{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,23]],"date-time":"2026-09-23T01:33:47Z","timestamp":1790127227115,"version":"4.0.1"},"reference-count":56,"publisher":"Wiley","issue":"4","license":[{"start":{"date-parts":[[2018,4,6]],"date-time":"2018-04-06T00:00:00Z","timestamp":1522972800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"name":"New Zealand Dental Association Research Foundation"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["J of Periodontal Research"],"published-print":{"date-parts":[[2018,8]]},"abstract":"<jats:sec><jats:title>Background and Objective<\/jats:title><jats:p>T cells are known to play a pivotal role in periodontal disease; however, less is known about the T\u2010helper subsets of regulatory T cells (Tregs) and Th17 cells. The aim of this study was to investigate the cell types expressing FoxP3 and interleukin (<jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>)\u201017A within periodontal disease tissues and to determine gene and protein expression profiles associated with periodontitis.<\/jats:p><\/jats:sec><jats:sec><jats:title>Material and Methods<\/jats:title><jats:p>A total of 10 healthy\/gingivitis and 10 chronic periodontitis tissues were investigated. Immunohistochemistry and immunofluorescence techniques were used to identify the FoxP3 and <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>17\u2010positive cells and to determine the cell types respectively. Gene expression was determined using semi\u2010quantitative polymerase chain reaction array technology that allowed the analysis of 84 pathway\u2010focused genes known to be associated with Tregs and Th17 cells. Transforming growth factor (<jats:styled-content style=\"fixed-case\">TGF<\/jats:styled-content>)\u2010\u03b21, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>10 and <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>17A protein levels were determined using enzyme\u2010linked immunosorbent assay.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Double immunofluorescence labeling revealed that all FoxP3<jats:sup>+<\/jats:sup> cells were <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4<jats:sup>+<\/jats:sup>, while <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>17<jats:sup>+<\/jats:sup> cells were neither <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4<jats:sup>+<\/jats:sup> nor <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>8<jats:sup>+<\/jats:sup> but were tryptase<jats:sup>+<\/jats:sup>, suggestive of mast cells. More FoxP3<jats:sup>+<\/jats:sup> cells than <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>17<jats:sup>+<\/jats:sup> cells were found in all the tissues examined and overall there were few <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>17<jats:sup>+<\/jats:sup> cells. Statistically significant increases in gene expression were found for <jats:styled-content style=\"fixed-case\">STAT<\/jats:styled-content>5A, <jats:styled-content style=\"fixed-case\">STAT<\/jats:styled-content>3, <jats:styled-content style=\"fixed-case\">SOCS<\/jats:styled-content>1, <jats:styled-content style=\"fixed-case\">TGF<\/jats:styled-content>\u03b21 and <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>10 in the chronic periodontitis specimens predominantly infiltrated with B cells and plasma cells when compared with healthy\/gingivitis specimens predominantly infiltrated with T cells. Protein analysis demonstrated higher levels of the <jats:styled-content style=\"fixed-case\">TGF<\/jats:styled-content>\u03b21 and <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>10 cytokines in periodontitis tissues and in B\u2010cell and plasma cell predominant gingival tissues than in healthy\/gingivitis tissues and T\u2010cell predominant gingival tissues. <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>17A gene and protein expression was not detected in any of the tissues.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>Based on the findings of this study, we suggest that the source of low levels of <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>17A in periodontal tissues is mast cells not Th17 cells and that Tregs may have a more prominent role in the pathogenesis of periodontal disease than Th17 cells.<\/jats:p><\/jats:sec>","DOI":"10.1111\/jre.12552","type":"journal-article","created":{"date-parts":[[2018,4,10]],"date-time":"2018-04-10T00:57:23Z","timestamp":1523321843000},"page":"622-635","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":20,"title":["FoxP3<sup>+<\/sup> regulatory T cells, interleukin 17 and mast cells in chronic inflammatory periodontal disease"],"prefix":"10.1111","volume":"53","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-1301-5047","authenticated-orcid":false,"given":"V. 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