Cell membrane-encapsulated magnetic nanoparticles for enhancing natural killer cell-mediated cancer immunotherapy
Natural killer (NK) cells have exhibited therapeutic potential for various malignant tumors. However, the cytotoxic effect of NK cells is relatively weak and less specific compared to other immunotherapy approaches such as chimeric antigen receptor T-Cell (CART) therapy, constituting a great challen...
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Veröffentlicht in: | Nanomedicine 2021-02, Vol.32, p.102333-102333, Article 102333 |
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creator | Wu, Dan Shou, Xin Zhang, Yalan Li, Zihan Wu, Guohua Wu, Di Wu, Jianguo Shi, Shengyu Wang, Shuqi |
description | Natural killer (NK) cells have exhibited therapeutic potential for various malignant tumors. However, the cytotoxic effect of NK cells is relatively weak and less specific compared to other immunotherapy approaches such as chimeric antigen receptor T-Cell (CART) therapy, constituting a great challenge for adoptive immunotherapy. Here, we report cell membrane-encapsulated magnetic nanoparticles for activating NK cells and enhancing anti-tumor effects. Magnetic nanoparticles were coated with silicon dioxide (SiO2), and cancer cell membranes were mixed with Fe3O4@SiO2 to construct cancer cell membrane coated Fe3O4@SiO2 magnetic nanoparticles (CMNPs). The functionalized nanoparticles bearing cancer-specific antigens on the surface effectively stimulated NK cells by enhancing expression of surface activating receptors and boosting anti-tumor function through the secretion of soluble cytotoxic effectors. To conclude, the biomimetic magnetic nanoparticles offer a versatile and powerful tool to present tumor-specific antigens, priming anti-tumor capability, which is promising to enhance NK cell-based adoptive cancer immunotherapy.
Novel tumor cell-derived membrane coated Fe3O4@SiO2 magnetic nanoparticles, containing tumor-specific antigens, serve an antigen presenting platform to activate NK cells by enhancing the expression level of surface activating receptors as well as markers (i.e., NKG2D, NKp30, NKp44, NKp46, and CD69), and increasing the secretion of cytotoxic factors including granzyme B, perforin and interferon-γ (IFN-γ) for enhanced NK cells-based immunotherapy. [Display omitted] |
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Novel tumor cell-derived membrane coated Fe3O4@SiO2 magnetic nanoparticles, containing tumor-specific antigens, serve an antigen presenting platform to activate NK cells by enhancing the expression level of surface activating receptors as well as markers (i.e., NKG2D, NKp30, NKp44, NKp46, and CD69), and increasing the secretion of cytotoxic factors including granzyme B, perforin and interferon-γ (IFN-γ) for enhanced NK cells-based immunotherapy. [Display omitted]</description><identifier>ISSN: 1549-9634</identifier><identifier>EISSN: 1549-9642</identifier><identifier>DOI: 10.1016/j.nano.2020.102333</identifier><identifier>PMID: 33188908</identifier><language>eng</language><publisher>AMSTERDAM: Elsevier Inc</publisher><subject><![CDATA[Biomimetic ; Cellular membrane ; Immunotherapy ; Life Sciences & Biomedicine ; Magnetic nanoparticles ; Medicine, Research & Experimental ; Nanoscience & Nanotechnology ; Natural killer cells ; Research & Experimental Medicine ; Science & Technology ; Science & Technology - Other Topics]]></subject><ispartof>Nanomedicine, 2021-02, Vol.32, p.102333-102333, Article 102333</ispartof><rights>2020 Elsevier Inc.</rights><rights>Copyright © 2020 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>35</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000663748100014</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c356t-2dd7686033e80dec509dcb79818f00d8f69493aec66b6ae456477dccf842a9103</citedby><cites>FETCH-LOGICAL-c356t-2dd7686033e80dec509dcb79818f00d8f69493aec66b6ae456477dccf842a9103</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.nano.2020.102333$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,39263,46000</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33188908$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Dan</creatorcontrib><creatorcontrib>Shou, Xin</creatorcontrib><creatorcontrib>Zhang, Yalan</creatorcontrib><creatorcontrib>Li, Zihan</creatorcontrib><creatorcontrib>Wu, Guohua</creatorcontrib><creatorcontrib>Wu, Di</creatorcontrib><creatorcontrib>Wu, Jianguo</creatorcontrib><creatorcontrib>Shi, Shengyu</creatorcontrib><creatorcontrib>Wang, Shuqi</creatorcontrib><title>Cell membrane-encapsulated magnetic nanoparticles for enhancing natural killer cell-mediated cancer immunotherapy</title><title>Nanomedicine</title><addtitle>NANOMED-NANOTECHNOL</addtitle><addtitle>Nanomedicine</addtitle><description>Natural killer (NK) cells have exhibited therapeutic potential for various malignant tumors. However, the cytotoxic effect of NK cells is relatively weak and less specific compared to other immunotherapy approaches such as chimeric antigen receptor T-Cell (CART) therapy, constituting a great challenge for adoptive immunotherapy. Here, we report cell membrane-encapsulated magnetic nanoparticles for activating NK cells and enhancing anti-tumor effects. Magnetic nanoparticles were coated with silicon dioxide (SiO2), and cancer cell membranes were mixed with Fe3O4@SiO2 to construct cancer cell membrane coated Fe3O4@SiO2 magnetic nanoparticles (CMNPs). The functionalized nanoparticles bearing cancer-specific antigens on the surface effectively stimulated NK cells by enhancing expression of surface activating receptors and boosting anti-tumor function through the secretion of soluble cytotoxic effectors. To conclude, the biomimetic magnetic nanoparticles offer a versatile and powerful tool to present tumor-specific antigens, priming anti-tumor capability, which is promising to enhance NK cell-based adoptive cancer immunotherapy.
Novel tumor cell-derived membrane coated Fe3O4@SiO2 magnetic nanoparticles, containing tumor-specific antigens, serve an antigen presenting platform to activate NK cells by enhancing the expression level of surface activating receptors as well as markers (i.e., NKG2D, NKp30, NKp44, NKp46, and CD69), and increasing the secretion of cytotoxic factors including granzyme B, perforin and interferon-γ (IFN-γ) for enhanced NK cells-based immunotherapy. [Display omitted]</description><subject>Biomimetic</subject><subject>Cellular membrane</subject><subject>Immunotherapy</subject><subject>Life Sciences & Biomedicine</subject><subject>Magnetic nanoparticles</subject><subject>Medicine, Research & Experimental</subject><subject>Nanoscience & Nanotechnology</subject><subject>Natural killer cells</subject><subject>Research & Experimental Medicine</subject><subject>Science & Technology</subject><subject>Science & Technology - Other Topics</subject><issn>1549-9634</issn><issn>1549-9642</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>HGBXW</sourceid><recordid>eNqNkE-P1SAUxRujcf7oF3BhujQxfV4KpTRxYxodTSZxo2tC4XaGZwsdoJr59lL7fEvjipPL7xy4pyheETgQIPzd8eCU84ca6m1QU0qfFJekYV3VcVY_PWvKLoqrGI8AtAXonhcXlBIhOhCXxUOP01TOOA9BOazQabXEdVIJTTmrO4fJ6nJ7ZlEhywljOfpQortXTlt3l-_SGtRU_rDThKHUOa6a0dg_CTpDeWjneXU-3WNQy-OL4tmopogvT-d18f3Tx2_95-r2682X_sNtpWnDU1Ub03LBgVIUYFA30Bk9tJ0gYgQwYuQd66hCzfnAFbKGs7Y1Wo-C1aojQK-LN3vuEvzDijHJ2cbte3lPv0ZZMw4tr5tWZLTeUR18jAFHuQQ7q_AoCcitanmUWwdyq1ruVWfT61P-OuSFz5a_3Wbg7Q78wsGPUdtcLp4xAOCctkyQrAjLtPh_urdJJetd71eXsvX9bsVc50-LQZ7sxgbUSRpv_7XIbzj7sn8</recordid><startdate>20210201</startdate><enddate>20210201</enddate><creator>Wu, Dan</creator><creator>Shou, Xin</creator><creator>Zhang, Yalan</creator><creator>Li, Zihan</creator><creator>Wu, Guohua</creator><creator>Wu, Di</creator><creator>Wu, Jianguo</creator><creator>Shi, Shengyu</creator><creator>Wang, Shuqi</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>BLEPL</scope><scope>DTL</scope><scope>HGBXW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20210201</creationdate><title>Cell membrane-encapsulated magnetic nanoparticles for enhancing natural killer cell-mediated cancer immunotherapy</title><author>Wu, Dan ; Shou, Xin ; Zhang, Yalan ; Li, Zihan ; Wu, Guohua ; Wu, Di ; Wu, Jianguo ; Shi, Shengyu ; Wang, Shuqi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-2dd7686033e80dec509dcb79818f00d8f69493aec66b6ae456477dccf842a9103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Biomimetic</topic><topic>Cellular membrane</topic><topic>Immunotherapy</topic><topic>Life Sciences & Biomedicine</topic><topic>Magnetic nanoparticles</topic><topic>Medicine, Research & Experimental</topic><topic>Nanoscience & Nanotechnology</topic><topic>Natural killer cells</topic><topic>Research & Experimental Medicine</topic><topic>Science & Technology</topic><topic>Science & Technology - Other Topics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Dan</creatorcontrib><creatorcontrib>Shou, Xin</creatorcontrib><creatorcontrib>Zhang, Yalan</creatorcontrib><creatorcontrib>Li, Zihan</creatorcontrib><creatorcontrib>Wu, Guohua</creatorcontrib><creatorcontrib>Wu, Di</creatorcontrib><creatorcontrib>Wu, Jianguo</creatorcontrib><creatorcontrib>Shi, Shengyu</creatorcontrib><creatorcontrib>Wang, Shuqi</creatorcontrib><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>Web of Science - Science Citation Index Expanded - 2021</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Nanomedicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Dan</au><au>Shou, Xin</au><au>Zhang, Yalan</au><au>Li, Zihan</au><au>Wu, Guohua</au><au>Wu, Di</au><au>Wu, Jianguo</au><au>Shi, Shengyu</au><au>Wang, Shuqi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cell membrane-encapsulated magnetic nanoparticles for enhancing natural killer cell-mediated cancer immunotherapy</atitle><jtitle>Nanomedicine</jtitle><stitle>NANOMED-NANOTECHNOL</stitle><addtitle>Nanomedicine</addtitle><date>2021-02-01</date><risdate>2021</risdate><volume>32</volume><spage>102333</spage><epage>102333</epage><pages>102333-102333</pages><artnum>102333</artnum><issn>1549-9634</issn><eissn>1549-9642</eissn><abstract>Natural killer (NK) cells have exhibited therapeutic potential for various malignant tumors. However, the cytotoxic effect of NK cells is relatively weak and less specific compared to other immunotherapy approaches such as chimeric antigen receptor T-Cell (CART) therapy, constituting a great challenge for adoptive immunotherapy. Here, we report cell membrane-encapsulated magnetic nanoparticles for activating NK cells and enhancing anti-tumor effects. Magnetic nanoparticles were coated with silicon dioxide (SiO2), and cancer cell membranes were mixed with Fe3O4@SiO2 to construct cancer cell membrane coated Fe3O4@SiO2 magnetic nanoparticles (CMNPs). The functionalized nanoparticles bearing cancer-specific antigens on the surface effectively stimulated NK cells by enhancing expression of surface activating receptors and boosting anti-tumor function through the secretion of soluble cytotoxic effectors. To conclude, the biomimetic magnetic nanoparticles offer a versatile and powerful tool to present tumor-specific antigens, priming anti-tumor capability, which is promising to enhance NK cell-based adoptive cancer immunotherapy.
Novel tumor cell-derived membrane coated Fe3O4@SiO2 magnetic nanoparticles, containing tumor-specific antigens, serve an antigen presenting platform to activate NK cells by enhancing the expression level of surface activating receptors as well as markers (i.e., NKG2D, NKp30, NKp44, NKp46, and CD69), and increasing the secretion of cytotoxic factors including granzyme B, perforin and interferon-γ (IFN-γ) for enhanced NK cells-based immunotherapy. [Display omitted]</abstract><cop>AMSTERDAM</cop><pub>Elsevier Inc</pub><pmid>33188908</pmid><doi>10.1016/j.nano.2020.102333</doi><tpages>10</tpages></addata></record> |
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subjects | Biomimetic Cellular membrane Immunotherapy Life Sciences & Biomedicine Magnetic nanoparticles Medicine, Research & Experimental Nanoscience & Nanotechnology Natural killer cells Research & Experimental Medicine Science & Technology Science & Technology - Other Topics |
title | Cell membrane-encapsulated magnetic nanoparticles for enhancing natural killer cell-mediated cancer immunotherapy |
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