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
Hauptverfasser: Pirojsakul, Kwanchai, Desai, Dev, Lacelle, Chantale, Seikaly, Mouin G.
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container_issue 10
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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.
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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 &gt;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. 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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 &gt;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. 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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 &gt;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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