Shaping of Natural Killer Cell Antitumor Activity by Ex Vivo Cultivation

Natural killer (NK) cells are a promising tool for the use in adoptive immunotherapy, since they efficiently recognize and kill tumor cells. In this context, ex vivo cultivation is an attractive option to increase NK cells in numbers and to improve their antitumor potential prior to clinical applica...

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Main Authors: Markus Granzin, Evelyn Ullrich, Juliane Wagner, Ulrike Köhl, Adelheid Cerwenka, Volker Huppert
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-04-01
Series:Frontiers in Immunology
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fimmu.2017.00458/full
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spelling doaj-d8832f357c4a47bdb4e54faec42920dc2020-11-24T23:25:27ZengFrontiers Media S.A.Frontiers in Immunology1664-32242017-04-01810.3389/fimmu.2017.00458257309Shaping of Natural Killer Cell Antitumor Activity by Ex Vivo CultivationMarkus Granzin0Evelyn Ullrich1Evelyn Ullrich2Juliane Wagner3Juliane Wagner4Ulrike Köhl5Adelheid Cerwenka6Adelheid Cerwenka7Volker Huppert8Clinical Research, Miltenyi Biotec Inc., Gaithersburg, MD, USADivision for Stem Cell Transplantation and Immunology, Department for Children and Adolescents Medicine, Hospital of the Goethe University, Frankfurt, GermanyLOEWE Center for Cell and Gene Therapy, Cellular Immunology, Goethe University, Frankfurt, GermanyDivision for Stem Cell Transplantation and Immunology, Department for Children and Adolescents Medicine, Hospital of the Goethe University, Frankfurt, GermanyLOEWE Center for Cell and Gene Therapy, Cellular Immunology, Goethe University, Frankfurt, GermanyInstitute of Cellular Therapeutics, Integrated Research and Treatment Center Transplantation, Hannover Medical School, Hannover, GermanyInnate Immunity Group, German Cancer Research Center, Heidelberg, GermanyDivision of Immunbiochemistry, Medical Faculty Mannheim, Heidelberg University, Heidelberg, GermanyR&D Reagents, Miltenyi Biotec GmbH, Bergisch Gladbach, GermanyNatural killer (NK) cells are a promising tool for the use in adoptive immunotherapy, since they efficiently recognize and kill tumor cells. In this context, ex vivo cultivation is an attractive option to increase NK cells in numbers and to improve their antitumor potential prior to clinical applications. Consequently, various strategies to generate NK cells for adoptive immunotherapy have been developed. Here, we give an overview of different NK cell cultivation approaches and their impact on shaping the NK cell antitumor activity. So far, the cytokines interleukin (IL)-2, IL-12, IL-15, IL-18, and IL-21 are used to culture and expand NK cells. The selection of the respective cytokine combination is an important factor that directly affects NK cell maturation, proliferation, survival, distribution of NK cell subpopulations, activation, and function in terms of cytokine production and cytotoxic potential. Importantly, cytokines can upregulate the expression of certain activating receptors on NK cells, thereby increasing their responsiveness against tumor cells that express the corresponding ligands. Apart from using cytokines, cocultivation with autologous accessory non-NK cells or addition of growth-inactivated feeder cells are approaches for NK cell cultivation with pronounced effects on NK cell activation and expansion. Furthermore, ex vivo cultivation was reported to prime NK cells for the killing of tumor cells that were previously resistant to NK cell attack. In general, NK cells become frequently dysfunctional in cancer patients, for instance, by downregulation of NK cell activating receptors, disabling them in their antitumor response. In such scenario, ex vivo cultivation can be helpful to arm NK cells with enhanced antitumor properties to overcome immunosuppression. In this review, we summarize the current knowledge on NK cell modulation by different ex vivo cultivation strategies focused on increasing NK cytotoxicity for clinical application in malignant diseases. Moreover, we critically discuss the technical and regulatory aspects and challenges underlying NK cell based therapeutic approaches in the clinics.http://journal.frontiersin.org/article/10.3389/fimmu.2017.00458/fullnatural killer cellsnatural killer cell cultivationnatural killer cell expansionnatural killer cell therapynatural killer cell cytotoxicityex vivo stimulation
collection DOAJ
language English
format Article
sources DOAJ
author Markus Granzin
Evelyn Ullrich
Evelyn Ullrich
Juliane Wagner
Juliane Wagner
Ulrike Köhl
Adelheid Cerwenka
Adelheid Cerwenka
Volker Huppert
spellingShingle Markus Granzin
Evelyn Ullrich
Evelyn Ullrich
Juliane Wagner
Juliane Wagner
Ulrike Köhl
Adelheid Cerwenka
Adelheid Cerwenka
Volker Huppert
Shaping of Natural Killer Cell Antitumor Activity by Ex Vivo Cultivation
Frontiers in Immunology
natural killer cells
natural killer cell cultivation
natural killer cell expansion
natural killer cell therapy
natural killer cell cytotoxicity
ex vivo stimulation
author_facet Markus Granzin
Evelyn Ullrich
Evelyn Ullrich
Juliane Wagner
Juliane Wagner
Ulrike Köhl
Adelheid Cerwenka
Adelheid Cerwenka
Volker Huppert
author_sort Markus Granzin
title Shaping of Natural Killer Cell Antitumor Activity by Ex Vivo Cultivation
title_short Shaping of Natural Killer Cell Antitumor Activity by Ex Vivo Cultivation
title_full Shaping of Natural Killer Cell Antitumor Activity by Ex Vivo Cultivation
title_fullStr Shaping of Natural Killer Cell Antitumor Activity by Ex Vivo Cultivation
title_full_unstemmed Shaping of Natural Killer Cell Antitumor Activity by Ex Vivo Cultivation
title_sort shaping of natural killer cell antitumor activity by ex vivo cultivation
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2017-04-01
description Natural killer (NK) cells are a promising tool for the use in adoptive immunotherapy, since they efficiently recognize and kill tumor cells. In this context, ex vivo cultivation is an attractive option to increase NK cells in numbers and to improve their antitumor potential prior to clinical applications. Consequently, various strategies to generate NK cells for adoptive immunotherapy have been developed. Here, we give an overview of different NK cell cultivation approaches and their impact on shaping the NK cell antitumor activity. So far, the cytokines interleukin (IL)-2, IL-12, IL-15, IL-18, and IL-21 are used to culture and expand NK cells. The selection of the respective cytokine combination is an important factor that directly affects NK cell maturation, proliferation, survival, distribution of NK cell subpopulations, activation, and function in terms of cytokine production and cytotoxic potential. Importantly, cytokines can upregulate the expression of certain activating receptors on NK cells, thereby increasing their responsiveness against tumor cells that express the corresponding ligands. Apart from using cytokines, cocultivation with autologous accessory non-NK cells or addition of growth-inactivated feeder cells are approaches for NK cell cultivation with pronounced effects on NK cell activation and expansion. Furthermore, ex vivo cultivation was reported to prime NK cells for the killing of tumor cells that were previously resistant to NK cell attack. In general, NK cells become frequently dysfunctional in cancer patients, for instance, by downregulation of NK cell activating receptors, disabling them in their antitumor response. In such scenario, ex vivo cultivation can be helpful to arm NK cells with enhanced antitumor properties to overcome immunosuppression. In this review, we summarize the current knowledge on NK cell modulation by different ex vivo cultivation strategies focused on increasing NK cytotoxicity for clinical application in malignant diseases. Moreover, we critically discuss the technical and regulatory aspects and challenges underlying NK cell based therapeutic approaches in the clinics.
topic natural killer cells
natural killer cell cultivation
natural killer cell expansion
natural killer cell therapy
natural killer cell cytotoxicity
ex vivo stimulation
url http://journal.frontiersin.org/article/10.3389/fimmu.2017.00458/full
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