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Synthesis and immunogenicity assessment of a gold nanoparticle conjugate for the delivery of a peptide from SARS-CoV-2
The development of vaccines is a crucial response against the COVID-19 pandemic and innovative nanovaccines could increase the potential to address this remarkable challenge. In the present study a B cell epitope (S(461-493)) from the spike protein of SARS-CoV-2 was selected and its immunogenicity v...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7920803/ https://www.ncbi.nlm.nih.gov/pubmed/33662593 http://dx.doi.org/10.1016/j.nano.2021.102372 |
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author | Farfán-Castro, Susan García-Soto, Mariano J. Comas-García, Mauricio Arévalo-Villalobos, Jaime I. Palestino, Gabriela González-Ortega, Omar Rosales-Mendoza, Sergio |
author_facet | Farfán-Castro, Susan García-Soto, Mariano J. Comas-García, Mauricio Arévalo-Villalobos, Jaime I. Palestino, Gabriela González-Ortega, Omar Rosales-Mendoza, Sergio |
author_sort | Farfán-Castro, Susan |
collection | PubMed |
description | The development of vaccines is a crucial response against the COVID-19 pandemic and innovative nanovaccines could increase the potential to address this remarkable challenge. In the present study a B cell epitope (S(461-493)) from the spike protein of SARS-CoV-2 was selected and its immunogenicity validated in sheep. This synthetic peptide was coupled to gold nanoparticles (AuNP) functionalized with SH-PEG-NH(2) via glutaraldehyde-mediated coupling to obtain the AuNP-S(461-493) candidate, which showed in s.c.-immunized mice a superior immunogenicity (IgG responses) when compared to soluble S(461-493); and led to increased expression of relevant cytokines in splenocyte cultures. Interestingly, the response triggered by AuNP-S(461-493) was similar in magnitude to that induced using a conventional strong adjuvant (Freund's adjuvant). This study provides a platform for the development of AuNP-based nanovaccines targeting specific SARS-CoV-2 epitopes. |
format | Online Article Text |
id | pubmed-7920803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79208032021-03-02 Synthesis and immunogenicity assessment of a gold nanoparticle conjugate for the delivery of a peptide from SARS-CoV-2 Farfán-Castro, Susan García-Soto, Mariano J. Comas-García, Mauricio Arévalo-Villalobos, Jaime I. Palestino, Gabriela González-Ortega, Omar Rosales-Mendoza, Sergio Nanomedicine Original Article The development of vaccines is a crucial response against the COVID-19 pandemic and innovative nanovaccines could increase the potential to address this remarkable challenge. In the present study a B cell epitope (S(461-493)) from the spike protein of SARS-CoV-2 was selected and its immunogenicity validated in sheep. This synthetic peptide was coupled to gold nanoparticles (AuNP) functionalized with SH-PEG-NH(2) via glutaraldehyde-mediated coupling to obtain the AuNP-S(461-493) candidate, which showed in s.c.-immunized mice a superior immunogenicity (IgG responses) when compared to soluble S(461-493); and led to increased expression of relevant cytokines in splenocyte cultures. Interestingly, the response triggered by AuNP-S(461-493) was similar in magnitude to that induced using a conventional strong adjuvant (Freund's adjuvant). This study provides a platform for the development of AuNP-based nanovaccines targeting specific SARS-CoV-2 epitopes. Elsevier Inc. 2021-06 2021-03-02 /pmc/articles/PMC7920803/ /pubmed/33662593 http://dx.doi.org/10.1016/j.nano.2021.102372 Text en © 2021 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Original Article Farfán-Castro, Susan García-Soto, Mariano J. Comas-García, Mauricio Arévalo-Villalobos, Jaime I. Palestino, Gabriela González-Ortega, Omar Rosales-Mendoza, Sergio Synthesis and immunogenicity assessment of a gold nanoparticle conjugate for the delivery of a peptide from SARS-CoV-2 |
title | Synthesis and immunogenicity assessment of a gold nanoparticle conjugate for the delivery of a peptide from SARS-CoV-2 |
title_full | Synthesis and immunogenicity assessment of a gold nanoparticle conjugate for the delivery of a peptide from SARS-CoV-2 |
title_fullStr | Synthesis and immunogenicity assessment of a gold nanoparticle conjugate for the delivery of a peptide from SARS-CoV-2 |
title_full_unstemmed | Synthesis and immunogenicity assessment of a gold nanoparticle conjugate for the delivery of a peptide from SARS-CoV-2 |
title_short | Synthesis and immunogenicity assessment of a gold nanoparticle conjugate for the delivery of a peptide from SARS-CoV-2 |
title_sort | synthesis and immunogenicity assessment of a gold nanoparticle conjugate for the delivery of a peptide from sars-cov-2 |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7920803/ https://www.ncbi.nlm.nih.gov/pubmed/33662593 http://dx.doi.org/10.1016/j.nano.2021.102372 |
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