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Comparative tissue proteomics reveals unique action mechanisms of vaccine adjuvants

Radiofrequency adjuvant (RFA) was recently developed to boost influenza vaccination without the safety concerns of chemical adjuvants due to their physical nature. Yet, the action mechanisms of RFA remain largely unknown. Omics techniques offer new opportunities to identify molecular mechanisms of R...

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Detalles Bibliográficos
Autores principales: Li, Yibo, Li, Zhuofan, Chen, Xinyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813788/
https://www.ncbi.nlm.nih.gov/pubmed/36619976
http://dx.doi.org/10.1016/j.isci.2022.105800
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author Li, Yibo
Li, Zhuofan
Chen, Xinyuan
author_facet Li, Yibo
Li, Zhuofan
Chen, Xinyuan
author_sort Li, Yibo
collection PubMed
description Radiofrequency adjuvant (RFA) was recently developed to boost influenza vaccination without the safety concerns of chemical adjuvants due to their physical nature. Yet, the action mechanisms of RFA remain largely unknown. Omics techniques offer new opportunities to identify molecular mechanisms of RFA. This study utilized comparative tissue proteomics to explore molecular mechanisms of the physical RFA. Comparison of RFA and chemical adjuvant (Alum, AddaVax, MPL, MPL/Alum)-induced tissue proteome changes identified 14 exclusively induced proteins by RFA, among which heat shock protein (HSP) 70 was selected for further analysis due to its known immune-modulating functions. RFA showed much weakened ability to boost ovalbumin and pandemic influenza vaccination in HSP70 knockout than wild-type mice, hinting crucial roles of HSP70 in RFA effects. This study supports comparative tissue proteomics to be an effective tool to study molecular mechanisms of vaccine adjuvants.
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spelling pubmed-98137882023-01-06 Comparative tissue proteomics reveals unique action mechanisms of vaccine adjuvants Li, Yibo Li, Zhuofan Chen, Xinyuan iScience Article Radiofrequency adjuvant (RFA) was recently developed to boost influenza vaccination without the safety concerns of chemical adjuvants due to their physical nature. Yet, the action mechanisms of RFA remain largely unknown. Omics techniques offer new opportunities to identify molecular mechanisms of RFA. This study utilized comparative tissue proteomics to explore molecular mechanisms of the physical RFA. Comparison of RFA and chemical adjuvant (Alum, AddaVax, MPL, MPL/Alum)-induced tissue proteome changes identified 14 exclusively induced proteins by RFA, among which heat shock protein (HSP) 70 was selected for further analysis due to its known immune-modulating functions. RFA showed much weakened ability to boost ovalbumin and pandemic influenza vaccination in HSP70 knockout than wild-type mice, hinting crucial roles of HSP70 in RFA effects. This study supports comparative tissue proteomics to be an effective tool to study molecular mechanisms of vaccine adjuvants. Elsevier 2022-12-14 /pmc/articles/PMC9813788/ /pubmed/36619976 http://dx.doi.org/10.1016/j.isci.2022.105800 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Li, Yibo
Li, Zhuofan
Chen, Xinyuan
Comparative tissue proteomics reveals unique action mechanisms of vaccine adjuvants
title Comparative tissue proteomics reveals unique action mechanisms of vaccine adjuvants
title_full Comparative tissue proteomics reveals unique action mechanisms of vaccine adjuvants
title_fullStr Comparative tissue proteomics reveals unique action mechanisms of vaccine adjuvants
title_full_unstemmed Comparative tissue proteomics reveals unique action mechanisms of vaccine adjuvants
title_short Comparative tissue proteomics reveals unique action mechanisms of vaccine adjuvants
title_sort comparative tissue proteomics reveals unique action mechanisms of vaccine adjuvants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813788/
https://www.ncbi.nlm.nih.gov/pubmed/36619976
http://dx.doi.org/10.1016/j.isci.2022.105800
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