Carrier Cell–mediated Delivery of a Replication-competent Adenovirus for Cancer Gene Therapy
Although replication-competent viruses have been developed to treat cancers, their cytotoxic effects are insufficient, as infection is inhibited by the generation of neutralizing antibodies. To address this limitation, we developed a carrier cell system to deliver a replication-competent adenovirus....
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Veröffentlicht in: | Molecular therapy 2007-06, Vol.15 (6), p.1121-1128 |
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creator | Hamada, Katsuyuki Desaki, Junzo Nakagawa, Kou Zhang, Ting Shirakawa, Toshiro Gotoh, Akinobu Tagawa, Masatoshi |
description | Although replication-competent viruses have been developed to treat cancers, their cytotoxic effects are insufficient, as infection is inhibited by the generation of neutralizing antibodies. To address this limitation, we developed a carrier cell system to deliver a replication-competent adenovirus. Carrier cells infected with replication-competent adenovirus were incubated with target cancer cells in a high titer of anti-adenovirus antibody. Carrier cells were injected into syngeneic subcutaneous tumors after immunization with adenovirus. Carrier cell–derived cell fragments containing viral particles were engulfed by proliferative target cancer cells. This engulfment-mediated transfer of adenovirus was not inhibited by the anti-adenovirus antibody and enabled repetitive infection. After the induction of anti-adenoviral cytotoxic T-lymphocyte (CTL) responses by immunization with adenovirus, administration of carrier cells infected with a replication-competent adenovirus induced complete tumor regression. Adenovirus-GM-CSF augmented the anti-tumor effect of carrier cells by increasing anti-adenoviral and anti-tumoral CTL responses and decreased the number of injections of carrier cells required to induce complete tumor regression. This novel carrier cell–mediated viral transfection system might prove useful in a variety of cancer therapies. |
doi_str_mv | 10.1038/sj.mt.6300128 |
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To address this limitation, we developed a carrier cell system to deliver a replication-competent adenovirus. Carrier cells infected with replication-competent adenovirus were incubated with target cancer cells in a high titer of anti-adenovirus antibody. Carrier cells were injected into syngeneic subcutaneous tumors after immunization with adenovirus. Carrier cell–derived cell fragments containing viral particles were engulfed by proliferative target cancer cells. This engulfment-mediated transfer of adenovirus was not inhibited by the anti-adenovirus antibody and enabled repetitive infection. After the induction of anti-adenoviral cytotoxic T-lymphocyte (CTL) responses by immunization with adenovirus, administration of carrier cells infected with a replication-competent adenovirus induced complete tumor regression. Adenovirus-GM-CSF augmented the anti-tumor effect of carrier cells by increasing anti-adenoviral and anti-tumoral CTL responses and decreased the number of injections of carrier cells required to induce complete tumor regression. This novel carrier cell–mediated viral transfection system might prove useful in a variety of cancer therapies.</description><identifier>ISSN: 1525-0016</identifier><identifier>EISSN: 1525-0024</identifier><identifier>DOI: 10.1038/sj.mt.6300128</identifier><identifier>PMID: 17387337</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adenoviridae - genetics ; Adenoviridae - immunology ; Adenoviruses ; Animals ; Antibodies ; Breast cancer ; Cancer Vaccines - administration & dosage ; Cancer Vaccines - immunology ; Cell Line ; Cell Line, Tumor ; Cell Proliferation ; Cell Survival ; Clinical trials ; Cytotoxicity ; Female ; Gene therapy ; Gene Transfer Techniques ; Genetic Therapy - methods ; Genetic Vectors - administration & dosage ; Genetic Vectors - genetics ; Granulocyte-Macrophage Colony-Stimulating Factor - genetics ; Gynecology ; HT29 Cells ; Humans ; Immunization ; Infections ; Medicine ; Metastasis ; Mice ; Mice, Inbred C3H ; Mice, Inbred C57BL ; Mice, Nude ; Microscopy, Electron, Transmission ; Neoplasms - immunology ; Neoplasms - pathology ; Neoplasms - therapy ; Obstetrics ; Ovarian cancer ; Ovarian Neoplasms - metabolism ; Ovarian Neoplasms - pathology ; T-Lymphocytes, Cytotoxic - immunology ; Tumors ; Vectors (Biology) ; Viral infections ; Viral Vaccines - administration & dosage ; Viral Vaccines - immunology ; Virus Replication - genetics ; Viruses ; Xenograft Model Antitumor Assays - methods</subject><ispartof>Molecular therapy, 2007-06, Vol.15 (6), p.1121-1128</ispartof><rights>2007 The American Society of Gene Therapy</rights><rights>Copyright Nature Publishing Group Jun 2007</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c406t-c8da524cfe4fea1bee8d6190f2c86a86076b650b19afc788b46022562fd6f10f3</citedby><cites>FETCH-LOGICAL-c406t-c8da524cfe4fea1bee8d6190f2c86a86076b650b19afc788b46022562fd6f10f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/1792607798?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,777,781,27905,27906,64364,64366,64368,72218</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17387337$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hamada, Katsuyuki</creatorcontrib><creatorcontrib>Desaki, Junzo</creatorcontrib><creatorcontrib>Nakagawa, Kou</creatorcontrib><creatorcontrib>Zhang, Ting</creatorcontrib><creatorcontrib>Shirakawa, Toshiro</creatorcontrib><creatorcontrib>Gotoh, Akinobu</creatorcontrib><creatorcontrib>Tagawa, Masatoshi</creatorcontrib><title>Carrier Cell–mediated Delivery of a Replication-competent Adenovirus for Cancer Gene Therapy</title><title>Molecular therapy</title><addtitle>Mol Ther</addtitle><description>Although replication-competent viruses have been developed to treat cancers, their cytotoxic effects are insufficient, as infection is inhibited by the generation of neutralizing antibodies. To address this limitation, we developed a carrier cell system to deliver a replication-competent adenovirus. Carrier cells infected with replication-competent adenovirus were incubated with target cancer cells in a high titer of anti-adenovirus antibody. Carrier cells were injected into syngeneic subcutaneous tumors after immunization with adenovirus. Carrier cell–derived cell fragments containing viral particles were engulfed by proliferative target cancer cells. This engulfment-mediated transfer of adenovirus was not inhibited by the anti-adenovirus antibody and enabled repetitive infection. After the induction of anti-adenoviral cytotoxic T-lymphocyte (CTL) responses by immunization with adenovirus, administration of carrier cells infected with a replication-competent adenovirus induced complete tumor regression. Adenovirus-GM-CSF augmented the anti-tumor effect of carrier cells by increasing anti-adenoviral and anti-tumoral CTL responses and decreased the number of injections of carrier cells required to induce complete tumor regression. This novel carrier cell–mediated viral transfection system might prove useful in a variety of cancer therapies.</description><subject>Adenoviridae - genetics</subject><subject>Adenoviridae - immunology</subject><subject>Adenoviruses</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Breast cancer</subject><subject>Cancer Vaccines - administration & dosage</subject><subject>Cancer Vaccines - immunology</subject><subject>Cell Line</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation</subject><subject>Cell Survival</subject><subject>Clinical trials</subject><subject>Cytotoxicity</subject><subject>Female</subject><subject>Gene therapy</subject><subject>Gene Transfer Techniques</subject><subject>Genetic Therapy - methods</subject><subject>Genetic Vectors - administration & dosage</subject><subject>Genetic Vectors - genetics</subject><subject>Granulocyte-Macrophage Colony-Stimulating Factor - genetics</subject><subject>Gynecology</subject><subject>HT29 Cells</subject><subject>Humans</subject><subject>Immunization</subject><subject>Infections</subject><subject>Medicine</subject><subject>Metastasis</subject><subject>Mice</subject><subject>Mice, Inbred C3H</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Nude</subject><subject>Microscopy, Electron, Transmission</subject><subject>Neoplasms - immunology</subject><subject>Neoplasms - pathology</subject><subject>Neoplasms - therapy</subject><subject>Obstetrics</subject><subject>Ovarian cancer</subject><subject>Ovarian Neoplasms - metabolism</subject><subject>Ovarian Neoplasms - pathology</subject><subject>T-Lymphocytes, Cytotoxic - immunology</subject><subject>Tumors</subject><subject>Vectors (Biology)</subject><subject>Viral infections</subject><subject>Viral Vaccines - administration & dosage</subject><subject>Viral Vaccines - immunology</subject><subject>Virus Replication - genetics</subject><subject>Viruses</subject><subject>Xenograft Model Antitumor Assays - methods</subject><issn>1525-0016</issn><issn>1525-0024</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kMtq3DAUQEVoyKRJltkGQ6E7TyTZeng5TNukEAiEZBshy1dUg205kjwwu_5D_zBfEpUZGgh0pbs4nHt1ELokeElwJa_jZjmkJa8wJlQeoVPCKCsxpvWnfzPhC_Q5xk2eCGv4CVoQUUlRVeIUPa91CA5CsYa-f_39Z4DO6QRd8Q16t4WwK7wtdPEAU--MTs6PpfHDBAnGVKw6GP3WhTkW1meFHk023cAIxeMvCHranaNjq_sIF4f3DD39-P64vi3v7m9-rld3pakxT6WRnWa0NhZqC5q0ALLjpMGWGsm15FjwljPckkZbI6Rsa44pZZzajluCbXWGvu69U_AvM8SkBhdN_pIewc9RCcyIYKzJ4JcP4MbPYcy3KSIamjeJRmaq3FMm-BgDWDUFN-iwUwSrv9lV3KghqUP2zF8drHObC77Th84ZEHsAcoRt7q2icZBzdS6ASarz7j_qN_I7kjI</recordid><startdate>200706</startdate><enddate>200706</enddate><creator>Hamada, Katsuyuki</creator><creator>Desaki, Junzo</creator><creator>Nakagawa, Kou</creator><creator>Zhang, Ting</creator><creator>Shirakawa, Toshiro</creator><creator>Gotoh, Akinobu</creator><creator>Tagawa, Masatoshi</creator><general>Elsevier Inc</general><general>Elsevier Limited</general><scope>6I.</scope><scope>AAFTH</scope><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</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>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>200706</creationdate><title>Carrier Cell–mediated Delivery of a Replication-competent Adenovirus for Cancer Gene Therapy</title><author>Hamada, Katsuyuki ; Desaki, Junzo ; Nakagawa, Kou ; Zhang, Ting ; Shirakawa, Toshiro ; Gotoh, Akinobu ; Tagawa, Masatoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c406t-c8da524cfe4fea1bee8d6190f2c86a86076b650b19afc788b46022562fd6f10f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adenoviridae - 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Academic</collection><jtitle>Molecular therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hamada, Katsuyuki</au><au>Desaki, Junzo</au><au>Nakagawa, Kou</au><au>Zhang, Ting</au><au>Shirakawa, Toshiro</au><au>Gotoh, Akinobu</au><au>Tagawa, Masatoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Carrier Cell–mediated Delivery of a Replication-competent Adenovirus for Cancer Gene Therapy</atitle><jtitle>Molecular therapy</jtitle><addtitle>Mol Ther</addtitle><date>2007-06</date><risdate>2007</risdate><volume>15</volume><issue>6</issue><spage>1121</spage><epage>1128</epage><pages>1121-1128</pages><issn>1525-0016</issn><eissn>1525-0024</eissn><abstract>Although replication-competent viruses have been developed to treat cancers, their cytotoxic effects are insufficient, as infection is inhibited by the generation of neutralizing antibodies. To address this limitation, we developed a carrier cell system to deliver a replication-competent adenovirus. Carrier cells infected with replication-competent adenovirus were incubated with target cancer cells in a high titer of anti-adenovirus antibody. Carrier cells were injected into syngeneic subcutaneous tumors after immunization with adenovirus. Carrier cell–derived cell fragments containing viral particles were engulfed by proliferative target cancer cells. This engulfment-mediated transfer of adenovirus was not inhibited by the anti-adenovirus antibody and enabled repetitive infection. After the induction of anti-adenoviral cytotoxic T-lymphocyte (CTL) responses by immunization with adenovirus, administration of carrier cells infected with a replication-competent adenovirus induced complete tumor regression. Adenovirus-GM-CSF augmented the anti-tumor effect of carrier cells by increasing anti-adenoviral and anti-tumoral CTL responses and decreased the number of injections of carrier cells required to induce complete tumor regression. This novel carrier cell–mediated viral transfection system might prove useful in a variety of cancer therapies.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>17387337</pmid><doi>10.1038/sj.mt.6300128</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adenoviridae - genetics Adenoviridae - immunology Adenoviruses Animals Antibodies Breast cancer Cancer Vaccines - administration & dosage Cancer Vaccines - immunology Cell Line Cell Line, Tumor Cell Proliferation Cell Survival Clinical trials Cytotoxicity Female Gene therapy Gene Transfer Techniques Genetic Therapy - methods Genetic Vectors - administration & dosage Genetic Vectors - genetics Granulocyte-Macrophage Colony-Stimulating Factor - genetics Gynecology HT29 Cells Humans Immunization Infections Medicine Metastasis Mice Mice, Inbred C3H Mice, Inbred C57BL Mice, Nude Microscopy, Electron, Transmission Neoplasms - immunology Neoplasms - pathology Neoplasms - therapy Obstetrics Ovarian cancer Ovarian Neoplasms - metabolism Ovarian Neoplasms - pathology T-Lymphocytes, Cytotoxic - immunology Tumors Vectors (Biology) Viral infections Viral Vaccines - administration & dosage Viral Vaccines - immunology Virus Replication - genetics Viruses Xenograft Model Antitumor Assays - methods |
title | Carrier Cell–mediated Delivery of a Replication-competent Adenovirus for Cancer Gene Therapy |
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