Th17 cells and IL-17 in protective immunity to vaginal candidiasis.

BACKGROUND: Th17 cells play a major role in coordinating the host defence in oropharyngeal candidiasis. In this study we investigated the involvement of the Th17 response in an animal model of vulvovaginal candidiasis (VVC). METHODS: To monitor the course of infection we exploited a new in vivo imag...

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Main Authors: Donatella Pietrella, Anna Rachini, Mark Pines, Neelam Pandey, Paolo Mosci, Francesco Bistoni, Cristophe d'Enfert, Anna Vecchiarelli
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3144947?pdf=render
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spelling doaj-8c658e73451c48b6a21ac70ebe685acc2020-11-25T02:39:02ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0167e2277010.1371/journal.pone.0022770Th17 cells and IL-17 in protective immunity to vaginal candidiasis.Donatella PietrellaAnna RachiniMark PinesNeelam PandeyPaolo MosciFrancesco BistoniCristophe d'EnfertAnna VecchiarelliBACKGROUND: Th17 cells play a major role in coordinating the host defence in oropharyngeal candidiasis. In this study we investigated the involvement of the Th17 response in an animal model of vulvovaginal candidiasis (VVC). METHODS: To monitor the course of infection we exploited a new in vivo imaging technique. RESULTS: i) The progression of VVC leads to a strong influx of neutrophils in the vagina soon after the challenge which persisted despite the resolution of infection; ii) IL-17, produced by vaginal cells, particularly CD4 T cells, was detected in the vaginal wash during the infection, reaching a maximum 14 days after the challenge; iii) The amount and kinetics of IL-23 in vaginal fluids were comparable to those in vaginal cells; iv) The inhibition of Th17 differentiation led to significant inhibition of IL-17 production with consequent exacerbation of infection; v) An increased production of βdefensin 2 was manifested in cells of infected mice. This production was strongly reduced when Th17 differentiation was inhibited and was increased by rIL-17 treatment. CONCLUSIONS: These results imply that IL-17 and Th17, along with innate antimicrobial factors, have a role in the immune response to vaginal candidiasis.http://europepmc.org/articles/PMC3144947?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Donatella Pietrella
Anna Rachini
Mark Pines
Neelam Pandey
Paolo Mosci
Francesco Bistoni
Cristophe d'Enfert
Anna Vecchiarelli
spellingShingle Donatella Pietrella
Anna Rachini
Mark Pines
Neelam Pandey
Paolo Mosci
Francesco Bistoni
Cristophe d'Enfert
Anna Vecchiarelli
Th17 cells and IL-17 in protective immunity to vaginal candidiasis.
PLoS ONE
author_facet Donatella Pietrella
Anna Rachini
Mark Pines
Neelam Pandey
Paolo Mosci
Francesco Bistoni
Cristophe d'Enfert
Anna Vecchiarelli
author_sort Donatella Pietrella
title Th17 cells and IL-17 in protective immunity to vaginal candidiasis.
title_short Th17 cells and IL-17 in protective immunity to vaginal candidiasis.
title_full Th17 cells and IL-17 in protective immunity to vaginal candidiasis.
title_fullStr Th17 cells and IL-17 in protective immunity to vaginal candidiasis.
title_full_unstemmed Th17 cells and IL-17 in protective immunity to vaginal candidiasis.
title_sort th17 cells and il-17 in protective immunity to vaginal candidiasis.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description BACKGROUND: Th17 cells play a major role in coordinating the host defence in oropharyngeal candidiasis. In this study we investigated the involvement of the Th17 response in an animal model of vulvovaginal candidiasis (VVC). METHODS: To monitor the course of infection we exploited a new in vivo imaging technique. RESULTS: i) The progression of VVC leads to a strong influx of neutrophils in the vagina soon after the challenge which persisted despite the resolution of infection; ii) IL-17, produced by vaginal cells, particularly CD4 T cells, was detected in the vaginal wash during the infection, reaching a maximum 14 days after the challenge; iii) The amount and kinetics of IL-23 in vaginal fluids were comparable to those in vaginal cells; iv) The inhibition of Th17 differentiation led to significant inhibition of IL-17 production with consequent exacerbation of infection; v) An increased production of βdefensin 2 was manifested in cells of infected mice. This production was strongly reduced when Th17 differentiation was inhibited and was increased by rIL-17 treatment. CONCLUSIONS: These results imply that IL-17 and Th17, along with innate antimicrobial factors, have a role in the immune response to vaginal candidiasis.
url http://europepmc.org/articles/PMC3144947?pdf=render
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