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Comparison of the Immunogenicity of HIV-1 CRF07_BC Gag Antigen With or Without a Seven Amino Acid Deletion in p6 Region

HIV-1 CRF07_BC-p6Δ7, a strain with a seven amino acid deletion in the p6 region of the Gag protein, is becoming the dominant strain of HIV transmission among men who have sex with men (MSM) in China. Previous studies demonstrated that HIV-1 patients infected by CRF07_BC-p6Δ7 strain had lower viral l...

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Autores principales: Li, Minchao, Yuan, Yue, Li, Pingchao, Deng, Zhaomin, Wen, Ziyu, Wang, Haiying, Feng, Fengling, Zou, Huachun, Chen, Ling, Tang, Shixing, Sun, Caijun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017423/
https://www.ncbi.nlm.nih.gov/pubmed/35450078
http://dx.doi.org/10.3389/fimmu.2022.850719
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author Li, Minchao
Yuan, Yue
Li, Pingchao
Deng, Zhaomin
Wen, Ziyu
Wang, Haiying
Feng, Fengling
Zou, Huachun
Chen, Ling
Tang, Shixing
Sun, Caijun
author_facet Li, Minchao
Yuan, Yue
Li, Pingchao
Deng, Zhaomin
Wen, Ziyu
Wang, Haiying
Feng, Fengling
Zou, Huachun
Chen, Ling
Tang, Shixing
Sun, Caijun
author_sort Li, Minchao
collection PubMed
description HIV-1 CRF07_BC-p6Δ7, a strain with a seven amino acid deletion in the p6 region of the Gag protein, is becoming the dominant strain of HIV transmission among men who have sex with men (MSM) in China. Previous studies demonstrated that HIV-1 patients infected by CRF07_BC-p6Δ7 strain had lower viral load and slower disease progression than those patients infected with CRF07_BC wild-type strain. However, the underlying mechanism for this observation is not fully clarified yet. In this study, we constructed the recombinant DNA plasmid and adenovirus type 2 (Ad2) vector-based constructs to express the HIV-1 CRF07_BC Gag antigen with or without p6Δ7 mutation and then investigated their immunogenicity in mice. Our results showed that HIV-1 CRF07_BC Gag antigen with p6Δ7 mutation induced a comparable level of Gag-specific antibodies but stronger CD4(+) and CD8(+) T-cell immune responses than that of CRF07_BC Gag (07_BC-wt). Furthermore, we identified a series of T-cell epitopes, which induced strong T-cell immune response and cross-immunity with CRF01_AE Gag. These findings implied that the p6(Gag) protein with a seven amino acid deletion might enhance the Gag immunogenicity in particular cellular immunity, which provides valuable information to clarify the pathogenic mechanism of HIV-1 CRF07_BC-p6Δ7 and to develop precise vaccine strategies against HIV-1 infection.
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spelling pubmed-90174232022-04-20 Comparison of the Immunogenicity of HIV-1 CRF07_BC Gag Antigen With or Without a Seven Amino Acid Deletion in p6 Region Li, Minchao Yuan, Yue Li, Pingchao Deng, Zhaomin Wen, Ziyu Wang, Haiying Feng, Fengling Zou, Huachun Chen, Ling Tang, Shixing Sun, Caijun Front Immunol Immunology HIV-1 CRF07_BC-p6Δ7, a strain with a seven amino acid deletion in the p6 region of the Gag protein, is becoming the dominant strain of HIV transmission among men who have sex with men (MSM) in China. Previous studies demonstrated that HIV-1 patients infected by CRF07_BC-p6Δ7 strain had lower viral load and slower disease progression than those patients infected with CRF07_BC wild-type strain. However, the underlying mechanism for this observation is not fully clarified yet. In this study, we constructed the recombinant DNA plasmid and adenovirus type 2 (Ad2) vector-based constructs to express the HIV-1 CRF07_BC Gag antigen with or without p6Δ7 mutation and then investigated their immunogenicity in mice. Our results showed that HIV-1 CRF07_BC Gag antigen with p6Δ7 mutation induced a comparable level of Gag-specific antibodies but stronger CD4(+) and CD8(+) T-cell immune responses than that of CRF07_BC Gag (07_BC-wt). Furthermore, we identified a series of T-cell epitopes, which induced strong T-cell immune response and cross-immunity with CRF01_AE Gag. These findings implied that the p6(Gag) protein with a seven amino acid deletion might enhance the Gag immunogenicity in particular cellular immunity, which provides valuable information to clarify the pathogenic mechanism of HIV-1 CRF07_BC-p6Δ7 and to develop precise vaccine strategies against HIV-1 infection. Frontiers Media S.A. 2022-04-05 /pmc/articles/PMC9017423/ /pubmed/35450078 http://dx.doi.org/10.3389/fimmu.2022.850719 Text en Copyright © 2022 Li, Yuan, Li, Deng, Wen, Wang, Feng, Zou, Chen, Tang and Sun 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 Immunology
Li, Minchao
Yuan, Yue
Li, Pingchao
Deng, Zhaomin
Wen, Ziyu
Wang, Haiying
Feng, Fengling
Zou, Huachun
Chen, Ling
Tang, Shixing
Sun, Caijun
Comparison of the Immunogenicity of HIV-1 CRF07_BC Gag Antigen With or Without a Seven Amino Acid Deletion in p6 Region
title Comparison of the Immunogenicity of HIV-1 CRF07_BC Gag Antigen With or Without a Seven Amino Acid Deletion in p6 Region
title_full Comparison of the Immunogenicity of HIV-1 CRF07_BC Gag Antigen With or Without a Seven Amino Acid Deletion in p6 Region
title_fullStr Comparison of the Immunogenicity of HIV-1 CRF07_BC Gag Antigen With or Without a Seven Amino Acid Deletion in p6 Region
title_full_unstemmed Comparison of the Immunogenicity of HIV-1 CRF07_BC Gag Antigen With or Without a Seven Amino Acid Deletion in p6 Region
title_short Comparison of the Immunogenicity of HIV-1 CRF07_BC Gag Antigen With or Without a Seven Amino Acid Deletion in p6 Region
title_sort comparison of the immunogenicity of hiv-1 crf07_bc gag antigen with or without a seven amino acid deletion in p6 region
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017423/
https://www.ncbi.nlm.nih.gov/pubmed/35450078
http://dx.doi.org/10.3389/fimmu.2022.850719
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