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Eighty\u2010four patients with <jats:styled-content style=\"fixed-case\">PNS<\/jats:styled-content> and 51 healthy age\u2010matched controls were included in this study. The percentage of \u03b3\u03b4 T cells, \u03b3\u03b4 T cell subsets, Th17 cells and Treg cells in peripheral blood mononuclear cells (<jats:styled-content style=\"fixed-case\">PBMC<\/jats:styled-content>s) were analysed by fluorescence\u2010activated cell sorting. <jats:styled-content style=\"fixed-case\">PMBC<\/jats:styled-content>s from <jats:styled-content style=\"fixed-case\">PNS<\/jats:styled-content> patients with active disease were cultured in the presence of <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201023, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201023 and an <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201023 antagonist, or <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>23 and an anti\u2010<jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201021 monoclonal antibody (<jats:styled-content style=\"fixed-case\">mA<\/jats:styled-content>b). The percentage of \u03b3\u03b4 T cells, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201023R<jats:sup>+<\/jats:sup> \u03b3\u03b4 T cells and <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201017<jats:sup>+<\/jats:sup> \u03b3\u03b4 T cells were significantly increased in <jats:styled-content style=\"fixed-case\">PNS<\/jats:styled-content> patients with active disease. There was a positive correlation between the percentage of \u03b3\u03b4 T cells, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201023R<jats:sup>+<\/jats:sup> \u03b3\u03b4 T cells, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201017<jats:sup>+<\/jats:sup> \u03b3\u03b4 T cells and the Th17\/Treg ratio. <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201023 increased the percentage of \u03b3\u03b4 T cells and Th17 cells and decreased the percentage of Treg cells in <jats:styled-content style=\"fixed-case\">PBMC<\/jats:styled-content>s isolated from <jats:styled-content style=\"fixed-case\">PNS<\/jats:styled-content> patients with active disease. Anti\u2010<jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201021 <jats:styled-content style=\"fixed-case\">mA<\/jats:styled-content>b reduced the percentage of \u03b3\u03b4 T cells and Th17 cells, but increased the percentage of Treg cells. \u03b3\u03b4 T cells, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201017<jats:sup>+<\/jats:sup> \u03b3\u03b4 T cells and <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201023R<jats:sup>+<\/jats:sup> \u03b3\u03b4 T cells may be involved in the pathogenesis of paediatric <jats:styled-content style=\"fixed-case\">PNS<\/jats:styled-content> by modulating the balance of Th17\/Treg cells. \u03b3\u03b4 T cells may cause an imbalance in Th17\/Treg cells by secreting <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201021 in the presence of <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201023.<\/jats:p>","DOI":"10.1111\/sji.12629","type":"journal-article","created":{"date-parts":[[2017,11,9]],"date-time":"2017-11-09T07:46:38Z","timestamp":1510213598000},"page":"36-45","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":20,"title":["<scp>IL<\/scp>\u201023 Activated \u03b3\u03b4 T Cells Affect Th17 Cells and Regulatory T Cells by Secreting <scp>IL<\/scp>\u201021 in Children with Primary Nephrotic Syndrome"],"prefix":"10.1111","volume":"87","author":[{"given":"L.","family":"Zhang","sequence":"first","affiliation":[{"name":"Ministry of Education Key Laboratory of Child Development and Disorders Key Laboratory of Pediatrics in Chongqing Chongqing International Science and Technology Cooperation Center for Child Development and Disorders Chongqing 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