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Establishment of an experimental model for MHC homo-to-hetero transplantation
Preventing rejection is a major challenge in transplantation medicine, even when using pluripotent stem cell-derived grafts. In iPS cell (iPSC)-based transplantation, to reduce the risk of rejection, it is thought to be optimal that preparing the cells from donors whose human leukocyte antigen-haplo...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7421494/ https://www.ncbi.nlm.nih.gov/pubmed/32782297 http://dx.doi.org/10.1038/s41598-020-69784-4 |
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author | Murata, Tomoki Wada, Haruka Otsuka, Ryo Sasaki, Airi Tsuji, Hyuma Itoh, Mizuho Eguchi, Nanami Kawai, Tatsuo Seino, Ken-ichiro |
author_facet | Murata, Tomoki Wada, Haruka Otsuka, Ryo Sasaki, Airi Tsuji, Hyuma Itoh, Mizuho Eguchi, Nanami Kawai, Tatsuo Seino, Ken-ichiro |
author_sort | Murata, Tomoki |
collection | PubMed |
description | Preventing rejection is a major challenge in transplantation medicine, even when using pluripotent stem cell-derived grafts. In iPS cell (iPSC)-based transplantation, to reduce the risk of rejection, it is thought to be optimal that preparing the cells from donors whose human leukocyte antigen-haplotype are homozygous. Generally, this approach is referred to as major histocompatibility complex (MHC) homo-to-hetero transplantation, which is MHC-matched but minor antigen-mismatched. To investigate the immune response in the MHC homo-to-hetero transplantation, we established a murine experimental system in which MHC-matched but minor antigen-mismatched tissue (skin) grafts were transplanted into MHC-heterozygous recipients. Unexpectedly, only minor antigen-mismatched grafts were rejected at the same time points as rejection of fully allogeneic grafts. A vigorous anti-donor type T cell response was detected in vitro and conventional immunosuppressants targeting T cell activation had limited effects on controlling rejection. However, anti-donor antibodies were not detected only in the minor antigen-mismatched transplantation. This murine transplantation model can be used to further analyze immunological subjects for MHC homo-to-hetero iPSC-based transplantation. |
format | Online Article Text |
id | pubmed-7421494 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74214942020-08-13 Establishment of an experimental model for MHC homo-to-hetero transplantation Murata, Tomoki Wada, Haruka Otsuka, Ryo Sasaki, Airi Tsuji, Hyuma Itoh, Mizuho Eguchi, Nanami Kawai, Tatsuo Seino, Ken-ichiro Sci Rep Article Preventing rejection is a major challenge in transplantation medicine, even when using pluripotent stem cell-derived grafts. In iPS cell (iPSC)-based transplantation, to reduce the risk of rejection, it is thought to be optimal that preparing the cells from donors whose human leukocyte antigen-haplotype are homozygous. Generally, this approach is referred to as major histocompatibility complex (MHC) homo-to-hetero transplantation, which is MHC-matched but minor antigen-mismatched. To investigate the immune response in the MHC homo-to-hetero transplantation, we established a murine experimental system in which MHC-matched but minor antigen-mismatched tissue (skin) grafts were transplanted into MHC-heterozygous recipients. Unexpectedly, only minor antigen-mismatched grafts were rejected at the same time points as rejection of fully allogeneic grafts. A vigorous anti-donor type T cell response was detected in vitro and conventional immunosuppressants targeting T cell activation had limited effects on controlling rejection. However, anti-donor antibodies were not detected only in the minor antigen-mismatched transplantation. This murine transplantation model can be used to further analyze immunological subjects for MHC homo-to-hetero iPSC-based transplantation. Nature Publishing Group UK 2020-08-11 /pmc/articles/PMC7421494/ /pubmed/32782297 http://dx.doi.org/10.1038/s41598-020-69784-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Murata, Tomoki Wada, Haruka Otsuka, Ryo Sasaki, Airi Tsuji, Hyuma Itoh, Mizuho Eguchi, Nanami Kawai, Tatsuo Seino, Ken-ichiro Establishment of an experimental model for MHC homo-to-hetero transplantation |
title | Establishment of an experimental model for MHC homo-to-hetero transplantation |
title_full | Establishment of an experimental model for MHC homo-to-hetero transplantation |
title_fullStr | Establishment of an experimental model for MHC homo-to-hetero transplantation |
title_full_unstemmed | Establishment of an experimental model for MHC homo-to-hetero transplantation |
title_short | Establishment of an experimental model for MHC homo-to-hetero transplantation |
title_sort | establishment of an experimental model for mhc homo-to-hetero transplantation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7421494/ https://www.ncbi.nlm.nih.gov/pubmed/32782297 http://dx.doi.org/10.1038/s41598-020-69784-4 |
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