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HLA and Histo-Blood Group Antigen Expression in Human Pluripotent Stem Cells and their Derivatives

One prerequisite for a successful clinical outcome of human pluripotent stem cell (hPSC) based therapies is immune compatibility between grafted cells/tissue and recipient. This study explores immune determinants of human embryonic stem cell lines (hESC) and induced human pluripotent stem cell (hiPS...

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Autores principales: Säljö, Karin, Barone, Angela, Mölne, Johan, Rydberg, Lennart, Teneberg, Susann, Breimer, Michael E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5638960/
https://www.ncbi.nlm.nih.gov/pubmed/29026098
http://dx.doi.org/10.1038/s41598-017-12231-8
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author Säljö, Karin
Barone, Angela
Mölne, Johan
Rydberg, Lennart
Teneberg, Susann
Breimer, Michael E.
author_facet Säljö, Karin
Barone, Angela
Mölne, Johan
Rydberg, Lennart
Teneberg, Susann
Breimer, Michael E.
author_sort Säljö, Karin
collection PubMed
description One prerequisite for a successful clinical outcome of human pluripotent stem cell (hPSC) based therapies is immune compatibility between grafted cells/tissue and recipient. This study explores immune determinants of human embryonic stem cell lines (hESC) and induced human pluripotent stem cell (hiPSC) lines and hepatocyte- and cardiomyocyte-like cells derived from these cells. HLA class I was expressed on all pluripotent hPSC lines which upon differentiation into hepatocyte-like cells was considerably reduced in contrast to cardiomyocyte-like cells which retained class I antigens. No HLA class II antigens were found in the pluripotent or differentiated cells. Histo-blood group carbohydrate antigens SSEA-3/SSEA-4/SSEA-5, Globo H, A, Le(x)/Le(y) and sialyl-lactotetra were expressed on all hPSC lines. Blood group AB(O)H antigen expression was in accordance with ABO genotype. Interestingly, only a subpopulation of A1O1 cells expressed A. During differentiation of hPSC, some histo-blood group antigens showed congruent alteration patterns while expression of other antigens differed between the cell lines. No systematic difference in the hPSC cell surface tissue antigen expression was detected. In conclusion, hPSC and their derivatives express cell surface antigens that may cause an immune rejection. Furthermore, tissue antigen expression must be established for each individual stem cell line prior to clinical application.
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spelling pubmed-56389602017-10-18 HLA and Histo-Blood Group Antigen Expression in Human Pluripotent Stem Cells and their Derivatives Säljö, Karin Barone, Angela Mölne, Johan Rydberg, Lennart Teneberg, Susann Breimer, Michael E. Sci Rep Article One prerequisite for a successful clinical outcome of human pluripotent stem cell (hPSC) based therapies is immune compatibility between grafted cells/tissue and recipient. This study explores immune determinants of human embryonic stem cell lines (hESC) and induced human pluripotent stem cell (hiPSC) lines and hepatocyte- and cardiomyocyte-like cells derived from these cells. HLA class I was expressed on all pluripotent hPSC lines which upon differentiation into hepatocyte-like cells was considerably reduced in contrast to cardiomyocyte-like cells which retained class I antigens. No HLA class II antigens were found in the pluripotent or differentiated cells. Histo-blood group carbohydrate antigens SSEA-3/SSEA-4/SSEA-5, Globo H, A, Le(x)/Le(y) and sialyl-lactotetra were expressed on all hPSC lines. Blood group AB(O)H antigen expression was in accordance with ABO genotype. Interestingly, only a subpopulation of A1O1 cells expressed A. During differentiation of hPSC, some histo-blood group antigens showed congruent alteration patterns while expression of other antigens differed between the cell lines. No systematic difference in the hPSC cell surface tissue antigen expression was detected. In conclusion, hPSC and their derivatives express cell surface antigens that may cause an immune rejection. Furthermore, tissue antigen expression must be established for each individual stem cell line prior to clinical application. Nature Publishing Group UK 2017-10-12 /pmc/articles/PMC5638960/ /pubmed/29026098 http://dx.doi.org/10.1038/s41598-017-12231-8 Text en © The Author(s) 2017 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
Säljö, Karin
Barone, Angela
Mölne, Johan
Rydberg, Lennart
Teneberg, Susann
Breimer, Michael E.
HLA and Histo-Blood Group Antigen Expression in Human Pluripotent Stem Cells and their Derivatives
title HLA and Histo-Blood Group Antigen Expression in Human Pluripotent Stem Cells and their Derivatives
title_full HLA and Histo-Blood Group Antigen Expression in Human Pluripotent Stem Cells and their Derivatives
title_fullStr HLA and Histo-Blood Group Antigen Expression in Human Pluripotent Stem Cells and their Derivatives
title_full_unstemmed HLA and Histo-Blood Group Antigen Expression in Human Pluripotent Stem Cells and their Derivatives
title_short HLA and Histo-Blood Group Antigen Expression in Human Pluripotent Stem Cells and their Derivatives
title_sort hla and histo-blood group antigen expression in human pluripotent stem cells and their derivatives
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5638960/
https://www.ncbi.nlm.nih.gov/pubmed/29026098
http://dx.doi.org/10.1038/s41598-017-12231-8
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