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Chimeric 2C10R4 anti-CD40 antibody therapy is critical for long-term survival of GTKO.hCD46.hTBM pig-to-primate cardiac xenograft
Preventing xenograft rejection is one of the greatest challenges of transplantation medicine. Here, we describe a reproducible, long-term survival of cardiac xenografts from alpha 1-3 galactosyltransferase gene knockout pigs, which express human complement regulatory protein CD46 and human thrombomo...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4822024/ https://www.ncbi.nlm.nih.gov/pubmed/27045379 http://dx.doi.org/10.1038/ncomms11138 |
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author | Mohiuddin, Muhammad M. Singh, Avneesh K. Corcoran, Philip C. Thomas III, Marvin L. Clark, Tannia Lewis, Billeta G. Hoyt, Robert F. Eckhaus, Michael Pierson III, Richard N. Belli, Aaron J. Wolf, Eckhard Klymiuk, Nikolai Phelps, Carol Reimann, Keith A. Ayares, David Horvath, Keith A. |
author_facet | Mohiuddin, Muhammad M. Singh, Avneesh K. Corcoran, Philip C. Thomas III, Marvin L. Clark, Tannia Lewis, Billeta G. Hoyt, Robert F. Eckhaus, Michael Pierson III, Richard N. Belli, Aaron J. Wolf, Eckhard Klymiuk, Nikolai Phelps, Carol Reimann, Keith A. Ayares, David Horvath, Keith A. |
author_sort | Mohiuddin, Muhammad M. |
collection | PubMed |
description | Preventing xenograft rejection is one of the greatest challenges of transplantation medicine. Here, we describe a reproducible, long-term survival of cardiac xenografts from alpha 1-3 galactosyltransferase gene knockout pigs, which express human complement regulatory protein CD46 and human thrombomodulin (GTKO.hCD46.hTBM), that were transplanted into baboons. Our immunomodulatory drug regimen includes induction with anti-thymocyte globulin and αCD20 antibody, followed by maintenance with mycophenolate mofetil and an intensively dosed αCD40 (2C10R4) antibody. Median (298 days) and longest (945 days) graft survival in five consecutive recipients using this regimen is significantly prolonged over our recently established survival benchmarks (180 and 500 days, respectively). Remarkably, the reduction of αCD40 antibody dose on day 100 or after 1 year resulted in recrudescence of anti-pig antibody and graft failure. In conclusion, genetic modifications (GTKO.hCD46.hTBM) combined with the treatment regimen tested here consistently prevent humoral rejection and systemic coagulation pathway dysregulation, sustaining long-term cardiac xenograft survival beyond 900 days. |
format | Online Article Text |
id | pubmed-4822024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48220242016-04-17 Chimeric 2C10R4 anti-CD40 antibody therapy is critical for long-term survival of GTKO.hCD46.hTBM pig-to-primate cardiac xenograft Mohiuddin, Muhammad M. Singh, Avneesh K. Corcoran, Philip C. Thomas III, Marvin L. Clark, Tannia Lewis, Billeta G. Hoyt, Robert F. Eckhaus, Michael Pierson III, Richard N. Belli, Aaron J. Wolf, Eckhard Klymiuk, Nikolai Phelps, Carol Reimann, Keith A. Ayares, David Horvath, Keith A. Nat Commun Article Preventing xenograft rejection is one of the greatest challenges of transplantation medicine. Here, we describe a reproducible, long-term survival of cardiac xenografts from alpha 1-3 galactosyltransferase gene knockout pigs, which express human complement regulatory protein CD46 and human thrombomodulin (GTKO.hCD46.hTBM), that were transplanted into baboons. Our immunomodulatory drug regimen includes induction with anti-thymocyte globulin and αCD20 antibody, followed by maintenance with mycophenolate mofetil and an intensively dosed αCD40 (2C10R4) antibody. Median (298 days) and longest (945 days) graft survival in five consecutive recipients using this regimen is significantly prolonged over our recently established survival benchmarks (180 and 500 days, respectively). Remarkably, the reduction of αCD40 antibody dose on day 100 or after 1 year resulted in recrudescence of anti-pig antibody and graft failure. In conclusion, genetic modifications (GTKO.hCD46.hTBM) combined with the treatment regimen tested here consistently prevent humoral rejection and systemic coagulation pathway dysregulation, sustaining long-term cardiac xenograft survival beyond 900 days. Nature Publishing Group 2016-04-05 /pmc/articles/PMC4822024/ /pubmed/27045379 http://dx.doi.org/10.1038/ncomms11138 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Mohiuddin, Muhammad M. Singh, Avneesh K. Corcoran, Philip C. Thomas III, Marvin L. Clark, Tannia Lewis, Billeta G. Hoyt, Robert F. Eckhaus, Michael Pierson III, Richard N. Belli, Aaron J. Wolf, Eckhard Klymiuk, Nikolai Phelps, Carol Reimann, Keith A. Ayares, David Horvath, Keith A. Chimeric 2C10R4 anti-CD40 antibody therapy is critical for long-term survival of GTKO.hCD46.hTBM pig-to-primate cardiac xenograft |
title | Chimeric 2C10R4 anti-CD40 antibody therapy is critical for long-term survival of GTKO.hCD46.hTBM pig-to-primate cardiac xenograft |
title_full | Chimeric 2C10R4 anti-CD40 antibody therapy is critical for long-term survival of GTKO.hCD46.hTBM pig-to-primate cardiac xenograft |
title_fullStr | Chimeric 2C10R4 anti-CD40 antibody therapy is critical for long-term survival of GTKO.hCD46.hTBM pig-to-primate cardiac xenograft |
title_full_unstemmed | Chimeric 2C10R4 anti-CD40 antibody therapy is critical for long-term survival of GTKO.hCD46.hTBM pig-to-primate cardiac xenograft |
title_short | Chimeric 2C10R4 anti-CD40 antibody therapy is critical for long-term survival of GTKO.hCD46.hTBM pig-to-primate cardiac xenograft |
title_sort | chimeric 2c10r4 anti-cd40 antibody therapy is critical for long-term survival of gtko.hcd46.htbm pig-to-primate cardiac xenograft |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4822024/ https://www.ncbi.nlm.nih.gov/pubmed/27045379 http://dx.doi.org/10.1038/ncomms11138 |
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