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A Phased Desensitization Protocol With Rituximab and Bortezomib for Highly Sensitized Kidney Transplant Candidates

Desensitization protocols comprising plasmapheresis, IVIGs, and rituximab and/or bortezomib have allowed for successful kidney transplantation in some highly HLA-sensitized patients with end-stage renal disease. However, the optimal combination of these therapies and their proper timing remains enti...

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Autores principales: Ide, Kentaro, Tanaka, Yuka, Sasaki, Yu, Tahara, Hiroyuki, Ohira, Masahiro, Ishiyama, Kohei, Tashiro, Hirotaka, Ohdan, Hideki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4946466/
https://www.ncbi.nlm.nih.gov/pubmed/27500219
http://dx.doi.org/10.1097/TXD.0000000000000526
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author Ide, Kentaro
Tanaka, Yuka
Sasaki, Yu
Tahara, Hiroyuki
Ohira, Masahiro
Ishiyama, Kohei
Tashiro, Hirotaka
Ohdan, Hideki
author_facet Ide, Kentaro
Tanaka, Yuka
Sasaki, Yu
Tahara, Hiroyuki
Ohira, Masahiro
Ishiyama, Kohei
Tashiro, Hirotaka
Ohdan, Hideki
author_sort Ide, Kentaro
collection PubMed
description Desensitization protocols comprising plasmapheresis, IVIGs, and rituximab and/or bortezomib have allowed for successful kidney transplantation in some highly HLA-sensitized patients with end-stage renal disease. However, the optimal combination of these therapies and their proper timing remains entirely unknown. We propose a phased desensitization strategy using rituximab followed by bortezomib as a safer method. METHODS: Three sensitized kidney transplant candidates who could not be desensitized using our conventional protocol, which consists of a single rituximab dose combined with plasmapheresis, were enrolled in this study. When IgM(+) CD27(−) naive B cells reappeared but IgM(+) CD27(+) memory B cells remained undetectable in their peripheral blood, the patients were treated with 1 cycle of bortezomib followed by plasmapheresis. RESULTS: After bortezomib treatment, patients' donor-specific anti-HLA antibodies (DSA) values were decreased, and cross-match tests were consistently negative. All 3 patients underwent living donor kidney transplantation. They showed immediate renal function, and both DSA and non-DSA were undetectable during the observation period. Neither antibody-mediated rejection nor severe acute cellular rejection was encountered in these patients after transplantation. CONCLUSIONS: The present cases suggest that a phased use of rituximab and bortezomib can safely desensitize highly sensitized kidney transplant candidates.
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spelling pubmed-49464662016-08-05 A Phased Desensitization Protocol With Rituximab and Bortezomib for Highly Sensitized Kidney Transplant Candidates Ide, Kentaro Tanaka, Yuka Sasaki, Yu Tahara, Hiroyuki Ohira, Masahiro Ishiyama, Kohei Tashiro, Hirotaka Ohdan, Hideki Transplant Direct Original Clinical Science Desensitization protocols comprising plasmapheresis, IVIGs, and rituximab and/or bortezomib have allowed for successful kidney transplantation in some highly HLA-sensitized patients with end-stage renal disease. However, the optimal combination of these therapies and their proper timing remains entirely unknown. We propose a phased desensitization strategy using rituximab followed by bortezomib as a safer method. METHODS: Three sensitized kidney transplant candidates who could not be desensitized using our conventional protocol, which consists of a single rituximab dose combined with plasmapheresis, were enrolled in this study. When IgM(+) CD27(−) naive B cells reappeared but IgM(+) CD27(+) memory B cells remained undetectable in their peripheral blood, the patients were treated with 1 cycle of bortezomib followed by plasmapheresis. RESULTS: After bortezomib treatment, patients' donor-specific anti-HLA antibodies (DSA) values were decreased, and cross-match tests were consistently negative. All 3 patients underwent living donor kidney transplantation. They showed immediate renal function, and both DSA and non-DSA were undetectable during the observation period. Neither antibody-mediated rejection nor severe acute cellular rejection was encountered in these patients after transplantation. CONCLUSIONS: The present cases suggest that a phased use of rituximab and bortezomib can safely desensitize highly sensitized kidney transplant candidates. Lippincott Williams & Wilkins 2015-06-05 /pmc/articles/PMC4946466/ /pubmed/27500219 http://dx.doi.org/10.1097/TXD.0000000000000526 Text en Copyright © 2015 The Authors. Transplantation Direct. Published by Wolters Kluwer Health, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License, where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/3.0.
spellingShingle Original Clinical Science
Ide, Kentaro
Tanaka, Yuka
Sasaki, Yu
Tahara, Hiroyuki
Ohira, Masahiro
Ishiyama, Kohei
Tashiro, Hirotaka
Ohdan, Hideki
A Phased Desensitization Protocol With Rituximab and Bortezomib for Highly Sensitized Kidney Transplant Candidates
title A Phased Desensitization Protocol With Rituximab and Bortezomib for Highly Sensitized Kidney Transplant Candidates
title_full A Phased Desensitization Protocol With Rituximab and Bortezomib for Highly Sensitized Kidney Transplant Candidates
title_fullStr A Phased Desensitization Protocol With Rituximab and Bortezomib for Highly Sensitized Kidney Transplant Candidates
title_full_unstemmed A Phased Desensitization Protocol With Rituximab and Bortezomib for Highly Sensitized Kidney Transplant Candidates
title_short A Phased Desensitization Protocol With Rituximab and Bortezomib for Highly Sensitized Kidney Transplant Candidates
title_sort phased desensitization protocol with rituximab and bortezomib for highly sensitized kidney transplant candidates
topic Original Clinical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4946466/
https://www.ncbi.nlm.nih.gov/pubmed/27500219
http://dx.doi.org/10.1097/TXD.0000000000000526
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