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A single immunization with spike-functionalized ferritin vaccines elicits neutralizing antibody responses against SARS-CoV-2 in mice
Development of a safe and effective SARS-CoV-2 vaccine is a public health priority. We designed subunit vaccine candidates using self-assembling ferritin nanoparticles displaying one of two multimerized SARS-CoV-2 spikes: full-length ectodomain (S-Fer) or a C-terminal 70 amino-acid deletion (SΔC-Fer...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7457616/ https://www.ncbi.nlm.nih.gov/pubmed/32869030 http://dx.doi.org/10.1101/2020.08.28.272518 |
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author | Powell, Abigail E. Zhang, Kaiming Sanyal, Mrinmoy Tang, Shaogeng Weidenbacher, Payton A. Li, Shanshan Pham, Tho D. Pak, John E. Chiu, Wah Kim, Peter S. |
author_facet | Powell, Abigail E. Zhang, Kaiming Sanyal, Mrinmoy Tang, Shaogeng Weidenbacher, Payton A. Li, Shanshan Pham, Tho D. Pak, John E. Chiu, Wah Kim, Peter S. |
author_sort | Powell, Abigail E. |
collection | PubMed |
description | Development of a safe and effective SARS-CoV-2 vaccine is a public health priority. We designed subunit vaccine candidates using self-assembling ferritin nanoparticles displaying one of two multimerized SARS-CoV-2 spikes: full-length ectodomain (S-Fer) or a C-terminal 70 amino-acid deletion (SΔC-Fer). Ferritin is an attractive nanoparticle platform for production of vaccines and ferritin-based vaccines have been investigated in humans in two separate clinical trials. We confirmed proper folding and antigenicity of spike on the surface of ferritin by cryo-EM and binding to conformation-specific monoclonal antibodies. After a single immunization of mice with either of the two spike ferritin particles, a lentiviral SARS-CoV-2 pseudovirus assay revealed mean neutralizing antibody titers at least 2-fold greater than those in convalescent plasma from COVID-19 patients. Additionally, a single dose of SΔC-Fer elicited significantly higher neutralizing responses as compared to immunization with the spike receptor binding domain (RBD) monomer or spike ectodomain trimer alone. After a second dose, mice immunized with SΔC-Fer exhibited higher neutralizing titers than all other groups. Taken together, these results demonstrate that multivalent presentation of SARS-CoV-2 spike on ferritin can notably enhance elicitation of neutralizing antibodies, thus constituting a viable strategy for single-dose vaccination against COVID-19. |
format | Online Article Text |
id | pubmed-7457616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-74576162020-09-01 A single immunization with spike-functionalized ferritin vaccines elicits neutralizing antibody responses against SARS-CoV-2 in mice Powell, Abigail E. Zhang, Kaiming Sanyal, Mrinmoy Tang, Shaogeng Weidenbacher, Payton A. Li, Shanshan Pham, Tho D. Pak, John E. Chiu, Wah Kim, Peter S. bioRxiv Article Development of a safe and effective SARS-CoV-2 vaccine is a public health priority. We designed subunit vaccine candidates using self-assembling ferritin nanoparticles displaying one of two multimerized SARS-CoV-2 spikes: full-length ectodomain (S-Fer) or a C-terminal 70 amino-acid deletion (SΔC-Fer). Ferritin is an attractive nanoparticle platform for production of vaccines and ferritin-based vaccines have been investigated in humans in two separate clinical trials. We confirmed proper folding and antigenicity of spike on the surface of ferritin by cryo-EM and binding to conformation-specific monoclonal antibodies. After a single immunization of mice with either of the two spike ferritin particles, a lentiviral SARS-CoV-2 pseudovirus assay revealed mean neutralizing antibody titers at least 2-fold greater than those in convalescent plasma from COVID-19 patients. Additionally, a single dose of SΔC-Fer elicited significantly higher neutralizing responses as compared to immunization with the spike receptor binding domain (RBD) monomer or spike ectodomain trimer alone. After a second dose, mice immunized with SΔC-Fer exhibited higher neutralizing titers than all other groups. Taken together, these results demonstrate that multivalent presentation of SARS-CoV-2 spike on ferritin can notably enhance elicitation of neutralizing antibodies, thus constituting a viable strategy for single-dose vaccination against COVID-19. Cold Spring Harbor Laboratory 2020-08-28 /pmc/articles/PMC7457616/ /pubmed/32869030 http://dx.doi.org/10.1101/2020.08.28.272518 Text en https://creativecommons.org/licenses/by/4.0/It is made available under a CC-BY 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Powell, Abigail E. Zhang, Kaiming Sanyal, Mrinmoy Tang, Shaogeng Weidenbacher, Payton A. Li, Shanshan Pham, Tho D. Pak, John E. Chiu, Wah Kim, Peter S. A single immunization with spike-functionalized ferritin vaccines elicits neutralizing antibody responses against SARS-CoV-2 in mice |
title | A single immunization with spike-functionalized ferritin vaccines elicits neutralizing antibody responses against SARS-CoV-2 in mice |
title_full | A single immunization with spike-functionalized ferritin vaccines elicits neutralizing antibody responses against SARS-CoV-2 in mice |
title_fullStr | A single immunization with spike-functionalized ferritin vaccines elicits neutralizing antibody responses against SARS-CoV-2 in mice |
title_full_unstemmed | A single immunization with spike-functionalized ferritin vaccines elicits neutralizing antibody responses against SARS-CoV-2 in mice |
title_short | A single immunization with spike-functionalized ferritin vaccines elicits neutralizing antibody responses against SARS-CoV-2 in mice |
title_sort | single immunization with spike-functionalized ferritin vaccines elicits neutralizing antibody responses against sars-cov-2 in mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7457616/ https://www.ncbi.nlm.nih.gov/pubmed/32869030 http://dx.doi.org/10.1101/2020.08.28.272518 |
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