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Development of Spike Receptor-Binding Domain Nanoparticles as a Vaccine Candidate against SARS-CoV-2 Infection in Ferrets
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), a causative agent of the CoV disease 2019 (COVID-19) pandemic, enters host cells via the interaction of its receptor-binding domain (RBD) of the spike protein with host angiotensin-converting enzyme 2 (ACE2). Therefore, the RBD is a promi...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092224/ https://www.ncbi.nlm.nih.gov/pubmed/33653891 http://dx.doi.org/10.1128/mBio.00230-21 |
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author | Kim, Young-Il Kim, Dokyun Yu, Kwang-Min Seo, Hogyu David Lee, Shin-Ae Casel, Mark Anthony B. Jang, Seung-Gyu Kim, Stephanie Jung, WooRam Lai, Chih-Jen Choi, Young Ki Jung, Jae U. |
author_facet | Kim, Young-Il Kim, Dokyun Yu, Kwang-Min Seo, Hogyu David Lee, Shin-Ae Casel, Mark Anthony B. Jang, Seung-Gyu Kim, Stephanie Jung, WooRam Lai, Chih-Jen Choi, Young Ki Jung, Jae U. |
author_sort | Kim, Young-Il |
collection | PubMed |
description | Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), a causative agent of the CoV disease 2019 (COVID-19) pandemic, enters host cells via the interaction of its receptor-binding domain (RBD) of the spike protein with host angiotensin-converting enzyme 2 (ACE2). Therefore, the RBD is a promising vaccine target to induce protective immunity against SARS-CoV-2 infection. In this study, we report the development of an RBD protein-based vaccine candidate against SARS-CoV-2 using self-assembling Helicobacter pylori-bullfrog ferritin nanoparticles as an antigen delivery system. RBD-ferritin protein purified from mammalian cells efficiently assembled into 24-mer nanoparticles. Sixteen- to 20-month-old ferrets were vaccinated with RBD-ferritin nanoparticles (RBD nanoparticles) by intramuscular or intranasal inoculation. All vaccinated ferrets with RBD nanoparticles produced potent neutralizing antibodies against SARS-CoV-2. Strikingly, vaccinated ferrets demonstrated efficient protection from SARS-CoV-2 challenge, showing no fever, body weight loss, or clinical symptoms. Furthermore, vaccinated ferrets showed rapid clearance of infectious virus in nasal washes and lungs as well as of viral RNA in respiratory organs. This study demonstrates that spike RBD-nanoparticles are an effective protein vaccine candidate against SARS-CoV-2. |
format | Online Article Text |
id | pubmed-8092224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-80922242021-05-04 Development of Spike Receptor-Binding Domain Nanoparticles as a Vaccine Candidate against SARS-CoV-2 Infection in Ferrets Kim, Young-Il Kim, Dokyun Yu, Kwang-Min Seo, Hogyu David Lee, Shin-Ae Casel, Mark Anthony B. Jang, Seung-Gyu Kim, Stephanie Jung, WooRam Lai, Chih-Jen Choi, Young Ki Jung, Jae U. mBio Research Article Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), a causative agent of the CoV disease 2019 (COVID-19) pandemic, enters host cells via the interaction of its receptor-binding domain (RBD) of the spike protein with host angiotensin-converting enzyme 2 (ACE2). Therefore, the RBD is a promising vaccine target to induce protective immunity against SARS-CoV-2 infection. In this study, we report the development of an RBD protein-based vaccine candidate against SARS-CoV-2 using self-assembling Helicobacter pylori-bullfrog ferritin nanoparticles as an antigen delivery system. RBD-ferritin protein purified from mammalian cells efficiently assembled into 24-mer nanoparticles. Sixteen- to 20-month-old ferrets were vaccinated with RBD-ferritin nanoparticles (RBD nanoparticles) by intramuscular or intranasal inoculation. All vaccinated ferrets with RBD nanoparticles produced potent neutralizing antibodies against SARS-CoV-2. Strikingly, vaccinated ferrets demonstrated efficient protection from SARS-CoV-2 challenge, showing no fever, body weight loss, or clinical symptoms. Furthermore, vaccinated ferrets showed rapid clearance of infectious virus in nasal washes and lungs as well as of viral RNA in respiratory organs. This study demonstrates that spike RBD-nanoparticles are an effective protein vaccine candidate against SARS-CoV-2. American Society for Microbiology 2021-03-02 /pmc/articles/PMC8092224/ /pubmed/33653891 http://dx.doi.org/10.1128/mBio.00230-21 Text en Copyright © 2021 Kim et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Kim, Young-Il Kim, Dokyun Yu, Kwang-Min Seo, Hogyu David Lee, Shin-Ae Casel, Mark Anthony B. Jang, Seung-Gyu Kim, Stephanie Jung, WooRam Lai, Chih-Jen Choi, Young Ki Jung, Jae U. Development of Spike Receptor-Binding Domain Nanoparticles as a Vaccine Candidate against SARS-CoV-2 Infection in Ferrets |
title | Development of Spike Receptor-Binding Domain Nanoparticles as a Vaccine Candidate against SARS-CoV-2 Infection in Ferrets |
title_full | Development of Spike Receptor-Binding Domain Nanoparticles as a Vaccine Candidate against SARS-CoV-2 Infection in Ferrets |
title_fullStr | Development of Spike Receptor-Binding Domain Nanoparticles as a Vaccine Candidate against SARS-CoV-2 Infection in Ferrets |
title_full_unstemmed | Development of Spike Receptor-Binding Domain Nanoparticles as a Vaccine Candidate against SARS-CoV-2 Infection in Ferrets |
title_short | Development of Spike Receptor-Binding Domain Nanoparticles as a Vaccine Candidate against SARS-CoV-2 Infection in Ferrets |
title_sort | development of spike receptor-binding domain nanoparticles as a vaccine candidate against sars-cov-2 infection in ferrets |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8092224/ https://www.ncbi.nlm.nih.gov/pubmed/33653891 http://dx.doi.org/10.1128/mBio.00230-21 |
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