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Immune Escape Mechanism and Vaccine Research Progress of African Swine Fever Virus

African swine fever virus (ASFV) is the causative agent of the epidemic of African swine fever (ASF), with virulent strains having a mortality rate of up to 100% and presenting devastating impacts on animal farming. Since ASF was first reported in China in 2018, ASFV still exists and poses a potenti...

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Autores principales: Wang, Zhaoyang, Ai, Qiangyun, Huang, Shenglin, Ou, Yating, Gao, Yinze, Tong, Tiezhu, Fan, Huiying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8949402/
https://www.ncbi.nlm.nih.gov/pubmed/35334976
http://dx.doi.org/10.3390/vaccines10030344
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author Wang, Zhaoyang
Ai, Qiangyun
Huang, Shenglin
Ou, Yating
Gao, Yinze
Tong, Tiezhu
Fan, Huiying
author_facet Wang, Zhaoyang
Ai, Qiangyun
Huang, Shenglin
Ou, Yating
Gao, Yinze
Tong, Tiezhu
Fan, Huiying
author_sort Wang, Zhaoyang
collection PubMed
description African swine fever virus (ASFV) is the causative agent of the epidemic of African swine fever (ASF), with virulent strains having a mortality rate of up to 100% and presenting devastating impacts on animal farming. Since ASF was first reported in China in 2018, ASFV still exists and poses a potential threat to the current pig industry. Low-virulence and genotype I strains of ASFV have been reported in China, and the prevention and control of ASF is more complicated. Insufficient understanding of the interaction of ASFV with the host immune system hinders vaccine development. Physical barriers, nonspecific immune response and acquired immunity are the three barriers of the host against infection. To escape the innate immune response, ASFV invades monocytes/macrophages and dendritic cells, thereby inhibiting IFN expression, regulating cytokine expression and the body’s inflammatory response process. Meanwhile, in order to evade the adaptive immune response, ASFV inhibits antigen presentation, induces the production of non-neutralizing antibodies, and inhibits apoptosis. Recently, significant advances have been achieved in vaccine development around the world. Live attenuated vaccines (LAVs) based on artificially deleting specific virulence genes can achieve 100% homologous protection and partial heterologous protection. The key of subunit vaccines is identifying the combination of antigens that can effectively provide protection and selecting carriers that can effectively deliver the antigens. In this review, we introduce the epidemic trend of ASF and the impact on the pig industry, analyze the interaction mechanism between ASFV and the body’s immune system, and compare the current status of potential vaccines in order to provide a reference for the development of effective ASF vaccines.
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spelling pubmed-89494022022-03-26 Immune Escape Mechanism and Vaccine Research Progress of African Swine Fever Virus Wang, Zhaoyang Ai, Qiangyun Huang, Shenglin Ou, Yating Gao, Yinze Tong, Tiezhu Fan, Huiying Vaccines (Basel) Review African swine fever virus (ASFV) is the causative agent of the epidemic of African swine fever (ASF), with virulent strains having a mortality rate of up to 100% and presenting devastating impacts on animal farming. Since ASF was first reported in China in 2018, ASFV still exists and poses a potential threat to the current pig industry. Low-virulence and genotype I strains of ASFV have been reported in China, and the prevention and control of ASF is more complicated. Insufficient understanding of the interaction of ASFV with the host immune system hinders vaccine development. Physical barriers, nonspecific immune response and acquired immunity are the three barriers of the host against infection. To escape the innate immune response, ASFV invades monocytes/macrophages and dendritic cells, thereby inhibiting IFN expression, regulating cytokine expression and the body’s inflammatory response process. Meanwhile, in order to evade the adaptive immune response, ASFV inhibits antigen presentation, induces the production of non-neutralizing antibodies, and inhibits apoptosis. Recently, significant advances have been achieved in vaccine development around the world. Live attenuated vaccines (LAVs) based on artificially deleting specific virulence genes can achieve 100% homologous protection and partial heterologous protection. The key of subunit vaccines is identifying the combination of antigens that can effectively provide protection and selecting carriers that can effectively deliver the antigens. In this review, we introduce the epidemic trend of ASF and the impact on the pig industry, analyze the interaction mechanism between ASFV and the body’s immune system, and compare the current status of potential vaccines in order to provide a reference for the development of effective ASF vaccines. MDPI 2022-02-22 /pmc/articles/PMC8949402/ /pubmed/35334976 http://dx.doi.org/10.3390/vaccines10030344 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Wang, Zhaoyang
Ai, Qiangyun
Huang, Shenglin
Ou, Yating
Gao, Yinze
Tong, Tiezhu
Fan, Huiying
Immune Escape Mechanism and Vaccine Research Progress of African Swine Fever Virus
title Immune Escape Mechanism and Vaccine Research Progress of African Swine Fever Virus
title_full Immune Escape Mechanism and Vaccine Research Progress of African Swine Fever Virus
title_fullStr Immune Escape Mechanism and Vaccine Research Progress of African Swine Fever Virus
title_full_unstemmed Immune Escape Mechanism and Vaccine Research Progress of African Swine Fever Virus
title_short Immune Escape Mechanism and Vaccine Research Progress of African Swine Fever Virus
title_sort immune escape mechanism and vaccine research progress of african swine fever virus
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8949402/
https://www.ncbi.nlm.nih.gov/pubmed/35334976
http://dx.doi.org/10.3390/vaccines10030344
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