Immune Response of A Novel ATR-AP205-001 Conjugate Anti-hypertensive Vaccine

Abstract We developed a virus-like particle (VLP)-based therapeutic vaccine against angiotensin II receptor type 1, ATR-AP205-001, which could significantly reduce the blood pressure and protect target organs of hypertensive animals. In this study, we focused on the immunological effect and safety o...

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Autores principales: Xiajun Hu, Yihuan Deng, Xiao Chen, Yanzhao Zhou, Hongrong Zhang, Hailang Wu, Shijun Yang, Fen Chen, Zihua Zhou, Min Wang, Zhihua Qiu, Yuhua Liao
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Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/462bb5a5eafc4ab8b2d68050165b2407
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spelling oai:doaj.org-article:462bb5a5eafc4ab8b2d68050165b24072021-12-02T15:05:50ZImmune Response of A Novel ATR-AP205-001 Conjugate Anti-hypertensive Vaccine10.1038/s41598-017-12996-y2045-2322https://doaj.org/article/462bb5a5eafc4ab8b2d68050165b24072017-10-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-12996-yhttps://doaj.org/toc/2045-2322Abstract We developed a virus-like particle (VLP)-based therapeutic vaccine against angiotensin II receptor type 1, ATR-AP205-001, which could significantly reduce the blood pressure and protect target organs of hypertensive animals. In this study, we focused on the immunological effect and safety of the VLP-based vaccine. By comparing to the depolymerized dimeric vaccine ATR-Dimer-001, we found that ATR-AP205-001 reached subcapsular sinus of lymph node shortly after administration, followed by accumulation on follicle dendritic cells via follicle B cell transportation, while ATR-Dimer-001 vaccine showed no association with FDCs. ATR-AP205-001 vaccine strongly activated dendritic cells, which promoted T cells differentiation to follicular helper T cells. ATR-AP205-001 vaccine induced powerful germinal center reaction, which was translated to a boost of specific antibody production and long-lasting B cell memory, far superior to ATR-Dimer-001 vaccine. Moreover, neither cytotoxic T cells, nor Th1/Th17 cell-mediated inflammation was observed in ATR-AP205-001 vaccine, similar to ATR-Dimer-001 vaccine. We concluded that ATR-AP205-001 vaccine quickly induced potent humoral immunity through collaboration of B cells, follicular dendritic cells and follicular helper T cells, providing an effective and safe intervention for hypertension in the future clinical application.Xiajun HuYihuan DengXiao ChenYanzhao ZhouHongrong ZhangHailang WuShijun YangFen ChenZihua ZhouMin WangZhihua QiuYuhua LiaoNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-13 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Xiajun Hu
Yihuan Deng
Xiao Chen
Yanzhao Zhou
Hongrong Zhang
Hailang Wu
Shijun Yang
Fen Chen
Zihua Zhou
Min Wang
Zhihua Qiu
Yuhua Liao
Immune Response of A Novel ATR-AP205-001 Conjugate Anti-hypertensive Vaccine
description Abstract We developed a virus-like particle (VLP)-based therapeutic vaccine against angiotensin II receptor type 1, ATR-AP205-001, which could significantly reduce the blood pressure and protect target organs of hypertensive animals. In this study, we focused on the immunological effect and safety of the VLP-based vaccine. By comparing to the depolymerized dimeric vaccine ATR-Dimer-001, we found that ATR-AP205-001 reached subcapsular sinus of lymph node shortly after administration, followed by accumulation on follicle dendritic cells via follicle B cell transportation, while ATR-Dimer-001 vaccine showed no association with FDCs. ATR-AP205-001 vaccine strongly activated dendritic cells, which promoted T cells differentiation to follicular helper T cells. ATR-AP205-001 vaccine induced powerful germinal center reaction, which was translated to a boost of specific antibody production and long-lasting B cell memory, far superior to ATR-Dimer-001 vaccine. Moreover, neither cytotoxic T cells, nor Th1/Th17 cell-mediated inflammation was observed in ATR-AP205-001 vaccine, similar to ATR-Dimer-001 vaccine. We concluded that ATR-AP205-001 vaccine quickly induced potent humoral immunity through collaboration of B cells, follicular dendritic cells and follicular helper T cells, providing an effective and safe intervention for hypertension in the future clinical application.
format article
author Xiajun Hu
Yihuan Deng
Xiao Chen
Yanzhao Zhou
Hongrong Zhang
Hailang Wu
Shijun Yang
Fen Chen
Zihua Zhou
Min Wang
Zhihua Qiu
Yuhua Liao
author_facet Xiajun Hu
Yihuan Deng
Xiao Chen
Yanzhao Zhou
Hongrong Zhang
Hailang Wu
Shijun Yang
Fen Chen
Zihua Zhou
Min Wang
Zhihua Qiu
Yuhua Liao
author_sort Xiajun Hu
title Immune Response of A Novel ATR-AP205-001 Conjugate Anti-hypertensive Vaccine
title_short Immune Response of A Novel ATR-AP205-001 Conjugate Anti-hypertensive Vaccine
title_full Immune Response of A Novel ATR-AP205-001 Conjugate Anti-hypertensive Vaccine
title_fullStr Immune Response of A Novel ATR-AP205-001 Conjugate Anti-hypertensive Vaccine
title_full_unstemmed Immune Response of A Novel ATR-AP205-001 Conjugate Anti-hypertensive Vaccine
title_sort immune response of a novel atr-ap205-001 conjugate anti-hypertensive vaccine
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/462bb5a5eafc4ab8b2d68050165b2407
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