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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...

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Autores principales: Zhuo, Shao-Hua, Wu, Jun-Jun, Zhao, Lang, Li, Wen-Hao, Zhao, Yu-Fen, Li, Yan-Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tsinghua University Press 2022
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.
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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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