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During temporomandibular joint osteoarthritis (<jats:styled-content style=\"fixed-case\">TMJ<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">OA<\/jats:styled-content>), <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20101\u03b2 and <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201017 have been implicated in the inflammation and resorption of sub\u2010chondral bone; however, the role of Th22 response in the <jats:styled-content style=\"fixed-case\">TMJ<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">OA<\/jats:styled-content> pathophysiology has not been established. This study aimed to compare the expression of Th1\/Th17\/Th22\u2010type cytokines, chemokines and chemokine receptors in synovial fluid samples obtained from <jats:styled-content style=\"fixed-case\">TMJ<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">OA<\/jats:styled-content> or disk displacement with reduction (<jats:styled-content style=\"fixed-case\">DDWR<\/jats:styled-content>) patients. In addition, it aimed to associate these levels with joint pain, imagenological signs of bone degeneration, <jats:styled-content style=\"fixed-case\">RANKL<\/jats:styled-content> production, osteoclastogenesis and osteoclast\u2010induced bone resorption. Higher levels of <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20101\u03b2, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201017 and <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201022 were expressed in <jats:styled-content style=\"fixed-case\">TMJ<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">OA<\/jats:styled-content> compared with <jats:styled-content style=\"fixed-case\">DDWR<\/jats:styled-content> subjects, and these increased levels significantly correlated with <jats:styled-content style=\"fixed-case\">RANKL<\/jats:styled-content> expression, joint pain and articular bone degeneration. Higher levels of <jats:styled-content style=\"fixed-case\">CCR<\/jats:styled-content>5, <jats:styled-content style=\"fixed-case\">CCR<\/jats:styled-content>6 and <jats:styled-content style=\"fixed-case\">CCR<\/jats:styled-content>7, as well as their respective ligands <jats:styled-content style=\"fixed-case\">CCL<\/jats:styled-content>5 and <jats:styled-content style=\"fixed-case\">CCL<\/jats:styled-content>20, responsible for recruitment of <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20101\u03b2, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201017 and <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201022\u2010producing cells, were over\u2010expressed in <jats:styled-content style=\"fixed-case\">TMJ<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">OA<\/jats:styled-content> compared with <jats:styled-content style=\"fixed-case\">DDWR<\/jats:styled-content> subjects. Osteoclastogenesis and osteoclast\u2010induced bone resorption were significantly greater in presence of synovial fluid from <jats:styled-content style=\"fixed-case\">TMJ<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">OA<\/jats:styled-content> compared with <jats:styled-content style=\"fixed-case\">DDWR<\/jats:styled-content> subjects. These data demonstrate that cytokines, <jats:styled-content style=\"fixed-case\">CCL<\/jats:styled-content>s and <jats:styled-content style=\"fixed-case\">CCR<\/jats:styled-content>s associated with the Th1\/Th17\/Th22 axis of immuno\u2010inflammatory response are involved in <jats:styled-content style=\"fixed-case\">TMJ<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">OA<\/jats:styled-content> pathogenesis. These findings suggest that <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201022 is involved in the <jats:styled-content style=\"fixed-case\">RANKL<\/jats:styled-content> expression in <jats:styled-content style=\"fixed-case\">TMJ<\/jats:styled-content>\u2010<jats:styled-content style=\"fixed-case\">OA<\/jats:styled-content>, which in turn induces differentiation of osteoclasts and subsequent resorption of sub\u2010chondral bone.<\/jats:p>","DOI":"10.1111\/joor.12649","type":"journal-article","created":{"date-parts":[[2018,5,15]],"date-time":"2018-05-15T11:20:45Z","timestamp":1526383245000},"page":"589-597","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":63,"title":["Th1\/Th17\/Th22 immune response and their association with joint pain, imagenological bone loss, RANKL expression and osteoclast activity in temporomandibular joint osteoarthritis: A preliminary report"],"prefix":"10.1111","volume":"45","author":[{"given":"G.","family":"Monasterio","sequence":"first","affiliation":[{"name":"Periodontal Biology Laboratory Faculty of Dentistry Universidad de Chile  Santiago Chile"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"F.","family":"Castillo","sequence":"additional","affiliation":[{"name":"Periodontal Biology Laboratory Faculty of Dentistry Universidad de Chile  Santiago Chile"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"L.","family":"Rojas","sequence":"additional","affiliation":[{"name":"Periodontal Biology Laboratory Faculty of Dentistry Universidad de Chile  Santiago Chile"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"E. 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