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Effects of lysed Enterococcus faecalis FK-23 on experimental allergic rhinitis in a murine model

In the current study, we sought to investigate whether lysed Enterococcus faecalis FK-23 (LFK), a heat-killed probiotic preparation, attenuated eosinophil influx into the upper airway and had immunomodulatory activity in a murine allergic rhinitis model. Eighteen BALB/c mice were divided into three...

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Autores principales: Zhu, Luping, Shimada, Takashi, Chen, Ruoxi, Lu, Meiping, Zhang, Qingzhao, Lu, Wenmin, Yin, Min, Enomoto, Tadao, Cheng, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial Department of Journal of Biomedical Research 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596073/
https://www.ncbi.nlm.nih.gov/pubmed/23554753
http://dx.doi.org/10.7555/JBR.26.20120023
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author Zhu, Luping
Shimada, Takashi
Chen, Ruoxi
Lu, Meiping
Zhang, Qingzhao
Lu, Wenmin
Yin, Min
Enomoto, Tadao
Cheng, Lei
author_facet Zhu, Luping
Shimada, Takashi
Chen, Ruoxi
Lu, Meiping
Zhang, Qingzhao
Lu, Wenmin
Yin, Min
Enomoto, Tadao
Cheng, Lei
author_sort Zhu, Luping
collection PubMed
description In the current study, we sought to investigate whether lysed Enterococcus faecalis FK-23 (LFK), a heat-killed probiotic preparation, attenuated eosinophil influx into the upper airway and had immunomodulatory activity in a murine allergic rhinitis model. Eighteen BALB/c mice were divided into three groups; the ovalbumin (OVA)-sensitized/challenged group, which received saline orally for 6 weeks (OVA group), the OVA-sensitized/challenged group, which received LFK orally for 6 weeks (LFK-fed group), and the non-sensitized group, which received saline for 6 weeks (saline control group). Nasal rubbing and sneezing were monitored during the study. After the final challenge, interleukin (IL)-4, interferon (IFN)-γ, and OVA-specific IgE levels in the sera and splenocyte culture supernatants were determined, eosinophilic infiltrate into the upper airway was quantified, and splenic CD4+CD25+ regulatory T cells (Tregs) were examined by flow cytometry. We found that nasal rubbing was significantly reduced in LFK-fed mice compared to the OVA group on d 27 and 35, and sneezing was significantly inhibited by LFK administration for 35 d. LFK-fed mice had significantly less eosinophil influx into the nasal mucosa than the OVA group. There were no significant differences between the LFK-fed group and OVA group in the serum and splenocyte culture supernatant levels of IL-4, IFN-γ, and OVA-specific IgE. Interestingly, the LFK-fed mice had a significantly greater percentage of splenic CD4+CD25+ Tregs than OVA group. Our results indicate that oral administration of LFK may alleviate nasal symptoms, reduce nasal eosinophilia, and increase the percentage of CD4+CD25+ Tregs in experimental allergic rhinitis.
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spelling pubmed-35960732013-04-02 Effects of lysed Enterococcus faecalis FK-23 on experimental allergic rhinitis in a murine model Zhu, Luping Shimada, Takashi Chen, Ruoxi Lu, Meiping Zhang, Qingzhao Lu, Wenmin Yin, Min Enomoto, Tadao Cheng, Lei J Biomed Res Research Paper In the current study, we sought to investigate whether lysed Enterococcus faecalis FK-23 (LFK), a heat-killed probiotic preparation, attenuated eosinophil influx into the upper airway and had immunomodulatory activity in a murine allergic rhinitis model. Eighteen BALB/c mice were divided into three groups; the ovalbumin (OVA)-sensitized/challenged group, which received saline orally for 6 weeks (OVA group), the OVA-sensitized/challenged group, which received LFK orally for 6 weeks (LFK-fed group), and the non-sensitized group, which received saline for 6 weeks (saline control group). Nasal rubbing and sneezing were monitored during the study. After the final challenge, interleukin (IL)-4, interferon (IFN)-γ, and OVA-specific IgE levels in the sera and splenocyte culture supernatants were determined, eosinophilic infiltrate into the upper airway was quantified, and splenic CD4+CD25+ regulatory T cells (Tregs) were examined by flow cytometry. We found that nasal rubbing was significantly reduced in LFK-fed mice compared to the OVA group on d 27 and 35, and sneezing was significantly inhibited by LFK administration for 35 d. LFK-fed mice had significantly less eosinophil influx into the nasal mucosa than the OVA group. There were no significant differences between the LFK-fed group and OVA group in the serum and splenocyte culture supernatant levels of IL-4, IFN-γ, and OVA-specific IgE. Interestingly, the LFK-fed mice had a significantly greater percentage of splenic CD4+CD25+ Tregs than OVA group. Our results indicate that oral administration of LFK may alleviate nasal symptoms, reduce nasal eosinophilia, and increase the percentage of CD4+CD25+ Tregs in experimental allergic rhinitis. Editorial Department of Journal of Biomedical Research 2012-05 2012-05-09 /pmc/articles/PMC3596073/ /pubmed/23554753 http://dx.doi.org/10.7555/JBR.26.20120023 Text en © 2012 by the Journal of Biomedical Research. All rights reserved. This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/
spellingShingle Research Paper
Zhu, Luping
Shimada, Takashi
Chen, Ruoxi
Lu, Meiping
Zhang, Qingzhao
Lu, Wenmin
Yin, Min
Enomoto, Tadao
Cheng, Lei
Effects of lysed Enterococcus faecalis FK-23 on experimental allergic rhinitis in a murine model
title Effects of lysed Enterococcus faecalis FK-23 on experimental allergic rhinitis in a murine model
title_full Effects of lysed Enterococcus faecalis FK-23 on experimental allergic rhinitis in a murine model
title_fullStr Effects of lysed Enterococcus faecalis FK-23 on experimental allergic rhinitis in a murine model
title_full_unstemmed Effects of lysed Enterococcus faecalis FK-23 on experimental allergic rhinitis in a murine model
title_short Effects of lysed Enterococcus faecalis FK-23 on experimental allergic rhinitis in a murine model
title_sort effects of lysed enterococcus faecalis fk-23 on experimental allergic rhinitis in a murine model
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596073/
https://www.ncbi.nlm.nih.gov/pubmed/23554753
http://dx.doi.org/10.7555/JBR.26.20120023
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