Bovine herpesvirus type 1 as a novel oncolytic virus
Oncolytic virotherapy is a promising avenue of cancer gene therapy. Current vectors include human viruses that have been engineered to replicate in tumor cells or nonhuman viruses that are naturally oncotropic and preferentially replicate in tumor cells harboring defects in innate immune pathways su...
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Veröffentlicht in: | Cancer gene therapy 2010-05, Vol.17 (5), p.344-355 |
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description | Oncolytic virotherapy is a promising avenue of cancer gene therapy. Current vectors include human viruses that have been engineered to replicate in tumor cells or nonhuman viruses that are naturally oncotropic and preferentially replicate in tumor cells harboring defects in innate immune pathways such as the type 1 interferon (IFN) pathway. Bovine herpesvirus type 1 (BHV-1) is a species-specific herpesvirus closely related to the human herpes simplex virus type 1 (HSV-1). Although BHV-1 does not efficiently replicate in and affect cellular viability of normal human cells, it is capable of infecting and killing various immortalized and transformed human cell types. Surprisingly, BHV-1 infection of human cells fails to elicit IFN production at the mRNA or protein level and the ability of BHV-1 to kill immortalized and transformed human cells does not correlate with defects in IFN pathways. Furthermore, although some cross-reactivity between BHV-1 and HSV-1 exists, the majority of human antibody or serum samples tested failed to neutralize BHV-1 despite possessing HSV-1 neutralizing capacity. Thus, BHV-1 is a novel candidate oncolytic virus with a distinct mechanism of tumor targeting. |
doi_str_mv | 10.1038/cgt.2009.77 |
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Current vectors include human viruses that have been engineered to replicate in tumor cells or nonhuman viruses that are naturally oncotropic and preferentially replicate in tumor cells harboring defects in innate immune pathways such as the type 1 interferon (IFN) pathway. Bovine herpesvirus type 1 (BHV-1) is a species-specific herpesvirus closely related to the human herpes simplex virus type 1 (HSV-1). Although BHV-1 does not efficiently replicate in and affect cellular viability of normal human cells, it is capable of infecting and killing various immortalized and transformed human cell types. Surprisingly, BHV-1 infection of human cells fails to elicit IFN production at the mRNA or protein level and the ability of BHV-1 to kill immortalized and transformed human cells does not correlate with defects in IFN pathways. Furthermore, although some cross-reactivity between BHV-1 and HSV-1 exists, the majority of human antibody or serum samples tested failed to neutralize BHV-1 despite possessing HSV-1 neutralizing capacity. Thus, BHV-1 is a novel candidate oncolytic virus with a distinct mechanism of tumor targeting.</description><identifier>ISSN: 0929-1903</identifier><identifier>EISSN: 1476-5500</identifier><identifier>DOI: 10.1038/cgt.2009.77</identifier><identifier>PMID: 19893594</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>Animals ; Biomedical and Life Sciences ; Biomedicine ; Cancer ; Care and treatment ; Cattle ; Cell Line ; Cell Line, Tumor ; Cell Survival - genetics ; Cell Survival - physiology ; Cell viability ; Cross-reactivity ; Expression vectors ; Gene Expression ; Gene Therapy ; Genetic aspects ; Health aspects ; Herpes simplex ; Herpes simplex virus 1 ; Herpes viruses ; Herpesvirus ; Herpesvirus 1, Human - genetics ; Herpesvirus 1, Human - physiology ; Herpesviruses ; Humans ; Interferon ; Interferon-alpha - genetics ; Interferon-alpha - metabolism ; mRNA ; Neoplasms - metabolism ; Neoplasms - therapy ; Oncolysis ; Oncolytic Virotherapy - adverse effects ; Oncolytic Virotherapy - methods ; original-article ; Tumor cells ; Tumors ; Virus Replication - genetics ; Virus Replication - physiology ; Viruses</subject><ispartof>Cancer gene therapy, 2010-05, Vol.17 (5), p.344-355</ispartof><rights>Springer Nature America, Inc. 2010</rights><rights>COPYRIGHT 2010 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group May 2010</rights><rights>Nature Publishing Group 2010.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c571t-42b6d54300df48a5f7a73e0fc6b4b85b6f96d5fdaf72c59e546e9f8609d8ed5e3</citedby><cites>FETCH-LOGICAL-c571t-42b6d54300df48a5f7a73e0fc6b4b85b6f96d5fdaf72c59e546e9f8609d8ed5e3</cites></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/19893594$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rodrigues, R</creatorcontrib><creatorcontrib>Cuddington, B</creatorcontrib><creatorcontrib>Mossman, K</creatorcontrib><title>Bovine herpesvirus type 1 as a novel oncolytic virus</title><title>Cancer gene therapy</title><addtitle>Cancer Gene Ther</addtitle><addtitle>Cancer Gene Ther</addtitle><description>Oncolytic virotherapy is a promising avenue of cancer gene therapy. Current vectors include human viruses that have been engineered to replicate in tumor cells or nonhuman viruses that are naturally oncotropic and preferentially replicate in tumor cells harboring defects in innate immune pathways such as the type 1 interferon (IFN) pathway. Bovine herpesvirus type 1 (BHV-1) is a species-specific herpesvirus closely related to the human herpes simplex virus type 1 (HSV-1). Although BHV-1 does not efficiently replicate in and affect cellular viability of normal human cells, it is capable of infecting and killing various immortalized and transformed human cell types. Surprisingly, BHV-1 infection of human cells fails to elicit IFN production at the mRNA or protein level and the ability of BHV-1 to kill immortalized and transformed human cells does not correlate with defects in IFN pathways. Furthermore, although some cross-reactivity between BHV-1 and HSV-1 exists, the majority of human antibody or serum samples tested failed to neutralize BHV-1 despite possessing HSV-1 neutralizing capacity. Thus, BHV-1 is a novel candidate oncolytic virus with a distinct mechanism of tumor targeting.</description><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer</subject><subject>Care and treatment</subject><subject>Cattle</subject><subject>Cell Line</subject><subject>Cell Line, Tumor</subject><subject>Cell Survival - genetics</subject><subject>Cell Survival - physiology</subject><subject>Cell viability</subject><subject>Cross-reactivity</subject><subject>Expression vectors</subject><subject>Gene Expression</subject><subject>Gene Therapy</subject><subject>Genetic aspects</subject><subject>Health aspects</subject><subject>Herpes simplex</subject><subject>Herpes simplex virus 1</subject><subject>Herpes viruses</subject><subject>Herpesvirus</subject><subject>Herpesvirus 1, Human - genetics</subject><subject>Herpesvirus 1, Human - physiology</subject><subject>Herpesviruses</subject><subject>Humans</subject><subject>Interferon</subject><subject>Interferon-alpha - genetics</subject><subject>Interferon-alpha - metabolism</subject><subject>mRNA</subject><subject>Neoplasms - metabolism</subject><subject>Neoplasms - therapy</subject><subject>Oncolysis</subject><subject>Oncolytic Virotherapy - adverse effects</subject><subject>Oncolytic Virotherapy - methods</subject><subject>original-article</subject><subject>Tumor cells</subject><subject>Tumors</subject><subject>Virus Replication - genetics</subject><subject>Virus Replication - physiology</subject><subject>Viruses</subject><issn>0929-1903</issn><issn>1476-5500</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</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>eNqF0kGPEyEUAGBi3Li1evKuE030oFNhgAGO60Z3TTbxomfCMI92NlOowDTpv5duG-uaNYYDCe_jPV54CL0geEEwlR_tMi8ajNVCiEdoRphoa84xfoxmWDWqJgrTc_Q0pVuMS1DQJ-icKKkoV2yG2KewHTxUK4gbSNshTqnKuw1UpDKpMpUPWxir4G0Yd3mw1Z14hs6cGRM8P-5z9OPL5--X1_XNt6uvlxc3teWC5Jo1XdtzRjHuHZOGO2EEBexs27FO8q51qsRdb5xoLFfAWQvKyRarXkLPgc7Ru0PeTQw_J0hZr4dkYRyNhzAlLRgTuOWS_F_S0i4RTBX55i95G6boSxu6aRkRhNHy5Dl6_U9FBMeSSnpKtTQj6MG7kKOx-8L6omlKLSqYLGrxgCqrh_Vggwc3lPN7F97-cWEFZsyrFMYpD8Gn-_D9AdoYUorg9CYOaxN3mmC9Hw1dRkPvR0OXb5-jl8eWpm4N_ckeZ6GADweQSsgvIZ56fjjfqwP3Jk8RfucrZk-K-AV5G8i6</recordid><startdate>20100501</startdate><enddate>20100501</enddate><creator>Rodrigues, R</creator><creator>Cuddington, B</creator><creator>Mossman, K</creator><general>Nature Publishing Group US</general><general>Nature Publishing Group</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>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</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>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>7QO</scope><scope>7T5</scope></search><sort><creationdate>20100501</creationdate><title>Bovine herpesvirus type 1 as a novel oncolytic virus</title><author>Rodrigues, R ; Cuddington, B ; Mossman, K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c571t-42b6d54300df48a5f7a73e0fc6b4b85b6f96d5fdaf72c59e546e9f8609d8ed5e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer</topic><topic>Care and treatment</topic><topic>Cattle</topic><topic>Cell Line</topic><topic>Cell Line, Tumor</topic><topic>Cell Survival - genetics</topic><topic>Cell Survival - physiology</topic><topic>Cell viability</topic><topic>Cross-reactivity</topic><topic>Expression vectors</topic><topic>Gene Expression</topic><topic>Gene Therapy</topic><topic>Genetic aspects</topic><topic>Health aspects</topic><topic>Herpes simplex</topic><topic>Herpes simplex virus 1</topic><topic>Herpes viruses</topic><topic>Herpesvirus</topic><topic>Herpesvirus 1, Human - genetics</topic><topic>Herpesvirus 1, Human - physiology</topic><topic>Herpesviruses</topic><topic>Humans</topic><topic>Interferon</topic><topic>Interferon-alpha - genetics</topic><topic>Interferon-alpha - metabolism</topic><topic>mRNA</topic><topic>Neoplasms - metabolism</topic><topic>Neoplasms - therapy</topic><topic>Oncolysis</topic><topic>Oncolytic Virotherapy - adverse effects</topic><topic>Oncolytic Virotherapy - methods</topic><topic>original-article</topic><topic>Tumor cells</topic><topic>Tumors</topic><topic>Virus Replication - genetics</topic><topic>Virus Replication - physiology</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rodrigues, R</creatorcontrib><creatorcontrib>Cuddington, B</creatorcontrib><creatorcontrib>Mossman, K</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</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 Edition)</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>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</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>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</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>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><jtitle>Cancer gene therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rodrigues, R</au><au>Cuddington, B</au><au>Mossman, K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bovine herpesvirus type 1 as a novel oncolytic virus</atitle><jtitle>Cancer gene therapy</jtitle><stitle>Cancer Gene Ther</stitle><addtitle>Cancer Gene Ther</addtitle><date>2010-05-01</date><risdate>2010</risdate><volume>17</volume><issue>5</issue><spage>344</spage><epage>355</epage><pages>344-355</pages><issn>0929-1903</issn><eissn>1476-5500</eissn><abstract>Oncolytic virotherapy is a promising avenue of cancer gene therapy. Current vectors include human viruses that have been engineered to replicate in tumor cells or nonhuman viruses that are naturally oncotropic and preferentially replicate in tumor cells harboring defects in innate immune pathways such as the type 1 interferon (IFN) pathway. Bovine herpesvirus type 1 (BHV-1) is a species-specific herpesvirus closely related to the human herpes simplex virus type 1 (HSV-1). Although BHV-1 does not efficiently replicate in and affect cellular viability of normal human cells, it is capable of infecting and killing various immortalized and transformed human cell types. Surprisingly, BHV-1 infection of human cells fails to elicit IFN production at the mRNA or protein level and the ability of BHV-1 to kill immortalized and transformed human cells does not correlate with defects in IFN pathways. Furthermore, although some cross-reactivity between BHV-1 and HSV-1 exists, the majority of human antibody or serum samples tested failed to neutralize BHV-1 despite possessing HSV-1 neutralizing capacity. Thus, BHV-1 is a novel candidate oncolytic virus with a distinct mechanism of tumor targeting.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>19893594</pmid><doi>10.1038/cgt.2009.77</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biomedical and Life Sciences Biomedicine Cancer Care and treatment Cattle Cell Line Cell Line, Tumor Cell Survival - genetics Cell Survival - physiology Cell viability Cross-reactivity Expression vectors Gene Expression Gene Therapy Genetic aspects Health aspects Herpes simplex Herpes simplex virus 1 Herpes viruses Herpesvirus Herpesvirus 1, Human - genetics Herpesvirus 1, Human - physiology Herpesviruses Humans Interferon Interferon-alpha - genetics Interferon-alpha - metabolism mRNA Neoplasms - metabolism Neoplasms - therapy Oncolysis Oncolytic Virotherapy - adverse effects Oncolytic Virotherapy - methods original-article Tumor cells Tumors Virus Replication - genetics Virus Replication - physiology Viruses |
title | Bovine herpesvirus type 1 as a novel oncolytic virus |
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