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Design, Immune Responses and Anti-Tumor Potential of an HPV16 E6E7 Multi-Epitope Vaccine

Cervical cancer is a common type of cancer among women worldwide and infection with high-risk human papillomavirus (HPVs) types represents the major risk factor for the etiopathogenesis of the disease. HPV-16 is the most frequently identified HPV type in cervical lesions and expression of E6 and E7...

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Autores principales: de Oliveira, Liliane Maria Fernandes, Morale, Mirian Galliote, Chaves, Agatha A. Muniz, Cavalher, Aline Marques, Lopes, Aline Soriano, Diniz, Mariana de Oliveira, Schanoski, Alessandra Soares, de Melo, Robson Lopes, Ferreira, Luís Carlos de Souza, de Oliveira, Maria Leonor S., Demasi, Marilene, Ho, Paulo Lee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4577214/
https://www.ncbi.nlm.nih.gov/pubmed/26390407
http://dx.doi.org/10.1371/journal.pone.0138686
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author de Oliveira, Liliane Maria Fernandes
Morale, Mirian Galliote
Chaves, Agatha A. Muniz
Cavalher, Aline Marques
Lopes, Aline Soriano
Diniz, Mariana de Oliveira
Schanoski, Alessandra Soares
de Melo, Robson Lopes
Ferreira, Luís Carlos de Souza
de Oliveira, Maria Leonor S.
Demasi, Marilene
Ho, Paulo Lee
author_facet de Oliveira, Liliane Maria Fernandes
Morale, Mirian Galliote
Chaves, Agatha A. Muniz
Cavalher, Aline Marques
Lopes, Aline Soriano
Diniz, Mariana de Oliveira
Schanoski, Alessandra Soares
de Melo, Robson Lopes
Ferreira, Luís Carlos de Souza
de Oliveira, Maria Leonor S.
Demasi, Marilene
Ho, Paulo Lee
author_sort de Oliveira, Liliane Maria Fernandes
collection PubMed
description Cervical cancer is a common type of cancer among women worldwide and infection with high-risk human papillomavirus (HPVs) types represents the major risk factor for the etiopathogenesis of the disease. HPV-16 is the most frequently identified HPV type in cervical lesions and expression of E6 and E7 oncoproteins is required for the uncontrolled cellular proliferation. In the present study we report the design and experimental testing of a recombinant multi-epitope protein containing immunogenic epitopes of HPV-16 E6 and E7. Tumor preventive assays, based on the engraftment of TC-1 cells in mice, showed that the E6E7 multi-epitope protein induced a full preventive anti-tumor protection in wild-type mice, as well as in mice deficient in expression of CD4(+) T cells and TLR4 receptor. Nonetheless, no anti-tumor protection was observed in mice deficient in CD8(+) T cells. Also, the vaccine promoted high activation of E6/E7-specific T cells and in a therapeutic-approach, E6E7 protein conferred full anti-tumor protection in mice. These results show a potential use of this E6E7 multi-epitope antigen as a new and promising antigen for the development of a therapeutic vaccine against tumors induced by HPV.
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spelling pubmed-45772142015-09-25 Design, Immune Responses and Anti-Tumor Potential of an HPV16 E6E7 Multi-Epitope Vaccine de Oliveira, Liliane Maria Fernandes Morale, Mirian Galliote Chaves, Agatha A. Muniz Cavalher, Aline Marques Lopes, Aline Soriano Diniz, Mariana de Oliveira Schanoski, Alessandra Soares de Melo, Robson Lopes Ferreira, Luís Carlos de Souza de Oliveira, Maria Leonor S. Demasi, Marilene Ho, Paulo Lee PLoS One Research Article Cervical cancer is a common type of cancer among women worldwide and infection with high-risk human papillomavirus (HPVs) types represents the major risk factor for the etiopathogenesis of the disease. HPV-16 is the most frequently identified HPV type in cervical lesions and expression of E6 and E7 oncoproteins is required for the uncontrolled cellular proliferation. In the present study we report the design and experimental testing of a recombinant multi-epitope protein containing immunogenic epitopes of HPV-16 E6 and E7. Tumor preventive assays, based on the engraftment of TC-1 cells in mice, showed that the E6E7 multi-epitope protein induced a full preventive anti-tumor protection in wild-type mice, as well as in mice deficient in expression of CD4(+) T cells and TLR4 receptor. Nonetheless, no anti-tumor protection was observed in mice deficient in CD8(+) T cells. Also, the vaccine promoted high activation of E6/E7-specific T cells and in a therapeutic-approach, E6E7 protein conferred full anti-tumor protection in mice. These results show a potential use of this E6E7 multi-epitope antigen as a new and promising antigen for the development of a therapeutic vaccine against tumors induced by HPV. Public Library of Science 2015-09-21 /pmc/articles/PMC4577214/ /pubmed/26390407 http://dx.doi.org/10.1371/journal.pone.0138686 Text en © 2015 de Oliveira et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
de Oliveira, Liliane Maria Fernandes
Morale, Mirian Galliote
Chaves, Agatha A. Muniz
Cavalher, Aline Marques
Lopes, Aline Soriano
Diniz, Mariana de Oliveira
Schanoski, Alessandra Soares
de Melo, Robson Lopes
Ferreira, Luís Carlos de Souza
de Oliveira, Maria Leonor S.
Demasi, Marilene
Ho, Paulo Lee
Design, Immune Responses and Anti-Tumor Potential of an HPV16 E6E7 Multi-Epitope Vaccine
title Design, Immune Responses and Anti-Tumor Potential of an HPV16 E6E7 Multi-Epitope Vaccine
title_full Design, Immune Responses and Anti-Tumor Potential of an HPV16 E6E7 Multi-Epitope Vaccine
title_fullStr Design, Immune Responses and Anti-Tumor Potential of an HPV16 E6E7 Multi-Epitope Vaccine
title_full_unstemmed Design, Immune Responses and Anti-Tumor Potential of an HPV16 E6E7 Multi-Epitope Vaccine
title_short Design, Immune Responses and Anti-Tumor Potential of an HPV16 E6E7 Multi-Epitope Vaccine
title_sort design, immune responses and anti-tumor potential of an hpv16 e6e7 multi-epitope vaccine
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4577214/
https://www.ncbi.nlm.nih.gov/pubmed/26390407
http://dx.doi.org/10.1371/journal.pone.0138686
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