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iPSC-Derived Natural Killer Cell Therapies - Expansion and Targeting
Treatment of cancer with allogeneic natural killer (NK) cell therapies has seen rapid development, especially use against hematologic malignancies. Clinical trials of NK cell-based adoptive transfer to treat relapsed or refractory malignancies have used peripheral blood, umbilical cord blood and plu...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8851389/ https://www.ncbi.nlm.nih.gov/pubmed/35185932 http://dx.doi.org/10.3389/fimmu.2022.841107 |
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author | Goldenson, Benjamin H. Hor, Pooja Kaufman, Dan S. |
author_facet | Goldenson, Benjamin H. Hor, Pooja Kaufman, Dan S. |
author_sort | Goldenson, Benjamin H. |
collection | PubMed |
description | Treatment of cancer with allogeneic natural killer (NK) cell therapies has seen rapid development, especially use against hematologic malignancies. Clinical trials of NK cell-based adoptive transfer to treat relapsed or refractory malignancies have used peripheral blood, umbilical cord blood and pluripotent stem cell-derived NK cells, with each approach undergoing continued clinical development. Improving the potency of these therapies relies on genetic modifications to improve tumor targeting and to enhance expansion and persistence of the NK cells. Induced pluripotent stem cell (iPSC)-derived NK cells allow for routine targeted introduction of genetic modifications and expansion of the resulting NK cells derived from a clonal starting cell population. In this review, we discuss and summarize recent important advances in the development of new iPSC-derived NK cell therapies, with a focus on improved targeting of cancer. We then discuss improvements in methods to expand iPSC-derived NK cells and how persistence of iPSC-NK cells can be enhanced. Finally, we describe how these advances may combine in future NK cell-based therapy products for the treatment of both hematologic malignancies and solid tumors. |
format | Online Article Text |
id | pubmed-8851389 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88513892022-02-18 iPSC-Derived Natural Killer Cell Therapies - Expansion and Targeting Goldenson, Benjamin H. Hor, Pooja Kaufman, Dan S. Front Immunol Immunology Treatment of cancer with allogeneic natural killer (NK) cell therapies has seen rapid development, especially use against hematologic malignancies. Clinical trials of NK cell-based adoptive transfer to treat relapsed or refractory malignancies have used peripheral blood, umbilical cord blood and pluripotent stem cell-derived NK cells, with each approach undergoing continued clinical development. Improving the potency of these therapies relies on genetic modifications to improve tumor targeting and to enhance expansion and persistence of the NK cells. Induced pluripotent stem cell (iPSC)-derived NK cells allow for routine targeted introduction of genetic modifications and expansion of the resulting NK cells derived from a clonal starting cell population. In this review, we discuss and summarize recent important advances in the development of new iPSC-derived NK cell therapies, with a focus on improved targeting of cancer. We then discuss improvements in methods to expand iPSC-derived NK cells and how persistence of iPSC-NK cells can be enhanced. Finally, we describe how these advances may combine in future NK cell-based therapy products for the treatment of both hematologic malignancies and solid tumors. Frontiers Media S.A. 2022-02-03 /pmc/articles/PMC8851389/ /pubmed/35185932 http://dx.doi.org/10.3389/fimmu.2022.841107 Text en Copyright © 2022 Goldenson, Hor and Kaufman https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Goldenson, Benjamin H. Hor, Pooja Kaufman, Dan S. iPSC-Derived Natural Killer Cell Therapies - Expansion and Targeting |
title | iPSC-Derived Natural Killer Cell Therapies - Expansion and Targeting |
title_full | iPSC-Derived Natural Killer Cell Therapies - Expansion and Targeting |
title_fullStr | iPSC-Derived Natural Killer Cell Therapies - Expansion and Targeting |
title_full_unstemmed | iPSC-Derived Natural Killer Cell Therapies - Expansion and Targeting |
title_short | iPSC-Derived Natural Killer Cell Therapies - Expansion and Targeting |
title_sort | ipsc-derived natural killer cell therapies - expansion and targeting |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8851389/ https://www.ncbi.nlm.nih.gov/pubmed/35185932 http://dx.doi.org/10.3389/fimmu.2022.841107 |
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