Perspectives for cancer immunotherapy mediated by p19Arf plus interferon-beta gene transfer

Detalhes bibliográficos
Autor(a) principal: Strauss, Bryan E.
Data de Publicação: 2019
Outros Autores: Silva, Gissele Rolemberg Oliveira, Vieira, Igor de Luna, Cerqueira, Otto Luiz Dutra, Del Valle, Paulo Roberto, Medrano, Ruan Felipe Vieira, Mendonça, Samir Andrade
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Clinics
Texto Completo: https://www.revistas.usp.br/clinics/article/view/154791
Resumo: While cancer immunotherapy has gained much deserved attention in recent years, many areas regarding the optimization of such modalities remain unexplored, including the development of novel approaches and the strategic combination of therapies that target multiple aspects of the cancer-immunity cycle. Our own work involves the use of gene transfer technology to promote cell death and immune stimulation. Such immunogenic cell death, mediated by the combined transfer of the alternate reading frame (p14ARF in humans and p19Arf in mice) and the interferon-b cDNA in our case, was shown to promote an antitumor immune response in mouse models of melanoma and lung carcinoma. With these encouraging results, we are now setting out on the road toward translational and preclinical development of our novel immunotherapeutic approach. Here, we outline the perspectives and challenges that we face, including the use of human tumor and immune cells to verify the response seen in mouse models and the incorporation of clinically relevant models, such as patient-derived xenografts and spontaneous tumors in animals. In addition, we seek to combine our immunotherapeutic approach with other treatments, such as chemotherapy or checkpoint blockade, with the goal of reducing dosage and increasing efficacy. The success of any translational research requires the cooperation of a multidisciplinary team of professionals involved in laboratory and clinical research, a relationship that is fostered at the Cancer Institute of Sao Paulo.
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spelling Perspectives for cancer immunotherapy mediated by p19Arf plus interferon-beta gene transferMelanomaImmunotherapyImmunogenic Cell DeathTranslational MedicineViral VectorsWhile cancer immunotherapy has gained much deserved attention in recent years, many areas regarding the optimization of such modalities remain unexplored, including the development of novel approaches and the strategic combination of therapies that target multiple aspects of the cancer-immunity cycle. Our own work involves the use of gene transfer technology to promote cell death and immune stimulation. Such immunogenic cell death, mediated by the combined transfer of the alternate reading frame (p14ARF in humans and p19Arf in mice) and the interferon-b cDNA in our case, was shown to promote an antitumor immune response in mouse models of melanoma and lung carcinoma. With these encouraging results, we are now setting out on the road toward translational and preclinical development of our novel immunotherapeutic approach. Here, we outline the perspectives and challenges that we face, including the use of human tumor and immune cells to verify the response seen in mouse models and the incorporation of clinically relevant models, such as patient-derived xenografts and spontaneous tumors in animals. In addition, we seek to combine our immunotherapeutic approach with other treatments, such as chemotherapy or checkpoint blockade, with the goal of reducing dosage and increasing efficacy. The success of any translational research requires the cooperation of a multidisciplinary team of professionals involved in laboratory and clinical research, a relationship that is fostered at the Cancer Institute of Sao Paulo.Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2019-02-15info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/15479110.6061/clinics/2018/e479sClinics; Vol. 73 No. Suppl. 1 (2018); e479sClinics; v. 73 n. Suppl. 1 (2018); e479sClinics; Vol. 73 Núm. Suppl. 1 (2018); e479s1980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/154791/150789Copyright (c) 2019 Clinicsinfo:eu-repo/semantics/openAccessStrauss, Bryan E.Silva, Gissele Rolemberg OliveiraVieira, Igor de LunaCerqueira, Otto Luiz DutraDel Valle, Paulo RobertoMedrano, Ruan Felipe VieiraMendonça, Samir Andrade2019-05-14T11:48:25Zoai:revistas.usp.br:article/154791Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2019-05-14T11:48:25Clinics - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Perspectives for cancer immunotherapy mediated by p19Arf plus interferon-beta gene transfer
title Perspectives for cancer immunotherapy mediated by p19Arf plus interferon-beta gene transfer
spellingShingle Perspectives for cancer immunotherapy mediated by p19Arf plus interferon-beta gene transfer
Strauss, Bryan E.
Melanoma
Immunotherapy
Immunogenic Cell Death
Translational Medicine
Viral Vectors
title_short Perspectives for cancer immunotherapy mediated by p19Arf plus interferon-beta gene transfer
title_full Perspectives for cancer immunotherapy mediated by p19Arf plus interferon-beta gene transfer
title_fullStr Perspectives for cancer immunotherapy mediated by p19Arf plus interferon-beta gene transfer
title_full_unstemmed Perspectives for cancer immunotherapy mediated by p19Arf plus interferon-beta gene transfer
title_sort Perspectives for cancer immunotherapy mediated by p19Arf plus interferon-beta gene transfer
author Strauss, Bryan E.
author_facet Strauss, Bryan E.
Silva, Gissele Rolemberg Oliveira
Vieira, Igor de Luna
Cerqueira, Otto Luiz Dutra
Del Valle, Paulo Roberto
Medrano, Ruan Felipe Vieira
Mendonça, Samir Andrade
author_role author
author2 Silva, Gissele Rolemberg Oliveira
Vieira, Igor de Luna
Cerqueira, Otto Luiz Dutra
Del Valle, Paulo Roberto
Medrano, Ruan Felipe Vieira
Mendonça, Samir Andrade
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Strauss, Bryan E.
Silva, Gissele Rolemberg Oliveira
Vieira, Igor de Luna
Cerqueira, Otto Luiz Dutra
Del Valle, Paulo Roberto
Medrano, Ruan Felipe Vieira
Mendonça, Samir Andrade
dc.subject.por.fl_str_mv Melanoma
Immunotherapy
Immunogenic Cell Death
Translational Medicine
Viral Vectors
topic Melanoma
Immunotherapy
Immunogenic Cell Death
Translational Medicine
Viral Vectors
description While cancer immunotherapy has gained much deserved attention in recent years, many areas regarding the optimization of such modalities remain unexplored, including the development of novel approaches and the strategic combination of therapies that target multiple aspects of the cancer-immunity cycle. Our own work involves the use of gene transfer technology to promote cell death and immune stimulation. Such immunogenic cell death, mediated by the combined transfer of the alternate reading frame (p14ARF in humans and p19Arf in mice) and the interferon-b cDNA in our case, was shown to promote an antitumor immune response in mouse models of melanoma and lung carcinoma. With these encouraging results, we are now setting out on the road toward translational and preclinical development of our novel immunotherapeutic approach. Here, we outline the perspectives and challenges that we face, including the use of human tumor and immune cells to verify the response seen in mouse models and the incorporation of clinically relevant models, such as patient-derived xenografts and spontaneous tumors in animals. In addition, we seek to combine our immunotherapeutic approach with other treatments, such as chemotherapy or checkpoint blockade, with the goal of reducing dosage and increasing efficacy. The success of any translational research requires the cooperation of a multidisciplinary team of professionals involved in laboratory and clinical research, a relationship that is fostered at the Cancer Institute of Sao Paulo.
publishDate 2019
dc.date.none.fl_str_mv 2019-02-15
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/clinics/article/view/154791
10.6061/clinics/2018/e479s
url https://www.revistas.usp.br/clinics/article/view/154791
identifier_str_mv 10.6061/clinics/2018/e479s
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/clinics/article/view/154791/150789
dc.rights.driver.fl_str_mv Copyright (c) 2019 Clinics
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2019 Clinics
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
dc.source.none.fl_str_mv Clinics; Vol. 73 No. Suppl. 1 (2018); e479s
Clinics; v. 73 n. Suppl. 1 (2018); e479s
Clinics; Vol. 73 Núm. Suppl. 1 (2018); e479s
1980-5322
1807-5932
reponame:Clinics
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Clinics
collection Clinics
repository.name.fl_str_mv Clinics - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||clinics@hc.fm.usp.br
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