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Novel Nanoparticulate and Ionic Titanium Antigens for Hypersensitivity Testing

Titanium is used in a wide variety of materials ranging from medical devices to materials used in everyday life. Adverse biological reactions that could occur in patients, consumers, and workers should be monitored and prevented. There is a lack of available agents to test and predict titanium-relat...

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Autores principales: Høl, Paul Johan, Kristoffersen, Einar K., Gjerdet, Nils Roar, Pellowe, Amanda S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5979587/
https://www.ncbi.nlm.nih.gov/pubmed/29642398
http://dx.doi.org/10.3390/ijms19041101
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author Høl, Paul Johan
Kristoffersen, Einar K.
Gjerdet, Nils Roar
Pellowe, Amanda S.
author_facet Høl, Paul Johan
Kristoffersen, Einar K.
Gjerdet, Nils Roar
Pellowe, Amanda S.
author_sort Høl, Paul Johan
collection PubMed
description Titanium is used in a wide variety of materials ranging from medical devices to materials used in everyday life. Adverse biological reactions that could occur in patients, consumers, and workers should be monitored and prevented. There is a lack of available agents to test and predict titanium-related hypersensitivity. The aim of this study was to develop two bioavailable titanium substances in ionic and nanoparticulate form to serve as antigens for hypersensitivity testing in vitro. Peripheral blood mononuclear cells from 20 test subjects were stimulated with the antigens and secretion of monocytic and lymphatic cytokines and chemokines were measured by a multiplex bead assay. Lymphocyte stimulation indices were also determined in a subset of test subjects by measuring CD69 and HLA-DR expression by flow cytometry. Cytokine profiling revealed that both antigens increased production of typical monocyte and macrophage secreted cytokines after 24 h, with significant increases in IL-1β, IL-7, IL-10, IL-12, IL-2R, IL-6, GM-CSF, TNF-α, IL-1RA, MIP-1α, MIP-1β, IFN-α, and IL-15. Lymphatic cytokines and chemokines were not significantly induced by activation. After seven days of stimulation, ionic-Ti (2.5 μg/mL) caused proliferation (stimulation index > 2) of CD4+ cells and CD8+ cells in all persons tested (N = 6), while titanium dioxide nanoparticles (50 μg/mL) only caused significant proliferation of CD4+ cells. Our preliminary results show that the experimental titanium antigens, especially the ionic form, induce a general inflammatory response in vitro. A relevant cohort of test subjects is required to further elucidate their potential for predictive hypersensitivity testing.
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spelling pubmed-59795872018-06-10 Novel Nanoparticulate and Ionic Titanium Antigens for Hypersensitivity Testing Høl, Paul Johan Kristoffersen, Einar K. Gjerdet, Nils Roar Pellowe, Amanda S. Int J Mol Sci Article Titanium is used in a wide variety of materials ranging from medical devices to materials used in everyday life. Adverse biological reactions that could occur in patients, consumers, and workers should be monitored and prevented. There is a lack of available agents to test and predict titanium-related hypersensitivity. The aim of this study was to develop two bioavailable titanium substances in ionic and nanoparticulate form to serve as antigens for hypersensitivity testing in vitro. Peripheral blood mononuclear cells from 20 test subjects were stimulated with the antigens and secretion of monocytic and lymphatic cytokines and chemokines were measured by a multiplex bead assay. Lymphocyte stimulation indices were also determined in a subset of test subjects by measuring CD69 and HLA-DR expression by flow cytometry. Cytokine profiling revealed that both antigens increased production of typical monocyte and macrophage secreted cytokines after 24 h, with significant increases in IL-1β, IL-7, IL-10, IL-12, IL-2R, IL-6, GM-CSF, TNF-α, IL-1RA, MIP-1α, MIP-1β, IFN-α, and IL-15. Lymphatic cytokines and chemokines were not significantly induced by activation. After seven days of stimulation, ionic-Ti (2.5 μg/mL) caused proliferation (stimulation index > 2) of CD4+ cells and CD8+ cells in all persons tested (N = 6), while titanium dioxide nanoparticles (50 μg/mL) only caused significant proliferation of CD4+ cells. Our preliminary results show that the experimental titanium antigens, especially the ionic form, induce a general inflammatory response in vitro. A relevant cohort of test subjects is required to further elucidate their potential for predictive hypersensitivity testing. MDPI 2018-04-06 /pmc/articles/PMC5979587/ /pubmed/29642398 http://dx.doi.org/10.3390/ijms19041101 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Høl, Paul Johan
Kristoffersen, Einar K.
Gjerdet, Nils Roar
Pellowe, Amanda S.
Novel Nanoparticulate and Ionic Titanium Antigens for Hypersensitivity Testing
title Novel Nanoparticulate and Ionic Titanium Antigens for Hypersensitivity Testing
title_full Novel Nanoparticulate and Ionic Titanium Antigens for Hypersensitivity Testing
title_fullStr Novel Nanoparticulate and Ionic Titanium Antigens for Hypersensitivity Testing
title_full_unstemmed Novel Nanoparticulate and Ionic Titanium Antigens for Hypersensitivity Testing
title_short Novel Nanoparticulate and Ionic Titanium Antigens for Hypersensitivity Testing
title_sort novel nanoparticulate and ionic titanium antigens for hypersensitivity testing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5979587/
https://www.ncbi.nlm.nih.gov/pubmed/29642398
http://dx.doi.org/10.3390/ijms19041101
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