Perspectives for cancer immunotherapy mediated by p19Arf plus interferon-beta gene transfer
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , , , |
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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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 |
_version_ |
1800222763766513664 |