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Th2 biased upper airway inflammation is associated with an impaired response to viral infection with Herpes simplex virus 1

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机构: [1]Ghent Univ Hosp, Dept Otorhinolaryngol, Upper Airway Res Lab, De Pintelaan 185, B-9000 Ghent, Belgium [2]Univ Ghent, Fac Vet Med, Virol Lab, Merelbeke, Belgium [3]Capital Med Univ, Beijing TongRen Hosp, Dept Otolaryngol Head & Neck Surg, Beijing, Peoples R China [4]Univ London Imperial Coll Sci Technol & Med, Natl Heart & Lung Inst, Airway Dis Infect Sect, London SW7 2AZ, England [5]Univ Athens, Pediat Clin 2, Dept Allergy, GR-10679 Athens, Greece [6]Univ Manchester, Inst Human Dev, Ctr Paediat & Child Hlth, Manchester M13 9PL, Lancs, England [7]Karolinska Inst, Clintec, Div ENT Dis, Stockholm, Sweden
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关键词: human ex vivo mucosa model herpes simplex virus 1 infection nasal polyps interferon-gamma

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Background: We aimed to elucidate possible differences in antiviral defense in chronic rhinosinusitis with nasal polyps (CRSwNP) mucosal tissue compared to healthy mucosal tissue (HMT) upon herpes simplex virus 1 (HSV1) exposure. Methodology: HMT and CRSwNP samples were infected with HSV1. We visualized the virus location by immunofluorescence and monitored invasion by a score. The mediators Interferon (IFN)-alpha, IFN-beta, IFN-lambda, IFN-gamma, Interleukin (IL)-6, IL-1 beta, Tumor necrosis factor (TNF)-alpha, IL-17, IL-5, IL-10 were measured in culture supernatants at baseline and at 24h, 48h and 72h after virus incubation. Results: CRSwNP mucosal tissue showed a significant deficit in IFN-gamma and IL-17 release within 24 to 72 hours after infection in comparison to HMT, at the same time releasing significantly more pro-inflammatory cytokines including IL-1 beta and TNF-alpha. These findings were associated with significantly higher viral invasion scores at 48 and 72 h in CRSwNP mucosa compared to those for the HMT. Conclusions: We demonstrate for the first time in a human ex-vivo mucosal model that the inadequate response of CRSwNP may be associated with a deeper intrusion of viruses into the mucosal tissue, and may contribute to more and longer symptoms upon acute infection, but also to the persistence of inflammation in CRSwNP tissue.

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出版当年[2015]版:
大类 | 3 区 医学
小类 | 2 区 耳鼻喉科学
最新[2023]版:
大类 | 2 区 医学
小类 | 1 区 耳鼻喉科学
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出版当年[2014]版:
Q1 OTORHINOLARYNGOLOGY
最新[2023]版:
Q1 OTORHINOLARYNGOLOGY

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第一作者机构: [1]Ghent Univ Hosp, Dept Otorhinolaryngol, Upper Airway Res Lab, De Pintelaan 185, B-9000 Ghent, Belgium
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通讯机构: [1]Ghent Univ Hosp, Dept Otorhinolaryngol, Upper Airway Res Lab, De Pintelaan 185, B-9000 Ghent, Belgium [*1]Upper Airway Research Laboratory Department of OtorhinolaryngologyGhent University HospitalDe Pintelaan 1859000 GhentBelgium
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