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IFN-γ immune priming of macrophages in vivo induces prolonged STAT1 binding and protection against Cryptococcus neoformans

Development of vaccines against opportunistic infections is difficult as patients most at risk of developing disease are deficient in aspects of the adaptive immune system. Here, we utilized an experimental immunization strategy to induce innate memory in macrophages in vivo. Unlike current trained...

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Autores principales: Leopold Wager, Chrissy M., Hole, Camaron R., Campuzano, Althea, Castro-Lopez, Natalia, Cai, Hong, Caballero Van Dyke, Marley C., Wozniak, Karen L., Wang, Yufeng, Wormley, Floyd L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6197699/
https://www.ncbi.nlm.nih.gov/pubmed/30304063
http://dx.doi.org/10.1371/journal.ppat.1007358
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author Leopold Wager, Chrissy M.
Hole, Camaron R.
Campuzano, Althea
Castro-Lopez, Natalia
Cai, Hong
Caballero Van Dyke, Marley C.
Wozniak, Karen L.
Wang, Yufeng
Wormley, Floyd L.
author_facet Leopold Wager, Chrissy M.
Hole, Camaron R.
Campuzano, Althea
Castro-Lopez, Natalia
Cai, Hong
Caballero Van Dyke, Marley C.
Wozniak, Karen L.
Wang, Yufeng
Wormley, Floyd L.
author_sort Leopold Wager, Chrissy M.
collection PubMed
description Development of vaccines against opportunistic infections is difficult as patients most at risk of developing disease are deficient in aspects of the adaptive immune system. Here, we utilized an experimental immunization strategy to induce innate memory in macrophages in vivo. Unlike current trained immunity models, we present an innate memory-like phenotype in macrophages that is maintained for at least 70 days post-immunization and results in complete protection against secondary challenge in the absence of adaptive immune cells. RNA-seq analysis of in vivo IFN-γ primed macrophages revealed a rapid up-regulation of IFN-γ and STAT1 signaling pathways following secondary challenge. The enhanced cytokine recall responses appeared to be pathogen-specific, dependent on changes in histone methylation and acetylation, and correlated with increased STAT1 binding to promoter regions of genes associated with protective anti-fungal immunity. Thus, we demonstrate an alternative mechanism to induce macrophage innate memory in vivo that facilitates pathogen-specific vaccine-mediated immune responses.
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spelling pubmed-61976992018-11-05 IFN-γ immune priming of macrophages in vivo induces prolonged STAT1 binding and protection against Cryptococcus neoformans Leopold Wager, Chrissy M. Hole, Camaron R. Campuzano, Althea Castro-Lopez, Natalia Cai, Hong Caballero Van Dyke, Marley C. Wozniak, Karen L. Wang, Yufeng Wormley, Floyd L. PLoS Pathog Research Article Development of vaccines against opportunistic infections is difficult as patients most at risk of developing disease are deficient in aspects of the adaptive immune system. Here, we utilized an experimental immunization strategy to induce innate memory in macrophages in vivo. Unlike current trained immunity models, we present an innate memory-like phenotype in macrophages that is maintained for at least 70 days post-immunization and results in complete protection against secondary challenge in the absence of adaptive immune cells. RNA-seq analysis of in vivo IFN-γ primed macrophages revealed a rapid up-regulation of IFN-γ and STAT1 signaling pathways following secondary challenge. The enhanced cytokine recall responses appeared to be pathogen-specific, dependent on changes in histone methylation and acetylation, and correlated with increased STAT1 binding to promoter regions of genes associated with protective anti-fungal immunity. Thus, we demonstrate an alternative mechanism to induce macrophage innate memory in vivo that facilitates pathogen-specific vaccine-mediated immune responses. Public Library of Science 2018-10-10 /pmc/articles/PMC6197699/ /pubmed/30304063 http://dx.doi.org/10.1371/journal.ppat.1007358 Text en © 2018 Leopold Wager et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Leopold Wager, Chrissy M.
Hole, Camaron R.
Campuzano, Althea
Castro-Lopez, Natalia
Cai, Hong
Caballero Van Dyke, Marley C.
Wozniak, Karen L.
Wang, Yufeng
Wormley, Floyd L.
IFN-γ immune priming of macrophages in vivo induces prolonged STAT1 binding and protection against Cryptococcus neoformans
title IFN-γ immune priming of macrophages in vivo induces prolonged STAT1 binding and protection against Cryptococcus neoformans
title_full IFN-γ immune priming of macrophages in vivo induces prolonged STAT1 binding and protection against Cryptococcus neoformans
title_fullStr IFN-γ immune priming of macrophages in vivo induces prolonged STAT1 binding and protection against Cryptococcus neoformans
title_full_unstemmed IFN-γ immune priming of macrophages in vivo induces prolonged STAT1 binding and protection against Cryptococcus neoformans
title_short IFN-γ immune priming of macrophages in vivo induces prolonged STAT1 binding and protection against Cryptococcus neoformans
title_sort ifn-γ immune priming of macrophages in vivo induces prolonged stat1 binding and protection against cryptococcus neoformans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6197699/
https://www.ncbi.nlm.nih.gov/pubmed/30304063
http://dx.doi.org/10.1371/journal.ppat.1007358
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