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The Invisible Enemy – How Human Papillomaviruses Avoid Recognition and Clearance by the Host Immune System

Human papillomavirus (HPV) needs to persist in squamous epithelia for a certain amount of time to complete its reproductive cycle. Therefore, the virus has evolved multiple immune evasion strategies. The interplay of these immune evasion mechanisms with the host immune system decides whether a HPV i...

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Detalles Bibliográficos
Autores principales: Grabowska, Agnieszka K, Riemer, Angelika B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Open 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3547646/
https://www.ncbi.nlm.nih.gov/pubmed/23341860
http://dx.doi.org/10.2174/1874357901206010249
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author Grabowska, Agnieszka K
Riemer, Angelika B
author_facet Grabowska, Agnieszka K
Riemer, Angelika B
author_sort Grabowska, Agnieszka K
collection PubMed
description Human papillomavirus (HPV) needs to persist in squamous epithelia for a certain amount of time to complete its reproductive cycle. Therefore, the virus has evolved multiple immune evasion strategies. The interplay of these immune evasion mechanisms with the host immune system decides whether a HPV infection is cleared or becomes persistent. Clearance of HPV-induced lesions is mediated by a cellular immune response, consisting of both cytotoxic T lymphocyte and T helper cell responses. Persistent HPV infection, on the other hand, is the single most important risk factor for the development of HPV-associated premalignant lesions and HPV-driven cancers. This article reviews the immune evasion mechanisms employed by high-risk HPVs to escape host immune recognition and attack.
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spelling pubmed-35476462013-01-22 The Invisible Enemy – How Human Papillomaviruses Avoid Recognition and Clearance by the Host Immune System Grabowska, Agnieszka K Riemer, Angelika B Open Virol J Article Human papillomavirus (HPV) needs to persist in squamous epithelia for a certain amount of time to complete its reproductive cycle. Therefore, the virus has evolved multiple immune evasion strategies. The interplay of these immune evasion mechanisms with the host immune system decides whether a HPV infection is cleared or becomes persistent. Clearance of HPV-induced lesions is mediated by a cellular immune response, consisting of both cytotoxic T lymphocyte and T helper cell responses. Persistent HPV infection, on the other hand, is the single most important risk factor for the development of HPV-associated premalignant lesions and HPV-driven cancers. This article reviews the immune evasion mechanisms employed by high-risk HPVs to escape host immune recognition and attack. Bentham Open 2012-12-28 /pmc/articles/PMC3547646/ /pubmed/23341860 http://dx.doi.org/10.2174/1874357901206010249 Text en © Grabowska and Riemer.; Licensee Bentham Open. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Grabowska, Agnieszka K
Riemer, Angelika B
The Invisible Enemy – How Human Papillomaviruses Avoid Recognition and Clearance by the Host Immune System
title The Invisible Enemy – How Human Papillomaviruses Avoid Recognition and Clearance by the Host Immune System
title_full The Invisible Enemy – How Human Papillomaviruses Avoid Recognition and Clearance by the Host Immune System
title_fullStr The Invisible Enemy – How Human Papillomaviruses Avoid Recognition and Clearance by the Host Immune System
title_full_unstemmed The Invisible Enemy – How Human Papillomaviruses Avoid Recognition and Clearance by the Host Immune System
title_short The Invisible Enemy – How Human Papillomaviruses Avoid Recognition and Clearance by the Host Immune System
title_sort invisible enemy – how human papillomaviruses avoid recognition and clearance by the host immune system
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3547646/
https://www.ncbi.nlm.nih.gov/pubmed/23341860
http://dx.doi.org/10.2174/1874357901206010249
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