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Alemtuzumab induction in pediatric kidney transplantation
Recipient parenchymal lymphatic cells are crucial for direct and indirect pathways of allorecognition. We proposed that alemtuzumab, being infused several weeks pretransplant could eradicate peripheral lymphatic cells and promote donor-specific tolerance. We present here a single center, retrospecti...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3644867/ https://www.ncbi.nlm.nih.gov/pubmed/23442101 http://dx.doi.org/10.1111/petr.12048 |
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author | Kaabak, Michael M Babenko, Nadezda N Samsonov, Dmitry V Sandrikov, Valery A Maschan, Alexey A Zokoev, Alan K |
author_facet | Kaabak, Michael M Babenko, Nadezda N Samsonov, Dmitry V Sandrikov, Valery A Maschan, Alexey A Zokoev, Alan K |
author_sort | Kaabak, Michael M |
collection | PubMed |
description | Recipient parenchymal lymphatic cells are crucial for direct and indirect pathways of allorecognition. We proposed that alemtuzumab, being infused several weeks pretransplant could eradicate peripheral lymphatic cells and promote donor-specific tolerance. We present here a single center, retrospective review of 101 consecutive living-donor kidney transplantations to pediatric patients aged from seven month to 18 yr, performed between September 2006 and April 2010. Immunosupression protocol included two 30 mg doses of alemtuzumab: first given 12–29 d prior to transplantation and second at the time of transplantation. Maintenance immunosupression was based on combination of low dose and wide range CNI and mycophenolate. Patients were followed for 3.8 ± 1.4 yr and protocol biopsies were taken one month, one, and three yr post transplant. The Kaplan–Meier graft and patient survival was 96% and 97% for one yr, 89% and 93% for three yr. Biopsy proven acute rejection developed in 26% patients at one yr and in 35% at two yr, no rejections occurred beyond two yr. We conclude that alemtuzumab pretreatment prior to living related donor kidney transplantation allows to reach satisfactory middle-term results in pediatric patients with wide range and low CNI concentrations. |
format | Online Article Text |
id | pubmed-3644867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-36448672013-05-06 Alemtuzumab induction in pediatric kidney transplantation Kaabak, Michael M Babenko, Nadezda N Samsonov, Dmitry V Sandrikov, Valery A Maschan, Alexey A Zokoev, Alan K Pediatr Transplant Original Articles Recipient parenchymal lymphatic cells are crucial for direct and indirect pathways of allorecognition. We proposed that alemtuzumab, being infused several weeks pretransplant could eradicate peripheral lymphatic cells and promote donor-specific tolerance. We present here a single center, retrospective review of 101 consecutive living-donor kidney transplantations to pediatric patients aged from seven month to 18 yr, performed between September 2006 and April 2010. Immunosupression protocol included two 30 mg doses of alemtuzumab: first given 12–29 d prior to transplantation and second at the time of transplantation. Maintenance immunosupression was based on combination of low dose and wide range CNI and mycophenolate. Patients were followed for 3.8 ± 1.4 yr and protocol biopsies were taken one month, one, and three yr post transplant. The Kaplan–Meier graft and patient survival was 96% and 97% for one yr, 89% and 93% for three yr. Biopsy proven acute rejection developed in 26% patients at one yr and in 35% at two yr, no rejections occurred beyond two yr. We conclude that alemtuzumab pretreatment prior to living related donor kidney transplantation allows to reach satisfactory middle-term results in pediatric patients with wide range and low CNI concentrations. Blackwell Publishing Ltd 2013-03 2013-02-26 /pmc/articles/PMC3644867/ /pubmed/23442101 http://dx.doi.org/10.1111/petr.12048 Text en © 2013 John Wiley & Sons A/S. http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Original Articles Kaabak, Michael M Babenko, Nadezda N Samsonov, Dmitry V Sandrikov, Valery A Maschan, Alexey A Zokoev, Alan K Alemtuzumab induction in pediatric kidney transplantation |
title | Alemtuzumab induction in pediatric kidney transplantation |
title_full | Alemtuzumab induction in pediatric kidney transplantation |
title_fullStr | Alemtuzumab induction in pediatric kidney transplantation |
title_full_unstemmed | Alemtuzumab induction in pediatric kidney transplantation |
title_short | Alemtuzumab induction in pediatric kidney transplantation |
title_sort | alemtuzumab induction in pediatric kidney transplantation |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3644867/ https://www.ncbi.nlm.nih.gov/pubmed/23442101 http://dx.doi.org/10.1111/petr.12048 |
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