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Long-Term Hematopoietic Engraftment of Congenic Amniotic Fluid Stem Cells After in Utero Intraperitoneal Transplantation to Immune Competent Mice

Clinical success of in utero transplantation (IUT) using allogeneic hematopoietic stem cells (HSCs) has been limited to fetuses that lack an immune response to allogeneic cells due to severe immunological defects, and where transplanted genetically normal cells have a proliferative or survival advan...

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Autores principales: Shangaris, Panicos, Loukogeorgakis, Stavros P., Blundell, Michael P., Petra, Eleni, Shaw, Steven W., Ramachandra, Durrgah L., Maghsoudlou, Panagiotis, Urbani, Luca, Thrasher, Adrian J., De Coppi, Paolo, David, Anna L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5910037/
https://www.ncbi.nlm.nih.gov/pubmed/29482456
http://dx.doi.org/10.1089/scd.2017.0116
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author Shangaris, Panicos
Loukogeorgakis, Stavros P.
Blundell, Michael P.
Petra, Eleni
Shaw, Steven W.
Ramachandra, Durrgah L.
Maghsoudlou, Panagiotis
Urbani, Luca
Thrasher, Adrian J.
De Coppi, Paolo
David, Anna L.
author_facet Shangaris, Panicos
Loukogeorgakis, Stavros P.
Blundell, Michael P.
Petra, Eleni
Shaw, Steven W.
Ramachandra, Durrgah L.
Maghsoudlou, Panagiotis
Urbani, Luca
Thrasher, Adrian J.
De Coppi, Paolo
David, Anna L.
author_sort Shangaris, Panicos
collection PubMed
description Clinical success of in utero transplantation (IUT) using allogeneic hematopoietic stem cells (HSCs) has been limited to fetuses that lack an immune response to allogeneic cells due to severe immunological defects, and where transplanted genetically normal cells have a proliferative or survival advantage. Amniotic fluid (AF) is an autologous source of stem cells with hematopoietic potential that could be used to treat congenital blood disorders. We compared the ability of congenic and allogeneic mouse AF stem cells (AFSC) to engraft the hematopoietic system of time-mated C57BL/6J mice (E13.5). At 4 and 16 weeks of age, multilineage donor engraftment was higher in congenic versus allogeneic animals. In vitro mixed lymphocyte reaction confirmed an immune response in the allogeneic group with higher CD4 and CD8 cell counts and increased proliferation of stimulated lymphocytes. IUT with congenic cells resulted in 100% of donor animals having chimerism of around 8% and successful hematopoietic long-term engraftment in immune-competent mice when compared with IUT with allogeneic cells. AFSCs may be useful for autologous cell/gene therapy approaches in fetuses diagnosed with congenital hematopoietic disorders.
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spelling pubmed-59100372018-04-23 Long-Term Hematopoietic Engraftment of Congenic Amniotic Fluid Stem Cells After in Utero Intraperitoneal Transplantation to Immune Competent Mice Shangaris, Panicos Loukogeorgakis, Stavros P. Blundell, Michael P. Petra, Eleni Shaw, Steven W. Ramachandra, Durrgah L. Maghsoudlou, Panagiotis Urbani, Luca Thrasher, Adrian J. De Coppi, Paolo David, Anna L. Stem Cells Dev Original Research Reports Clinical success of in utero transplantation (IUT) using allogeneic hematopoietic stem cells (HSCs) has been limited to fetuses that lack an immune response to allogeneic cells due to severe immunological defects, and where transplanted genetically normal cells have a proliferative or survival advantage. Amniotic fluid (AF) is an autologous source of stem cells with hematopoietic potential that could be used to treat congenital blood disorders. We compared the ability of congenic and allogeneic mouse AF stem cells (AFSC) to engraft the hematopoietic system of time-mated C57BL/6J mice (E13.5). At 4 and 16 weeks of age, multilineage donor engraftment was higher in congenic versus allogeneic animals. In vitro mixed lymphocyte reaction confirmed an immune response in the allogeneic group with higher CD4 and CD8 cell counts and increased proliferation of stimulated lymphocytes. IUT with congenic cells resulted in 100% of donor animals having chimerism of around 8% and successful hematopoietic long-term engraftment in immune-competent mice when compared with IUT with allogeneic cells. AFSCs may be useful for autologous cell/gene therapy approaches in fetuses diagnosed with congenital hematopoietic disorders. Mary Ann Liebert, Inc. 2018-04-15 2018-04-15 /pmc/articles/PMC5910037/ /pubmed/29482456 http://dx.doi.org/10.1089/scd.2017.0116 Text en © Panicos Shangaris et al. 2018; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Reports
Shangaris, Panicos
Loukogeorgakis, Stavros P.
Blundell, Michael P.
Petra, Eleni
Shaw, Steven W.
Ramachandra, Durrgah L.
Maghsoudlou, Panagiotis
Urbani, Luca
Thrasher, Adrian J.
De Coppi, Paolo
David, Anna L.
Long-Term Hematopoietic Engraftment of Congenic Amniotic Fluid Stem Cells After in Utero Intraperitoneal Transplantation to Immune Competent Mice
title Long-Term Hematopoietic Engraftment of Congenic Amniotic Fluid Stem Cells After in Utero Intraperitoneal Transplantation to Immune Competent Mice
title_full Long-Term Hematopoietic Engraftment of Congenic Amniotic Fluid Stem Cells After in Utero Intraperitoneal Transplantation to Immune Competent Mice
title_fullStr Long-Term Hematopoietic Engraftment of Congenic Amniotic Fluid Stem Cells After in Utero Intraperitoneal Transplantation to Immune Competent Mice
title_full_unstemmed Long-Term Hematopoietic Engraftment of Congenic Amniotic Fluid Stem Cells After in Utero Intraperitoneal Transplantation to Immune Competent Mice
title_short Long-Term Hematopoietic Engraftment of Congenic Amniotic Fluid Stem Cells After in Utero Intraperitoneal Transplantation to Immune Competent Mice
title_sort long-term hematopoietic engraftment of congenic amniotic fluid stem cells after in utero intraperitoneal transplantation to immune competent mice
topic Original Research Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5910037/
https://www.ncbi.nlm.nih.gov/pubmed/29482456
http://dx.doi.org/10.1089/scd.2017.0116
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