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...
Main Authors: | , , , , , , , |
---|---|
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 |
id |
doaj-8c658e73451c48b6a21ac70ebe685acc |
---|---|
record_format |
Article |
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 |
work_keys_str_mv |
AT donatellapietrella th17cellsandil17inprotectiveimmunitytovaginalcandidiasis AT annarachini th17cellsandil17inprotectiveimmunitytovaginalcandidiasis AT markpines th17cellsandil17inprotectiveimmunitytovaginalcandidiasis AT neelampandey th17cellsandil17inprotectiveimmunitytovaginalcandidiasis AT paolomosci th17cellsandil17inprotectiveimmunitytovaginalcandidiasis AT francescobistoni th17cellsandil17inprotectiveimmunitytovaginalcandidiasis AT cristophedenfert th17cellsandil17inprotectiveimmunitytovaginalcandidiasis AT annavecchiarelli th17cellsandil17inprotectiveimmunitytovaginalcandidiasis |
_version_ |
1724788028404137984 |