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Allogeneic natural killer cell therapy
Interest in adoptive cell therapy for treating cancer is exploding owing to early clinical successes of autologous chimeric antigen receptor (CAR) T lymphocyte therapy. However, limitations using T cells and autologous cell products are apparent as they (1) take weeks to generate, (2) utilize a 1:1...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The American Society of Hematology
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10023727/ https://www.ncbi.nlm.nih.gov/pubmed/36416736 http://dx.doi.org/10.1182/blood.2022016200 |
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author | Berrien-Elliott, Melissa M. Jacobs, Miriam T. Fehniger, Todd A. |
author_facet | Berrien-Elliott, Melissa M. Jacobs, Miriam T. Fehniger, Todd A. |
author_sort | Berrien-Elliott, Melissa M. |
collection | PubMed |
description | Interest in adoptive cell therapy for treating cancer is exploding owing to early clinical successes of autologous chimeric antigen receptor (CAR) T lymphocyte therapy. However, limitations using T cells and autologous cell products are apparent as they (1) take weeks to generate, (2) utilize a 1:1 donor-to-patient model, (3) are expensive, and (4) are prone to heterogeneity and manufacturing failures. CAR T cells are also associated with significant toxicities, including cytokine release syndrome, immune effector cell–associated neurotoxicity syndrome, and prolonged cytopenias. To overcome these issues, natural killer (NK) cells are being explored as an alternative cell source for allogeneic cell therapies. NK cells have an inherent ability to recognize cancers, mediate immune functions of killing and communication, and do not induce graft-versus-host disease, cytokine release syndrome, or immune effector cell–associated neurotoxicity syndrome. NK cells can be obtained from blood or cord blood or be derived from hematopoietic stem and progenitor cells or induced pluripotent stem cells, and can be expanded and cryopreserved for off-the-shelf availability. The first wave of point-of-care NK cell therapies led to the current allogeneic NK cell products being investigated in clinical trials with promising preliminary results. Basic advances in NK cell biology and cellular engineering have led to new translational strategies to block inhibition, enhance and broaden target cell recognition, optimize functional persistence, and provide stealth from patients’ immunity. This review details NK cell biology, as well as NK cell product manufacturing, engineering, and combination therapies explored in the clinic leading to the next generation of potent, off-the-shelf cellular therapies for blood cancers. |
format | Online Article Text |
id | pubmed-10023727 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The American Society of Hematology |
record_format | MEDLINE/PubMed |
spelling | pubmed-100237272023-03-19 Allogeneic natural killer cell therapy Berrien-Elliott, Melissa M. Jacobs, Miriam T. Fehniger, Todd A. Blood Banked Allogeneic Immune Effector Cells Interest in adoptive cell therapy for treating cancer is exploding owing to early clinical successes of autologous chimeric antigen receptor (CAR) T lymphocyte therapy. However, limitations using T cells and autologous cell products are apparent as they (1) take weeks to generate, (2) utilize a 1:1 donor-to-patient model, (3) are expensive, and (4) are prone to heterogeneity and manufacturing failures. CAR T cells are also associated with significant toxicities, including cytokine release syndrome, immune effector cell–associated neurotoxicity syndrome, and prolonged cytopenias. To overcome these issues, natural killer (NK) cells are being explored as an alternative cell source for allogeneic cell therapies. NK cells have an inherent ability to recognize cancers, mediate immune functions of killing and communication, and do not induce graft-versus-host disease, cytokine release syndrome, or immune effector cell–associated neurotoxicity syndrome. NK cells can be obtained from blood or cord blood or be derived from hematopoietic stem and progenitor cells or induced pluripotent stem cells, and can be expanded and cryopreserved for off-the-shelf availability. The first wave of point-of-care NK cell therapies led to the current allogeneic NK cell products being investigated in clinical trials with promising preliminary results. Basic advances in NK cell biology and cellular engineering have led to new translational strategies to block inhibition, enhance and broaden target cell recognition, optimize functional persistence, and provide stealth from patients’ immunity. This review details NK cell biology, as well as NK cell product manufacturing, engineering, and combination therapies explored in the clinic leading to the next generation of potent, off-the-shelf cellular therapies for blood cancers. The American Society of Hematology 2023-02-23 2022-11-24 /pmc/articles/PMC10023727/ /pubmed/36416736 http://dx.doi.org/10.1182/blood.2022016200 Text en © 2023 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Banked Allogeneic Immune Effector Cells Berrien-Elliott, Melissa M. Jacobs, Miriam T. Fehniger, Todd A. Allogeneic natural killer cell therapy |
title | Allogeneic natural killer cell therapy |
title_full | Allogeneic natural killer cell therapy |
title_fullStr | Allogeneic natural killer cell therapy |
title_full_unstemmed | Allogeneic natural killer cell therapy |
title_short | Allogeneic natural killer cell therapy |
title_sort | allogeneic natural killer cell therapy |
topic | Banked Allogeneic Immune Effector Cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10023727/ https://www.ncbi.nlm.nih.gov/pubmed/36416736 http://dx.doi.org/10.1182/blood.2022016200 |
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