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dc.contributor.authorGould, SJ
dc.contributor.authorFoey, AD
dc.contributor.authorSalih, VM
dc.date.accessioned2023-11-01T15:04:15Z
dc.date.available2023-11-01T15:04:15Z
dc.date.issued2023-01
dc.identifier.issn2041-7314
dc.identifier.issn2041-7314
dc.identifier.otherARTN 20417314231197310
dc.identifier.urihttps://pearl.plymouth.ac.uk/handle/10026.1/21504
dc.description.abstract

Early in vitro oral mucosal infection models (OMMs) failed to consider the suitability of the model environment to represent the host immune response. Denture stomatitis (DS) is mediated by Candida albicans, but the role of Staphylococcus aureus remains uncertain. A collagen hydrogel-based OMM containing HaCaT and HGF cell types was developed, characterised and employed to study of tissue invasion and pro-inflammatory cytokine production in response to pathogens. Models formed a robust epithelium. Despite their inflammatory baseline, 24-h infection with C. albicans, and/or S. aureus led to tissue invasion, and significantly upregulated IL-6 and IL-8 production by OMMs when compared to the unstimulated control. No significant difference in IL-6 or IL-8 production by OMMs was observed between single and dual infections. These attributes indicate that this newly developed OMM is suitable for the study of DS and could be implemented for the wider study of oral infection.

dc.format.extent20417314231197310-
dc.format.mediumElectronic-eCollection
dc.languageen
dc.publisherSAGE Publications
dc.subjectCandida albicans
dc.subjectStaphylococcus aureus
dc.subjectorganotypic
dc.subjectoral mucosa
dc.subjectinfection model
dc.subjecttissue-engineering
dc.subjectdenture stomatitis
dc.titleAn organotypic oral mucosal infection model to study host-pathogen interactions
dc.typejournal-article
dc.typeArticle
plymouth.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/37873034
plymouth.volume14
plymouth.publisher-urlhttp://dx.doi.org/10.1177/20417314231197310
plymouth.publication-statusPublished
plymouth.journalJournal of Tissue Engineering
dc.identifier.doi10.1177/20417314231197310
plymouth.organisational-group|Plymouth
plymouth.organisational-group|Plymouth|Research Groups
plymouth.organisational-group|Plymouth|Faculty of Health
plymouth.organisational-group|Plymouth|Research Groups|Institute of Translational and Stratified Medicine (ITSMED)
plymouth.organisational-group|Plymouth|Research Groups|Institute of Translational and Stratified Medicine (ITSMED)|CBR
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA
plymouth.organisational-group|Plymouth|Users by role
plymouth.organisational-group|Plymouth|Users by role|Academics
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA|UoA01 Clinical Medicine
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA|UoA03 Allied Health Professions, Dentistry, Nursing and Pharmacy
plymouth.organisational-group|Plymouth|Faculty of Health|Peninsula Dental School
plymouth.organisational-group|Plymouth|Faculty of Health|School of Biomedical Sciences
plymouth.organisational-group|Plymouth|REF 2021 Researchers by UoA|UoA01 Clinical Medicine|UoA01 Clinical Medicine
dc.publisher.placeEngland
dcterms.dateAccepted2023-08-10
dc.date.updated2023-11-01T15:04:08Z
dc.rights.embargodate2023-11-2
dc.identifier.eissn2041-7314
rioxxterms.versionofrecord10.1177/20417314231197310


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