A prophylactic effect of aluminium-based adjuvants against respiratory viruses via priming local innate immunity.
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Authors
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Wang, Xin1, 2
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Yin, Xiaochen1
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Zhang, Boya1
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Liu, Chenfeng3
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Lin, Yahua1
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Huang, Xiaofen1
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Li, Yufang1
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Shen, Chenguang1
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Zheng, Weibin4
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Fu, Guofeng4
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Chen, Junyu1
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Wen, Yanling2
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Zhang, Wei1
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Pan, Bo-Sheng5
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Fang, Mujin1
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Zheng, Zizheng1
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Zhang, Zheng2
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Yuan, Quan1
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Fu, Guo4
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Li, Shaowei1
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Zhang, Jun1
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Chen, Yixin1
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Xia, Ningshao1
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Zhao, Qinjian1, 6
And 4 more
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1
State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, National Institute of Diagnostics and Vaccine Development in Infectious Diseases, School of Public Health, Xiamen University, Xiamen, People's Republic of China.
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(China)
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2
Institute for Hepatology, National Clinical Research Center for Infectious Disease, Shenzhen Third People's Hospital; The Second Affiliated Hospital, School of Medicine, Southern University of Science and Technology, Shenzhen, People's Republic of China.
,
(China)
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3
Department of Cell Biology, School of Life Science, Anhui Medical University, Hefei, People's Republic of China.
,
(China)
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4
School of Life Science, Xiamen University, Xiamen, People's Republic of China.
,
(China)
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5
Reverie Labs, Cambridge, MA, USA.
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6
College of Pharmacy, Chongqing Medical University, Chongqing, People's Republic of China.
,
(China)
- Type
- Published Article
- Journal
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Emerging microbes & infections
- Publication Date
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Dec 01, 2022
- Volume
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11
- Issue
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1
- Pages
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914–925
- Identifiers
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DOI: 10.1080/22221751.2022.2050951
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PMID: 35254215
- Source
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Medline
- Keywords
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- Language
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English
- License
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Unknown
Abstract
Infection caused by respiratory viruses can lead to a severe respiratory disease and even death. Vaccination is the most effective way to prevent the disease, but it cannot be quickly applied when facing an emerging infectious disease. Here, we demonstrated that immunization with an aluminium-zinc hybrid particulate adjuvant (FH-001) alone, bearing great resemblance in morphology with commonly used aluminium-based adjuvants in vaccines, could quickly induce mice to generate a broadly protective immune response to resist the lethal challenge of influenza B viruses. Furthermore, a multi-omics-based analysis revealed that the alveolar macrophage and type I interferon pathway, rather than adaptive immunity and type II interferon pathway, were essential for the observed prophylactic effect of FH-001. More importantly, a similar protective effect was observed against influenza A virus strain A/Shanghai/02/2013(H7N9), A/California/04/2009(H1N1) and respiratory syncytial virus. Therefore, we introduced here a new and promising strategy that can be quickly applied during the outbreak of emerging respiratory viruses.
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
This record was last updated on 04/06/2022 and may not reflect the most current and accurate biomedical/scientific data available from NLM.
The corresponding record at NLM can be accessed at
https://www.ncbi.nlm.nih.gov/pubmed/35254215
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