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Control of Adaptive Immune Responses by Staphylococcus aureus through IL-10, PD-L1, and TLR2

Microbes induce innate immune responses in hosts. It is critical to know how different microbes control adaptive responses through innate pathways. The impact of gram-positive bacteria on the innate and adaptive responses is unclear. Herein we report that Staphylococcus aureus induces IL-10, Th17-in...

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Detalles Bibliográficos
Autores principales: Wang, Jinhai, Roderiquez, Gregory, Norcross, Michael A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428601/
https://www.ncbi.nlm.nih.gov/pubmed/22930672
http://dx.doi.org/10.1038/srep00606
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author Wang, Jinhai
Roderiquez, Gregory
Norcross, Michael A.
author_facet Wang, Jinhai
Roderiquez, Gregory
Norcross, Michael A.
author_sort Wang, Jinhai
collection PubMed
description Microbes induce innate immune responses in hosts. It is critical to know how different microbes control adaptive responses through innate pathways. The impact of gram-positive bacteria on the innate and adaptive responses is unclear. Herein we report that Staphylococcus aureus induces IL-10, Th17-inducing cytokines IL-6 and IL-23, chemokines, and regulates dendritic cell markers. S. aureus inhibits T-cell IL-2 responses through modulation of HLA-DR, CD86 and PD-L1. IFN-gamma, Src kinase inhibitors, or TLR2 antibodies prevented the down-modulation of HLA-DR by S. aureus. Our data demonstrate that innate TLR signaling induces multi-dimensional inhibition of adaptive immune responses, which may contribute to the lack of protective immunity to bacteria or microbe tolerance. IL-10 and PD-L1 antagonists may boost immunity to vaccines for S. aureus and other microbes.
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spelling pubmed-34286012012-08-28 Control of Adaptive Immune Responses by Staphylococcus aureus through IL-10, PD-L1, and TLR2 Wang, Jinhai Roderiquez, Gregory Norcross, Michael A. Sci Rep Article Microbes induce innate immune responses in hosts. It is critical to know how different microbes control adaptive responses through innate pathways. The impact of gram-positive bacteria on the innate and adaptive responses is unclear. Herein we report that Staphylococcus aureus induces IL-10, Th17-inducing cytokines IL-6 and IL-23, chemokines, and regulates dendritic cell markers. S. aureus inhibits T-cell IL-2 responses through modulation of HLA-DR, CD86 and PD-L1. IFN-gamma, Src kinase inhibitors, or TLR2 antibodies prevented the down-modulation of HLA-DR by S. aureus. Our data demonstrate that innate TLR signaling induces multi-dimensional inhibition of adaptive immune responses, which may contribute to the lack of protective immunity to bacteria or microbe tolerance. IL-10 and PD-L1 antagonists may boost immunity to vaccines for S. aureus and other microbes. Nature Publishing Group 2012-08-28 /pmc/articles/PMC3428601/ /pubmed/22930672 http://dx.doi.org/10.1038/srep00606 Text en Copyright © 2012, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareALike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Article
Wang, Jinhai
Roderiquez, Gregory
Norcross, Michael A.
Control of Adaptive Immune Responses by Staphylococcus aureus through IL-10, PD-L1, and TLR2
title Control of Adaptive Immune Responses by Staphylococcus aureus through IL-10, PD-L1, and TLR2
title_full Control of Adaptive Immune Responses by Staphylococcus aureus through IL-10, PD-L1, and TLR2
title_fullStr Control of Adaptive Immune Responses by Staphylococcus aureus through IL-10, PD-L1, and TLR2
title_full_unstemmed Control of Adaptive Immune Responses by Staphylococcus aureus through IL-10, PD-L1, and TLR2
title_short Control of Adaptive Immune Responses by Staphylococcus aureus through IL-10, PD-L1, and TLR2
title_sort control of adaptive immune responses by staphylococcus aureus through il-10, pd-l1, and tlr2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3428601/
https://www.ncbi.nlm.nih.gov/pubmed/22930672
http://dx.doi.org/10.1038/srep00606
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