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Rituximab, plasma exchange and immunoglobulins: an ineffective treatment for chronic active antibody-mediated rejection
BACKGROUND: Chronic active antibody-mediated rejection (c-aABMR) is an important cause of allograft failure and graft loss in long-term kidney transplants. METHODS: To determine the efficacy and safety of combined therapy with rituximab, plasma exchange (PE) and intravenous immunoglobulins (IVIG), a...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182805/ https://www.ncbi.nlm.nih.gov/pubmed/30309322 http://dx.doi.org/10.1186/s12882-018-1057-4 |
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author | Piñeiro, Gastón J De Sousa-Amorim, Erika Solé, Manel Ríos, José Lozano, Miguel Cofán, Frederic Ventura-Aguiar, Pedro Cucchiari, David Revuelta, Ignacio Cid, Joan Palou, Eduard Campistol, Josep M Oppenheimer, Federico Rovira, Jordi Diekmann, Fritz |
author_facet | Piñeiro, Gastón J De Sousa-Amorim, Erika Solé, Manel Ríos, José Lozano, Miguel Cofán, Frederic Ventura-Aguiar, Pedro Cucchiari, David Revuelta, Ignacio Cid, Joan Palou, Eduard Campistol, Josep M Oppenheimer, Federico Rovira, Jordi Diekmann, Fritz |
author_sort | Piñeiro, Gastón J |
collection | PubMed |
description | BACKGROUND: Chronic active antibody-mediated rejection (c-aABMR) is an important cause of allograft failure and graft loss in long-term kidney transplants. METHODS: To determine the efficacy and safety of combined therapy with rituximab, plasma exchange (PE) and intravenous immunoglobulins (IVIG), a cohort of patients with transplant glomerulopathy (TG) that met criteria of active cABMR, according to BANFF’17 classification, was identified. RESULTS: We identified 62 patients with active c-aABMR and TG (cg ≥ 1). Twenty-three patients were treated with the combination therapy and, 39 patients did not receive treatment and were considered the control group. There were no significant differences in the graft survival between the two groups. The number of graft losses at 12 and 24 months and the decline of eGFR were not different and independent of the treatment. A decrease of eGFR≥13 ml/min between 6 months before and c-aABMR diagnosis, was an independent risk factor for graft loss at 24 months (OR = 5; P = 0.01). Infections that required hospitalization during the first year after c-aABMR diagnosis were significantly more frequent in treated patients (OR = 4.22; P = 0.013), with a ratio infection/patient-year of 0.65 and 0.20 respectively. CONCLUSIONS: Treatment with rituximab, PE, and IVIG in kidney transplants with c-aABMR did not improve graft survival and was associated with a significant increase in severe infectious complications. TRIAL REGISTRATION: Agencia Española de Medicametos y Productos Sanitarios (AEMPS): 14566/RG 24161. Study code: UTR-INM-2017-01. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12882-018-1057-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6182805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61828052018-10-18 Rituximab, plasma exchange and immunoglobulins: an ineffective treatment for chronic active antibody-mediated rejection Piñeiro, Gastón J De Sousa-Amorim, Erika Solé, Manel Ríos, José Lozano, Miguel Cofán, Frederic Ventura-Aguiar, Pedro Cucchiari, David Revuelta, Ignacio Cid, Joan Palou, Eduard Campistol, Josep M Oppenheimer, Federico Rovira, Jordi Diekmann, Fritz BMC Nephrol Research Article BACKGROUND: Chronic active antibody-mediated rejection (c-aABMR) is an important cause of allograft failure and graft loss in long-term kidney transplants. METHODS: To determine the efficacy and safety of combined therapy with rituximab, plasma exchange (PE) and intravenous immunoglobulins (IVIG), a cohort of patients with transplant glomerulopathy (TG) that met criteria of active cABMR, according to BANFF’17 classification, was identified. RESULTS: We identified 62 patients with active c-aABMR and TG (cg ≥ 1). Twenty-three patients were treated with the combination therapy and, 39 patients did not receive treatment and were considered the control group. There were no significant differences in the graft survival between the two groups. The number of graft losses at 12 and 24 months and the decline of eGFR were not different and independent of the treatment. A decrease of eGFR≥13 ml/min between 6 months before and c-aABMR diagnosis, was an independent risk factor for graft loss at 24 months (OR = 5; P = 0.01). Infections that required hospitalization during the first year after c-aABMR diagnosis were significantly more frequent in treated patients (OR = 4.22; P = 0.013), with a ratio infection/patient-year of 0.65 and 0.20 respectively. CONCLUSIONS: Treatment with rituximab, PE, and IVIG in kidney transplants with c-aABMR did not improve graft survival and was associated with a significant increase in severe infectious complications. TRIAL REGISTRATION: Agencia Española de Medicametos y Productos Sanitarios (AEMPS): 14566/RG 24161. Study code: UTR-INM-2017-01. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12882-018-1057-4) contains supplementary material, which is available to authorized users. BioMed Central 2018-10-11 /pmc/articles/PMC6182805/ /pubmed/30309322 http://dx.doi.org/10.1186/s12882-018-1057-4 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Piñeiro, Gastón J De Sousa-Amorim, Erika Solé, Manel Ríos, José Lozano, Miguel Cofán, Frederic Ventura-Aguiar, Pedro Cucchiari, David Revuelta, Ignacio Cid, Joan Palou, Eduard Campistol, Josep M Oppenheimer, Federico Rovira, Jordi Diekmann, Fritz Rituximab, plasma exchange and immunoglobulins: an ineffective treatment for chronic active antibody-mediated rejection |
title | Rituximab, plasma exchange and immunoglobulins: an ineffective treatment for chronic active antibody-mediated rejection |
title_full | Rituximab, plasma exchange and immunoglobulins: an ineffective treatment for chronic active antibody-mediated rejection |
title_fullStr | Rituximab, plasma exchange and immunoglobulins: an ineffective treatment for chronic active antibody-mediated rejection |
title_full_unstemmed | Rituximab, plasma exchange and immunoglobulins: an ineffective treatment for chronic active antibody-mediated rejection |
title_short | Rituximab, plasma exchange and immunoglobulins: an ineffective treatment for chronic active antibody-mediated rejection |
title_sort | rituximab, plasma exchange and immunoglobulins: an ineffective treatment for chronic active antibody-mediated rejection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182805/ https://www.ncbi.nlm.nih.gov/pubmed/30309322 http://dx.doi.org/10.1186/s12882-018-1057-4 |
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