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DNA origami presenting the receptor binding domain of SARS-CoV-2 elicit robust protective immune response
Effective and safe vaccines are invaluable tools in the arsenal to fight infectious diseases. The rapid spreading of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) responsible for the coronavirus disease 2019 pandemic has highlighted the need to develop methods for rapid and efficient...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10034259/ https://www.ncbi.nlm.nih.gov/pubmed/36959304 http://dx.doi.org/10.1038/s42003-023-04689-2 |
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author | Oktay, Esra Alem, Farhang Hernandez, Keziah Girgis, Michael Green, Christopher Mathur, Divita Medintz, Igor L. Narayanan, Aarthi Veneziano, Remi |
author_facet | Oktay, Esra Alem, Farhang Hernandez, Keziah Girgis, Michael Green, Christopher Mathur, Divita Medintz, Igor L. Narayanan, Aarthi Veneziano, Remi |
author_sort | Oktay, Esra |
collection | PubMed |
description | Effective and safe vaccines are invaluable tools in the arsenal to fight infectious diseases. The rapid spreading of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) responsible for the coronavirus disease 2019 pandemic has highlighted the need to develop methods for rapid and efficient vaccine development. DNA origami nanoparticles (DNA-NPs) presenting multiple antigens in prescribed nanoscale patterns have recently emerged as a safe, efficient, and easily scalable alternative for rational design of vaccines. Here, we are leveraging the unique properties of these DNA-NPs and demonstrate that precisely patterning ten copies of a reconstituted trimer of the receptor binding domain (RBD) of SARS-CoV-2 along with CpG adjuvants on the DNA-NPs is able to elicit a robust protective immunity against SARS-CoV-2 in a mouse model. Our results demonstrate the potential of our DNA-NP-based approach for developing safe and effective nanovaccines against infectious diseases with prolonged antibody response and effective protection in the context of a viral challenge. |
format | Online Article Text |
id | pubmed-10034259 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100342592023-03-23 DNA origami presenting the receptor binding domain of SARS-CoV-2 elicit robust protective immune response Oktay, Esra Alem, Farhang Hernandez, Keziah Girgis, Michael Green, Christopher Mathur, Divita Medintz, Igor L. Narayanan, Aarthi Veneziano, Remi Commun Biol Article Effective and safe vaccines are invaluable tools in the arsenal to fight infectious diseases. The rapid spreading of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) responsible for the coronavirus disease 2019 pandemic has highlighted the need to develop methods for rapid and efficient vaccine development. DNA origami nanoparticles (DNA-NPs) presenting multiple antigens in prescribed nanoscale patterns have recently emerged as a safe, efficient, and easily scalable alternative for rational design of vaccines. Here, we are leveraging the unique properties of these DNA-NPs and demonstrate that precisely patterning ten copies of a reconstituted trimer of the receptor binding domain (RBD) of SARS-CoV-2 along with CpG adjuvants on the DNA-NPs is able to elicit a robust protective immunity against SARS-CoV-2 in a mouse model. Our results demonstrate the potential of our DNA-NP-based approach for developing safe and effective nanovaccines against infectious diseases with prolonged antibody response and effective protection in the context of a viral challenge. Nature Publishing Group UK 2023-03-23 /pmc/articles/PMC10034259/ /pubmed/36959304 http://dx.doi.org/10.1038/s42003-023-04689-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Oktay, Esra Alem, Farhang Hernandez, Keziah Girgis, Michael Green, Christopher Mathur, Divita Medintz, Igor L. Narayanan, Aarthi Veneziano, Remi DNA origami presenting the receptor binding domain of SARS-CoV-2 elicit robust protective immune response |
title | DNA origami presenting the receptor binding domain of SARS-CoV-2 elicit robust protective immune response |
title_full | DNA origami presenting the receptor binding domain of SARS-CoV-2 elicit robust protective immune response |
title_fullStr | DNA origami presenting the receptor binding domain of SARS-CoV-2 elicit robust protective immune response |
title_full_unstemmed | DNA origami presenting the receptor binding domain of SARS-CoV-2 elicit robust protective immune response |
title_short | DNA origami presenting the receptor binding domain of SARS-CoV-2 elicit robust protective immune response |
title_sort | dna origami presenting the receptor binding domain of sars-cov-2 elicit robust protective immune response |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10034259/ https://www.ncbi.nlm.nih.gov/pubmed/36959304 http://dx.doi.org/10.1038/s42003-023-04689-2 |
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