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Specific immunotherapy in combination with Clostridium butyricum inhibits allergic inflammation in the mouse intestine

The current therapy on allergic inflammation is unsatisfactory. Probiotics improve the immunity in the body. This study aims to test a hypothesis that administration with Clostridium butyricum (C. butyricum) enforces the effect of specific immunotherapy (SIT) on intestinal allergic inflammation. In...

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Autores principales: Shi, Yanhong, Xu, Ling-Zhi, Peng, Kangsheng, Wu, Wei, Wu, Ruijin, Liu, Zhi-Qiang, Yang, Gui, Geng, Xiao-Rui, Liu, Jun, Liu, Zhi-Gang, Liu, Zhanju, Yang, Ping-Chang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667269/
https://www.ncbi.nlm.nih.gov/pubmed/26627845
http://dx.doi.org/10.1038/srep17651
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author Shi, Yanhong
Xu, Ling-Zhi
Peng, Kangsheng
Wu, Wei
Wu, Ruijin
Liu, Zhi-Qiang
Yang, Gui
Geng, Xiao-Rui
Liu, Jun
Liu, Zhi-Gang
Liu, Zhanju
Yang, Ping-Chang
author_facet Shi, Yanhong
Xu, Ling-Zhi
Peng, Kangsheng
Wu, Wei
Wu, Ruijin
Liu, Zhi-Qiang
Yang, Gui
Geng, Xiao-Rui
Liu, Jun
Liu, Zhi-Gang
Liu, Zhanju
Yang, Ping-Chang
author_sort Shi, Yanhong
collection PubMed
description The current therapy on allergic inflammation is unsatisfactory. Probiotics improve the immunity in the body. This study aims to test a hypothesis that administration with Clostridium butyricum (C. butyricum) enforces the effect of specific immunotherapy (SIT) on intestinal allergic inflammation. In this study, an ovalbumin (OVA) specific allergic inflammation mouse model was created. The mice were treated with SIT or/and C. butyricum. The results showed that the intestinal allergic inflammation was only moderately alleviated by SIT, which was significantly enforced by a combination with C. butyricum; treating with C. butyricum alone did not show much inhibitory efficacy. The increase in the frequency of the interleukin (IL)-10-producing OVA-specific B cell (OVAsBC) was observed in mice in parallel to the inhibitory effect on the intestinal allergic inflammation. The in vitro treatment of the OVAsBCs with OVA increased the histone deacetylase-1 (HDAC1) phosphorylation, modulated the transcription of the Bcl6 gene, and triggered the OVAsBCs to differentiate to the IgE-producing plasma cells. Exposure to both OVA and butyrate sodium in the culture increased the expression of IL-10 in OVAsBCs. In conclusion, administration with C. butyricum enforces the inhibitory effect of SIT on allergic inflammation in the mouse intestine.
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spelling pubmed-46672692015-12-08 Specific immunotherapy in combination with Clostridium butyricum inhibits allergic inflammation in the mouse intestine Shi, Yanhong Xu, Ling-Zhi Peng, Kangsheng Wu, Wei Wu, Ruijin Liu, Zhi-Qiang Yang, Gui Geng, Xiao-Rui Liu, Jun Liu, Zhi-Gang Liu, Zhanju Yang, Ping-Chang Sci Rep Article The current therapy on allergic inflammation is unsatisfactory. Probiotics improve the immunity in the body. This study aims to test a hypothesis that administration with Clostridium butyricum (C. butyricum) enforces the effect of specific immunotherapy (SIT) on intestinal allergic inflammation. In this study, an ovalbumin (OVA) specific allergic inflammation mouse model was created. The mice were treated with SIT or/and C. butyricum. The results showed that the intestinal allergic inflammation was only moderately alleviated by SIT, which was significantly enforced by a combination with C. butyricum; treating with C. butyricum alone did not show much inhibitory efficacy. The increase in the frequency of the interleukin (IL)-10-producing OVA-specific B cell (OVAsBC) was observed in mice in parallel to the inhibitory effect on the intestinal allergic inflammation. The in vitro treatment of the OVAsBCs with OVA increased the histone deacetylase-1 (HDAC1) phosphorylation, modulated the transcription of the Bcl6 gene, and triggered the OVAsBCs to differentiate to the IgE-producing plasma cells. Exposure to both OVA and butyrate sodium in the culture increased the expression of IL-10 in OVAsBCs. In conclusion, administration with C. butyricum enforces the inhibitory effect of SIT on allergic inflammation in the mouse intestine. Nature Publishing Group 2015-12-02 /pmc/articles/PMC4667269/ /pubmed/26627845 http://dx.doi.org/10.1038/srep17651 Text en Copyright © 2015, Macmillan Publishers Limited 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
Shi, Yanhong
Xu, Ling-Zhi
Peng, Kangsheng
Wu, Wei
Wu, Ruijin
Liu, Zhi-Qiang
Yang, Gui
Geng, Xiao-Rui
Liu, Jun
Liu, Zhi-Gang
Liu, Zhanju
Yang, Ping-Chang
Specific immunotherapy in combination with Clostridium butyricum inhibits allergic inflammation in the mouse intestine
title Specific immunotherapy in combination with Clostridium butyricum inhibits allergic inflammation in the mouse intestine
title_full Specific immunotherapy in combination with Clostridium butyricum inhibits allergic inflammation in the mouse intestine
title_fullStr Specific immunotherapy in combination with Clostridium butyricum inhibits allergic inflammation in the mouse intestine
title_full_unstemmed Specific immunotherapy in combination with Clostridium butyricum inhibits allergic inflammation in the mouse intestine
title_short Specific immunotherapy in combination with Clostridium butyricum inhibits allergic inflammation in the mouse intestine
title_sort specific immunotherapy in combination with clostridium butyricum inhibits allergic inflammation in the mouse intestine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667269/
https://www.ncbi.nlm.nih.gov/pubmed/26627845
http://dx.doi.org/10.1038/srep17651
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