Orally administered <it>Lactobacillus rhamnosus</it> modulates the respiratory immune response triggered by the viral pathogen-associated molecular pattern poly(I:C)

<p>Abstract</p> <p>Background</p> <p>Some studies have shown that probiotics, including <it>Lactobacillus rhamnosus</it> CRL1505, had the potential to beneficially modulate the outcome of certain bacterial and viral respiratory infections. However, these stu...

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Main Authors: Villena Julio, Chiba Eriko, Tomosada Yohsuke, Salva Susana, Marranzino Gabriela, Kitazawa Haruki, Alvarez Susana
Format: Article
Language:English
Published: BMC 2012-09-01
Series:BMC Immunology
Subjects:
Online Access:http://www.biomedcentral.com/1471-2172/13/53
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spelling doaj-d2de9211c76e4cc3bda1351ec96196d62020-11-25T01:38:37ZengBMCBMC Immunology1471-21722012-09-011315310.1186/1471-2172-13-53Orally administered <it>Lactobacillus rhamnosus</it> modulates the respiratory immune response triggered by the viral pathogen-associated molecular pattern poly(I:C)Villena JulioChiba ErikoTomosada YohsukeSalva SusanaMarranzino GabrielaKitazawa HarukiAlvarez Susana<p>Abstract</p> <p>Background</p> <p>Some studies have shown that probiotics, including <it>Lactobacillus rhamnosus</it> CRL1505, had the potential to beneficially modulate the outcome of certain bacterial and viral respiratory infections. However, these studies did not determine the mechanism(s) by which probiotics contribute to host defense against respiratory viruses.</p> <p>Results</p> <p>In this work we demonstrated that orally administered <it>Lactobacillus rhamnosus</it> CRL1505 (Lr1505) was able to increase the levels of IFN-γ, IL-10 and IL-6 in the respiratory tract and the number of lung CD3<sup>+</sup>CD4<sup>+</sup>IFN-γ<sup>+</sup> T cells. To mimic the pro-inflammatory and physiopathological consecuences of RNA viral infections in the lung, we used an experimental model of lung inflammation based on the administration of the artificial viral pathogen-associated molecular pattern poly(I:C). Nasal administration of poly(I:C) to mice induced a marked impairment of lung function that was accompanied by the production of pro-inflammatory mediators and inflammatory cell recruitment into the airways. The preventive administration of Lr1505 reduced lung injuries and the production of TNF-α, IL-6, IL-8 and MCP-1 in the respiratory tract after the challenge with poly(I:C). Moreover, Lr1505 induced a significant increase in lung and serum IL-10. We also observed that Lr1505 was able to increase respiratory IFN-γ levels and the number of lung CD3<sup>+</sup>CD4<sup>+</sup>IFN-γ<sup>+</sup> T cells after poly(I:C) challenge. Moreover, higher numbers of both CD103<sup>+</sup> and CD11b<sup>high</sup> dendritic cells and increased expression of MHC-II, IL-12 and IFN-γ in these cell populations were found in lungs of Lr1505-treated mice. Therefore, Lr1505 treatment would beneficially regulate the balance between pro-inflammatory mediators and IL-10, allowing an effective inflammatory response against infection and avoiding tissue damage.</p> <p>Conclusions</p> <p>Results showed that Lr1505 would induce a mobilization of cells from intestine and changes in cytokine profile that would be able to beneficially modulate the respiratory mucosal immunity. Although deeper studies are needed using challenges with respiratory viruses, the results in this study suggest that Lr1505, a potent inducer of antiviral cytokines, may be useful as a prophylactic agent to control respiratory virus infection.</p> http://www.biomedcentral.com/1471-2172/13/53<it>L. rhamnosus</it> CRL1505Poly(I:C)Antiviral immunityRespiratory tract
collection DOAJ
language English
format Article
sources DOAJ
author Villena Julio
Chiba Eriko
Tomosada Yohsuke
Salva Susana
Marranzino Gabriela
Kitazawa Haruki
Alvarez Susana
spellingShingle Villena Julio
Chiba Eriko
Tomosada Yohsuke
Salva Susana
Marranzino Gabriela
Kitazawa Haruki
Alvarez Susana
Orally administered <it>Lactobacillus rhamnosus</it> modulates the respiratory immune response triggered by the viral pathogen-associated molecular pattern poly(I:C)
BMC Immunology
<it>L. rhamnosus</it> CRL1505
Poly(I:C)
Antiviral immunity
Respiratory tract
author_facet Villena Julio
Chiba Eriko
Tomosada Yohsuke
Salva Susana
Marranzino Gabriela
Kitazawa Haruki
Alvarez Susana
author_sort Villena Julio
title Orally administered <it>Lactobacillus rhamnosus</it> modulates the respiratory immune response triggered by the viral pathogen-associated molecular pattern poly(I:C)
title_short Orally administered <it>Lactobacillus rhamnosus</it> modulates the respiratory immune response triggered by the viral pathogen-associated molecular pattern poly(I:C)
title_full Orally administered <it>Lactobacillus rhamnosus</it> modulates the respiratory immune response triggered by the viral pathogen-associated molecular pattern poly(I:C)
title_fullStr Orally administered <it>Lactobacillus rhamnosus</it> modulates the respiratory immune response triggered by the viral pathogen-associated molecular pattern poly(I:C)
title_full_unstemmed Orally administered <it>Lactobacillus rhamnosus</it> modulates the respiratory immune response triggered by the viral pathogen-associated molecular pattern poly(I:C)
title_sort orally administered <it>lactobacillus rhamnosus</it> modulates the respiratory immune response triggered by the viral pathogen-associated molecular pattern poly(i:c)
publisher BMC
series BMC Immunology
issn 1471-2172
publishDate 2012-09-01
description <p>Abstract</p> <p>Background</p> <p>Some studies have shown that probiotics, including <it>Lactobacillus rhamnosus</it> CRL1505, had the potential to beneficially modulate the outcome of certain bacterial and viral respiratory infections. However, these studies did not determine the mechanism(s) by which probiotics contribute to host defense against respiratory viruses.</p> <p>Results</p> <p>In this work we demonstrated that orally administered <it>Lactobacillus rhamnosus</it> CRL1505 (Lr1505) was able to increase the levels of IFN-γ, IL-10 and IL-6 in the respiratory tract and the number of lung CD3<sup>+</sup>CD4<sup>+</sup>IFN-γ<sup>+</sup> T cells. To mimic the pro-inflammatory and physiopathological consecuences of RNA viral infections in the lung, we used an experimental model of lung inflammation based on the administration of the artificial viral pathogen-associated molecular pattern poly(I:C). Nasal administration of poly(I:C) to mice induced a marked impairment of lung function that was accompanied by the production of pro-inflammatory mediators and inflammatory cell recruitment into the airways. The preventive administration of Lr1505 reduced lung injuries and the production of TNF-α, IL-6, IL-8 and MCP-1 in the respiratory tract after the challenge with poly(I:C). Moreover, Lr1505 induced a significant increase in lung and serum IL-10. We also observed that Lr1505 was able to increase respiratory IFN-γ levels and the number of lung CD3<sup>+</sup>CD4<sup>+</sup>IFN-γ<sup>+</sup> T cells after poly(I:C) challenge. Moreover, higher numbers of both CD103<sup>+</sup> and CD11b<sup>high</sup> dendritic cells and increased expression of MHC-II, IL-12 and IFN-γ in these cell populations were found in lungs of Lr1505-treated mice. Therefore, Lr1505 treatment would beneficially regulate the balance between pro-inflammatory mediators and IL-10, allowing an effective inflammatory response against infection and avoiding tissue damage.</p> <p>Conclusions</p> <p>Results showed that Lr1505 would induce a mobilization of cells from intestine and changes in cytokine profile that would be able to beneficially modulate the respiratory mucosal immunity. Although deeper studies are needed using challenges with respiratory viruses, the results in this study suggest that Lr1505, a potent inducer of antiviral cytokines, may be useful as a prophylactic agent to control respiratory virus infection.</p>
topic <it>L. rhamnosus</it> CRL1505
Poly(I:C)
Antiviral immunity
Respiratory tract
url http://www.biomedcentral.com/1471-2172/13/53
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