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一种壳聚糖介导的抗SARS-CoV-2可吸入纳米疫苗。

A chitosan-mediated inhalable nanovaccine against SARS-CoV-2.

作者信息

Zhuo Shao-Hua, Wu Jun-Jun, Zhao Lang, Li Wen-Hao, Zhao Yu-Fen, Li Yan-Mei

机构信息

Key Lab of Bioorganic Phosphorus Chemistry & Chemical Biology, Department of Chemistry, Tsinghua University, Beijing, 100084 China.

Institute of Drug Discovery Technology, Ningbo University, Ningbo, 315221 China.

出版信息

Nano Res. 2022;15(5):4191-4200. doi: 10.1007/s12274-021-4012-9. Epub 2022 Feb 2.

DOI:10.1007/s12274-021-4012-9
PMID:35126879
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8809230/
Abstract

UNLABELLED

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.

摘要

未标记

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)及其多种抗原变体已成为一项全球性挑战,迅速建立免疫屏障对于实现对该病毒的长期控制至关重要。这导致对易于制备且可扩展的疫苗有巨大需求,尤其是在低收入国家。在此,我们展示了一种由壳聚糖和SARS-CoV-2刺突蛋白组成的可吸入纳米疫苗。壳聚糖介导的纳米疫苗能够引发强烈的刺突特异性抗体免疫反应,并增强支气管肺泡灌洗和肺部的局部黏膜免疫,这可能能够保护宿主免受感染且无全身毒性。此外,壳聚糖刺激产生的增强的适应性免疫显示出对SARS-CoV-2的潜在保护作用。此外,与肌肉注射相比,吸入纳米疫苗诱导出相当的抗体反应。这种针对SARS-CoV-2的可吸入纳米疫苗提供了一种方便且合规的策略,可减少针头的使用以及对医护人员的需求。

电子补充材料

补充材料(壳聚糖介导的纳米疫苗对骨髓来源树突状细胞的免疫激活、细胞活力、肺部和支气管肺泡灌洗中的免疫反应、血清化学以及苏木精和伊红组织病理学分析)可在本文的在线版本中获取,链接为10.1007/s12274-021-4012-9。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be09/8809230/bce7b5466680/12274_2021_4012_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be09/8809230/bce7b5466680/12274_2021_4012_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be09/8809230/bce7b5466680/12274_2021_4012_Fig1_HTML.jpg

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