A Thermostable Oral SARS-CoV-2 Vaccine Induces Mucosal and Protective Immunity
An ideal protective vaccine against SARS-CoV-2 should not only be effective in preventing disease, but also in preventing virus transmission. It should also be well accepted by the population and have a simple logistic chain. To fulfill these criteria, we developed a thermostable, orally administere...
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Frontiers Media S.A.
2022
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Acceso en línea: | http://pa.bibdigital.ucc.edu.ar/3253/1/A_Saura_Luj%C3%A1n_Luj%C3%A1n.pdf |
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I38-R144-3253 |
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Universidad Católica de Córdoba |
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I-38 |
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R-144 |
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Producción Académica Universidad Católica de Córdoba (UCCor) |
language |
Español |
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topic |
Q Ciencia (General) QR180 Inmunología QR355 Virología |
spellingShingle |
Q Ciencia (General) QR180 Inmunología QR355 Virología Bellier, Bertrand Saura, Alicia Luján, Lucas A. Molina, Cecilia R. Luján, Hugo Daniel Klatzmann, David A Thermostable Oral SARS-CoV-2 Vaccine Induces Mucosal and Protective Immunity |
topic_facet |
Q Ciencia (General) QR180 Inmunología QR355 Virología |
description |
An ideal protective vaccine against SARS-CoV-2 should not only be effective in preventing disease, but also in preventing virus transmission. It should also be well accepted by the population and have a simple logistic chain. To fulfill these criteria, we developed a thermostable, orally administered vaccine that can induce a robust mucosal neutralizing immune response. We used our platform based on retrovirus-derived enveloped virus-like particles (eVLPs) harnessed with variable surface proteins (VSPs) from the intestinal parasite Giardia lamblia, affording them resistance to degradation and the triggering of robust mucosal cellular and antibody immune responses after oral administration. We made eVLPs expressing various forms of the SARS-CoV-2 Spike protein (S), with or without membrane protein (M) expression. We found that prime-boost administration of VSP-decorated eVLPs expressing a pre-fusion stabilized form of S and M triggers robust mucosal responses against SARS-CoV-2 in mice and hamsters, which translate into complete protection from a viral challenge. Moreover, they dramatically boosted the IgA mucosal response of intramuscularly injected vaccines. We conclude that our thermostable orally administered eVLP vaccine could be a valuable addition to the current arsenal against SARS-CoV-2, in a stand-alone prime-boost vaccination strategy or as a boost for existing vaccines. |
format |
Artículo Artículo |
author |
Bellier, Bertrand Saura, Alicia Luján, Lucas A. Molina, Cecilia R. Luján, Hugo Daniel Klatzmann, David |
author_facet |
Bellier, Bertrand Saura, Alicia Luján, Lucas A. Molina, Cecilia R. Luján, Hugo Daniel Klatzmann, David |
author_sort |
Bellier, Bertrand |
title |
A Thermostable Oral SARS-CoV-2 Vaccine Induces Mucosal and Protective Immunity |
title_short |
A Thermostable Oral SARS-CoV-2 Vaccine Induces Mucosal and Protective Immunity |
title_full |
A Thermostable Oral SARS-CoV-2 Vaccine Induces Mucosal and Protective Immunity |
title_fullStr |
A Thermostable Oral SARS-CoV-2 Vaccine Induces Mucosal and Protective Immunity |
title_full_unstemmed |
A Thermostable Oral SARS-CoV-2 Vaccine Induces Mucosal and Protective Immunity |
title_sort |
thermostable oral sars-cov-2 vaccine induces mucosal and protective immunity |
publisher |
Frontiers Media S.A. |
publishDate |
2022 |
url |
http://pa.bibdigital.ucc.edu.ar/3253/1/A_Saura_Luj%C3%A1n_Luj%C3%A1n.pdf |
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Repositorios |
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