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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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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. |
format | Online Article Text |
id | pubmed-6197699 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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