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Evaluation of Cellular Immunity with ASFV Infection by Swine Leukocyte Antigen (SLA)—Peptide Tetramers

African swine fever virus (ASFV) causes acute hemorrhagic fever in domestic pigs and wild boars, resulting in incalculable economic losses to the pig industry. As the mechanism of viral infection is not clear, protective antigens have not been discovered or identified. In this study, we determined t...

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Autores principales: Sun, Wenqiang, Zhang, He, Fan, Wenhui, He, Lihong, Chen, Teng, Zhou, Xintao, Qi, Yu, Sun, Lei, Hu, Rongliang, Luo, Tingrong, Liu, Wenjun, Li, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8617699/
https://www.ncbi.nlm.nih.gov/pubmed/34835070
http://dx.doi.org/10.3390/v13112264
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author Sun, Wenqiang
Zhang, He
Fan, Wenhui
He, Lihong
Chen, Teng
Zhou, Xintao
Qi, Yu
Sun, Lei
Hu, Rongliang
Luo, Tingrong
Liu, Wenjun
Li, Jing
author_facet Sun, Wenqiang
Zhang, He
Fan, Wenhui
He, Lihong
Chen, Teng
Zhou, Xintao
Qi, Yu
Sun, Lei
Hu, Rongliang
Luo, Tingrong
Liu, Wenjun
Li, Jing
author_sort Sun, Wenqiang
collection PubMed
description African swine fever virus (ASFV) causes acute hemorrhagic fever in domestic pigs and wild boars, resulting in incalculable economic losses to the pig industry. As the mechanism of viral infection is not clear, protective antigens have not been discovered or identified. In this study, we determined that the p30, pp62, p72, and CD2v proteins were all involved in the T cell immune response of live pigs infected with ASFV, among which p72 and pp62 proteins were the strongest. Panoramic scanning was performed on T cell epitopes of the p72 protein, and three high-frequency positive epitopes were selected to construct a swine leukocyte antigen (SLA)-tetramer, and ASFV-specific T cells were detected. Subsequently, the specific T cell and humoral immune responses of ASFV-infected pigs and surviving pigs were compared. The results demonstrate that the specific T cellular immunity responses gradually increased during the infection and were higher than that in the surviving pigs in the late stages of infection. The same trend was observed in specific humoral immune responses, which were highest in surviving pigs. In general, our study provides key information for the exploration of ASFV-specific immune responses and the development of an ASFV vaccine.
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spelling pubmed-86176992021-11-27 Evaluation of Cellular Immunity with ASFV Infection by Swine Leukocyte Antigen (SLA)—Peptide Tetramers Sun, Wenqiang Zhang, He Fan, Wenhui He, Lihong Chen, Teng Zhou, Xintao Qi, Yu Sun, Lei Hu, Rongliang Luo, Tingrong Liu, Wenjun Li, Jing Viruses Article African swine fever virus (ASFV) causes acute hemorrhagic fever in domestic pigs and wild boars, resulting in incalculable economic losses to the pig industry. As the mechanism of viral infection is not clear, protective antigens have not been discovered or identified. In this study, we determined that the p30, pp62, p72, and CD2v proteins were all involved in the T cell immune response of live pigs infected with ASFV, among which p72 and pp62 proteins were the strongest. Panoramic scanning was performed on T cell epitopes of the p72 protein, and three high-frequency positive epitopes were selected to construct a swine leukocyte antigen (SLA)-tetramer, and ASFV-specific T cells were detected. Subsequently, the specific T cell and humoral immune responses of ASFV-infected pigs and surviving pigs were compared. The results demonstrate that the specific T cellular immunity responses gradually increased during the infection and were higher than that in the surviving pigs in the late stages of infection. The same trend was observed in specific humoral immune responses, which were highest in surviving pigs. In general, our study provides key information for the exploration of ASFV-specific immune responses and the development of an ASFV vaccine. MDPI 2021-11-12 /pmc/articles/PMC8617699/ /pubmed/34835070 http://dx.doi.org/10.3390/v13112264 Text en © 2021 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 Article
Sun, Wenqiang
Zhang, He
Fan, Wenhui
He, Lihong
Chen, Teng
Zhou, Xintao
Qi, Yu
Sun, Lei
Hu, Rongliang
Luo, Tingrong
Liu, Wenjun
Li, Jing
Evaluation of Cellular Immunity with ASFV Infection by Swine Leukocyte Antigen (SLA)—Peptide Tetramers
title Evaluation of Cellular Immunity with ASFV Infection by Swine Leukocyte Antigen (SLA)—Peptide Tetramers
title_full Evaluation of Cellular Immunity with ASFV Infection by Swine Leukocyte Antigen (SLA)—Peptide Tetramers
title_fullStr Evaluation of Cellular Immunity with ASFV Infection by Swine Leukocyte Antigen (SLA)—Peptide Tetramers
title_full_unstemmed Evaluation of Cellular Immunity with ASFV Infection by Swine Leukocyte Antigen (SLA)—Peptide Tetramers
title_short Evaluation of Cellular Immunity with ASFV Infection by Swine Leukocyte Antigen (SLA)—Peptide Tetramers
title_sort evaluation of cellular immunity with asfv infection by swine leukocyte antigen (sla)—peptide tetramers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8617699/
https://www.ncbi.nlm.nih.gov/pubmed/34835070
http://dx.doi.org/10.3390/v13112264
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