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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...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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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. |
format | Online Article Text |
id | pubmed-4577214 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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