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NK cells encapsulated in micro/macropore-forming hydrogels via 3D bioprinting for tumor immunotherapy
Patients face a serious threat if a solid tumor leaves behind partial residuals or cannot be completely removed after surgical resection. Immunotherapy has attracted attention as a method to prevent this condition. However, the conventional immunotherapy method targeting solid tumors, that is, intra...
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Published in: | Biomaterials research 2023, 27(00), , pp.1572-1587 |
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description | Patients face a serious threat if a solid tumor leaves behind partial residuals or cannot be completely removed after surgical resection. Immunotherapy has attracted attention as a method to prevent this condition. However, the conventional immunotherapy method targeting solid tumors, that is, intravenous injection, has limitations in homing in on the tumor and in vivo expansion and has not shown effective clinical results.
To overcome these limitations, NK cells (Natural killer cells) were encapsulated in micro/macropore-forming hydrogels using 3D bioprinting to target solid tumors. Sodium alginate and gelatin were used to prepare micro-macroporous hydrogels. The gelatin contained in the alginate hydrogel was removed because of the thermal sensitivity of the gelatin, which can generate interconnected micropores where the gelatin was released. Therefore, macropores can be formed through bioprinting and micropores can be formed using thermally sensitive gelatin to make macroporous hydrogels.
It was confirmed that intentionally formed micropores could help NK cells to aggregate easily, which enhances cell viability, lysis activity, and cytokine release. Macropores can be formed using 3D bioprinting, which enables NK cells to receive the essential elements. We also characterized the functionality of NK 92 and zEGFR-CAR-NK cells in the pore-forming hydrogel. The antitumor effects on leukemia and solid tumors were investigated using an in vitro model.
We demonstrated that the hydrogel encapsulating NK cells created an appropriate micro-macro environment for clinical applications of NK cell therapy for both leukemia and solid tumors via 3D bioprinting. 3D bioprinting makes macro-scale clinical applications possible, and the automatic process shows potential for development as an off-the-shelf immunotherapy product. This immunotherapy system could provide a clinical option for preventing tumor relapse and metastasis after tumor resection. Micro/macropore-forming hydrogel with NK cells fabricated by 3D bioprinting and implanted into the tumor site. |
doi_str_mv | 10.1186/s40824-023-00403-9 |
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To overcome these limitations, NK cells (Natural killer cells) were encapsulated in micro/macropore-forming hydrogels using 3D bioprinting to target solid tumors. Sodium alginate and gelatin were used to prepare micro-macroporous hydrogels. The gelatin contained in the alginate hydrogel was removed because of the thermal sensitivity of the gelatin, which can generate interconnected micropores where the gelatin was released. Therefore, macropores can be formed through bioprinting and micropores can be formed using thermally sensitive gelatin to make macroporous hydrogels.
It was confirmed that intentionally formed micropores could help NK cells to aggregate easily, which enhances cell viability, lysis activity, and cytokine release. Macropores can be formed using 3D bioprinting, which enables NK cells to receive the essential elements. We also characterized the functionality of NK 92 and zEGFR-CAR-NK cells in the pore-forming hydrogel. The antitumor effects on leukemia and solid tumors were investigated using an in vitro model.
We demonstrated that the hydrogel encapsulating NK cells created an appropriate micro-macro environment for clinical applications of NK cell therapy for both leukemia and solid tumors via 3D bioprinting. 3D bioprinting makes macro-scale clinical applications possible, and the automatic process shows potential for development as an off-the-shelf immunotherapy product. This immunotherapy system could provide a clinical option for preventing tumor relapse and metastasis after tumor resection. Micro/macropore-forming hydrogel with NK cells fabricated by 3D bioprinting and implanted into the tumor site.</description><identifier>ISSN: 1226-4601</identifier><identifier>ISSN: 2055-7124</identifier><identifier>EISSN: 2055-7124</identifier><identifier>DOI: 10.1186/s40824-023-00403-9</identifier><identifier>PMID: 37349810</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>3-D printers ; 3D bioprinting ; Alginic acid ; Antitumor activity ; Cancer therapies ; Cell culture ; Cell therapy ; Cell viability ; Cytokines ; Drug therapy ; Gelatin ; Hydrogels ; Immunotherapy ; Killer cells ; Leukemia ; Lysis ; Metastases ; Micro/macropore-forming ; Natural killer cells ; NK cells ; Prevention ; Sodium ; Sodium alginate ; Solid tumor ; Solid tumors ; Therapeutic applications ; Tumors ; 의공학</subject><ispartof>생체재료학회지, 2023, 27(00), , pp.1572-1587</ispartof><rights>2023. The Author(s).</rights><rights>COPYRIGHT 2023 BioMed Central Ltd.</rights><rights>2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c633t-a59ec63abee201a9b30cb6b5c64510acba52d4dcf4a61739ae1babc50f5a8d393</citedby><cites>FETCH-LOGICAL-c633t-a59ec63abee201a9b30cb6b5c64510acba52d4dcf4a61739ae1babc50f5a8d393</cites><orcidid>0000-0001-5878-8054</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10286468/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2838779358?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37349810$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART003005654$$DAccess content in National Research Foundation of Korea (NRF)$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Dahong</creatorcontrib><creatorcontrib>Jo, Seona</creatorcontrib><creatorcontrib>Lee, Dongjin</creatorcontrib><creatorcontrib>Kim, Seok-Min</creatorcontrib><creatorcontrib>Seok, Ji Min</creatorcontrib><creatorcontrib>Yeo, Seon Ju</creatorcontrib><creatorcontrib>Lee, Jun Hee</creatorcontrib><creatorcontrib>Lee, Jae Jong</creatorcontrib><creatorcontrib>Lee, Kangwon</creatorcontrib><creatorcontrib>Kim, Tae-Don</creatorcontrib><creatorcontrib>Park, Su A</creatorcontrib><title>NK cells encapsulated in micro/macropore-forming hydrogels via 3D bioprinting for tumor immunotherapy</title><title>Biomaterials research</title><addtitle>Biomater Res</addtitle><description>Patients face a serious threat if a solid tumor leaves behind partial residuals or cannot be completely removed after surgical resection. Immunotherapy has attracted attention as a method to prevent this condition. However, the conventional immunotherapy method targeting solid tumors, that is, intravenous injection, has limitations in homing in on the tumor and in vivo expansion and has not shown effective clinical results.
To overcome these limitations, NK cells (Natural killer cells) were encapsulated in micro/macropore-forming hydrogels using 3D bioprinting to target solid tumors. Sodium alginate and gelatin were used to prepare micro-macroporous hydrogels. The gelatin contained in the alginate hydrogel was removed because of the thermal sensitivity of the gelatin, which can generate interconnected micropores where the gelatin was released. Therefore, macropores can be formed through bioprinting and micropores can be formed using thermally sensitive gelatin to make macroporous hydrogels.
It was confirmed that intentionally formed micropores could help NK cells to aggregate easily, which enhances cell viability, lysis activity, and cytokine release. Macropores can be formed using 3D bioprinting, which enables NK cells to receive the essential elements. We also characterized the functionality of NK 92 and zEGFR-CAR-NK cells in the pore-forming hydrogel. The antitumor effects on leukemia and solid tumors were investigated using an in vitro model.
We demonstrated that the hydrogel encapsulating NK cells created an appropriate micro-macro environment for clinical applications of NK cell therapy for both leukemia and solid tumors via 3D bioprinting. 3D bioprinting makes macro-scale clinical applications possible, and the automatic process shows potential for development as an off-the-shelf immunotherapy product. This immunotherapy system could provide a clinical option for preventing tumor relapse and metastasis after tumor resection. Micro/macropore-forming hydrogel with NK cells fabricated by 3D bioprinting and implanted into the tumor site.</description><subject>3-D printers</subject><subject>3D bioprinting</subject><subject>Alginic acid</subject><subject>Antitumor activity</subject><subject>Cancer therapies</subject><subject>Cell culture</subject><subject>Cell therapy</subject><subject>Cell viability</subject><subject>Cytokines</subject><subject>Drug therapy</subject><subject>Gelatin</subject><subject>Hydrogels</subject><subject>Immunotherapy</subject><subject>Killer cells</subject><subject>Leukemia</subject><subject>Lysis</subject><subject>Metastases</subject><subject>Micro/macropore-forming</subject><subject>Natural killer cells</subject><subject>NK cells</subject><subject>Prevention</subject><subject>Sodium</subject><subject>Sodium alginate</subject><subject>Solid tumor</subject><subject>Solid tumors</subject><subject>Therapeutic applications</subject><subject>Tumors</subject><subject>의공학</subject><issn>1226-4601</issn><issn>2055-7124</issn><issn>2055-7124</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkl1v0zAUhiMEYlPZH-ACReIGkLL5O84VqsZXxQTSGNfWseOk7pK42MlE_z1OOwZFKJId2c_72j7nzbLnGJ1jLMVFZEgSViBCC4QYokX1KDsliPOixIQ9zk4xIaJgAuGT7CzGDUIIM1wxXj3NTmhJWSUxOs3sl8-5sV0XczsY2Mapg9HWuRvy3pngL3pI49YHWzQ-9G5o8_WuDr61SXHnIKfvcu38NrhhnDcTlI9Tn0bX99Pgx7UNsN09y5400EV7dj8vsu8f3t9cfiquvn5cXS6vCiMoHQvglU1_oK0lCEOlKTJaaG4E4xiB0cBJzWrTMBC4pBVYrEEbjhoOsqYVXWRvDr5DaNStccqD28-tV7dBLa9vVgojigWVJMGrA1x72Kj0hB7Cbq_YL_jQKgijM51VTNZNI7DlFCSzFdKazidjKiXX2LDk9fbgtZ10b2tjhzFAd2R6vDO4dbrUXboNkYIJmRxe3TsE_2OycVS9i3NnYLB-iopIUjEiytTqRfbyH3TjpzCkwiaKyrKsKJd_qBbSC9zQ-HSwmU3VsuSMSEbKmTr_D5W-2qYA-ME2Lq0fCV4fCRIz2p9jC1OMavXt-pglBzZlKMZgm4eCYKTmFKtDilVKsdqnWM09fPF3KR8kvzNLfwE3POv4</recordid><startdate>20230622</startdate><enddate>20230622</enddate><creator>Kim, Dahong</creator><creator>Jo, Seona</creator><creator>Lee, Dongjin</creator><creator>Kim, Seok-Min</creator><creator>Seok, Ji Min</creator><creator>Yeo, Seon Ju</creator><creator>Lee, Jun Hee</creator><creator>Lee, Jae Jong</creator><creator>Lee, Kangwon</creator><creator>Kim, Tae-Don</creator><creator>Park, Su A</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>American Association for the Advancement of Science (AAAS)</general><general>한국생체재료학회</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><scope>ACYCR</scope><orcidid>https://orcid.org/0000-0001-5878-8054</orcidid></search><sort><creationdate>20230622</creationdate><title>NK cells encapsulated in micro/macropore-forming hydrogels via 3D bioprinting for tumor immunotherapy</title><author>Kim, Dahong ; Jo, Seona ; Lee, Dongjin ; Kim, Seok-Min ; Seok, Ji Min ; Yeo, Seon Ju ; Lee, Jun Hee ; Lee, Jae Jong ; Lee, Kangwon ; Kim, Tae-Don ; Park, Su A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c633t-a59ec63abee201a9b30cb6b5c64510acba52d4dcf4a61739ae1babc50f5a8d393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>3-D printers</topic><topic>3D bioprinting</topic><topic>Alginic acid</topic><topic>Antitumor activity</topic><topic>Cancer therapies</topic><topic>Cell culture</topic><topic>Cell therapy</topic><topic>Cell viability</topic><topic>Cytokines</topic><topic>Drug therapy</topic><topic>Gelatin</topic><topic>Hydrogels</topic><topic>Immunotherapy</topic><topic>Killer cells</topic><topic>Leukemia</topic><topic>Lysis</topic><topic>Metastases</topic><topic>Micro/macropore-forming</topic><topic>Natural killer cells</topic><topic>NK cells</topic><topic>Prevention</topic><topic>Sodium</topic><topic>Sodium alginate</topic><topic>Solid tumor</topic><topic>Solid tumors</topic><topic>Therapeutic applications</topic><topic>Tumors</topic><topic>의공학</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Dahong</creatorcontrib><creatorcontrib>Jo, Seona</creatorcontrib><creatorcontrib>Lee, Dongjin</creatorcontrib><creatorcontrib>Kim, Seok-Min</creatorcontrib><creatorcontrib>Seok, Ji Min</creatorcontrib><creatorcontrib>Yeo, Seon Ju</creatorcontrib><creatorcontrib>Lee, Jun Hee</creatorcontrib><creatorcontrib>Lee, Jae Jong</creatorcontrib><creatorcontrib>Lee, Kangwon</creatorcontrib><creatorcontrib>Kim, Tae-Don</creatorcontrib><creatorcontrib>Park, Su A</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale in Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><collection>Korean Citation Index</collection><jtitle>Biomaterials research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Dahong</au><au>Jo, Seona</au><au>Lee, Dongjin</au><au>Kim, Seok-Min</au><au>Seok, Ji Min</au><au>Yeo, Seon Ju</au><au>Lee, Jun Hee</au><au>Lee, Jae Jong</au><au>Lee, Kangwon</au><au>Kim, Tae-Don</au><au>Park, Su A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>NK cells encapsulated in micro/macropore-forming hydrogels via 3D bioprinting for tumor immunotherapy</atitle><jtitle>Biomaterials research</jtitle><addtitle>Biomater Res</addtitle><date>2023-06-22</date><risdate>2023</risdate><volume>27</volume><issue>1</issue><spage>60</spage><epage>60</epage><pages>60-60</pages><issn>1226-4601</issn><issn>2055-7124</issn><eissn>2055-7124</eissn><abstract>Patients face a serious threat if a solid tumor leaves behind partial residuals or cannot be completely removed after surgical resection. Immunotherapy has attracted attention as a method to prevent this condition. However, the conventional immunotherapy method targeting solid tumors, that is, intravenous injection, has limitations in homing in on the tumor and in vivo expansion and has not shown effective clinical results.
To overcome these limitations, NK cells (Natural killer cells) were encapsulated in micro/macropore-forming hydrogels using 3D bioprinting to target solid tumors. Sodium alginate and gelatin were used to prepare micro-macroporous hydrogels. The gelatin contained in the alginate hydrogel was removed because of the thermal sensitivity of the gelatin, which can generate interconnected micropores where the gelatin was released. Therefore, macropores can be formed through bioprinting and micropores can be formed using thermally sensitive gelatin to make macroporous hydrogels.
It was confirmed that intentionally formed micropores could help NK cells to aggregate easily, which enhances cell viability, lysis activity, and cytokine release. Macropores can be formed using 3D bioprinting, which enables NK cells to receive the essential elements. We also characterized the functionality of NK 92 and zEGFR-CAR-NK cells in the pore-forming hydrogel. The antitumor effects on leukemia and solid tumors were investigated using an in vitro model.
We demonstrated that the hydrogel encapsulating NK cells created an appropriate micro-macro environment for clinical applications of NK cell therapy for both leukemia and solid tumors via 3D bioprinting. 3D bioprinting makes macro-scale clinical applications possible, and the automatic process shows potential for development as an off-the-shelf immunotherapy product. This immunotherapy system could provide a clinical option for preventing tumor relapse and metastasis after tumor resection. Micro/macropore-forming hydrogel with NK cells fabricated by 3D bioprinting and implanted into the tumor site.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>37349810</pmid><doi>10.1186/s40824-023-00403-9</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-5878-8054</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 3-D printers 3D bioprinting Alginic acid Antitumor activity Cancer therapies Cell culture Cell therapy Cell viability Cytokines Drug therapy Gelatin Hydrogels Immunotherapy Killer cells Leukemia Lysis Metastases Micro/macropore-forming Natural killer cells NK cells Prevention Sodium Sodium alginate Solid tumor Solid tumors Therapeutic applications Tumors 의공학 |
title | NK cells encapsulated in micro/macropore-forming hydrogels via 3D bioprinting for tumor immunotherapy |
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