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Immunity induced by a broad class of inorganic crystalline materials is directly controlled by their chemistry
There is currently no paradigm in immunology that enables an accurate prediction of how the immune system will respond to any given agent. Here we show that the immunological responses induced by members of a broad class of inorganic crystalline materials are controlled purely by their physicochemic...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4042647/ https://www.ncbi.nlm.nih.gov/pubmed/24799501 http://dx.doi.org/10.1084/jem.20131768 |
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author | Williams, Gareth R. Fierens, Kaat Preston, Stephen G. Lunn, Daniel Rysnik, Oliwia De Prijck, Sofie Kool, Mirjam Buckley, Hannah C. Lambrecht, Bart N. O’Hare, Dermot Austyn, Jonathan M. |
author_facet | Williams, Gareth R. Fierens, Kaat Preston, Stephen G. Lunn, Daniel Rysnik, Oliwia De Prijck, Sofie Kool, Mirjam Buckley, Hannah C. Lambrecht, Bart N. O’Hare, Dermot Austyn, Jonathan M. |
author_sort | Williams, Gareth R. |
collection | PubMed |
description | There is currently no paradigm in immunology that enables an accurate prediction of how the immune system will respond to any given agent. Here we show that the immunological responses induced by members of a broad class of inorganic crystalline materials are controlled purely by their physicochemical properties in a highly predictable manner. We show that structurally and chemically homogeneous layered double hydroxides (LDHs) can elicit diverse human dendritic cell responses in vitro. Using a systems vaccinology approach, we find that every measured response can be modeled using a subset of just three physical and chemical properties for all compounds tested. This correlation can be reduced to a simple linear equation that enables the immunological responses stimulated by newly synthesized LDHs to be predicted in advance from these three parameters alone. We also show that mouse antigen–specific antibody responses in vivo and human macrophage responses in vitro are controlled by the same properties, suggesting they may control diverse responses at both individual component and global levels of immunity. This study demonstrates that immunity can be determined purely by chemistry and opens the possibility of rational manipulation of immunity for therapeutic purposes. |
format | Online Article Text |
id | pubmed-4042647 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-40426472014-12-02 Immunity induced by a broad class of inorganic crystalline materials is directly controlled by their chemistry Williams, Gareth R. Fierens, Kaat Preston, Stephen G. Lunn, Daniel Rysnik, Oliwia De Prijck, Sofie Kool, Mirjam Buckley, Hannah C. Lambrecht, Bart N. O’Hare, Dermot Austyn, Jonathan M. J Exp Med Brief Definitive Report There is currently no paradigm in immunology that enables an accurate prediction of how the immune system will respond to any given agent. Here we show that the immunological responses induced by members of a broad class of inorganic crystalline materials are controlled purely by their physicochemical properties in a highly predictable manner. We show that structurally and chemically homogeneous layered double hydroxides (LDHs) can elicit diverse human dendritic cell responses in vitro. Using a systems vaccinology approach, we find that every measured response can be modeled using a subset of just three physical and chemical properties for all compounds tested. This correlation can be reduced to a simple linear equation that enables the immunological responses stimulated by newly synthesized LDHs to be predicted in advance from these three parameters alone. We also show that mouse antigen–specific antibody responses in vivo and human macrophage responses in vitro are controlled by the same properties, suggesting they may control diverse responses at both individual component and global levels of immunity. This study demonstrates that immunity can be determined purely by chemistry and opens the possibility of rational manipulation of immunity for therapeutic purposes. The Rockefeller University Press 2014-06-02 /pmc/articles/PMC4042647/ /pubmed/24799501 http://dx.doi.org/10.1084/jem.20131768 Text en © 2014 Williams et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Brief Definitive Report Williams, Gareth R. Fierens, Kaat Preston, Stephen G. Lunn, Daniel Rysnik, Oliwia De Prijck, Sofie Kool, Mirjam Buckley, Hannah C. Lambrecht, Bart N. O’Hare, Dermot Austyn, Jonathan M. Immunity induced by a broad class of inorganic crystalline materials is directly controlled by their chemistry |
title | Immunity induced by a broad class of inorganic crystalline materials is directly controlled by their chemistry |
title_full | Immunity induced by a broad class of inorganic crystalline materials is directly controlled by their chemistry |
title_fullStr | Immunity induced by a broad class of inorganic crystalline materials is directly controlled by their chemistry |
title_full_unstemmed | Immunity induced by a broad class of inorganic crystalline materials is directly controlled by their chemistry |
title_short | Immunity induced by a broad class of inorganic crystalline materials is directly controlled by their chemistry |
title_sort | immunity induced by a broad class of inorganic crystalline materials is directly controlled by their chemistry |
topic | Brief Definitive Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4042647/ https://www.ncbi.nlm.nih.gov/pubmed/24799501 http://dx.doi.org/10.1084/jem.20131768 |
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