Publication: Trained immunity induction by the inactivated
mucosal vaccine MV130 protects
against experimental viral respiratory infections
Authors
Brandi, Paola ; Conejero, Laura ; Cueto, Francisco J. ; Martínez Cano, Sarai ; Dunphy, Gillian ; Gómez, Manuel J. ; Relaño, Carlos ; Saz Leal, Paula ; Enamorado, Michel ; Quintas, Ana ; Dopazo, Ana ; Amores Iniesta, Joaquín ; Fresno, Carlos del ; Nistal Villán, Estanislao ; Ardavín, Carlos ; Nieto, Antonio ; Casanovas, Miguel ; Subiza, José Luis ; Sancho, David
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Publisher
Cell Press
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DOI
https://doi.org/10.1016/j.celrep.2021.110184
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info:eu-repo/semantics/article
Description
© 2021 The Authors. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/
This document is the Published version of a Published Work that appeared in final form in Cell Reports. To access the final edited and published work see https://doi.org/10.1016/j.celrep.2021.110184
Abstract
MV130 is an inactivated polybacterial mucosal vaccine that confers protection to patients against recurrent respiratory infections, including those of viral etiology. However, its mechanism of action remains poorly un-derstood. Here, we find that intranasal prophylaxis with MV130 modulates the lung immune landscape and provides long-term heterologous protection against viral respiratory infections in mice. Intranasal adminis-tration of MV130 provides protection against systemic candidiasis in wild-type and Rag1-deficient mice lacking functional lymphocytes, indicative of innate immune-mediated protection. Moreover, pharmacolog-ical inhibition of trained immunity with metformin abrogates the protection conferred by MV130 against influ-enza A virus respiratory infection. MV130 induces reprogramming of both mouse bone marrow progenitor cells and in vitro human monocytes, promoting an enhanced cytokine production that relies on a metabolic shift. Our results unveil that the mucosal administration of a fully inactivated bacterial vaccine provides pro-tection against viral infections by a mechanism associated with the induction of trained immunity.
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