A potential bivalent mRNA vaccine candidate protects against both RSV and SARS-CoV-2 infections
Copyright © 2024 The American Society of Gene and Cell Therapy. Published by Elsevier Inc. All rights reserved..
As the world continues to confront severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), respiratory syncytial virus (RSV) is also causing severe respiratory illness in millions of infants, elderly individuals, and immunocompromised people globally. Exacerbating the situation is the fact that co-infection with multiple viruses is occurring, something which has greatly increased the clinical severity of the infections. Thus, our team developed a bivalent vaccine that delivered mRNAs encoding SARS-CoV-2 Omicron spike (S) and RSV fusion (F) proteins simultaneously, SF-LNP, which induced S and F protein-specific binding antibodies and cellular immune responses in BALB/c mice. Moreover, SF-LNP immunization effectively protected BALB/c mice from RSV infection and hamsters from SARS-CoV-2 Omicron infection. Notably, our study pointed out the antigenic competition problem of bivalent vaccines and provided a solution. Overall, our results demonstrated the potential of preventing two infectious diseases with a single vaccine and provided a paradigm for the subsequent design of multivalent vaccines.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2024 |
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Erschienen: |
2024 |
Enthalten in: |
Zur Gesamtaufnahme - volume:32 |
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Enthalten in: |
Molecular therapy : the journal of the American Society of Gene Therapy - 32(2024), 4 vom: 03. Apr., Seite 1033-1047 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Wu, Namei [VerfasserIn] |
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Links: |
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Anmerkungen: |
Date Completed 08.04.2024 Date Revised 08.04.2024 published: Print-Electronic Citation Status MEDLINE |
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doi: |
10.1016/j.ymthe.2024.02.011 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM368311236 |
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520 | |a Copyright © 2024 The American Society of Gene and Cell Therapy. Published by Elsevier Inc. All rights reserved. | ||
520 | |a As the world continues to confront severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), respiratory syncytial virus (RSV) is also causing severe respiratory illness in millions of infants, elderly individuals, and immunocompromised people globally. Exacerbating the situation is the fact that co-infection with multiple viruses is occurring, something which has greatly increased the clinical severity of the infections. Thus, our team developed a bivalent vaccine that delivered mRNAs encoding SARS-CoV-2 Omicron spike (S) and RSV fusion (F) proteins simultaneously, SF-LNP, which induced S and F protein-specific binding antibodies and cellular immune responses in BALB/c mice. Moreover, SF-LNP immunization effectively protected BALB/c mice from RSV infection and hamsters from SARS-CoV-2 Omicron infection. Notably, our study pointed out the antigenic competition problem of bivalent vaccines and provided a solution. Overall, our results demonstrated the potential of preventing two infectious diseases with a single vaccine and provided a paradigm for the subsequent design of multivalent vaccines | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a antigen competition | |
650 | 4 | |a bivalent vaccine | |
650 | 4 | |a lipid nanoparticle | |
650 | 4 | |a mRNA | |
650 | 4 | |a respiratory infectious disease | |
650 | 4 | |a respiratory syncytial virus | |
650 | 4 | |a severe acute respiratory syndrome coronavirus 2 | |
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650 | 7 | |a Vaccines, Combined |2 NLM | |
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700 | 1 | |a Zhang, Jiachen |e verfasserin |4 aut | |
700 | 1 | |a Shen, Yanqiong |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Xinghai |e verfasserin |4 aut | |
700 | 1 | |a Zhou, Jinge |e verfasserin |4 aut | |
700 | 1 | |a Wu, Yan |e verfasserin |4 aut | |
700 | 1 | |a Li, Entao |e verfasserin |4 aut | |
700 | 1 | |a Meng, Xiaoming |e verfasserin |4 aut | |
700 | 1 | |a Chuai, Xia |e verfasserin |4 aut | |
700 | 1 | |a Chiu, Sandra |e verfasserin |4 aut | |
700 | 1 | |a Wang, Yucai |e verfasserin |4 aut | |
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