Immunological enhancement of micro-nanoparticle formulated with risedronate and zinc as vaccine adjuvant in aged mice

Abstract Background Elderly individuals face heightened susceptibility to infectious diseases and diminished vaccine responses. Vaccine adjuvants offer a solution. Despite aluminum adjuvant’s long history, its limitations in inducing strong cellular immunity and protecting immunocompromised individu...

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Main Authors: Yue Liu, Man Yang, Meifeng Nie, Shuyu Wu, Rong Su, Dekui Qiu, Shouneng Lu, Hualong Xiong, Jinlei Zhang, Shengxiang Ge, Quan Yuan, Qinjian Zhao, Tianying Zhang, Yingbin Wang, Ningshao Xia
Format: Article
Language:English
Published: BMC 2025-05-01
Series:Immunity & Ageing
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Online Access:https://doi.org/10.1186/s12979-025-00512-0
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author Yue Liu
Man Yang
Meifeng Nie
Shuyu Wu
Rong Su
Dekui Qiu
Shouneng Lu
Hualong Xiong
Jinlei Zhang
Shengxiang Ge
Quan Yuan
Qinjian Zhao
Tianying Zhang
Yingbin Wang
Ningshao Xia
author_facet Yue Liu
Man Yang
Meifeng Nie
Shuyu Wu
Rong Su
Dekui Qiu
Shouneng Lu
Hualong Xiong
Jinlei Zhang
Shengxiang Ge
Quan Yuan
Qinjian Zhao
Tianying Zhang
Yingbin Wang
Ningshao Xia
author_sort Yue Liu
collection DOAJ
description Abstract Background Elderly individuals face heightened susceptibility to infectious diseases and diminished vaccine responses. Vaccine adjuvants offer a solution. Despite aluminum adjuvant’s long history, its limitations in inducing strong cellular immunity and protecting immunocompromised individuals restrict its application. Building upon our previous development of zinc salt particle-based risedronate (Zn-RS), we systematically investigated the immunoenhancing effects of Zn-RS in aged mice and thoroughly explored the underlying mechanisms responsible for these observations in this study. Results Compared to formulations using aluminum adjuvant, Zn-RS combined with either varicella-zoster virus glycoprotein E (gE) or SARS-CoV-2 monovalent STFK protein (STFK) elicited significantly higher IgG and neutralization titers, as well as superior long-term humoral immunity. Moreover, Zn-RS induced greater quantities of dendritic cells (DCs), antigen-presenting cells (APCs), follicular helper T (TFH) cells, Th1/Th2/Th9/Th17 type immune cells, germinal center B cells (GCBs) and plasma cells. Conclusions These findings support Zn-RS as a promising adjuvant candidate for elderly populations, warranting further exploration of its mechanisms and potential applications.
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spelling doaj-art-bcadc9dd257e463693f5749755d3869b2025-08-20T02:25:17ZengBMCImmunity & Ageing1742-49332025-05-0122111510.1186/s12979-025-00512-0Immunological enhancement of micro-nanoparticle formulated with risedronate and zinc as vaccine adjuvant in aged miceYue Liu0Man Yang1Meifeng Nie2Shuyu Wu3Rong Su4Dekui Qiu5Shouneng Lu6Hualong Xiong7Jinlei Zhang8Shengxiang Ge9Quan Yuan10Qinjian Zhao11Tianying Zhang12Yingbin Wang13Ningshao Xia14State Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, School of Public Health & School of Life Sciences, Xiamen UniversityState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, School of Public Health & School of Life Sciences, Xiamen UniversityState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, School of Public Health & School of Life Sciences, Xiamen UniversityState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, School of Public Health & School of Life Sciences, Xiamen UniversityState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, School of Public Health & School of Life Sciences, Xiamen UniversityState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, School of Public Health & School of Life Sciences, Xiamen UniversityState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, School of Public Health & School of Life Sciences, Xiamen UniversityState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, School of Public Health & School of Life Sciences, Xiamen UniversityState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, School of Public Health & School of Life Sciences, Xiamen UniversityState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, School of Public Health & School of Life Sciences, Xiamen UniversityState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, School of Public Health & School of Life Sciences, Xiamen UniversityCollege of Pharmacy, Chongqing Medical UniversityState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, School of Public Health & School of Life Sciences, Xiamen UniversityState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, School of Public Health & School of Life Sciences, Xiamen UniversityState Key Laboratory of Vaccines for Infectious Diseases, Xiang An Biomedicine Laboratory, School of Public Health & School of Life Sciences, Xiamen UniversityAbstract Background Elderly individuals face heightened susceptibility to infectious diseases and diminished vaccine responses. Vaccine adjuvants offer a solution. Despite aluminum adjuvant’s long history, its limitations in inducing strong cellular immunity and protecting immunocompromised individuals restrict its application. Building upon our previous development of zinc salt particle-based risedronate (Zn-RS), we systematically investigated the immunoenhancing effects of Zn-RS in aged mice and thoroughly explored the underlying mechanisms responsible for these observations in this study. Results Compared to formulations using aluminum adjuvant, Zn-RS combined with either varicella-zoster virus glycoprotein E (gE) or SARS-CoV-2 monovalent STFK protein (STFK) elicited significantly higher IgG and neutralization titers, as well as superior long-term humoral immunity. Moreover, Zn-RS induced greater quantities of dendritic cells (DCs), antigen-presenting cells (APCs), follicular helper T (TFH) cells, Th1/Th2/Th9/Th17 type immune cells, germinal center B cells (GCBs) and plasma cells. Conclusions These findings support Zn-RS as a promising adjuvant candidate for elderly populations, warranting further exploration of its mechanisms and potential applications.https://doi.org/10.1186/s12979-025-00512-0RisedronateVaccine adjuvantAged miceImmune enhancementMechanism
spellingShingle Yue Liu
Man Yang
Meifeng Nie
Shuyu Wu
Rong Su
Dekui Qiu
Shouneng Lu
Hualong Xiong
Jinlei Zhang
Shengxiang Ge
Quan Yuan
Qinjian Zhao
Tianying Zhang
Yingbin Wang
Ningshao Xia
Immunological enhancement of micro-nanoparticle formulated with risedronate and zinc as vaccine adjuvant in aged mice
Immunity & Ageing
Risedronate
Vaccine adjuvant
Aged mice
Immune enhancement
Mechanism
title Immunological enhancement of micro-nanoparticle formulated with risedronate and zinc as vaccine adjuvant in aged mice
title_full Immunological enhancement of micro-nanoparticle formulated with risedronate and zinc as vaccine adjuvant in aged mice
title_fullStr Immunological enhancement of micro-nanoparticle formulated with risedronate and zinc as vaccine adjuvant in aged mice
title_full_unstemmed Immunological enhancement of micro-nanoparticle formulated with risedronate and zinc as vaccine adjuvant in aged mice
title_short Immunological enhancement of micro-nanoparticle formulated with risedronate and zinc as vaccine adjuvant in aged mice
title_sort immunological enhancement of micro nanoparticle formulated with risedronate and zinc as vaccine adjuvant in aged mice
topic Risedronate
Vaccine adjuvant
Aged mice
Immune enhancement
Mechanism
url https://doi.org/10.1186/s12979-025-00512-0
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