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Immunopathogenesis of HPV-Associated Cancers and Prospects for Immunotherapy
Human papillomavirus (HPV) infection is a causative factor for various cancers of the anogenital region and oropharynx, and is supposed to play an important cofactor role for skin carcinogenesis. Evasion from immunosurveillance favors viral persistence. However, there is evidence that the mere prese...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618020/ https://www.ncbi.nlm.nih.gov/pubmed/28895886 http://dx.doi.org/10.3390/v9090254 |
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author | Smola, Sigrun |
author_facet | Smola, Sigrun |
author_sort | Smola, Sigrun |
collection | PubMed |
description | Human papillomavirus (HPV) infection is a causative factor for various cancers of the anogenital region and oropharynx, and is supposed to play an important cofactor role for skin carcinogenesis. Evasion from immunosurveillance favors viral persistence. However, there is evidence that the mere presence of oncogenic HPV is not sufficient for malignant progression and that additional tumor-promoting steps are required. Recent studies have demonstrated that HPV-transformed cells actively promote chronic stromal inflammation and conspire with cells in the local microenvironment to promote carcinogenesis. This review highlights the complex interplay between HPV-infected cells and the local immune microenvironment during oncogenic HPV infection, persistence, and malignant progression, and discusses new prospects for diagnosis and immunotherapy of HPV-associated cancers. |
format | Online Article Text |
id | pubmed-5618020 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-56180202017-09-29 Immunopathogenesis of HPV-Associated Cancers and Prospects for Immunotherapy Smola, Sigrun Viruses Review Human papillomavirus (HPV) infection is a causative factor for various cancers of the anogenital region and oropharynx, and is supposed to play an important cofactor role for skin carcinogenesis. Evasion from immunosurveillance favors viral persistence. However, there is evidence that the mere presence of oncogenic HPV is not sufficient for malignant progression and that additional tumor-promoting steps are required. Recent studies have demonstrated that HPV-transformed cells actively promote chronic stromal inflammation and conspire with cells in the local microenvironment to promote carcinogenesis. This review highlights the complex interplay between HPV-infected cells and the local immune microenvironment during oncogenic HPV infection, persistence, and malignant progression, and discusses new prospects for diagnosis and immunotherapy of HPV-associated cancers. MDPI 2017-09-12 /pmc/articles/PMC5618020/ /pubmed/28895886 http://dx.doi.org/10.3390/v9090254 Text en © 2017 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Smola, Sigrun Immunopathogenesis of HPV-Associated Cancers and Prospects for Immunotherapy |
title | Immunopathogenesis of HPV-Associated Cancers and Prospects for Immunotherapy |
title_full | Immunopathogenesis of HPV-Associated Cancers and Prospects for Immunotherapy |
title_fullStr | Immunopathogenesis of HPV-Associated Cancers and Prospects for Immunotherapy |
title_full_unstemmed | Immunopathogenesis of HPV-Associated Cancers and Prospects for Immunotherapy |
title_short | Immunopathogenesis of HPV-Associated Cancers and Prospects for Immunotherapy |
title_sort | immunopathogenesis of hpv-associated cancers and prospects for immunotherapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618020/ https://www.ncbi.nlm.nih.gov/pubmed/28895886 http://dx.doi.org/10.3390/v9090254 |
work_keys_str_mv | AT smolasigrun immunopathogenesisofhpvassociatedcancersandprospectsforimmunotherapy |