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Interleukin 10 inhibits pro-inflammatory cytokine responses and killing of Burkholderia pseudomallei

Melioidosis, caused by Burkholderia pseudomallei, is endemic in northeastern Thailand and Northern Australia. Severe septicemic melioidosis is associated with high levels of pro-inflammatory cytokines and is correlated with poor clinical outcomes. IL-10 is an immunoregulatory cytokine, which in othe...

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Autores principales: Kessler, Bianca, Rinchai, Darawan, Kewcharoenwong, Chidchamai, Nithichanon, Arnone, Biggart, Rachael, Hawrylowicz, Catherine M., Bancroft, Gregory J., Lertmemongkolchai, Ganjana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5316963/
https://www.ncbi.nlm.nih.gov/pubmed/28216665
http://dx.doi.org/10.1038/srep42791
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author Kessler, Bianca
Rinchai, Darawan
Kewcharoenwong, Chidchamai
Nithichanon, Arnone
Biggart, Rachael
Hawrylowicz, Catherine M.
Bancroft, Gregory J.
Lertmemongkolchai, Ganjana
author_facet Kessler, Bianca
Rinchai, Darawan
Kewcharoenwong, Chidchamai
Nithichanon, Arnone
Biggart, Rachael
Hawrylowicz, Catherine M.
Bancroft, Gregory J.
Lertmemongkolchai, Ganjana
author_sort Kessler, Bianca
collection PubMed
description Melioidosis, caused by Burkholderia pseudomallei, is endemic in northeastern Thailand and Northern Australia. Severe septicemic melioidosis is associated with high levels of pro-inflammatory cytokines and is correlated with poor clinical outcomes. IL-10 is an immunoregulatory cytokine, which in other infections can control the expression of pro-inflammatory cytokines, but its role in melioidosis has not been addressed. Here, whole blood of healthy seropositive individuals (n = 75), living in N. E. Thailand was co-cultured with B. pseudomallei and production of IL-10 and IFN-γ detected and the cellular sources identified. CD3(−) CD14(+) monocytes were the main source of IL-10. Neutralization of IL-10 increased IFN-γ, IL-6 and TNF-α production and improved bacteria killing. IFN-γ production and microbicidal activity were impaired in individuals with diabetes mellitus (DM). In contrast, IL-10 production was unimpaired in individuals with DM, resulting in an IL-10 dominant cytokine balance. Neutralization of IL-10 restored the IFN-γ response of individuals with DM to similar levels observed in healthy individuals and improved killing of B. pseudomallei in vitro. These results demonstrate that monocyte derived IL-10 acts to inhibit potentially protective cell mediated immune responses against B. pseudomallei, but may also moderate the pathological effects of excessive cytokine production during sepsis.
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spelling pubmed-53169632017-02-24 Interleukin 10 inhibits pro-inflammatory cytokine responses and killing of Burkholderia pseudomallei Kessler, Bianca Rinchai, Darawan Kewcharoenwong, Chidchamai Nithichanon, Arnone Biggart, Rachael Hawrylowicz, Catherine M. Bancroft, Gregory J. Lertmemongkolchai, Ganjana Sci Rep Article Melioidosis, caused by Burkholderia pseudomallei, is endemic in northeastern Thailand and Northern Australia. Severe septicemic melioidosis is associated with high levels of pro-inflammatory cytokines and is correlated with poor clinical outcomes. IL-10 is an immunoregulatory cytokine, which in other infections can control the expression of pro-inflammatory cytokines, but its role in melioidosis has not been addressed. Here, whole blood of healthy seropositive individuals (n = 75), living in N. E. Thailand was co-cultured with B. pseudomallei and production of IL-10 and IFN-γ detected and the cellular sources identified. CD3(−) CD14(+) monocytes were the main source of IL-10. Neutralization of IL-10 increased IFN-γ, IL-6 and TNF-α production and improved bacteria killing. IFN-γ production and microbicidal activity were impaired in individuals with diabetes mellitus (DM). In contrast, IL-10 production was unimpaired in individuals with DM, resulting in an IL-10 dominant cytokine balance. Neutralization of IL-10 restored the IFN-γ response of individuals with DM to similar levels observed in healthy individuals and improved killing of B. pseudomallei in vitro. These results demonstrate that monocyte derived IL-10 acts to inhibit potentially protective cell mediated immune responses against B. pseudomallei, but may also moderate the pathological effects of excessive cytokine production during sepsis. Nature Publishing Group 2017-02-20 /pmc/articles/PMC5316963/ /pubmed/28216665 http://dx.doi.org/10.1038/srep42791 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Kessler, Bianca
Rinchai, Darawan
Kewcharoenwong, Chidchamai
Nithichanon, Arnone
Biggart, Rachael
Hawrylowicz, Catherine M.
Bancroft, Gregory J.
Lertmemongkolchai, Ganjana
Interleukin 10 inhibits pro-inflammatory cytokine responses and killing of Burkholderia pseudomallei
title Interleukin 10 inhibits pro-inflammatory cytokine responses and killing of Burkholderia pseudomallei
title_full Interleukin 10 inhibits pro-inflammatory cytokine responses and killing of Burkholderia pseudomallei
title_fullStr Interleukin 10 inhibits pro-inflammatory cytokine responses and killing of Burkholderia pseudomallei
title_full_unstemmed Interleukin 10 inhibits pro-inflammatory cytokine responses and killing of Burkholderia pseudomallei
title_short Interleukin 10 inhibits pro-inflammatory cytokine responses and killing of Burkholderia pseudomallei
title_sort interleukin 10 inhibits pro-inflammatory cytokine responses and killing of burkholderia pseudomallei
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5316963/
https://www.ncbi.nlm.nih.gov/pubmed/28216665
http://dx.doi.org/10.1038/srep42791
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