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Desensitization Using Bortezomib and High-dose Immunoglobulin Increases Rate of Deceased Donor Kidney Transplantation

Combination therapy of intravenous immunoglobulin (IVIG) and rituximab showed a good transplant rate in highly sensitized wait-listed patients for deceased donor kidney transplantation (DDKT), but carried the risk of antibody-mediated rejection. The authors investigated the impact of a new combinati...

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Autores principales: Jeong, Jong Cheol, Jambaldorj, Enkthuya, Kwon, Hyuk Yong, Kim, Myung-Gyu, Im, Hye Jin, Jeon, Hee Jung, In, Ji Won, Han, Miyeun, Koo, Tai Yeon, Chung, Junho, Song, Eun Young, Ahn, Curie, Yang, Jaeseok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748896/
https://www.ncbi.nlm.nih.gov/pubmed/26844479
http://dx.doi.org/10.1097/MD.0000000000002635
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author Jeong, Jong Cheol
Jambaldorj, Enkthuya
Kwon, Hyuk Yong
Kim, Myung-Gyu
Im, Hye Jin
Jeon, Hee Jung
In, Ji Won
Han, Miyeun
Koo, Tai Yeon
Chung, Junho
Song, Eun Young
Ahn, Curie
Yang, Jaeseok
author_facet Jeong, Jong Cheol
Jambaldorj, Enkthuya
Kwon, Hyuk Yong
Kim, Myung-Gyu
Im, Hye Jin
Jeon, Hee Jung
In, Ji Won
Han, Miyeun
Koo, Tai Yeon
Chung, Junho
Song, Eun Young
Ahn, Curie
Yang, Jaeseok
author_sort Jeong, Jong Cheol
collection PubMed
description Combination therapy of intravenous immunoglobulin (IVIG) and rituximab showed a good transplant rate in highly sensitized wait-listed patients for deceased donor kidney transplantation (DDKT), but carried the risk of antibody-mediated rejection. The authors investigated the impact of a new combination therapy of bortezomib, IVIG, and rituximab on transplantation rate. This study was a prospective, open-labeled clinical trial. The desensitization regimen consisted of 2 doses of IVIG (2 g/kg), a single dose of rituximab (375 mg/m(2)), and 4 doses of bortezomib (1.3 mg/m(2)). The transplant rate was analyzed. Anti-Human leukocyte antigen (HLA) DRB antibodies were determined by a Luminex solid-phase bead assay at baseline and after 2, 3, and 6 months in the desensitized patients. There were 19 highly sensitized patients who received desensitization and 17 patients in the control group. Baseline values of class I and II panel reactive antibody (%, peak mean fluorescence intensity) were 83 ± 16.0 (14952 ± 5820) and 63 ± 36.0 (10321 ± 7421), respectively. Deceased donor kidney transplantation was successfully performed in 8 patients (42.1%) in the desensitization group versus 4 (23.5%) in the control group. Multivariate time-varying covariate Cox regression analysis showed that desensitization increased the probability of DDKT (hazard ratio, 46.895; 95% confidence interval, 3.468–634.132; P = 0.004). Desensitization decreased mean fluorescence intensity values of class I panel reactive antibody by 15.5% (20.8%) at 2 months. In addition, a liberal mismatch strategy in post hoc analysis increased the benefit of desensitization in donor-specific antibody reduction. Desensitization was well tolerated, and acute rejection occurred only in the control group. In conclusion, a desensitization protocol using bortezomib, high-dose IVIG, and rituximab increased the DDKT rate in highly sensitized, wait-listed patients.
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spelling pubmed-47488962016-04-01 Desensitization Using Bortezomib and High-dose Immunoglobulin Increases Rate of Deceased Donor Kidney Transplantation Jeong, Jong Cheol Jambaldorj, Enkthuya Kwon, Hyuk Yong Kim, Myung-Gyu Im, Hye Jin Jeon, Hee Jung In, Ji Won Han, Miyeun Koo, Tai Yeon Chung, Junho Song, Eun Young Ahn, Curie Yang, Jaeseok Medicine (Baltimore) 4500 Combination therapy of intravenous immunoglobulin (IVIG) and rituximab showed a good transplant rate in highly sensitized wait-listed patients for deceased donor kidney transplantation (DDKT), but carried the risk of antibody-mediated rejection. The authors investigated the impact of a new combination therapy of bortezomib, IVIG, and rituximab on transplantation rate. This study was a prospective, open-labeled clinical trial. The desensitization regimen consisted of 2 doses of IVIG (2 g/kg), a single dose of rituximab (375 mg/m(2)), and 4 doses of bortezomib (1.3 mg/m(2)). The transplant rate was analyzed. Anti-Human leukocyte antigen (HLA) DRB antibodies were determined by a Luminex solid-phase bead assay at baseline and after 2, 3, and 6 months in the desensitized patients. There were 19 highly sensitized patients who received desensitization and 17 patients in the control group. Baseline values of class I and II panel reactive antibody (%, peak mean fluorescence intensity) were 83 ± 16.0 (14952 ± 5820) and 63 ± 36.0 (10321 ± 7421), respectively. Deceased donor kidney transplantation was successfully performed in 8 patients (42.1%) in the desensitization group versus 4 (23.5%) in the control group. Multivariate time-varying covariate Cox regression analysis showed that desensitization increased the probability of DDKT (hazard ratio, 46.895; 95% confidence interval, 3.468–634.132; P = 0.004). Desensitization decreased mean fluorescence intensity values of class I panel reactive antibody by 15.5% (20.8%) at 2 months. In addition, a liberal mismatch strategy in post hoc analysis increased the benefit of desensitization in donor-specific antibody reduction. Desensitization was well tolerated, and acute rejection occurred only in the control group. In conclusion, a desensitization protocol using bortezomib, high-dose IVIG, and rituximab increased the DDKT rate in highly sensitized, wait-listed patients. Wolters Kluwer Health 2016-02-08 /pmc/articles/PMC4748896/ /pubmed/26844479 http://dx.doi.org/10.1097/MD.0000000000002635 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0, where it is permissible to download, share and reproduce the work in any medium, provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle 4500
Jeong, Jong Cheol
Jambaldorj, Enkthuya
Kwon, Hyuk Yong
Kim, Myung-Gyu
Im, Hye Jin
Jeon, Hee Jung
In, Ji Won
Han, Miyeun
Koo, Tai Yeon
Chung, Junho
Song, Eun Young
Ahn, Curie
Yang, Jaeseok
Desensitization Using Bortezomib and High-dose Immunoglobulin Increases Rate of Deceased Donor Kidney Transplantation
title Desensitization Using Bortezomib and High-dose Immunoglobulin Increases Rate of Deceased Donor Kidney Transplantation
title_full Desensitization Using Bortezomib and High-dose Immunoglobulin Increases Rate of Deceased Donor Kidney Transplantation
title_fullStr Desensitization Using Bortezomib and High-dose Immunoglobulin Increases Rate of Deceased Donor Kidney Transplantation
title_full_unstemmed Desensitization Using Bortezomib and High-dose Immunoglobulin Increases Rate of Deceased Donor Kidney Transplantation
title_short Desensitization Using Bortezomib and High-dose Immunoglobulin Increases Rate of Deceased Donor Kidney Transplantation
title_sort desensitization using bortezomib and high-dose immunoglobulin increases rate of deceased donor kidney transplantation
topic 4500
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4748896/
https://www.ncbi.nlm.nih.gov/pubmed/26844479
http://dx.doi.org/10.1097/MD.0000000000002635
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