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Selective elimination of undifferentiated human pluripotent stem cells using pluripotent state-specific immunogenic antigen Glypican-3
Immunogenicity of immature pluripotent stem cells is a topic of intense debate. Immunogenic antigens, which are specific in pluripotent states, have not been described previously. In this study, we identified glypican-3 (GPC3), a known carcinoembryonic antigen, as a pluripotent state-specific immuno...
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Published in: | Biochemical and biophysical research communications 2019-04, Vol.511 (3), p.711-717 |
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creator | Okada, Marina Tada, Yoshitaka Seki, Tomohisa Tohyama, Shugo Fujita, Jun Suzuki, Toshihiro Shimomura, Manami Ofuji, Kazuya Kishino, Yoshikazu Nakajima, Kazuaki Tanosaki, Sho Someya, Shota Kanazawa, Hideaki Senju, Satoru Nakatsura, Tetsuya Fukuda, Keiichi |
description | Immunogenicity of immature pluripotent stem cells is a topic of intense debate. Immunogenic antigens, which are specific in pluripotent states, have not been described previously. In this study, we identified glypican-3 (GPC3), a known carcinoembryonic antigen, as a pluripotent state-specific immunogenic antigen. Additionally, we validated the applicability of human leukocyte antigen (HLA)-class I-restricted GPC3-reactive cytotoxic T lymphocytes (CTLs) in the removal of undifferentiated pluripotent stem cells (PSCs) from human induced pluripotent stem cell (hiPSC)-derivatives. HiPSCs uniquely express GPC3 in pluripotent states and were rejected by GPC3-reactive CTLs, which were sensitized with HLA-class I-restricted GPC3 peptides. Furthermore, GPC3-reactive CTLs selectively removed undifferentiated PSCs from hiPSC-derivatives in vitro and inhibited tumor formation in vivo. Our results demonstrate that GPC3 works as a pluripotent state-specific immunogenic antigen in hiPSCs and is applicable to regenerative medicine as a method of removing undifferentiated PSCs, which are the main cause of tumor formation.
•GPC3 is specifically expressed in hiPSCs.•GPC3-specific CTLs selectively remove undifferentiated hiPSCs in vitro.•GPC3-specific CTLs inhibit tumor formation in vivo. |
doi_str_mv | 10.1016/j.bbrc.2019.02.094 |
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•GPC3 is specifically expressed in hiPSCs.•GPC3-specific CTLs selectively remove undifferentiated hiPSCs in vitro.•GPC3-specific CTLs inhibit tumor formation in vivo.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/j.bbrc.2019.02.094</identifier><identifier>PMID: 30827508</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Cell Differentiation ; Cell Line ; Cytotoxic T lymphocytes ; Glypican-3 ; Glypicans - analysis ; Glypicans - immunology ; HLA-A2 Antigen - immunology ; Humans ; Immunotherapy ; Induced pluripotent stem cell ; Induced Pluripotent Stem Cells - cytology ; Induced Pluripotent Stem Cells - immunology ; Mice, Inbred NOD ; Mice, SCID ; Models, Molecular ; Neoplasms - immunology ; Regenerative medicine ; T-Lymphocytes, Cytotoxic - immunology ; Tumor formation</subject><ispartof>Biochemical and biophysical research communications, 2019-04, Vol.511 (3), p.711-717</ispartof><rights>2019 Elsevier Inc.</rights><rights>Copyright © 2019 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c422t-d4c5f0770fd146f00acaf4f014af8eb2f66deba8ad2b6e267391d07edeb48a953</citedby><cites>FETCH-LOGICAL-c422t-d4c5f0770fd146f00acaf4f014af8eb2f66deba8ad2b6e267391d07edeb48a953</cites><orcidid>0000-0003-3918-2385</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30827508$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Okada, Marina</creatorcontrib><creatorcontrib>Tada, Yoshitaka</creatorcontrib><creatorcontrib>Seki, Tomohisa</creatorcontrib><creatorcontrib>Tohyama, Shugo</creatorcontrib><creatorcontrib>Fujita, Jun</creatorcontrib><creatorcontrib>Suzuki, Toshihiro</creatorcontrib><creatorcontrib>Shimomura, Manami</creatorcontrib><creatorcontrib>Ofuji, Kazuya</creatorcontrib><creatorcontrib>Kishino, Yoshikazu</creatorcontrib><creatorcontrib>Nakajima, Kazuaki</creatorcontrib><creatorcontrib>Tanosaki, Sho</creatorcontrib><creatorcontrib>Someya, Shota</creatorcontrib><creatorcontrib>Kanazawa, Hideaki</creatorcontrib><creatorcontrib>Senju, Satoru</creatorcontrib><creatorcontrib>Nakatsura, Tetsuya</creatorcontrib><creatorcontrib>Fukuda, Keiichi</creatorcontrib><title>Selective elimination of undifferentiated human pluripotent stem cells using pluripotent state-specific immunogenic antigen Glypican-3</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>Immunogenicity of immature pluripotent stem cells is a topic of intense debate. Immunogenic antigens, which are specific in pluripotent states, have not been described previously. In this study, we identified glypican-3 (GPC3), a known carcinoembryonic antigen, as a pluripotent state-specific immunogenic antigen. Additionally, we validated the applicability of human leukocyte antigen (HLA)-class I-restricted GPC3-reactive cytotoxic T lymphocytes (CTLs) in the removal of undifferentiated pluripotent stem cells (PSCs) from human induced pluripotent stem cell (hiPSC)-derivatives. HiPSCs uniquely express GPC3 in pluripotent states and were rejected by GPC3-reactive CTLs, which were sensitized with HLA-class I-restricted GPC3 peptides. Furthermore, GPC3-reactive CTLs selectively removed undifferentiated PSCs from hiPSC-derivatives in vitro and inhibited tumor formation in vivo. Our results demonstrate that GPC3 works as a pluripotent state-specific immunogenic antigen in hiPSCs and is applicable to regenerative medicine as a method of removing undifferentiated PSCs, which are the main cause of tumor formation.
•GPC3 is specifically expressed in hiPSCs.•GPC3-specific CTLs selectively remove undifferentiated hiPSCs in vitro.•GPC3-specific CTLs inhibit tumor formation in vivo.</description><subject>Animals</subject><subject>Cell Differentiation</subject><subject>Cell Line</subject><subject>Cytotoxic T lymphocytes</subject><subject>Glypican-3</subject><subject>Glypicans - analysis</subject><subject>Glypicans - immunology</subject><subject>HLA-A2 Antigen - immunology</subject><subject>Humans</subject><subject>Immunotherapy</subject><subject>Induced pluripotent stem cell</subject><subject>Induced Pluripotent Stem Cells - cytology</subject><subject>Induced Pluripotent Stem Cells - immunology</subject><subject>Mice, Inbred NOD</subject><subject>Mice, SCID</subject><subject>Models, Molecular</subject><subject>Neoplasms - immunology</subject><subject>Regenerative medicine</subject><subject>T-Lymphocytes, Cytotoxic - immunology</subject><subject>Tumor formation</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kUtLJTEQhYOM6PXxB1xIlrPptpLbtx_gRmR8gOBCBXchnVS0Lt3pnqRb8A_4uyeX67hw4SpF1XcOnBPGTgTkAkR5ts7bNphcgmhykDk0xQ5bCGggkwKKX2wBAGUmG_G8zw5iXAMIUZTNHttfQi2rFdQL9vGAHZqJ3pBjRz15PdHg-eD47C05hwH9RHpCy1_nXns-dnOgcZjSmscJe26w6yKfI_mXb8ekyuKIhhwZTn0_--EFfZp1skwTv-7eRzLaZ8sjtut0F_H48z1kT1d_Hi9vsrv769vLi7vMFFJOmS3MykFVgbMpiQPQRrvCgSi0q7GVriwttrrWVrYlyrJaNsJChWlZ1LpZLQ_Z763vGIa_M8ZJ9RQ3CbTHYY5KirpKWNVUCZVb1IQhxoBOjYF6Hd6VALXpX63Vpn-16V-BVKn_JDr99J_bHu2X5H_hCTjfAphSvhEGFQ2hN2gppH9QdqCf_P8B77-bkw</recordid><startdate>20190409</startdate><enddate>20190409</enddate><creator>Okada, Marina</creator><creator>Tada, Yoshitaka</creator><creator>Seki, Tomohisa</creator><creator>Tohyama, Shugo</creator><creator>Fujita, Jun</creator><creator>Suzuki, Toshihiro</creator><creator>Shimomura, Manami</creator><creator>Ofuji, Kazuya</creator><creator>Kishino, Yoshikazu</creator><creator>Nakajima, Kazuaki</creator><creator>Tanosaki, Sho</creator><creator>Someya, Shota</creator><creator>Kanazawa, Hideaki</creator><creator>Senju, Satoru</creator><creator>Nakatsura, Tetsuya</creator><creator>Fukuda, Keiichi</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-3918-2385</orcidid></search><sort><creationdate>20190409</creationdate><title>Selective elimination of undifferentiated human pluripotent stem cells using pluripotent state-specific immunogenic antigen Glypican-3</title><author>Okada, Marina ; Tada, Yoshitaka ; Seki, Tomohisa ; Tohyama, Shugo ; Fujita, Jun ; Suzuki, Toshihiro ; Shimomura, Manami ; Ofuji, Kazuya ; Kishino, Yoshikazu ; Nakajima, Kazuaki ; Tanosaki, Sho ; Someya, Shota ; Kanazawa, Hideaki ; Senju, Satoru ; Nakatsura, Tetsuya ; Fukuda, Keiichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-d4c5f0770fd146f00acaf4f014af8eb2f66deba8ad2b6e267391d07edeb48a953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Cell Differentiation</topic><topic>Cell Line</topic><topic>Cytotoxic T lymphocytes</topic><topic>Glypican-3</topic><topic>Glypicans - analysis</topic><topic>Glypicans - immunology</topic><topic>HLA-A2 Antigen - immunology</topic><topic>Humans</topic><topic>Immunotherapy</topic><topic>Induced pluripotent stem cell</topic><topic>Induced Pluripotent Stem Cells - cytology</topic><topic>Induced Pluripotent Stem Cells - immunology</topic><topic>Mice, Inbred NOD</topic><topic>Mice, SCID</topic><topic>Models, Molecular</topic><topic>Neoplasms - immunology</topic><topic>Regenerative medicine</topic><topic>T-Lymphocytes, Cytotoxic - immunology</topic><topic>Tumor formation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Okada, Marina</creatorcontrib><creatorcontrib>Tada, Yoshitaka</creatorcontrib><creatorcontrib>Seki, Tomohisa</creatorcontrib><creatorcontrib>Tohyama, Shugo</creatorcontrib><creatorcontrib>Fujita, Jun</creatorcontrib><creatorcontrib>Suzuki, Toshihiro</creatorcontrib><creatorcontrib>Shimomura, Manami</creatorcontrib><creatorcontrib>Ofuji, Kazuya</creatorcontrib><creatorcontrib>Kishino, Yoshikazu</creatorcontrib><creatorcontrib>Nakajima, Kazuaki</creatorcontrib><creatorcontrib>Tanosaki, Sho</creatorcontrib><creatorcontrib>Someya, Shota</creatorcontrib><creatorcontrib>Kanazawa, Hideaki</creatorcontrib><creatorcontrib>Senju, Satoru</creatorcontrib><creatorcontrib>Nakatsura, Tetsuya</creatorcontrib><creatorcontrib>Fukuda, Keiichi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Okada, Marina</au><au>Tada, Yoshitaka</au><au>Seki, Tomohisa</au><au>Tohyama, Shugo</au><au>Fujita, Jun</au><au>Suzuki, Toshihiro</au><au>Shimomura, Manami</au><au>Ofuji, Kazuya</au><au>Kishino, Yoshikazu</au><au>Nakajima, Kazuaki</au><au>Tanosaki, Sho</au><au>Someya, Shota</au><au>Kanazawa, Hideaki</au><au>Senju, Satoru</au><au>Nakatsura, Tetsuya</au><au>Fukuda, Keiichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Selective elimination of undifferentiated human pluripotent stem cells using pluripotent state-specific immunogenic antigen Glypican-3</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2019-04-09</date><risdate>2019</risdate><volume>511</volume><issue>3</issue><spage>711</spage><epage>717</epage><pages>711-717</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>Immunogenicity of immature pluripotent stem cells is a topic of intense debate. Immunogenic antigens, which are specific in pluripotent states, have not been described previously. In this study, we identified glypican-3 (GPC3), a known carcinoembryonic antigen, as a pluripotent state-specific immunogenic antigen. Additionally, we validated the applicability of human leukocyte antigen (HLA)-class I-restricted GPC3-reactive cytotoxic T lymphocytes (CTLs) in the removal of undifferentiated pluripotent stem cells (PSCs) from human induced pluripotent stem cell (hiPSC)-derivatives. HiPSCs uniquely express GPC3 in pluripotent states and were rejected by GPC3-reactive CTLs, which were sensitized with HLA-class I-restricted GPC3 peptides. Furthermore, GPC3-reactive CTLs selectively removed undifferentiated PSCs from hiPSC-derivatives in vitro and inhibited tumor formation in vivo. Our results demonstrate that GPC3 works as a pluripotent state-specific immunogenic antigen in hiPSCs and is applicable to regenerative medicine as a method of removing undifferentiated PSCs, which are the main cause of tumor formation.
•GPC3 is specifically expressed in hiPSCs.•GPC3-specific CTLs selectively remove undifferentiated hiPSCs in vitro.•GPC3-specific CTLs inhibit tumor formation in vivo.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>30827508</pmid><doi>10.1016/j.bbrc.2019.02.094</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-3918-2385</orcidid></addata></record> |
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subjects | Animals Cell Differentiation Cell Line Cytotoxic T lymphocytes Glypican-3 Glypicans - analysis Glypicans - immunology HLA-A2 Antigen - immunology Humans Immunotherapy Induced pluripotent stem cell Induced Pluripotent Stem Cells - cytology Induced Pluripotent Stem Cells - immunology Mice, Inbred NOD Mice, SCID Models, Molecular Neoplasms - immunology Regenerative medicine T-Lymphocytes, Cytotoxic - immunology Tumor formation |
title | Selective elimination of undifferentiated human pluripotent stem cells using pluripotent state-specific immunogenic antigen Glypican-3 |
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