therapeutic use ; Urology</subject><ispartof>Pediatric nephrology (Berlin, West), 2016-10, Vol.31 (10), p.1691-1698</ispartof><rights>IPNA 2016</rights><rights>COPYRIGHT 2016 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c541t-27d08d2ff87aae27de8462fbdfb7cc2f289fa61b6a5f512b0c18e49d8e0568c93</citedby><cites>FETCH-LOGICAL-c541t-27d08d2ff87aae27de8462fbdfb7cc2f289fa61b6a5f512b0c18e49d8e0568c93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00467-015-3295-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00467-015-3295-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26801944$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pirojsakul, Kwanchai</creatorcontrib><creatorcontrib>Desai, Dev</creatorcontrib><creatorcontrib>Lacelle, Chantale</creatorcontrib><creatorcontrib>Seikaly, Mouin G.</creatorcontrib><title>Management of sensitized pediatric patients prior to renal transplantation</title><title>Pediatric nephrology (Berlin, West)</title><addtitle>Pediatr Nephrol</addtitle><addtitle>Pediatr Nephrol</addtitle><description>Background
Data on renal allograft outcome in sensitized children are scarce. We report the clinical courses of four children who received desensitization therapy prior to renal transplantation in our institution.
Methods
Between 2009 and 2011, four pediatric patients with stage 5 chronic kidney disease received desensitization therapy due to: (1) positive donor-specific antibodies (DSA) and/or crossmatches with potential living donors, (2) more than three positive crossmatches with deceased donors or (3) high calculated panel-reactive antibody of >80 %. Desensitization with rituximab, intravenous immunoglobulin and bortezomib was performed in all patients. Induction therapy included combinations of plasmapheresis and/or alemtuzumab or anti-thymocyte globulin. Standard post-transplant medications included tacrolimus, mycophenolate mofetil and prednisolone.
Results
Post-transplant screening revealed DSA in three patients. Biopsy showed no evidence of rejection at 1 month in two patients, one of whom developed chronic active antibody-mediated rejection 4.5 years later. One patient developed borderline acute cellular rejection at 1 month, but the serum creatinine level was stable and DSA disappeared without treatment 1 month later, with stable long-term allograft function at 3 years. Estimated or measured glomerular filtration rate of the patients ranged between 30 and 75 ml/min/1.73 m
2
after 1 to 4.5 years.
Conclusions
The four sensitized patients reported here who received desensitization therapy had successful renal transplants with a low risk of immediate post-transplant rejection. Overall, long-term allograft functions and complications from immunosuppression were encouraging.</description><subject>Adolescent</subject><subject>Antibodies</subject><subject>Apheresis</subject><subject>Bortezomib - therapeutic use</subject><subject>Care and treatment</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Chronic kidney failure</subject><subject>Desensitization, Immunologic - methods</subject><subject>Female</subject><subject>Genetic aspects</subject><subject>Glomerular Filtration Rate</subject><subject>Graft Rejection - drug therapy</subject><subject>Graft Rejection - pathology</subject><subject>Graft Rejection - prevention & control</subject><subject>Histocompatibility Testing</subject><subject>HLA antigens</subject><subject>HLA Antigens - immunology</subject><subject>Humans</subject><subject>Immunoglobulins</subject><subject>Immunoglobulins, Intravenous - therapeutic use</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Infant</subject><subject>Kidney diseases</subject><subject>Kidney transplantation</subject><subject>Kidney Transplantation - methods</subject><subject>Kidney transplants</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Methods</subject><subject>Nephrology</subject><subject>Original Article</subject><subject>Patients</subject><subject>Pediatrics</subject><subject>Physiological aspects</subject><subject>Plasmapheresis</subject><subject>Renal Insufficiency, Chronic - immunology</subject><subject>Renal Insufficiency, Chronic - surgery</subject><subject>Rituximab - therapeutic use</subject><subject>Tacrolimus - therapeutic use</subject><subject>Urology</subject><issn>0931-041X</issn><issn>1432-198X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqNkkFvFSEUhYmxsc_qD3BjJjExbqZeGGaGWTaNVpsaN5p0Rxjm8kozAyMwi75fL6-v1bZ5JoYFgfudCxwOIW8oHFOA9mME4E1bAq3LinV1uXlGVpRXrKSduHxOVtBVtAROLw_JyxivAUDUonlBDlkjgHacr8j5N-XUGid0qfCmiOiiTXaDQzHjYFUKVhezSjbXYzEH60ORfBHQqbFIQbk4j8qlDHj3ihwYNUZ8fTcfkZ-fP_04_VJefD_7enpyUeqa01SydgAxMGNEqxTmFQreMNMPpm-1ZoaJzqiG9o2qTU1ZD5oK5N0gEOpG6K46Ih92fefgfy0Yk5xs1Djmi6BfoqSCdpRDDc3_oDwbJiqW0XdP0Gu_hPzMW6rKRzcM_lJrNaK0zvhsgt42lSe8BV6B6NpMlXuoNToMavQOjc3bj_jjPXweA05W7xW8fyC4QjWmq-jHZfsN8TFId6AOPsaARuY_nFS4kRTkNkNylyGZMyS3GZKbrHl758TSTzj8UdyHJgNsB8RccmsMD6z6Z9ffAEzPgQ</recordid><startdate>20161001</startdate><enddate>20161001</enddate><creator>Pirojsakul, Kwanchai</creator><creator>Desai, Dev</creator><creator>Lacelle, Chantale</creator><creator>Seikaly, Mouin G.</creator><general>Springer Berlin Heidelberg</general><general>Springer</general><general>Springer Nature B.V</general><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>3V.</scope><scope>7QP</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>20161001</creationdate><title>Management of sensitized pediatric patients prior to renal transplantation</title><author>Pirojsakul, Kwanchai ; Desai, Dev ; Lacelle, Chantale ; Seikaly, Mouin G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c541t-27d08d2ff87aae27de8462fbdfb7cc2f289fa61b6a5f512b0c18e49d8e0568c93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adolescent</topic><topic>Antibodies</topic><topic>Apheresis</topic><topic>Bortezomib - therapeutic use</topic><topic>Care and treatment</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Chronic kidney failure</topic><topic>Desensitization, Immunologic - methods</topic><topic>Female</topic><topic>Genetic aspects</topic><topic>Glomerular Filtration Rate</topic><topic>Graft Rejection - drug therapy</topic><topic>Graft Rejection - pathology</topic><topic>Graft Rejection - prevention & control</topic><topic>Histocompatibility Testing</topic><topic>HLA antigens</topic><topic>HLA Antigens - immunology</topic><topic>Humans</topic><topic>Immunoglobulins</topic><topic>Immunoglobulins, Intravenous - therapeutic use</topic><topic>Immunosuppressive Agents - therapeutic use</topic><topic>Infant</topic><topic>Kidney diseases</topic><topic>Kidney transplantation</topic><topic>Kidney Transplantation - methods</topic><topic>Kidney transplants</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Methods</topic><topic>Nephrology</topic><topic>Original Article</topic><topic>Patients</topic><topic>Pediatrics</topic><topic>Physiological aspects</topic><topic>Plasmapheresis</topic><topic>Renal Insufficiency, Chronic - immunology</topic><topic>Renal Insufficiency, Chronic - surgery</topic><topic>Rituximab - therapeutic use</topic><topic>Tacrolimus - therapeutic use</topic><topic>Urology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pirojsakul, Kwanchai</creatorcontrib><creatorcontrib>Desai, Dev</creatorcontrib><creatorcontrib>Lacelle, Chantale</creatorcontrib><creatorcontrib>Seikaly, Mouin G.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric nephrology (Berlin, West)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pirojsakul, Kwanchai</au><au>Desai, Dev</au><au>Lacelle, Chantale</au><au>Seikaly, Mouin G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Management of sensitized pediatric patients prior to renal transplantation</atitle><jtitle>Pediatric nephrology (Berlin, West)</jtitle><stitle>Pediatr Nephrol</stitle><addtitle>Pediatr Nephrol</addtitle><date>2016-10-01</date><risdate>2016</risdate><volume>31</volume><issue>10</issue><spage>1691</spage><epage>1698</epage><pages>1691-1698</pages><issn>0931-041X</issn><eissn>1432-198X</eissn><abstract>Background
Data on renal allograft outcome in sensitized children are scarce. We report the clinical courses of four children who received desensitization therapy prior to renal transplantation in our institution.
Methods
Between 2009 and 2011, four pediatric patients with stage 5 chronic kidney disease received desensitization therapy due to: (1) positive donor-specific antibodies (DSA) and/or crossmatches with potential living donors, (2) more than three positive crossmatches with deceased donors or (3) high calculated panel-reactive antibody of >80 %. Desensitization with rituximab, intravenous immunoglobulin and bortezomib was performed in all patients. Induction therapy included combinations of plasmapheresis and/or alemtuzumab or anti-thymocyte globulin. Standard post-transplant medications included tacrolimus, mycophenolate mofetil and prednisolone.
Results
Post-transplant screening revealed DSA in three patients. Biopsy showed no evidence of rejection at 1 month in two patients, one of whom developed chronic active antibody-mediated rejection 4.5 years later. One patient developed borderline acute cellular rejection at 1 month, but the serum creatinine level was stable and DSA disappeared without treatment 1 month later, with stable long-term allograft function at 3 years. Estimated or measured glomerular filtration rate of the patients ranged between 30 and 75 ml/min/1.73 m
2
after 1 to 4.5 years.
Conclusions
The four sensitized patients reported here who received desensitization therapy had successful renal transplants with a low risk of immediate post-transplant rejection. Overall, long-term allograft functions and complications from immunosuppression were encouraging.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>26801944</pmid><doi>10.1007/s00467-015-3295-z</doi><tpages>8</tpages></addata></record> |
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subjects | Adolescent Antibodies Apheresis Bortezomib - therapeutic use Care and treatment Child Child, Preschool Chronic kidney failure Desensitization, Immunologic - methods Female Genetic aspects Glomerular Filtration Rate Graft Rejection - drug therapy Graft Rejection - pathology Graft Rejection - prevention & control Histocompatibility Testing HLA antigens HLA Antigens - immunology Humans Immunoglobulins Immunoglobulins, Intravenous - therapeutic use Immunosuppressive Agents - therapeutic use Infant Kidney diseases Kidney transplantation Kidney Transplantation - methods Kidney transplants Male Medicine Medicine & Public Health Methods Nephrology Original Article Patients Pediatrics Physiological aspects Plasmapheresis Renal Insufficiency, Chronic - immunology Renal Insufficiency, Chronic - surgery Rituximab - therapeutic use Tacrolimus - therapeutic use Urology |
title | Management of sensitized pediatric patients prior to renal transplantation |
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