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Human Polyomavirus Reactivation: Disease Pathogenesis and Treatment Approaches

JC and BK polyomaviruses were discovered over 40 years ago and have become increasingly prevalent causes of morbidity and mortality in a variety of distinct, immunocompromised patient cohorts. The recent discoveries of eight new members of the Polyomaviridae family that are capable of infecting huma...

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Detalles Bibliográficos
Autores principales: De Gascun, Cillian F., Carr, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659475/
https://www.ncbi.nlm.nih.gov/pubmed/23737811
http://dx.doi.org/10.1155/2013/373579
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author De Gascun, Cillian F.
Carr, Michael J.
author_facet De Gascun, Cillian F.
Carr, Michael J.
author_sort De Gascun, Cillian F.
collection PubMed
description JC and BK polyomaviruses were discovered over 40 years ago and have become increasingly prevalent causes of morbidity and mortality in a variety of distinct, immunocompromised patient cohorts. The recent discoveries of eight new members of the Polyomaviridae family that are capable of infecting humans suggest that there are more to be discovered and raise the possibility that they may play a more significant role in human disease than previously understood. In spite of this, there remains a dearth of specific therapeutic options for human polyomavirus infections and an incomplete understanding of the relationship between the virus and the host immune system. This review summarises the human polyomaviruses with particular emphasis on pathogenesis in those directly implicated in disease aetiology and the therapeutic options available for treatment in the immunocompromised host.
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spelling pubmed-36594752013-06-04 Human Polyomavirus Reactivation: Disease Pathogenesis and Treatment Approaches De Gascun, Cillian F. Carr, Michael J. Clin Dev Immunol Review Article JC and BK polyomaviruses were discovered over 40 years ago and have become increasingly prevalent causes of morbidity and mortality in a variety of distinct, immunocompromised patient cohorts. The recent discoveries of eight new members of the Polyomaviridae family that are capable of infecting humans suggest that there are more to be discovered and raise the possibility that they may play a more significant role in human disease than previously understood. In spite of this, there remains a dearth of specific therapeutic options for human polyomavirus infections and an incomplete understanding of the relationship between the virus and the host immune system. This review summarises the human polyomaviruses with particular emphasis on pathogenesis in those directly implicated in disease aetiology and the therapeutic options available for treatment in the immunocompromised host. Hindawi Publishing Corporation 2013 2013-05-02 /pmc/articles/PMC3659475/ /pubmed/23737811 http://dx.doi.org/10.1155/2013/373579 Text en Copyright © 2013 C. F. De Gascun and M. J. Carr. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
De Gascun, Cillian F.
Carr, Michael J.
Human Polyomavirus Reactivation: Disease Pathogenesis and Treatment Approaches
title Human Polyomavirus Reactivation: Disease Pathogenesis and Treatment Approaches
title_full Human Polyomavirus Reactivation: Disease Pathogenesis and Treatment Approaches
title_fullStr Human Polyomavirus Reactivation: Disease Pathogenesis and Treatment Approaches
title_full_unstemmed Human Polyomavirus Reactivation: Disease Pathogenesis and Treatment Approaches
title_short Human Polyomavirus Reactivation: Disease Pathogenesis and Treatment Approaches
title_sort human polyomavirus reactivation: disease pathogenesis and treatment approaches
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659475/
https://www.ncbi.nlm.nih.gov/pubmed/23737811
http://dx.doi.org/10.1155/2013/373579
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