Anti-Staphylococcal Humoral Immune Response in patients with chronic rhinosinusitis

dc.bibliographicCitation.firstPage50eng
dc.bibliographicCitation.journalTitleRhinology onlineeng
dc.bibliographicCitation.volume2eng
dc.contributor.authorThunberg, Ulrica
dc.contributor.authorHugosson, Svante
dc.contributor.authorFredlund, Hans
dc.contributor.authorCao, Yang
dc.contributor.authorEhricht, Ralf
dc.contributor.authorMonecke, Stefan
dc.contributor.authorMueller, Elke
dc.contributor.authorEngelmann, Susanne
dc.contributor.authorSöderquist, Bo
dc.date.accessioned2020-01-03T14:03:30Z
dc.date.available2020-01-03T14:03:30Z
dc.date.issued2019
dc.description.abstractBackground: Staphylococcus aureus (S. aureus) can behave both as a harmless commensal and as a pathogen. Its significance in the pathogenesis of chronic rhinosinusitis (CRS) is not yet fully understood. This study aimed to determine serum antibody responses to specific staphylococcal antigens in patients with CRS and healthy controls, and to investigate the correlation between specific antibody response and severity of symptoms. Methodology: Serum samples from 39 patients with CRS and 56 healthy controls were analysed using a protein microarray to investigate the antibody response to S. aureus specific antigens, with a focus on immunoglobulin G (IgG) directed toward staphylococcal components accessible to the immune system. Holm-Bonferroni corrections were applied in all analyses. Information about growth of S. aureus in nares and maxillary sinus was taken from a previous study based on the same individuals. Clinical symptoms were assessed using a scoring system. Results: IgG antibody levels toward staphylococcal TSST-1 and LukF-PV were significantly higher in the CRS patient group compared to healthy controls, and levels of anti-TSST-1 antibodies were significantly higher in the CRS patient group with S. aureus in maxillary sinus than in controls. There were no correlations between the severity of symptoms and levels of serum anti-staphylococcal IgG antibody levels for LukF-PV and TSST-1. Conclusions: TSST-1 and LukF-PV could be interesting markers for future studies of the pathogenesis of CRS.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://doi.org/10.34657/80
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/4809
dc.language.isoengeng
dc.publisherAmsterdam : European Rhinologic Societyeng
dc.relation.doihttps://doi.org/10.4193/RHINOL/19.002
dc.rights.licenseCC BY 4.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/eng
dc.subject.ddc610eng
dc.subject.otherantibodieseng
dc.subject.otherchronic rhinosinusitiseng
dc.subject.otherimmunoglobulineng
dc.subject.otherGeng
dc.subject.otherprotein microarrayeng
dc.subject.otherstaphylococcal antigeneng
dc.titleAnti-Staphylococcal Humoral Immune Response in patients with chronic rhinosinusitiseng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorIPHTeng
wgl.subjectIngenieurwissenschafteneng
wgl.typeZeitschriftenartikeleng
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