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A New Insight into Hepatitis C Vaccine Development
Chronic hepatitis C virus (HCV) infection remains a serious burden to public health worldwide. Currently, HCV-infected patients could undergo antiviral therapy by giving pegylated IFN-α with ribavirin. However, this therapy is only effective in around 50% of patients with HCV genotype 1, which accou...
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2896694/ https://www.ncbi.nlm.nih.gov/pubmed/20625493 http://dx.doi.org/10.1155/2010/548280 |
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author | Yu, Chun I Chiang, Bor-Luen |
author_facet | Yu, Chun I Chiang, Bor-Luen |
author_sort | Yu, Chun I |
collection | PubMed |
description | Chronic hepatitis C virus (HCV) infection remains a serious burden to public health worldwide. Currently, HCV-infected patients could undergo antiviral therapy by giving pegylated IFN-α with ribavirin. However, this therapy is only effective in around 50% of patients with HCV genotype 1, which accounts for more than 70% of all HCV infection, and it is not well tolerated for most patients. Moreover, there is no vaccine available. The efforts on identifying protective immunity against HCV have progressed recently. Neutralizing antibodies and robust T cell responses including both CD4(+) and CD8(+) have been shown to be related to the clearance of HCV, which have shed lights on the potential success of HCV vaccines. There are many vaccines developed and tested before entering clinical trials. Here, we would first discuss strategies of viral immune evasion and correlates of protective host immunity and finally review some prospective vaccine approaches against chronic HCV infection. |
format | Text |
id | pubmed-2896694 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-28966942010-07-12 A New Insight into Hepatitis C Vaccine Development Yu, Chun I Chiang, Bor-Luen J Biomed Biotechnol Review Article Chronic hepatitis C virus (HCV) infection remains a serious burden to public health worldwide. Currently, HCV-infected patients could undergo antiviral therapy by giving pegylated IFN-α with ribavirin. However, this therapy is only effective in around 50% of patients with HCV genotype 1, which accounts for more than 70% of all HCV infection, and it is not well tolerated for most patients. Moreover, there is no vaccine available. The efforts on identifying protective immunity against HCV have progressed recently. Neutralizing antibodies and robust T cell responses including both CD4(+) and CD8(+) have been shown to be related to the clearance of HCV, which have shed lights on the potential success of HCV vaccines. There are many vaccines developed and tested before entering clinical trials. Here, we would first discuss strategies of viral immune evasion and correlates of protective host immunity and finally review some prospective vaccine approaches against chronic HCV infection. Hindawi Publishing Corporation 2010 2010-06-13 /pmc/articles/PMC2896694/ /pubmed/20625493 http://dx.doi.org/10.1155/2010/548280 Text en Copyright © 2010 C. I. Yu and B.-L. Chiang. 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 Yu, Chun I Chiang, Bor-Luen A New Insight into Hepatitis C Vaccine Development |
title | A New Insight into Hepatitis C Vaccine Development |
title_full | A New Insight into Hepatitis C Vaccine Development |
title_fullStr | A New Insight into Hepatitis C Vaccine Development |
title_full_unstemmed | A New Insight into Hepatitis C Vaccine Development |
title_short | A New Insight into Hepatitis C Vaccine Development |
title_sort | new insight into hepatitis c vaccine development |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2896694/ https://www.ncbi.nlm.nih.gov/pubmed/20625493 http://dx.doi.org/10.1155/2010/548280 |
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