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Identification and Characterization of Circulating Naïve CD4+ and CD8+ T Cells Recognizing Nickel

Allergic contact dermatitis caused by contact sensitizers is a T-cell-mediated inflammatory skin disease. The most prevalent contact allergens is nickel. Whereas, memory T cells from nickel-allergic patients are well-characterized, little is known concerning nickel-specific naïve T-cell repertoire....

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Autores principales: Bechara, Rami, Pollastro, Sabrina, Azoury, Marie Eliane, Szely, Natacha, Maillère, Bernard, de Vries, Niek, Pallardy, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582854/
https://www.ncbi.nlm.nih.gov/pubmed/31249573
http://dx.doi.org/10.3389/fimmu.2019.01331
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author Bechara, Rami
Pollastro, Sabrina
Azoury, Marie Eliane
Szely, Natacha
Maillère, Bernard
de Vries, Niek
Pallardy, Marc
author_facet Bechara, Rami
Pollastro, Sabrina
Azoury, Marie Eliane
Szely, Natacha
Maillère, Bernard
de Vries, Niek
Pallardy, Marc
author_sort Bechara, Rami
collection PubMed
description Allergic contact dermatitis caused by contact sensitizers is a T-cell-mediated inflammatory skin disease. The most prevalent contact allergens is nickel. Whereas, memory T cells from nickel-allergic patients are well-characterized, little is known concerning nickel-specific naïve T-cell repertoire. The purpose of this study was to identify and quantify naïve CD4+ and CD8+ T cells recognizing nickel in the general population. Using a T-cell priming in vitro assay based on autologous co-cultures between naïve T cells and dendritic cells loaded with nickel, we were able to detect a naïve CD4+ and CD8+ T-cell repertoire for nickel in 10/11 and 7/8 of the tested donors. We calculated a mean frequency of 0.49 nickel-specific naïve CD4+ T cells and 0.37 nickel-specific naïve CD8+ T cells per million of circulating naïve T cells. The activation of these specific T cells requires MHC molecules and alongside IFN-γ production, some nickel-specific T-cells were able to produce granzyme-B. Interestingly, nickel-specific naïve CD4+ and CD8+ T cells showed a low rate of cross-reactivity with cobalt, another metallic hapten, frequently mixed with nickel in many alloys. Moreover, naïve CD4+ T cells showed a polyclonal TCRβ composition and the presence of highly expanded clones with an enrichment and/or preferentially expansion of some TRBV genes that was donor and T-cell specific. Our results contribute to a better understanding of the mechanism of immunization to nickel and propose the T-cell priming assay as a useful tool to identify antigen-specific naïve T cells.
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spelling pubmed-65828542019-06-27 Identification and Characterization of Circulating Naïve CD4+ and CD8+ T Cells Recognizing Nickel Bechara, Rami Pollastro, Sabrina Azoury, Marie Eliane Szely, Natacha Maillère, Bernard de Vries, Niek Pallardy, Marc Front Immunol Immunology Allergic contact dermatitis caused by contact sensitizers is a T-cell-mediated inflammatory skin disease. The most prevalent contact allergens is nickel. Whereas, memory T cells from nickel-allergic patients are well-characterized, little is known concerning nickel-specific naïve T-cell repertoire. The purpose of this study was to identify and quantify naïve CD4+ and CD8+ T cells recognizing nickel in the general population. Using a T-cell priming in vitro assay based on autologous co-cultures between naïve T cells and dendritic cells loaded with nickel, we were able to detect a naïve CD4+ and CD8+ T-cell repertoire for nickel in 10/11 and 7/8 of the tested donors. We calculated a mean frequency of 0.49 nickel-specific naïve CD4+ T cells and 0.37 nickel-specific naïve CD8+ T cells per million of circulating naïve T cells. The activation of these specific T cells requires MHC molecules and alongside IFN-γ production, some nickel-specific T-cells were able to produce granzyme-B. Interestingly, nickel-specific naïve CD4+ and CD8+ T cells showed a low rate of cross-reactivity with cobalt, another metallic hapten, frequently mixed with nickel in many alloys. Moreover, naïve CD4+ T cells showed a polyclonal TCRβ composition and the presence of highly expanded clones with an enrichment and/or preferentially expansion of some TRBV genes that was donor and T-cell specific. Our results contribute to a better understanding of the mechanism of immunization to nickel and propose the T-cell priming assay as a useful tool to identify antigen-specific naïve T cells. Frontiers Media S.A. 2019-06-12 /pmc/articles/PMC6582854/ /pubmed/31249573 http://dx.doi.org/10.3389/fimmu.2019.01331 Text en Copyright © 2019 Bechara, Pollastro, Azoury, Szely, Maillère, de Vries and Pallardy. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Bechara, Rami
Pollastro, Sabrina
Azoury, Marie Eliane
Szely, Natacha
Maillère, Bernard
de Vries, Niek
Pallardy, Marc
Identification and Characterization of Circulating Naïve CD4+ and CD8+ T Cells Recognizing Nickel
title Identification and Characterization of Circulating Naïve CD4+ and CD8+ T Cells Recognizing Nickel
title_full Identification and Characterization of Circulating Naïve CD4+ and CD8+ T Cells Recognizing Nickel
title_fullStr Identification and Characterization of Circulating Naïve CD4+ and CD8+ T Cells Recognizing Nickel
title_full_unstemmed Identification and Characterization of Circulating Naïve CD4+ and CD8+ T Cells Recognizing Nickel
title_short Identification and Characterization of Circulating Naïve CD4+ and CD8+ T Cells Recognizing Nickel
title_sort identification and characterization of circulating naïve cd4+ and cd8+ t cells recognizing nickel
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6582854/
https://www.ncbi.nlm.nih.gov/pubmed/31249573
http://dx.doi.org/10.3389/fimmu.2019.01331
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