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Desensitization using imlifidase and EndoS enables chimerism induction in allosensitized recipient mice
Mixed hematopoietic chimerism induction as a way to foster tolerance to donor organs in recipients who have been sensitized to donor antigens is challenging. Donor‐specific antibodies (DSA) are a dominant barrier toward successful donor bone marrow engraftment. Although desensitization methods are r...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496317/ https://www.ncbi.nlm.nih.gov/pubmed/32185855 http://dx.doi.org/10.1111/ajt.15851 |
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author | Lin, Jiaxin Boon, Louis Bockermann, Robert Robertson, Anna‐Karin Kjellman, Christian Anderson, Colin C. |
author_facet | Lin, Jiaxin Boon, Louis Bockermann, Robert Robertson, Anna‐Karin Kjellman, Christian Anderson, Colin C. |
author_sort | Lin, Jiaxin |
collection | PubMed |
description | Mixed hematopoietic chimerism induction as a way to foster tolerance to donor organs in recipients who have been sensitized to donor antigens is challenging. Donor‐specific antibodies (DSA) are a dominant barrier toward successful donor bone marrow engraftment. Although desensitization methods are routinely used in recipients with allosensitization for allogeneic bone marrow transplantation, engraftment is frequently unsuccessful. To overcome the barrier of prior sensitization we tested enzymatic desensitization of donor‐specific IgG using imlifidase and endoglycosidase of Streptococcus pyogenes (EndoS), which both partially block the function of DSA in mice, as a novel approach to improve murine bone marrow engraftment in primed hosts. We found that EndoS was capable of inhibiting antibody‐mediated killing of donor cells in vivo. Furthermore, the effect of EndoS depended on the titer of DSA and the genetic background of the recipients. In combination with imlifidase, EndoS improved the survival of donor bone marrow cells. Together with cyclophosphamide, bortezomib, T cell depletion, and nonlethal irradiation, imlifidase in combination with EndoS allowed allogeneic bone marrow engraftment in sensitized recipients. We conclude that enzymatic inactivation of DSA, using the combination of imlifidase and EndoS, can be used for inducing donor hematopoietic chimerism in allosensitized recipient mice in combination with other desensitization strategies. |
format | Online Article Text |
id | pubmed-7496317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74963172020-09-25 Desensitization using imlifidase and EndoS enables chimerism induction in allosensitized recipient mice Lin, Jiaxin Boon, Louis Bockermann, Robert Robertson, Anna‐Karin Kjellman, Christian Anderson, Colin C. Am J Transplant ORIGINAL ARTICLES Mixed hematopoietic chimerism induction as a way to foster tolerance to donor organs in recipients who have been sensitized to donor antigens is challenging. Donor‐specific antibodies (DSA) are a dominant barrier toward successful donor bone marrow engraftment. Although desensitization methods are routinely used in recipients with allosensitization for allogeneic bone marrow transplantation, engraftment is frequently unsuccessful. To overcome the barrier of prior sensitization we tested enzymatic desensitization of donor‐specific IgG using imlifidase and endoglycosidase of Streptococcus pyogenes (EndoS), which both partially block the function of DSA in mice, as a novel approach to improve murine bone marrow engraftment in primed hosts. We found that EndoS was capable of inhibiting antibody‐mediated killing of donor cells in vivo. Furthermore, the effect of EndoS depended on the titer of DSA and the genetic background of the recipients. In combination with imlifidase, EndoS improved the survival of donor bone marrow cells. Together with cyclophosphamide, bortezomib, T cell depletion, and nonlethal irradiation, imlifidase in combination with EndoS allowed allogeneic bone marrow engraftment in sensitized recipients. We conclude that enzymatic inactivation of DSA, using the combination of imlifidase and EndoS, can be used for inducing donor hematopoietic chimerism in allosensitized recipient mice in combination with other desensitization strategies. John Wiley and Sons Inc. 2020-04-07 2020-09 /pmc/articles/PMC7496317/ /pubmed/32185855 http://dx.doi.org/10.1111/ajt.15851 Text en © 2020 The Authors. American Journal of Transplantation published by Wiley Periodicals LLC on behalf of The American Society of Transplantation and the American Society of Transplant Surgeons This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | ORIGINAL ARTICLES Lin, Jiaxin Boon, Louis Bockermann, Robert Robertson, Anna‐Karin Kjellman, Christian Anderson, Colin C. Desensitization using imlifidase and EndoS enables chimerism induction in allosensitized recipient mice |
title | Desensitization using imlifidase and EndoS enables chimerism induction in allosensitized recipient mice |
title_full | Desensitization using imlifidase and EndoS enables chimerism induction in allosensitized recipient mice |
title_fullStr | Desensitization using imlifidase and EndoS enables chimerism induction in allosensitized recipient mice |
title_full_unstemmed | Desensitization using imlifidase and EndoS enables chimerism induction in allosensitized recipient mice |
title_short | Desensitization using imlifidase and EndoS enables chimerism induction in allosensitized recipient mice |
title_sort | desensitization using imlifidase and endos enables chimerism induction in allosensitized recipient mice |
topic | ORIGINAL ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496317/ https://www.ncbi.nlm.nih.gov/pubmed/32185855 http://dx.doi.org/10.1111/ajt.15851 |
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