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Staphylococcus aureus-Specific Tissue-Resident Memory CD4(+) T Cells Are Abundant in Healthy Human Skin
The skin is an immunocompetent tissue that harbors several kinds of immune cells and a plethora of commensal microbes constituting the skin microbiome. Staphylococcus aureus is a prominent skin pathogen that colonizes a large proportion of the human population. We currently have an incomplete unders...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008074/ https://www.ncbi.nlm.nih.gov/pubmed/33796109 http://dx.doi.org/10.3389/fimmu.2021.642711 |
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author | Hendriks, Astrid Mnich, Malgorzata Ewa Clemente, Bruna Cruz, Ana Rita Tavarini, Simona Bagnoli, Fabio Soldaini, Elisabetta |
author_facet | Hendriks, Astrid Mnich, Malgorzata Ewa Clemente, Bruna Cruz, Ana Rita Tavarini, Simona Bagnoli, Fabio Soldaini, Elisabetta |
author_sort | Hendriks, Astrid |
collection | PubMed |
description | The skin is an immunocompetent tissue that harbors several kinds of immune cells and a plethora of commensal microbes constituting the skin microbiome. Staphylococcus aureus is a prominent skin pathogen that colonizes a large proportion of the human population. We currently have an incomplete understanding of the correlates of protection against S. aureus infection, however genetic and experimental evidence has shown that CD4(+) T cells play a key role in orchestrating a protective anti-S. aureus immune response. A high S. aureus-specific memory CD4(+) T cell response has been reported in the blood of healthy subjects. Since T cells are more abundant in the skin than in blood, we hypothesized that S. aureus-specific CD4(+) T cells could be present in the skin of healthy individuals. Indeed, we observed proliferation of tissue-resident memory CD4(+) T cells and production of IL-17A, IL-22, IFN-γ and TNF-β by cells isolated from abdominal skin explants in response to heat-killed S. aureus. Remarkably, these cytokines were produced also during an ex vivo epicutaneous S. aureus infection of human skin explants. These findings highlight the importance of tissue-resident memory CD4(+) T cells present at barrier sites such as the skin, a primary entry site for S. aureus. Further phenotypical and functional characterization of these cells will ultimately aid in the development of novel vaccine strategies against this elusive pathogen. |
format | Online Article Text |
id | pubmed-8008074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80080742021-03-31 Staphylococcus aureus-Specific Tissue-Resident Memory CD4(+) T Cells Are Abundant in Healthy Human Skin Hendriks, Astrid Mnich, Malgorzata Ewa Clemente, Bruna Cruz, Ana Rita Tavarini, Simona Bagnoli, Fabio Soldaini, Elisabetta Front Immunol Immunology The skin is an immunocompetent tissue that harbors several kinds of immune cells and a plethora of commensal microbes constituting the skin microbiome. Staphylococcus aureus is a prominent skin pathogen that colonizes a large proportion of the human population. We currently have an incomplete understanding of the correlates of protection against S. aureus infection, however genetic and experimental evidence has shown that CD4(+) T cells play a key role in orchestrating a protective anti-S. aureus immune response. A high S. aureus-specific memory CD4(+) T cell response has been reported in the blood of healthy subjects. Since T cells are more abundant in the skin than in blood, we hypothesized that S. aureus-specific CD4(+) T cells could be present in the skin of healthy individuals. Indeed, we observed proliferation of tissue-resident memory CD4(+) T cells and production of IL-17A, IL-22, IFN-γ and TNF-β by cells isolated from abdominal skin explants in response to heat-killed S. aureus. Remarkably, these cytokines were produced also during an ex vivo epicutaneous S. aureus infection of human skin explants. These findings highlight the importance of tissue-resident memory CD4(+) T cells present at barrier sites such as the skin, a primary entry site for S. aureus. Further phenotypical and functional characterization of these cells will ultimately aid in the development of novel vaccine strategies against this elusive pathogen. Frontiers Media S.A. 2021-03-16 /pmc/articles/PMC8008074/ /pubmed/33796109 http://dx.doi.org/10.3389/fimmu.2021.642711 Text en Copyright © 2021 Hendriks, Mnich, Clemente, Cruz, Tavarini, Bagnoli and Soldaini. 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 Hendriks, Astrid Mnich, Malgorzata Ewa Clemente, Bruna Cruz, Ana Rita Tavarini, Simona Bagnoli, Fabio Soldaini, Elisabetta Staphylococcus aureus-Specific Tissue-Resident Memory CD4(+) T Cells Are Abundant in Healthy Human Skin |
title | Staphylococcus aureus-Specific Tissue-Resident Memory CD4(+) T Cells Are Abundant in Healthy Human Skin |
title_full | Staphylococcus aureus-Specific Tissue-Resident Memory CD4(+) T Cells Are Abundant in Healthy Human Skin |
title_fullStr | Staphylococcus aureus-Specific Tissue-Resident Memory CD4(+) T Cells Are Abundant in Healthy Human Skin |
title_full_unstemmed | Staphylococcus aureus-Specific Tissue-Resident Memory CD4(+) T Cells Are Abundant in Healthy Human Skin |
title_short | Staphylococcus aureus-Specific Tissue-Resident Memory CD4(+) T Cells Are Abundant in Healthy Human Skin |
title_sort | staphylococcus aureus-specific tissue-resident memory cd4(+) t cells are abundant in healthy human skin |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008074/ https://www.ncbi.nlm.nih.gov/pubmed/33796109 http://dx.doi.org/10.3389/fimmu.2021.642711 |
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