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Innate Immune Evasion Mediated by Flaviviridae Non-Structural Proteins
Flaviviridae-caused diseases are a critical, emerging public health problem worldwide. Flaviviridae infections usually cause severe, acute or chronic diseases, such as liver damage and liver cancer resulting from a hepatitis C virus (HCV) infection and high fever and shock caused by yellow fever. Ma...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691642/ https://www.ncbi.nlm.nih.gov/pubmed/28991176 http://dx.doi.org/10.3390/v9100291 |
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author | Chen, Shun Wu, Zhen Wang, Mingshu Cheng, Anchun |
author_facet | Chen, Shun Wu, Zhen Wang, Mingshu Cheng, Anchun |
author_sort | Chen, Shun |
collection | PubMed |
description | Flaviviridae-caused diseases are a critical, emerging public health problem worldwide. Flaviviridae infections usually cause severe, acute or chronic diseases, such as liver damage and liver cancer resulting from a hepatitis C virus (HCV) infection and high fever and shock caused by yellow fever. Many researchers worldwide are investigating the mechanisms by which Flaviviridae cause severe diseases. Flaviviridae can interfere with the host’s innate immunity to achieve their purpose of proliferation. For instance, dengue virus (DENV) NS2A, NS2B3, NS4A, NS4B and NS5; HCV NS2, NS3, NS3/4A, NS4B and NS5A; and West Nile virus (WNV) NS1 and NS4B proteins are involved in immune evasion. This review discusses the interplay between viral non-structural Flaviviridae proteins and relevant host proteins, which leads to the suppression of the host’s innate antiviral immunity. |
format | Online Article Text |
id | pubmed-5691642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-56916422017-11-22 Innate Immune Evasion Mediated by Flaviviridae Non-Structural Proteins Chen, Shun Wu, Zhen Wang, Mingshu Cheng, Anchun Viruses Review Flaviviridae-caused diseases are a critical, emerging public health problem worldwide. Flaviviridae infections usually cause severe, acute or chronic diseases, such as liver damage and liver cancer resulting from a hepatitis C virus (HCV) infection and high fever and shock caused by yellow fever. Many researchers worldwide are investigating the mechanisms by which Flaviviridae cause severe diseases. Flaviviridae can interfere with the host’s innate immunity to achieve their purpose of proliferation. For instance, dengue virus (DENV) NS2A, NS2B3, NS4A, NS4B and NS5; HCV NS2, NS3, NS3/4A, NS4B and NS5A; and West Nile virus (WNV) NS1 and NS4B proteins are involved in immune evasion. This review discusses the interplay between viral non-structural Flaviviridae proteins and relevant host proteins, which leads to the suppression of the host’s innate antiviral immunity. MDPI 2017-10-07 /pmc/articles/PMC5691642/ /pubmed/28991176 http://dx.doi.org/10.3390/v9100291 Text en © 2017 by the authors. 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 Chen, Shun Wu, Zhen Wang, Mingshu Cheng, Anchun Innate Immune Evasion Mediated by Flaviviridae Non-Structural Proteins |
title | Innate Immune Evasion Mediated by Flaviviridae Non-Structural Proteins |
title_full | Innate Immune Evasion Mediated by Flaviviridae Non-Structural Proteins |
title_fullStr | Innate Immune Evasion Mediated by Flaviviridae Non-Structural Proteins |
title_full_unstemmed | Innate Immune Evasion Mediated by Flaviviridae Non-Structural Proteins |
title_short | Innate Immune Evasion Mediated by Flaviviridae Non-Structural Proteins |
title_sort | innate immune evasion mediated by flaviviridae non-structural proteins |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691642/ https://www.ncbi.nlm.nih.gov/pubmed/28991176 http://dx.doi.org/10.3390/v9100291 |
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