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Stem Cell-Based Disease Models for Inborn Errors of Immunity

The intrinsic capacity of human hematopoietic stem cells (hHSCs) to reconstitute myeloid and lymphoid lineages combined with their self-renewal capacity hold enormous promises for gene therapy as a viable treatment option for a number of immune-mediated diseases, most prominently for inborn errors o...

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Autores principales: Zbinden, Aline, Canté-Barrett, Kirsten, Pike-Overzet, Karin, Staal, Frank J. T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8750661/
https://www.ncbi.nlm.nih.gov/pubmed/35011669
http://dx.doi.org/10.3390/cells11010108
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author Zbinden, Aline
Canté-Barrett, Kirsten
Pike-Overzet, Karin
Staal, Frank J. T.
author_facet Zbinden, Aline
Canté-Barrett, Kirsten
Pike-Overzet, Karin
Staal, Frank J. T.
author_sort Zbinden, Aline
collection PubMed
description The intrinsic capacity of human hematopoietic stem cells (hHSCs) to reconstitute myeloid and lymphoid lineages combined with their self-renewal capacity hold enormous promises for gene therapy as a viable treatment option for a number of immune-mediated diseases, most prominently for inborn errors of immunity (IEI). The current development of such therapies relies on disease models, both in vitro and in vivo, which allow the study of human pathophysiology in great detail. Here, we discuss the current challenges with regards to developmental origin, heterogeneity and the subsequent implications for disease modeling. We review models based on induced pluripotent stem cell technology and those relaying on use of adult hHSCs. We critically review the advantages and limitations of current models for IEI both in vitro and in vivo. We conclude that existing and future stem cell-based models are necessary tools for developing next generation therapies for IEI.
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spelling pubmed-87506612022-01-12 Stem Cell-Based Disease Models for Inborn Errors of Immunity Zbinden, Aline Canté-Barrett, Kirsten Pike-Overzet, Karin Staal, Frank J. T. Cells Review The intrinsic capacity of human hematopoietic stem cells (hHSCs) to reconstitute myeloid and lymphoid lineages combined with their self-renewal capacity hold enormous promises for gene therapy as a viable treatment option for a number of immune-mediated diseases, most prominently for inborn errors of immunity (IEI). The current development of such therapies relies on disease models, both in vitro and in vivo, which allow the study of human pathophysiology in great detail. Here, we discuss the current challenges with regards to developmental origin, heterogeneity and the subsequent implications for disease modeling. We review models based on induced pluripotent stem cell technology and those relaying on use of adult hHSCs. We critically review the advantages and limitations of current models for IEI both in vitro and in vivo. We conclude that existing and future stem cell-based models are necessary tools for developing next generation therapies for IEI. MDPI 2021-12-30 /pmc/articles/PMC8750661/ /pubmed/35011669 http://dx.doi.org/10.3390/cells11010108 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Zbinden, Aline
Canté-Barrett, Kirsten
Pike-Overzet, Karin
Staal, Frank J. T.
Stem Cell-Based Disease Models for Inborn Errors of Immunity
title Stem Cell-Based Disease Models for Inborn Errors of Immunity
title_full Stem Cell-Based Disease Models for Inborn Errors of Immunity
title_fullStr Stem Cell-Based Disease Models for Inborn Errors of Immunity
title_full_unstemmed Stem Cell-Based Disease Models for Inborn Errors of Immunity
title_short Stem Cell-Based Disease Models for Inborn Errors of Immunity
title_sort stem cell-based disease models for inborn errors of immunity
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8750661/
https://www.ncbi.nlm.nih.gov/pubmed/35011669
http://dx.doi.org/10.3390/cells11010108
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