Inhalable nanovaccine with biomimetic coronavirus structure to trigger mucosal immunity of respiratory tract against COVID-19
•The bionic-virus nanovaccine completely simulated the structure of SARS-CoV-2.•The nanovaccine induced innate immunity by stimulating TLR 3 pathway.•The bio-PS layer liposomes could effectively enter into alveolar epithelial cells.•The nanovaccine was delivered easily and painlessly through respira...
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Veröffentlicht in: | Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2021-08, Vol.418, p.129392-129392, Article 129392 |
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Sprache: | eng |
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Zusammenfassung: | •The bionic-virus nanovaccine completely simulated the structure of SARS-CoV-2.•The nanovaccine induced innate immunity by stimulating TLR 3 pathway.•The bio-PS layer liposomes could effectively enter into alveolar epithelial cells.•The nanovaccine was delivered easily and painlessly through respiratory route.•Nasal administration induced strong respiratory mucosal immunity.
The COVID-19 pandemic caused by SARS-CoV-2 seriously threatens global public health. It has previously been confirmed that SARS-CoV-2 is mainly transmitted between people through “respiratory droplets”. Therefore, the respiratory tract mucosa is the first barrier to prevent virus invasion. It is very important to stimulate mucosal immunity to protect the body from respiratory virus infection. Inspired by this, we designed a bionic-virus nanovaccine, which can induce mucosal immunity by nasal delivery to prevent virus infection from respiratory tract. The nanovaccine that mimic virosome is composed of poly(I:C) mimicking viral genetic material as immune adjuvant, biomimetic pulmonary surfactant (bio-PS) liposomes as capsid structure of virus and the receptor binding domains (RBDs) of SARS-CoV-2 as “spike” to completely simulate the structure of the coronavirus. The nanovaccine can be administered by inhaling to imitate the process of SARS-CoV-2 infection through the respiratory tract. Our results demonstrated that the inhalable nanovaccine with bionic virus-like structure has a stronger mucosal protective effect than routine muscle and subcutaneous inoculation. In particular, high titer of secretory immunoglobulin A (sIgA) was detected in respiratory secretions, which effectively neutralize the virus and prevent it from entering the body through the respiratory tract. Through imitating the structure and route of infection, this inhalable nanovaccine strategy might inspire a new approach to the precaution of respiratory viruses. |
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ISSN: | 1385-8947 1873-3212 1385-8947 |
DOI: | 10.1016/j.cej.2021.129392 |