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A novel endogenous CD16-Expressing Natural Killer Cell for cancer immunotherapy

Natural killer (NK) cells, as a potential source for off-the-shelf cell therapy, attack tumor cells with low risk of severe cytokine release syndrome (CRS) or graft-versus-host disease (GvHD). Fcγ receptor IIIA, also known as CD16, further confers NK cells with antibody-dependent cell-mediated cytot...

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Autores principales: Cheng, Zih-Fei, Li, Hao-Kang, Yang, Hsiu-Ping, Lee, Chia-Yun, Tang, Sai-Wen, Lin, Yan-Liang, Hsiao, Shih-Chia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7889824/
https://www.ncbi.nlm.nih.gov/pubmed/33644421
http://dx.doi.org/10.1016/j.bbrep.2021.100935
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author Cheng, Zih-Fei
Li, Hao-Kang
Yang, Hsiu-Ping
Lee, Chia-Yun
Tang, Sai-Wen
Lin, Yan-Liang
Hsiao, Shih-Chia
author_facet Cheng, Zih-Fei
Li, Hao-Kang
Yang, Hsiu-Ping
Lee, Chia-Yun
Tang, Sai-Wen
Lin, Yan-Liang
Hsiao, Shih-Chia
author_sort Cheng, Zih-Fei
collection PubMed
description Natural killer (NK) cells, as a potential source for off-the-shelf cell therapy, attack tumor cells with low risk of severe cytokine release syndrome (CRS) or graft-versus-host disease (GvHD). Fcγ receptor IIIA, also known as CD16, further confers NK cells with antibody-dependent cell-mediated cytotoxicity (ADCC), one mechanism of action of antibody-based immunotherapy. Here, we establish a novel human NK cell line, oNK-1, endogenously expressing CD16 along with high levels of NK activation markers and low levels of NK inhibitory markers. The long-term expansion and CD16 expression of oNK-1 cells were demonstrated. Furthermore, oNK-1 cells elicit superior cytotoxicity against cancer cells than primary NK cells. In conclusion, this study suggests that endogenous CD16-expressing oNK-1 has the potential to develop an effective NK-based therapy.
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spelling pubmed-78898242021-02-26 A novel endogenous CD16-Expressing Natural Killer Cell for cancer immunotherapy Cheng, Zih-Fei Li, Hao-Kang Yang, Hsiu-Ping Lee, Chia-Yun Tang, Sai-Wen Lin, Yan-Liang Hsiao, Shih-Chia Biochem Biophys Rep Research Article Natural killer (NK) cells, as a potential source for off-the-shelf cell therapy, attack tumor cells with low risk of severe cytokine release syndrome (CRS) or graft-versus-host disease (GvHD). Fcγ receptor IIIA, also known as CD16, further confers NK cells with antibody-dependent cell-mediated cytotoxicity (ADCC), one mechanism of action of antibody-based immunotherapy. Here, we establish a novel human NK cell line, oNK-1, endogenously expressing CD16 along with high levels of NK activation markers and low levels of NK inhibitory markers. The long-term expansion and CD16 expression of oNK-1 cells were demonstrated. Furthermore, oNK-1 cells elicit superior cytotoxicity against cancer cells than primary NK cells. In conclusion, this study suggests that endogenous CD16-expressing oNK-1 has the potential to develop an effective NK-based therapy. Elsevier 2021-02-03 /pmc/articles/PMC7889824/ /pubmed/33644421 http://dx.doi.org/10.1016/j.bbrep.2021.100935 Text en © 2021 The Authors http://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 Research Article
Cheng, Zih-Fei
Li, Hao-Kang
Yang, Hsiu-Ping
Lee, Chia-Yun
Tang, Sai-Wen
Lin, Yan-Liang
Hsiao, Shih-Chia
A novel endogenous CD16-Expressing Natural Killer Cell for cancer immunotherapy
title A novel endogenous CD16-Expressing Natural Killer Cell for cancer immunotherapy
title_full A novel endogenous CD16-Expressing Natural Killer Cell for cancer immunotherapy
title_fullStr A novel endogenous CD16-Expressing Natural Killer Cell for cancer immunotherapy
title_full_unstemmed A novel endogenous CD16-Expressing Natural Killer Cell for cancer immunotherapy
title_short A novel endogenous CD16-Expressing Natural Killer Cell for cancer immunotherapy
title_sort novel endogenous cd16-expressing natural killer cell for cancer immunotherapy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7889824/
https://www.ncbi.nlm.nih.gov/pubmed/33644421
http://dx.doi.org/10.1016/j.bbrep.2021.100935
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