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Development of Preventive Vaccines for Hepatitis C Virus E1/E2 Protein
Hepatitis C virus (HCV) is responsible for a vast majority of liver failure cases. HCV is a kind of blood disease estimated to chronically infect 3% of the worlds population, causing significant morbidity and mortality. Therefore, a complete knowledge of humoral responses against HCV, resulting anti...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Iranian Society of Pathology
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6339490/ https://www.ncbi.nlm.nih.gov/pubmed/30697280 |
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author | Ghasemi, Faezeh Ghayour-Mobarhan, Majid Gouklani, Hamed Meshkat, Zahra |
author_facet | Ghasemi, Faezeh Ghayour-Mobarhan, Majid Gouklani, Hamed Meshkat, Zahra |
author_sort | Ghasemi, Faezeh |
collection | PubMed |
description | Hepatitis C virus (HCV) is responsible for a vast majority of liver failure cases. HCV is a kind of blood disease estimated to chronically infect 3% of the worlds population, causing significant morbidity and mortality. Therefore, a complete knowledge of humoral responses against HCV, resulting antibodies, and virus-receptor and virus-antibody interactions, are essential to design a vaccine. HCV epitopes or full sequence of HCV proteins can induce HCV specific immune responses. In fact, structural proteins are usually the main target of humoral responses and non-structural proteins are usually the main target of cellular responses. Hence, various vaccines based on distinct antigenic combinations are developed to prevent HCV infection and the current study tried to summarize them. |
format | Online Article Text |
id | pubmed-6339490 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Iranian Society of Pathology |
record_format | MEDLINE/PubMed |
spelling | pubmed-63394902019-01-29 Development of Preventive Vaccines for Hepatitis C Virus E1/E2 Protein Ghasemi, Faezeh Ghayour-Mobarhan, Majid Gouklani, Hamed Meshkat, Zahra Iran J Pathol Review Article Hepatitis C virus (HCV) is responsible for a vast majority of liver failure cases. HCV is a kind of blood disease estimated to chronically infect 3% of the worlds population, causing significant morbidity and mortality. Therefore, a complete knowledge of humoral responses against HCV, resulting antibodies, and virus-receptor and virus-antibody interactions, are essential to design a vaccine. HCV epitopes or full sequence of HCV proteins can induce HCV specific immune responses. In fact, structural proteins are usually the main target of humoral responses and non-structural proteins are usually the main target of cellular responses. Hence, various vaccines based on distinct antigenic combinations are developed to prevent HCV infection and the current study tried to summarize them. Iranian Society of Pathology 2018 2018-07-17 /pmc/articles/PMC6339490/ /pubmed/30697280 Text en © 2018, IRANIAN JOURNAL OF PATHOLOGY This is an open-access article distributed under the terms of the Creative Commons Attribution-noncommercial 4.0 International License, (https://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited. |
spellingShingle | Review Article Ghasemi, Faezeh Ghayour-Mobarhan, Majid Gouklani, Hamed Meshkat, Zahra Development of Preventive Vaccines for Hepatitis C Virus E1/E2 Protein |
title | Development of Preventive Vaccines for Hepatitis C Virus E1/E2 Protein |
title_full | Development of Preventive Vaccines for Hepatitis C Virus E1/E2 Protein |
title_fullStr | Development of Preventive Vaccines for Hepatitis C Virus E1/E2 Protein |
title_full_unstemmed | Development of Preventive Vaccines for Hepatitis C Virus E1/E2 Protein |
title_short | Development of Preventive Vaccines for Hepatitis C Virus E1/E2 Protein |
title_sort | development of preventive vaccines for hepatitis c virus e1/e2 protein |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6339490/ https://www.ncbi.nlm.nih.gov/pubmed/30697280 |
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