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A chitosan-mediated inhalable nanovaccine against SARS-CoV-2
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), with several antigenic variants, has grown into a global challenge, and the rapid establishment of an immune barrier is crucial to achieving long-term control of the virus. This has led to a great demand for easy preparation and scalable...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Tsinghua University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8809230/ https://www.ncbi.nlm.nih.gov/pubmed/35126879 http://dx.doi.org/10.1007/s12274-021-4012-9 |
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author | Zhuo, Shao-Hua Wu, Jun-Jun Zhao, Lang Li, Wen-Hao Zhao, Yu-Fen Li, Yan-Mei |
author_facet | Zhuo, Shao-Hua Wu, Jun-Jun Zhao, Lang Li, Wen-Hao Zhao, Yu-Fen Li, Yan-Mei |
author_sort | Zhuo, Shao-Hua |
collection | PubMed |
description | Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), with several antigenic variants, has grown into a global challenge, and the rapid establishment of an immune barrier is crucial to achieving long-term control of the virus. This has led to a great demand for easy preparation and scalable vaccines, especially in low-income countries. Here, we present an inhalable nanovaccine comprising chitosan and SARS-CoV-2 spike protein. The chitosan-mediated nanovaccine enabled a strong spike-specific antibody immune response and augmented local mucosal immunity in bronchoalveolar lavage and lungs, which might be capable of protecting the host from infection without systemic toxicity. In addition, the enhanced adaptive immunity stimulated by chitosan showed potential protection against SARS-CoV-2. Furthermore, inhalation of the nanovaccine induced a comparable antibody response compared to intramuscular injection. This inhalable nanovaccine against SARS-CoV-2 offers a convenient and compliant strategy to reduce the use of needles and the need for medical staff. ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary material (the immune activation of CS-mediated nanovacccine on BMDCs, cell viability, immune responses in lungs and BALF, serum chemistry and H&E histopathological analysis.) is available in the online version of this article at 10.1007/s12274-021-4012-9. |
format | Online Article Text |
id | pubmed-8809230 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Tsinghua University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-88092302022-02-02 A chitosan-mediated inhalable nanovaccine against SARS-CoV-2 Zhuo, Shao-Hua Wu, Jun-Jun Zhao, Lang Li, Wen-Hao Zhao, Yu-Fen Li, Yan-Mei Nano Res Research Article Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), with several antigenic variants, has grown into a global challenge, and the rapid establishment of an immune barrier is crucial to achieving long-term control of the virus. This has led to a great demand for easy preparation and scalable vaccines, especially in low-income countries. Here, we present an inhalable nanovaccine comprising chitosan and SARS-CoV-2 spike protein. The chitosan-mediated nanovaccine enabled a strong spike-specific antibody immune response and augmented local mucosal immunity in bronchoalveolar lavage and lungs, which might be capable of protecting the host from infection without systemic toxicity. In addition, the enhanced adaptive immunity stimulated by chitosan showed potential protection against SARS-CoV-2. Furthermore, inhalation of the nanovaccine induced a comparable antibody response compared to intramuscular injection. This inhalable nanovaccine against SARS-CoV-2 offers a convenient and compliant strategy to reduce the use of needles and the need for medical staff. ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary material (the immune activation of CS-mediated nanovacccine on BMDCs, cell viability, immune responses in lungs and BALF, serum chemistry and H&E histopathological analysis.) is available in the online version of this article at 10.1007/s12274-021-4012-9. Tsinghua University Press 2022-02-02 2022 /pmc/articles/PMC8809230/ /pubmed/35126879 http://dx.doi.org/10.1007/s12274-021-4012-9 Text en © Tsinghua University Press and Springer-Verlag GmbH Germany, part of Springer Nature 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Research Article Zhuo, Shao-Hua Wu, Jun-Jun Zhao, Lang Li, Wen-Hao Zhao, Yu-Fen Li, Yan-Mei A chitosan-mediated inhalable nanovaccine against SARS-CoV-2 |
title | A chitosan-mediated inhalable nanovaccine against SARS-CoV-2 |
title_full | A chitosan-mediated inhalable nanovaccine against SARS-CoV-2 |
title_fullStr | A chitosan-mediated inhalable nanovaccine against SARS-CoV-2 |
title_full_unstemmed | A chitosan-mediated inhalable nanovaccine against SARS-CoV-2 |
title_short | A chitosan-mediated inhalable nanovaccine against SARS-CoV-2 |
title_sort | chitosan-mediated inhalable nanovaccine against sars-cov-2 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8809230/ https://www.ncbi.nlm.nih.gov/pubmed/35126879 http://dx.doi.org/10.1007/s12274-021-4012-9 |
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