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Development of spike receptor-binding domain nanoparticle as a vaccine candidate against SARS-CoV-2 infection in ferrets
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), a causative agent of COVID-19 pandemic, enters host cells via the interaction of its Receptor-Binding Domain (RBD) of Spike protein with host Angiotensin-Converting Enzyme 2 (ACE2). Therefore, RBD is a promising vaccine target to induce p...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7852231/ https://www.ncbi.nlm.nih.gov/pubmed/33532767 http://dx.doi.org/10.1101/2021.01.28.428743 |
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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 COVID-19 pandemic, enters host cells via the interaction of its Receptor-Binding Domain (RBD) of Spike protein with host Angiotensin-Converting Enzyme 2 (ACE2). Therefore, RBD is a promising vaccine target to induce protective immunity against SARS-CoV-2 infection. In this study, we report the development of RBD protein-based vaccine candidate against SARS-CoV-2 using self-assembling H. pylori-bullfrog ferritin nanoparticles as an antigen delivery. RBD-ferritin protein purified from mammalian cells efficiently assembled into 24-mer nanoparticles. 16–20 months-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 and clinical symptoms. Furthermore, vaccinated ferrets showed rapid clearance of infectious viruses in nasal washes and lungs as well as viral RNA in respiratory organs. This study demonstrates the Spike RBD-nanoparticle as an effective protein vaccine candidate against SARS-CoV-2. |
format | Online Article Text |
id | pubmed-7852231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-78522312021-02-03 Development of spike receptor-binding domain nanoparticle 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. bioRxiv Article Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), a causative agent of COVID-19 pandemic, enters host cells via the interaction of its Receptor-Binding Domain (RBD) of Spike protein with host Angiotensin-Converting Enzyme 2 (ACE2). Therefore, RBD is a promising vaccine target to induce protective immunity against SARS-CoV-2 infection. In this study, we report the development of RBD protein-based vaccine candidate against SARS-CoV-2 using self-assembling H. pylori-bullfrog ferritin nanoparticles as an antigen delivery. RBD-ferritin protein purified from mammalian cells efficiently assembled into 24-mer nanoparticles. 16–20 months-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 and clinical symptoms. Furthermore, vaccinated ferrets showed rapid clearance of infectious viruses in nasal washes and lungs as well as viral RNA in respiratory organs. This study demonstrates the Spike RBD-nanoparticle as an effective protein vaccine candidate against SARS-CoV-2. Cold Spring Harbor Laboratory 2021-01-29 /pmc/articles/PMC7852231/ /pubmed/33532767 http://dx.doi.org/10.1101/2021.01.28.428743 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | 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 nanoparticle as a vaccine candidate against SARS-CoV-2 infection in ferrets |
title | Development of spike receptor-binding domain nanoparticle as a vaccine candidate against SARS-CoV-2 infection in ferrets |
title_full | Development of spike receptor-binding domain nanoparticle as a vaccine candidate against SARS-CoV-2 infection in ferrets |
title_fullStr | Development of spike receptor-binding domain nanoparticle as a vaccine candidate against SARS-CoV-2 infection in ferrets |
title_full_unstemmed | Development of spike receptor-binding domain nanoparticle as a vaccine candidate against SARS-CoV-2 infection in ferrets |
title_short | Development of spike receptor-binding domain nanoparticle as a vaccine candidate against SARS-CoV-2 infection in ferrets |
title_sort | development of spike receptor-binding domain nanoparticle as a vaccine candidate against sars-cov-2 infection in ferrets |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7852231/ https://www.ncbi.nlm.nih.gov/pubmed/33532767 http://dx.doi.org/10.1101/2021.01.28.428743 |
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