Murine Models of Cancer Cytokine Gene Therapy Using Interleukin-12
Cytokine gene therapy, in particular IL-12 gene therapy, is one of the more novel and promising approaches in cancer therapy based on significant preclinical data derived mainly from murine tumor models. IL-12 is a heterodimeric cytokine that requires the simultaneous expression of both the p35 and...
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Veröffentlicht in: | Annals of the New York Academy of Sciences 1996-01, Vol.795 (1), p.275-283 |
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description | Cytokine gene therapy, in particular IL-12 gene therapy, is one of the more novel and promising approaches in cancer therapy based on significant preclinical data derived mainly from murine tumor models. IL-12 is a heterodimeric cytokine that requires the simultaneous expression of both the p35 and p40 chains from the same cell for production of biologically active IL-12. A variety of biological functions have been attributed to IL-12 including the induction of IFN-gamma production and the promotion of predominantly Th1-type immune responses to antigens. Our previous studies using systemic administration of recombinant murine IL-12 have demonstrated profound antitumor efficacy against all tumors tested with the concomitant long-lived specific antitumor immunity in some cases. To determine whether the local secretion of IL-12 achieved by gene transduction has significant antitumor effects, fibroblast cell lines or murine tumor cell lines were transduced with expression plasmids or the retroviral vector TFG-mIL-12-Neo and inoculated intradermally (i.d.). Our first study using IL-12-transfected NIH3T3 cells admixed with the murine melanoma, BL-6, showed that local IL-12 expression suppresses tumor growth and promotes the acquisition of specific antitumor immunity. Subsequent studies showed that IL-12 gene therapy is also effective in treating established day 3 tumors. CD4+ and CD8+ T cells, as well as NK cells, appear to play important roles in the observed antitumor effects resulting from IL-12 paracrine secretion. Administration of neutralizing antibody specific for IFN-gamma also abrogated some of the IL-12-associated antitumor effects. Finally, this IL-12 gene therapy strategy to elicit an antitumor immune response was more effective when used in combination with the transduction of tumor cells with B7.1. Based on these promising results, a clinical protocol for the treating patients with cancer using genetically engineered fibroblasts to express IL-12 has been initiated at our institution. |
doi_str_mv | 10.1111/j.1749-6632.1996.tb52677.x |
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IL-12 is a heterodimeric cytokine that requires the simultaneous expression of both the p35 and p40 chains from the same cell for production of biologically active IL-12. A variety of biological functions have been attributed to IL-12 including the induction of IFN-gamma production and the promotion of predominantly Th1-type immune responses to antigens. Our previous studies using systemic administration of recombinant murine IL-12 have demonstrated profound antitumor efficacy against all tumors tested with the concomitant long-lived specific antitumor immunity in some cases. To determine whether the local secretion of IL-12 achieved by gene transduction has significant antitumor effects, fibroblast cell lines or murine tumor cell lines were transduced with expression plasmids or the retroviral vector TFG-mIL-12-Neo and inoculated intradermally (i.d.). Our first study using IL-12-transfected NIH3T3 cells admixed with the murine melanoma, BL-6, showed that local IL-12 expression suppresses tumor growth and promotes the acquisition of specific antitumor immunity. Subsequent studies showed that IL-12 gene therapy is also effective in treating established day 3 tumors. CD4+ and CD8+ T cells, as well as NK cells, appear to play important roles in the observed antitumor effects resulting from IL-12 paracrine secretion. Administration of neutralizing antibody specific for IFN-gamma also abrogated some of the IL-12-associated antitumor effects. Finally, this IL-12 gene therapy strategy to elicit an antitumor immune response was more effective when used in combination with the transduction of tumor cells with B7.1. Based on these promising results, a clinical protocol for the treating patients with cancer using genetically engineered fibroblasts to express IL-12 has been initiated at our institution.</description><identifier>ISSN: 0077-8923</identifier><identifier>EISSN: 1749-6632</identifier><identifier>DOI: 10.1111/j.1749-6632.1996.tb52677.x</identifier><identifier>PMID: 8958939</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Animals ; Antineoplastic Agents - administration & dosage ; B7-1 Antigen - administration & dosage ; Genetic Therapy ; Genetic Vectors ; Immunity, Cellular ; Interferon-gamma - physiology ; Interleukin-12 - administration & dosage ; Killer Cells, Natural - immunology ; Mice ; Neoplasms, Experimental - therapy ; Transduction, Genetic ; Transfection</subject><ispartof>Annals of the New York Academy of Sciences, 1996-01, Vol.795 (1), p.275-283</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8958939$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>TAHARA, HIDEAKI</creatorcontrib><creatorcontrib>ZITVOGEL, LAURENCE</creatorcontrib><creatorcontrib>STORKUS, WALTER J.</creatorcontrib><creatorcontrib>ROBBINS, PAUL D.</creatorcontrib><creatorcontrib>LOTZE, MICHAEL T.</creatorcontrib><title>Murine Models of Cancer Cytokine Gene Therapy Using Interleukin-12</title><title>Annals of the New York Academy of Sciences</title><addtitle>Ann N Y Acad Sci</addtitle><description>Cytokine gene therapy, in particular IL-12 gene therapy, is one of the more novel and promising approaches in cancer therapy based on significant preclinical data derived mainly from murine tumor models. IL-12 is a heterodimeric cytokine that requires the simultaneous expression of both the p35 and p40 chains from the same cell for production of biologically active IL-12. A variety of biological functions have been attributed to IL-12 including the induction of IFN-gamma production and the promotion of predominantly Th1-type immune responses to antigens. Our previous studies using systemic administration of recombinant murine IL-12 have demonstrated profound antitumor efficacy against all tumors tested with the concomitant long-lived specific antitumor immunity in some cases. To determine whether the local secretion of IL-12 achieved by gene transduction has significant antitumor effects, fibroblast cell lines or murine tumor cell lines were transduced with expression plasmids or the retroviral vector TFG-mIL-12-Neo and inoculated intradermally (i.d.). Our first study using IL-12-transfected NIH3T3 cells admixed with the murine melanoma, BL-6, showed that local IL-12 expression suppresses tumor growth and promotes the acquisition of specific antitumor immunity. Subsequent studies showed that IL-12 gene therapy is also effective in treating established day 3 tumors. CD4+ and CD8+ T cells, as well as NK cells, appear to play important roles in the observed antitumor effects resulting from IL-12 paracrine secretion. Administration of neutralizing antibody specific for IFN-gamma also abrogated some of the IL-12-associated antitumor effects. Finally, this IL-12 gene therapy strategy to elicit an antitumor immune response was more effective when used in combination with the transduction of tumor cells with B7.1. Based on these promising results, a clinical protocol for the treating patients with cancer using genetically engineered fibroblasts to express IL-12 has been initiated at our institution.</description><subject>Animals</subject><subject>Antineoplastic Agents - administration & dosage</subject><subject>B7-1 Antigen - administration & dosage</subject><subject>Genetic Therapy</subject><subject>Genetic Vectors</subject><subject>Immunity, Cellular</subject><subject>Interferon-gamma - physiology</subject><subject>Interleukin-12 - administration & dosage</subject><subject>Killer Cells, Natural - immunology</subject><subject>Mice</subject><subject>Neoplasms, Experimental - therapy</subject><subject>Transduction, Genetic</subject><subject>Transfection</subject><issn>0077-8923</issn><issn>1749-6632</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9z8tKw0AUBuBBlFqrjyAEF-4S535ZatC20KpIS5fDZDLRtGlSZxJo395IS8_i_Ivv58AB4AHBBPXztE6QoCrmnOAEKcWTNmOYC5HsL8DwTJdgCKEQsVSYXIObENYQIiypGICBVEwqoobgZd75snbRvMldFaKmiFJTW-ej9NA2m38Zu34tfpw3u0O0DGX9HU3r1vnKdb3HCN-Cq8JUwd2dcgSWb6-LdBLPPsbT9HkWl4SoNqbc5sZiRqTNpHAFtNg5oVTRZ2E5xYzDXFoBDZU5MionDDLKuWQZozmVZAQej3d3vvntXGj1tgzWVZWpXdMFLSRHgkjYF-9PxS7bulzvfLk1_qBPT_ceH70Mrduf2fiN5oIIplfvYz2ZfM0-OXzRK_IHJ1Bp3A</recordid><startdate>19960101</startdate><enddate>19960101</enddate><creator>TAHARA, HIDEAKI</creator><creator>ZITVOGEL, LAURENCE</creator><creator>STORKUS, WALTER J.</creator><creator>ROBBINS, PAUL D.</creator><creator>LOTZE, MICHAEL T.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>19960101</creationdate><title>Murine Models of Cancer Cytokine Gene Therapy Using Interleukin-12</title><author>TAHARA, HIDEAKI ; ZITVOGEL, LAURENCE ; STORKUS, WALTER J. ; ROBBINS, PAUL D. ; LOTZE, MICHAEL T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i339t-46cdac2538cb87ef0c2ee799fc2efc642560d8c70a48d1a9d350546685b54d483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Animals</topic><topic>Antineoplastic Agents - administration & dosage</topic><topic>B7-1 Antigen - administration & dosage</topic><topic>Genetic Therapy</topic><topic>Genetic Vectors</topic><topic>Immunity, Cellular</topic><topic>Interferon-gamma - physiology</topic><topic>Interleukin-12 - administration & dosage</topic><topic>Killer Cells, Natural - immunology</topic><topic>Mice</topic><topic>Neoplasms, Experimental - therapy</topic><topic>Transduction, Genetic</topic><topic>Transfection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TAHARA, HIDEAKI</creatorcontrib><creatorcontrib>ZITVOGEL, LAURENCE</creatorcontrib><creatorcontrib>STORKUS, WALTER J.</creatorcontrib><creatorcontrib>ROBBINS, PAUL D.</creatorcontrib><creatorcontrib>LOTZE, MICHAEL T.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of the New York Academy of Sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>TAHARA, HIDEAKI</au><au>ZITVOGEL, LAURENCE</au><au>STORKUS, WALTER J.</au><au>ROBBINS, PAUL D.</au><au>LOTZE, MICHAEL T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Murine Models of Cancer Cytokine Gene Therapy Using Interleukin-12</atitle><jtitle>Annals of the New York Academy of Sciences</jtitle><addtitle>Ann N Y Acad Sci</addtitle><date>1996-01-01</date><risdate>1996</risdate><volume>795</volume><issue>1</issue><spage>275</spage><epage>283</epage><pages>275-283</pages><issn>0077-8923</issn><eissn>1749-6632</eissn><abstract>Cytokine gene therapy, in particular IL-12 gene therapy, is one of the more novel and promising approaches in cancer therapy based on significant preclinical data derived mainly from murine tumor models. IL-12 is a heterodimeric cytokine that requires the simultaneous expression of both the p35 and p40 chains from the same cell for production of biologically active IL-12. A variety of biological functions have been attributed to IL-12 including the induction of IFN-gamma production and the promotion of predominantly Th1-type immune responses to antigens. Our previous studies using systemic administration of recombinant murine IL-12 have demonstrated profound antitumor efficacy against all tumors tested with the concomitant long-lived specific antitumor immunity in some cases. To determine whether the local secretion of IL-12 achieved by gene transduction has significant antitumor effects, fibroblast cell lines or murine tumor cell lines were transduced with expression plasmids or the retroviral vector TFG-mIL-12-Neo and inoculated intradermally (i.d.). Our first study using IL-12-transfected NIH3T3 cells admixed with the murine melanoma, BL-6, showed that local IL-12 expression suppresses tumor growth and promotes the acquisition of specific antitumor immunity. Subsequent studies showed that IL-12 gene therapy is also effective in treating established day 3 tumors. CD4+ and CD8+ T cells, as well as NK cells, appear to play important roles in the observed antitumor effects resulting from IL-12 paracrine secretion. Administration of neutralizing antibody specific for IFN-gamma also abrogated some of the IL-12-associated antitumor effects. Finally, this IL-12 gene therapy strategy to elicit an antitumor immune response was more effective when used in combination with the transduction of tumor cells with B7.1. Based on these promising results, a clinical protocol for the treating patients with cancer using genetically engineered fibroblasts to express IL-12 has been initiated at our institution.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>8958939</pmid><doi>10.1111/j.1749-6632.1996.tb52677.x</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Antineoplastic Agents - administration & dosage B7-1 Antigen - administration & dosage Genetic Therapy Genetic Vectors Immunity, Cellular Interferon-gamma - physiology Interleukin-12 - administration & dosage Killer Cells, Natural - immunology Mice Neoplasms, Experimental - therapy Transduction, Genetic Transfection |
title | Murine Models of Cancer Cytokine Gene Therapy Using Interleukin-12 |
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