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Toll-like receptors, cytokines & nitric oxide synthase in patients with otitis media with effusion

BACKGROUND & OBJECTIVES: Microbial infections in the normally sterile environment of the middle ear cavity in patients with otitis media trigger expression of Toll-like receptors (TLRs), cytokines, and nitric oxide. We evaluated the expression levels of TLR-1, -2, -4, -5, -6, and -9, interleukin...

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Autores principales: Lee, Ho Yun, Chung, Ji Hyun, Lee, Sun Kyu, Byun, Jae Yong, Kim, Young Il, Yeo, Seung Geun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3868065/
https://www.ncbi.nlm.nih.gov/pubmed/24434259
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author Lee, Ho Yun
Chung, Ji Hyun
Lee, Sun Kyu
Byun, Jae Yong
Kim, Young Il
Yeo, Seung Geun
author_facet Lee, Ho Yun
Chung, Ji Hyun
Lee, Sun Kyu
Byun, Jae Yong
Kim, Young Il
Yeo, Seung Geun
author_sort Lee, Ho Yun
collection PubMed
description BACKGROUND & OBJECTIVES: Microbial infections in the normally sterile environment of the middle ear cavity in patients with otitis media trigger expression of Toll-like receptors (TLRs), cytokines, and nitric oxide. We evaluated the expression levels of TLR-1, -2, -4, -5, -6, and -9, interleukin (IL)-6, -8, -10, and -12, interferon-γ (IFN-γ), tumour necrosis factor-α (TNF-α), and nitric oxide (NO), in paediatric patients with otitis media with effusion (OME). METHODS: The levels of TLR, cytokine, and nitric oxide synthase (NOS) mRNAs in middle ear effusion were assessed by real-time polymerase chain reaction in 96 children with OME, 24 prone and 72 not prone to otitis. The level of expression of each mRNA was compared in the otitis-prone and non-otitis-prone groups, in patients with and without bacteria, and by frequency of ventilation tube insertion. RESULTS: The expression of TLR-1, -2, -4, -5, -6, and -9; IL-6, -8, -10, and -12; IFN-γ; TNF-α; and NOS mRNAs in the effusion fluid of both the otitis-prone and non-otitis-prone groups were measured. The expression levels of TLR-2, -4, -6, and -9 mRNA were significantly lower in the otitis-prone than in the non-otitis-prone group (P<0.05). Although higher levels of TLR, cytokine, and NOS mRNAs were generally observed in culture positive than in culture negative patients, none of these differences was statistically significant. No differences were observed in the expressions relative to the frequencies of ventilation tube insertion. INTERPRETATION & CONCLUSIONS: TLRs, cytokines, and NOS, which act cooperatively in the innate immune response, were closely associated with OME. Decreased expression of TLRs may be associated with increased susceptibility to OME.
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spelling pubmed-38680652013-12-30 Toll-like receptors, cytokines & nitric oxide synthase in patients with otitis media with effusion Lee, Ho Yun Chung, Ji Hyun Lee, Sun Kyu Byun, Jae Yong Kim, Young Il Yeo, Seung Geun Indian J Med Res Original Article BACKGROUND & OBJECTIVES: Microbial infections in the normally sterile environment of the middle ear cavity in patients with otitis media trigger expression of Toll-like receptors (TLRs), cytokines, and nitric oxide. We evaluated the expression levels of TLR-1, -2, -4, -5, -6, and -9, interleukin (IL)-6, -8, -10, and -12, interferon-γ (IFN-γ), tumour necrosis factor-α (TNF-α), and nitric oxide (NO), in paediatric patients with otitis media with effusion (OME). METHODS: The levels of TLR, cytokine, and nitric oxide synthase (NOS) mRNAs in middle ear effusion were assessed by real-time polymerase chain reaction in 96 children with OME, 24 prone and 72 not prone to otitis. The level of expression of each mRNA was compared in the otitis-prone and non-otitis-prone groups, in patients with and without bacteria, and by frequency of ventilation tube insertion. RESULTS: The expression of TLR-1, -2, -4, -5, -6, and -9; IL-6, -8, -10, and -12; IFN-γ; TNF-α; and NOS mRNAs in the effusion fluid of both the otitis-prone and non-otitis-prone groups were measured. The expression levels of TLR-2, -4, -6, and -9 mRNA were significantly lower in the otitis-prone than in the non-otitis-prone group (P<0.05). Although higher levels of TLR, cytokine, and NOS mRNAs were generally observed in culture positive than in culture negative patients, none of these differences was statistically significant. No differences were observed in the expressions relative to the frequencies of ventilation tube insertion. INTERPRETATION & CONCLUSIONS: TLRs, cytokines, and NOS, which act cooperatively in the innate immune response, were closely associated with OME. Decreased expression of TLRs may be associated with increased susceptibility to OME. Medknow Publications & Media Pvt Ltd 2013-10 /pmc/articles/PMC3868065/ /pubmed/24434259 Text en Copyright: © The Indian Journal of Medical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Ho Yun
Chung, Ji Hyun
Lee, Sun Kyu
Byun, Jae Yong
Kim, Young Il
Yeo, Seung Geun
Toll-like receptors, cytokines & nitric oxide synthase in patients with otitis media with effusion
title Toll-like receptors, cytokines & nitric oxide synthase in patients with otitis media with effusion
title_full Toll-like receptors, cytokines & nitric oxide synthase in patients with otitis media with effusion
title_fullStr Toll-like receptors, cytokines & nitric oxide synthase in patients with otitis media with effusion
title_full_unstemmed Toll-like receptors, cytokines & nitric oxide synthase in patients with otitis media with effusion
title_short Toll-like receptors, cytokines & nitric oxide synthase in patients with otitis media with effusion
title_sort toll-like receptors, cytokines & nitric oxide synthase in patients with otitis media with effusion
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3868065/
https://www.ncbi.nlm.nih.gov/pubmed/24434259
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