Gene Therapy against Murine Melanoma B16F10-Nex2 Using IL-13R alpha 2-Fc Chimera and Interleukin 12 in Association with a Cyclopalladated Drug

Detalhes bibliográficos
Autor(a) principal: Hebeler-Barbosa, Flavia [UNIFESP]
Data de Publicação: 2008
Outros Autores: Rodrigues, Elaine Guadalupe [UNIFESP], Puccia, Rosana [UNIFESP], Caires, Antonio Carlos Favero, Travassos, Luiz Rodolpho [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/30871
http://dx.doi.org/10.1593/tlo.08115
Resumo: Interleukin 13 (IL-13) is immunoregulatory in many diseases, including cancer. the protective or suppressive role of CD1-restricted natural killer T cells (NKT cells) in tumor immunosurveillance and immunity is well documented. Interleukin 12 (IL-12) can activate type I NKT cells to produce interferon-gamma (IFN-gamma), whereas type II NKT cells may produce IL-13. the high-affinity chain of IL-13R alpha 2 may act as negative inhibitor, suppressing the action of IL-13 and helping to maintain tumor immunosurveillance. We constructed an mIL-13R alpha 2-Fc chimera in a eukaryotic expression vector and confirmed the identity of the recombinant protein by immunoblot analysis and binding to IL-13 in chemiluminescent ELISA. Such DNA vaccine was tested against syngeneic B16F10-Nex2 murine melanoma. in vivo experiments showed a protective effect mediated by high production of IFN-gamma and down-regulation of anti-inflammatory interleukins mainly by NKT 1.1(+) T cells. Biochemoterapy in vivo with plasmid encoding mIL-13R alpha 2-Fc in association with plasmid encoding IL-12 and the 7A cyclopalladated drug led to a significant reduction in the tumor evolution with 30% tumor-free mice. We conclude that IL-12 gene therapy, followed by continuous administration of IL-13R alpha 2-Fc gene along with 7A-drug has antitumor activity involving the high production of proinflammatory cytokines and low immune suppression, specifically by NK1.1(+) T cells producing IL-13 and IL-10.
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spelling Hebeler-Barbosa, Flavia [UNIFESP]Rodrigues, Elaine Guadalupe [UNIFESP]Puccia, Rosana [UNIFESP]Caires, Antonio Carlos FaveroTravassos, Luiz Rodolpho [UNIFESP]Universidade Federal de São Paulo (UNIFESP)Univ Mogi das Cruzes2016-01-24T13:51:39Z2016-01-24T13:51:39Z2008-09-01Translational Oncology. Ann Arbor: Neoplasia Press, v. 1, n. 3, p. 110-120, 2008.1936-5233http://repositorio.unifesp.br/handle/11600/30871http://dx.doi.org/10.1593/tlo.0811510.1593/tlo.08115WOS:000272467200001Interleukin 13 (IL-13) is immunoregulatory in many diseases, including cancer. the protective or suppressive role of CD1-restricted natural killer T cells (NKT cells) in tumor immunosurveillance and immunity is well documented. Interleukin 12 (IL-12) can activate type I NKT cells to produce interferon-gamma (IFN-gamma), whereas type II NKT cells may produce IL-13. the high-affinity chain of IL-13R alpha 2 may act as negative inhibitor, suppressing the action of IL-13 and helping to maintain tumor immunosurveillance. We constructed an mIL-13R alpha 2-Fc chimera in a eukaryotic expression vector and confirmed the identity of the recombinant protein by immunoblot analysis and binding to IL-13 in chemiluminescent ELISA. Such DNA vaccine was tested against syngeneic B16F10-Nex2 murine melanoma. in vivo experiments showed a protective effect mediated by high production of IFN-gamma and down-regulation of anti-inflammatory interleukins mainly by NKT 1.1(+) T cells. Biochemoterapy in vivo with plasmid encoding mIL-13R alpha 2-Fc in association with plasmid encoding IL-12 and the 7A cyclopalladated drug led to a significant reduction in the tumor evolution with 30% tumor-free mice. We conclude that IL-12 gene therapy, followed by continuous administration of IL-13R alpha 2-Fc gene along with 7A-drug has antitumor activity involving the high production of proinflammatory cytokines and low immune suppression, specifically by NK1.1(+) T cells producing IL-13 and IL-10.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Brazilian National Research CouncilUniversidade Federal de São Paulo, Dept Microbiol Imunol & Parasitol, UNONEX, BR-04023062 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Microbiol Imunol & Parasitol, Disciplina Biol Celular, BR-04023062 São Paulo, BrazilUniv Mogi das Cruzes, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Microbiol Imunol & Parasitol, UNONEX, BR-04023062 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Microbiol Imunol & Parasitol, Disciplina Biol Celular, BR-04023062 São Paulo, BrazilWeb of Science110-120engNeoplasia PressTranslational OncologyGene Therapy against Murine Melanoma B16F10-Nex2 Using IL-13R alpha 2-Fc Chimera and Interleukin 12 in Association with a Cyclopalladated Druginfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP11600/308712022-09-27 12:00:37.209metadata only accessoai:repositorio.unifesp.br:11600/30871Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652022-09-27T15:00:37Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Gene Therapy against Murine Melanoma B16F10-Nex2 Using IL-13R alpha 2-Fc Chimera and Interleukin 12 in Association with a Cyclopalladated Drug
title Gene Therapy against Murine Melanoma B16F10-Nex2 Using IL-13R alpha 2-Fc Chimera and Interleukin 12 in Association with a Cyclopalladated Drug
spellingShingle Gene Therapy against Murine Melanoma B16F10-Nex2 Using IL-13R alpha 2-Fc Chimera and Interleukin 12 in Association with a Cyclopalladated Drug
Hebeler-Barbosa, Flavia [UNIFESP]
title_short Gene Therapy against Murine Melanoma B16F10-Nex2 Using IL-13R alpha 2-Fc Chimera and Interleukin 12 in Association with a Cyclopalladated Drug
title_full Gene Therapy against Murine Melanoma B16F10-Nex2 Using IL-13R alpha 2-Fc Chimera and Interleukin 12 in Association with a Cyclopalladated Drug
title_fullStr Gene Therapy against Murine Melanoma B16F10-Nex2 Using IL-13R alpha 2-Fc Chimera and Interleukin 12 in Association with a Cyclopalladated Drug
title_full_unstemmed Gene Therapy against Murine Melanoma B16F10-Nex2 Using IL-13R alpha 2-Fc Chimera and Interleukin 12 in Association with a Cyclopalladated Drug
title_sort Gene Therapy against Murine Melanoma B16F10-Nex2 Using IL-13R alpha 2-Fc Chimera and Interleukin 12 in Association with a Cyclopalladated Drug
author Hebeler-Barbosa, Flavia [UNIFESP]
author_facet Hebeler-Barbosa, Flavia [UNIFESP]
Rodrigues, Elaine Guadalupe [UNIFESP]
Puccia, Rosana [UNIFESP]
Caires, Antonio Carlos Favero
Travassos, Luiz Rodolpho [UNIFESP]
author_role author
author2 Rodrigues, Elaine Guadalupe [UNIFESP]
Puccia, Rosana [UNIFESP]
Caires, Antonio Carlos Favero
Travassos, Luiz Rodolpho [UNIFESP]
author2_role author
author
author
author
dc.contributor.institution.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
Univ Mogi das Cruzes
dc.contributor.author.fl_str_mv Hebeler-Barbosa, Flavia [UNIFESP]
Rodrigues, Elaine Guadalupe [UNIFESP]
Puccia, Rosana [UNIFESP]
Caires, Antonio Carlos Favero
Travassos, Luiz Rodolpho [UNIFESP]
description Interleukin 13 (IL-13) is immunoregulatory in many diseases, including cancer. the protective or suppressive role of CD1-restricted natural killer T cells (NKT cells) in tumor immunosurveillance and immunity is well documented. Interleukin 12 (IL-12) can activate type I NKT cells to produce interferon-gamma (IFN-gamma), whereas type II NKT cells may produce IL-13. the high-affinity chain of IL-13R alpha 2 may act as negative inhibitor, suppressing the action of IL-13 and helping to maintain tumor immunosurveillance. We constructed an mIL-13R alpha 2-Fc chimera in a eukaryotic expression vector and confirmed the identity of the recombinant protein by immunoblot analysis and binding to IL-13 in chemiluminescent ELISA. Such DNA vaccine was tested against syngeneic B16F10-Nex2 murine melanoma. in vivo experiments showed a protective effect mediated by high production of IFN-gamma and down-regulation of anti-inflammatory interleukins mainly by NKT 1.1(+) T cells. Biochemoterapy in vivo with plasmid encoding mIL-13R alpha 2-Fc in association with plasmid encoding IL-12 and the 7A cyclopalladated drug led to a significant reduction in the tumor evolution with 30% tumor-free mice. We conclude that IL-12 gene therapy, followed by continuous administration of IL-13R alpha 2-Fc gene along with 7A-drug has antitumor activity involving the high production of proinflammatory cytokines and low immune suppression, specifically by NK1.1(+) T cells producing IL-13 and IL-10.
publishDate 2008
dc.date.issued.fl_str_mv 2008-09-01
dc.date.accessioned.fl_str_mv 2016-01-24T13:51:39Z
dc.date.available.fl_str_mv 2016-01-24T13:51:39Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv Translational Oncology. Ann Arbor: Neoplasia Press, v. 1, n. 3, p. 110-120, 2008.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/30871
http://dx.doi.org/10.1593/tlo.08115
dc.identifier.issn.none.fl_str_mv 1936-5233
dc.identifier.doi.none.fl_str_mv 10.1593/tlo.08115
dc.identifier.wos.none.fl_str_mv WOS:000272467200001
identifier_str_mv Translational Oncology. Ann Arbor: Neoplasia Press, v. 1, n. 3, p. 110-120, 2008.
1936-5233
10.1593/tlo.08115
WOS:000272467200001
url http://repositorio.unifesp.br/handle/11600/30871
http://dx.doi.org/10.1593/tlo.08115
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Translational Oncology
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 110-120
dc.publisher.none.fl_str_mv Neoplasia Press
publisher.none.fl_str_mv Neoplasia Press
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv
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