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Immunological Identification and Characterization of the Capsid Scaffold Protein Encoded by UL26.5 of Herpes Simplex Virus Type 2
Herpes simplex virus type 2 (HSV2), a pathogen that causes genital herpes lesions, interferes with the host immune system via various known and unknown mechanisms. This virus has been used to study viral antigenic composition. Convalescent serum from HSV2-infected patients was used to identify viral...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8187855/ https://www.ncbi.nlm.nih.gov/pubmed/34123868 http://dx.doi.org/10.3389/fcimb.2021.649722 |
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author | Li, Xueqi Wang, Jianbin Mou, Tangwei Gao, Yang Wang, Lichun Fan, Shengtao Xu, Xingli Jiang, Guorun Cui, Pingfang Xu, Xiangxiong Duan, Suqin Zhang, Jingjing Li, Dandan Liao, Yun Yu, Li Zhao, Heng Lu, Ming Zhu, Hailian Gu, Ran Zhang, Ying Dong, Wei Li, Qihan |
author_facet | Li, Xueqi Wang, Jianbin Mou, Tangwei Gao, Yang Wang, Lichun Fan, Shengtao Xu, Xingli Jiang, Guorun Cui, Pingfang Xu, Xiangxiong Duan, Suqin Zhang, Jingjing Li, Dandan Liao, Yun Yu, Li Zhao, Heng Lu, Ming Zhu, Hailian Gu, Ran Zhang, Ying Dong, Wei Li, Qihan |
author_sort | Li, Xueqi |
collection | PubMed |
description | Herpes simplex virus type 2 (HSV2), a pathogen that causes genital herpes lesions, interferes with the host immune system via various known and unknown mechanisms. This virus has been used to study viral antigenic composition. Convalescent serum from HSV2-infected patients was used to identify viral antigens via 2-D protein electrophoresis and immunoblotting. The serum predominantly recognized several capsid scaffold proteins encoded by gene UL26.5, mainly ICP35. This protein has been primarily reported to function temporarily in viral assembly but is not expressed in mature virus particles. Further immunological studies suggested that this protein elicits specific antibody and cytotoxic T lymphocyte (CTL) responses in mice, but these responses do not result in a clinical protective effect in response to HSV2 challenge. The data suggested that immunodominance of ICP35 might be used to design an integrated antigen with other viral glycoproteins. |
format | Online Article Text |
id | pubmed-8187855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81878552021-06-10 Immunological Identification and Characterization of the Capsid Scaffold Protein Encoded by UL26.5 of Herpes Simplex Virus Type 2 Li, Xueqi Wang, Jianbin Mou, Tangwei Gao, Yang Wang, Lichun Fan, Shengtao Xu, Xingli Jiang, Guorun Cui, Pingfang Xu, Xiangxiong Duan, Suqin Zhang, Jingjing Li, Dandan Liao, Yun Yu, Li Zhao, Heng Lu, Ming Zhu, Hailian Gu, Ran Zhang, Ying Dong, Wei Li, Qihan Front Cell Infect Microbiol Cellular and Infection Microbiology Herpes simplex virus type 2 (HSV2), a pathogen that causes genital herpes lesions, interferes with the host immune system via various known and unknown mechanisms. This virus has been used to study viral antigenic composition. Convalescent serum from HSV2-infected patients was used to identify viral antigens via 2-D protein electrophoresis and immunoblotting. The serum predominantly recognized several capsid scaffold proteins encoded by gene UL26.5, mainly ICP35. This protein has been primarily reported to function temporarily in viral assembly but is not expressed in mature virus particles. Further immunological studies suggested that this protein elicits specific antibody and cytotoxic T lymphocyte (CTL) responses in mice, but these responses do not result in a clinical protective effect in response to HSV2 challenge. The data suggested that immunodominance of ICP35 might be used to design an integrated antigen with other viral glycoproteins. Frontiers Media S.A. 2021-05-26 /pmc/articles/PMC8187855/ /pubmed/34123868 http://dx.doi.org/10.3389/fcimb.2021.649722 Text en Copyright © 2021 Li, Wang, Mou, Gao, Wang, Fan, Xu, Jiang, Cui, Xu, Duan, Zhang, Li, Liao, Yu, Zhao, Lu, Zhu, Gu, Zhang, Dong and Li https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Li, Xueqi Wang, Jianbin Mou, Tangwei Gao, Yang Wang, Lichun Fan, Shengtao Xu, Xingli Jiang, Guorun Cui, Pingfang Xu, Xiangxiong Duan, Suqin Zhang, Jingjing Li, Dandan Liao, Yun Yu, Li Zhao, Heng Lu, Ming Zhu, Hailian Gu, Ran Zhang, Ying Dong, Wei Li, Qihan Immunological Identification and Characterization of the Capsid Scaffold Protein Encoded by UL26.5 of Herpes Simplex Virus Type 2 |
title | Immunological Identification and Characterization of the Capsid Scaffold Protein Encoded by UL26.5 of Herpes Simplex Virus Type 2 |
title_full | Immunological Identification and Characterization of the Capsid Scaffold Protein Encoded by UL26.5 of Herpes Simplex Virus Type 2 |
title_fullStr | Immunological Identification and Characterization of the Capsid Scaffold Protein Encoded by UL26.5 of Herpes Simplex Virus Type 2 |
title_full_unstemmed | Immunological Identification and Characterization of the Capsid Scaffold Protein Encoded by UL26.5 of Herpes Simplex Virus Type 2 |
title_short | Immunological Identification and Characterization of the Capsid Scaffold Protein Encoded by UL26.5 of Herpes Simplex Virus Type 2 |
title_sort | immunological identification and characterization of the capsid scaffold protein encoded by ul26.5 of herpes simplex virus type 2 |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8187855/ https://www.ncbi.nlm.nih.gov/pubmed/34123868 http://dx.doi.org/10.3389/fcimb.2021.649722 |
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