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Glycoengineering of Natural Killer Cells with CD22 Ligands for Enhanced Anticancer Immunotherapy
[Image: see text] Adoptive transfer of immune cells is being actively pursued for cancer treatment. Natural killer (NK) cells, a class of cytotoxic immune cells, generally lack inherent selectivities toward cancer. To bestow tumor-targeting abilities and enhance anticancer efficacy, a new strategy i...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7099595/ https://www.ncbi.nlm.nih.gov/pubmed/32232138 http://dx.doi.org/10.1021/acscentsci.9b00956 |
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author | Wang, Xianwu Lang, Shuyao Tian, Yunpeng Zhang, Jianghong Yan, Xu Fang, Zhihong Weng, Jian Lu, Na Wu, Xuanjun Li, Tianlu Cao, Hongzhi Li, Zhu Huang, Xuefei |
author_facet | Wang, Xianwu Lang, Shuyao Tian, Yunpeng Zhang, Jianghong Yan, Xu Fang, Zhihong Weng, Jian Lu, Na Wu, Xuanjun Li, Tianlu Cao, Hongzhi Li, Zhu Huang, Xuefei |
author_sort | Wang, Xianwu |
collection | PubMed |
description | [Image: see text] Adoptive transfer of immune cells is being actively pursued for cancer treatment. Natural killer (NK) cells, a class of cytotoxic immune cells, generally lack inherent selectivities toward cancer. To bestow tumor-targeting abilities and enhance anticancer efficacy, a new strategy is established to glycoengineer NK cells. Carbohydrate-based ligands for CD22, a marker for B cell lymphoma, are introduced onto NK cells through either metabolic engineering or glyco-polymer insertion. Such NK cells exhibited greatly enhanced cytotoxicities toward CD22(+) lymphoma cells in a CD22-dependent manner. Importantly, both CD22(+) lymphoma cell lines and primary lymphoma cells from human cancer patients can be effectively killed by the engineered NK cells. Furthermore, glycoengineered NK cells provided significant protection to tumor-bearing mice. Thus, NK cell glycoengineering is an exciting new approach for cancer treatment complementing the current immune cell genetic engineering strategy. |
format | Online Article Text |
id | pubmed-7099595 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-70995952020-03-30 Glycoengineering of Natural Killer Cells with CD22 Ligands for Enhanced Anticancer Immunotherapy Wang, Xianwu Lang, Shuyao Tian, Yunpeng Zhang, Jianghong Yan, Xu Fang, Zhihong Weng, Jian Lu, Na Wu, Xuanjun Li, Tianlu Cao, Hongzhi Li, Zhu Huang, Xuefei ACS Cent Sci [Image: see text] Adoptive transfer of immune cells is being actively pursued for cancer treatment. Natural killer (NK) cells, a class of cytotoxic immune cells, generally lack inherent selectivities toward cancer. To bestow tumor-targeting abilities and enhance anticancer efficacy, a new strategy is established to glycoengineer NK cells. Carbohydrate-based ligands for CD22, a marker for B cell lymphoma, are introduced onto NK cells through either metabolic engineering or glyco-polymer insertion. Such NK cells exhibited greatly enhanced cytotoxicities toward CD22(+) lymphoma cells in a CD22-dependent manner. Importantly, both CD22(+) lymphoma cell lines and primary lymphoma cells from human cancer patients can be effectively killed by the engineered NK cells. Furthermore, glycoengineered NK cells provided significant protection to tumor-bearing mice. Thus, NK cell glycoengineering is an exciting new approach for cancer treatment complementing the current immune cell genetic engineering strategy. American Chemical Society 2020-03-05 2020-03-25 /pmc/articles/PMC7099595/ /pubmed/32232138 http://dx.doi.org/10.1021/acscentsci.9b00956 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Wang, Xianwu Lang, Shuyao Tian, Yunpeng Zhang, Jianghong Yan, Xu Fang, Zhihong Weng, Jian Lu, Na Wu, Xuanjun Li, Tianlu Cao, Hongzhi Li, Zhu Huang, Xuefei Glycoengineering of Natural Killer Cells with CD22 Ligands for Enhanced Anticancer Immunotherapy |
title | Glycoengineering of Natural Killer Cells with CD22
Ligands for Enhanced Anticancer Immunotherapy |
title_full | Glycoengineering of Natural Killer Cells with CD22
Ligands for Enhanced Anticancer Immunotherapy |
title_fullStr | Glycoengineering of Natural Killer Cells with CD22
Ligands for Enhanced Anticancer Immunotherapy |
title_full_unstemmed | Glycoengineering of Natural Killer Cells with CD22
Ligands for Enhanced Anticancer Immunotherapy |
title_short | Glycoengineering of Natural Killer Cells with CD22
Ligands for Enhanced Anticancer Immunotherapy |
title_sort | glycoengineering of natural killer cells with cd22
ligands for enhanced anticancer immunotherapy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7099595/ https://www.ncbi.nlm.nih.gov/pubmed/32232138 http://dx.doi.org/10.1021/acscentsci.9b00956 |
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