tetano
Editor, Senior Moderator
Nano Res
. 2022 Feb 2;1-10.
doi: 10.1007/s12274-021-4012-9. Online ahead of print.
A chitosan-mediated inhalable nanovaccine against SARS-CoV-2
Shao-Hua Zhuo[SUP] #[/SUP][SUP] 1 [/SUP], Jun-Jun Wu[SUP] #[/SUP][SUP] 1 [/SUP], Lang Zhao[SUP] 1 [/SUP], Wen-Hao Li[SUP] 1 [/SUP], Yu-Fen Zhao[SUP] 1 2 [/SUP], Yan-Mei Li[SUP] 1 3 4 [/SUP]
Affiliations
Abstract
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.
. 2022 Feb 2;1-10.
doi: 10.1007/s12274-021-4012-9. Online ahead of print.
A chitosan-mediated inhalable nanovaccine against SARS-CoV-2
Shao-Hua Zhuo[SUP] #[/SUP][SUP] 1 [/SUP], Jun-Jun Wu[SUP] #[/SUP][SUP] 1 [/SUP], Lang Zhao[SUP] 1 [/SUP], Wen-Hao Li[SUP] 1 [/SUP], Yu-Fen Zhao[SUP] 1 2 [/SUP], Yan-Mei Li[SUP] 1 3 4 [/SUP]
Affiliations
- PMID: 35126879
- PMCID: PMC8809230
- DOI: 10.1007/s12274-021-4012-9
Abstract
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.