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Adaptive immunity against gut microbiota enhances apoE-mediated immune regulation and reduces atherosclerosis and western-diet-related inflammation

Common features of immune-metabolic and inflammatory diseases such as metabolic syndrome, diabetes, obesity and cardiovascular diseases are an altered gut microbiota composition and a systemic pro-inflammatory state. We demonstrate that active immunization against the outer membrane protein of bacte...

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Autores principales: Saita, Diego, Ferrarese, Roberto, Foglieni, Chiara, Esposito, Antonio, Canu, Tamara, Perani, Laura, Ceresola, Elisa Rita, Visconti, Laura, Burioni, Roberto, Clementi, Massimo, Canducci, Filippo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4935993/
https://www.ncbi.nlm.nih.gov/pubmed/27383250
http://dx.doi.org/10.1038/srep29353
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author Saita, Diego
Ferrarese, Roberto
Foglieni, Chiara
Esposito, Antonio
Canu, Tamara
Perani, Laura
Ceresola, Elisa Rita
Visconti, Laura
Burioni, Roberto
Clementi, Massimo
Canducci, Filippo
author_facet Saita, Diego
Ferrarese, Roberto
Foglieni, Chiara
Esposito, Antonio
Canu, Tamara
Perani, Laura
Ceresola, Elisa Rita
Visconti, Laura
Burioni, Roberto
Clementi, Massimo
Canducci, Filippo
author_sort Saita, Diego
collection PubMed
description Common features of immune-metabolic and inflammatory diseases such as metabolic syndrome, diabetes, obesity and cardiovascular diseases are an altered gut microbiota composition and a systemic pro-inflammatory state. We demonstrate that active immunization against the outer membrane protein of bacteria present in the gut enhances local and systemic immune control via apoE-mediated immune-modulation. Reduction of western-diet-associated inflammation was obtained for more than eighteen weeks after immunization. Immunized mice had reduced serum cytokine levels, reduced insulin and fasting glucose concentrations; and gene expression in both liver and visceral adipose tissue confirmed a reduced inflammatory steady-state after immunization. Moreover, both gut and atherosclerotic plaques of immunized mice showed reduced inflammatory cells and an increased M2 macrophage fraction. These results suggest that adaptive responses directed against microbes present in our microbiota have systemic beneficial consequences and demonstrate the key role of apoE in this mechanism that could be exploited to treat immune-metabolic diseases.
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spelling pubmed-49359932016-07-13 Adaptive immunity against gut microbiota enhances apoE-mediated immune regulation and reduces atherosclerosis and western-diet-related inflammation Saita, Diego Ferrarese, Roberto Foglieni, Chiara Esposito, Antonio Canu, Tamara Perani, Laura Ceresola, Elisa Rita Visconti, Laura Burioni, Roberto Clementi, Massimo Canducci, Filippo Sci Rep Article Common features of immune-metabolic and inflammatory diseases such as metabolic syndrome, diabetes, obesity and cardiovascular diseases are an altered gut microbiota composition and a systemic pro-inflammatory state. We demonstrate that active immunization against the outer membrane protein of bacteria present in the gut enhances local and systemic immune control via apoE-mediated immune-modulation. Reduction of western-diet-associated inflammation was obtained for more than eighteen weeks after immunization. Immunized mice had reduced serum cytokine levels, reduced insulin and fasting glucose concentrations; and gene expression in both liver and visceral adipose tissue confirmed a reduced inflammatory steady-state after immunization. Moreover, both gut and atherosclerotic plaques of immunized mice showed reduced inflammatory cells and an increased M2 macrophage fraction. These results suggest that adaptive responses directed against microbes present in our microbiota have systemic beneficial consequences and demonstrate the key role of apoE in this mechanism that could be exploited to treat immune-metabolic diseases. Nature Publishing Group 2016-07-07 /pmc/articles/PMC4935993/ /pubmed/27383250 http://dx.doi.org/10.1038/srep29353 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Saita, Diego
Ferrarese, Roberto
Foglieni, Chiara
Esposito, Antonio
Canu, Tamara
Perani, Laura
Ceresola, Elisa Rita
Visconti, Laura
Burioni, Roberto
Clementi, Massimo
Canducci, Filippo
Adaptive immunity against gut microbiota enhances apoE-mediated immune regulation and reduces atherosclerosis and western-diet-related inflammation
title Adaptive immunity against gut microbiota enhances apoE-mediated immune regulation and reduces atherosclerosis and western-diet-related inflammation
title_full Adaptive immunity against gut microbiota enhances apoE-mediated immune regulation and reduces atherosclerosis and western-diet-related inflammation
title_fullStr Adaptive immunity against gut microbiota enhances apoE-mediated immune regulation and reduces atherosclerosis and western-diet-related inflammation
title_full_unstemmed Adaptive immunity against gut microbiota enhances apoE-mediated immune regulation and reduces atherosclerosis and western-diet-related inflammation
title_short Adaptive immunity against gut microbiota enhances apoE-mediated immune regulation and reduces atherosclerosis and western-diet-related inflammation
title_sort adaptive immunity against gut microbiota enhances apoe-mediated immune regulation and reduces atherosclerosis and western-diet-related inflammation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4935993/
https://www.ncbi.nlm.nih.gov/pubmed/27383250
http://dx.doi.org/10.1038/srep29353
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