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HPV16 E6/E7 -based mRNA vaccine is therapeutic in mice bearing aggressive HPV-positive lesions
HPV (Human papillomavirus) affects 600,000 people worldwide each year. Almost all cervical cancers are associated with a past HPV infection. In particular, the positivity to the high-risk type HPV16 is detected in most of the invasive cervical cancers. FDA has approved prophylactic vaccines that pro...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10368880/ https://www.ncbi.nlm.nih.gov/pubmed/37503351 http://dx.doi.org/10.3389/fimmu.2023.1213285 |
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author | Zhou, Kun Yuzhakov, Olga Behloul, Nouredine Wang, Dehua Bhagat, Lakshmi Chu, Dafeng Zhang, Xinyue Cheng, Xinwei Fan, Lusheng Huang, Xinyu Mirabella, Teodelinda |
author_facet | Zhou, Kun Yuzhakov, Olga Behloul, Nouredine Wang, Dehua Bhagat, Lakshmi Chu, Dafeng Zhang, Xinyue Cheng, Xinwei Fan, Lusheng Huang, Xinyu Mirabella, Teodelinda |
author_sort | Zhou, Kun |
collection | PubMed |
description | HPV (Human papillomavirus) affects 600,000 people worldwide each year. Almost all cervical cancers are associated with a past HPV infection. In particular, the positivity to the high-risk type HPV16 is detected in most of the invasive cervical cancers. FDA has approved prophylactic vaccines that protect against new HPV16 infections, but do not induce immunity in those patients with established infections or neoplasms. To date, no therapeutic vaccine targeting HPV16-associated lesions has been authorized. We have developed an mRNA-based vaccine against the HPV16 late oncoproteins E6 and E7, which are abundantly and exclusively expressed in high-grade squamous intraepithelial lesions (HSILs), a stage of the cervical disease that precedes the progression to carcinoma. Our in vitro and in vivo studies demonstrated that the translated mRNA is functional and elicits an antigen-specific adaptive immune response. Upon immunization with the vaccine, mice with HPV16+ lesions exhibited tumor growth inhibition, extension of lifespan, and development of a protective immune memory. In light of these results and the remarkable clinical success of mRNA vaccines against SARS-CoV2, we believe that our mRNA-based therapeutic vaccine has the potential to offer a non-invasive treatment alternative to the current standard of care for HPV16+ HSILs. |
format | Online Article Text |
id | pubmed-10368880 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103688802023-07-27 HPV16 E6/E7 -based mRNA vaccine is therapeutic in mice bearing aggressive HPV-positive lesions Zhou, Kun Yuzhakov, Olga Behloul, Nouredine Wang, Dehua Bhagat, Lakshmi Chu, Dafeng Zhang, Xinyue Cheng, Xinwei Fan, Lusheng Huang, Xinyu Mirabella, Teodelinda Front Immunol Immunology HPV (Human papillomavirus) affects 600,000 people worldwide each year. Almost all cervical cancers are associated with a past HPV infection. In particular, the positivity to the high-risk type HPV16 is detected in most of the invasive cervical cancers. FDA has approved prophylactic vaccines that protect against new HPV16 infections, but do not induce immunity in those patients with established infections or neoplasms. To date, no therapeutic vaccine targeting HPV16-associated lesions has been authorized. We have developed an mRNA-based vaccine against the HPV16 late oncoproteins E6 and E7, which are abundantly and exclusively expressed in high-grade squamous intraepithelial lesions (HSILs), a stage of the cervical disease that precedes the progression to carcinoma. Our in vitro and in vivo studies demonstrated that the translated mRNA is functional and elicits an antigen-specific adaptive immune response. Upon immunization with the vaccine, mice with HPV16+ lesions exhibited tumor growth inhibition, extension of lifespan, and development of a protective immune memory. In light of these results and the remarkable clinical success of mRNA vaccines against SARS-CoV2, we believe that our mRNA-based therapeutic vaccine has the potential to offer a non-invasive treatment alternative to the current standard of care for HPV16+ HSILs. Frontiers Media S.A. 2023-07-12 /pmc/articles/PMC10368880/ /pubmed/37503351 http://dx.doi.org/10.3389/fimmu.2023.1213285 Text en Copyright © 2023 Zhou, Yuzhakov, Behloul, Wang, Bhagat, Chu, Zhang, Cheng, Fan, Huang and Mirabella https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Zhou, Kun Yuzhakov, Olga Behloul, Nouredine Wang, Dehua Bhagat, Lakshmi Chu, Dafeng Zhang, Xinyue Cheng, Xinwei Fan, Lusheng Huang, Xinyu Mirabella, Teodelinda HPV16 E6/E7 -based mRNA vaccine is therapeutic in mice bearing aggressive HPV-positive lesions |
title | HPV16 E6/E7 -based mRNA vaccine is therapeutic in mice bearing aggressive HPV-positive lesions |
title_full | HPV16 E6/E7 -based mRNA vaccine is therapeutic in mice bearing aggressive HPV-positive lesions |
title_fullStr | HPV16 E6/E7 -based mRNA vaccine is therapeutic in mice bearing aggressive HPV-positive lesions |
title_full_unstemmed | HPV16 E6/E7 -based mRNA vaccine is therapeutic in mice bearing aggressive HPV-positive lesions |
title_short | HPV16 E6/E7 -based mRNA vaccine is therapeutic in mice bearing aggressive HPV-positive lesions |
title_sort | hpv16 e6/e7 -based mrna vaccine is therapeutic in mice bearing aggressive hpv-positive lesions |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10368880/ https://www.ncbi.nlm.nih.gov/pubmed/37503351 http://dx.doi.org/10.3389/fimmu.2023.1213285 |
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