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Effect sizes were estimated with random\u2010effects models.<\/jats:p><\/jats:sec><jats:sec><jats:title>Result<\/jats:title><jats:p>Eighty\u2010two studies comprising 3212 participants with <jats:styled-content style=\"fixed-case\">MDD<\/jats:styled-content> and 2798 <jats:styled-content style=\"fixed-case\">HC<\/jats:styled-content>s met inclusion criteria. Peripheral levels of interleukin\u20106 (<jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20106), tumor necrosis factor (<jats:styled-content style=\"fixed-case\">TNF<\/jats:styled-content>)\u2010alpha, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201010, the soluble <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20102 receptor, C\u2010C chemokine ligand 2, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201013, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201018, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201012, the <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20101 receptor antagonist, and the soluble <jats:styled-content style=\"fixed-case\">TNF<\/jats:styled-content> receptor 2 were elevated in patients with <jats:styled-content style=\"fixed-case\">MDD<\/jats:styled-content> compared to <jats:styled-content style=\"fixed-case\">HC<\/jats:styled-content>s, whereas interferon\u2010gamma levels were lower in <jats:styled-content style=\"fixed-case\">MDD<\/jats:styled-content> (Hedge's <jats:italic>g<\/jats:italic> = \u22120.477, <jats:italic>P<\/jats:italic> = 0.043). Levels of <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20101\u03b2, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20102, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20104, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20108, the soluble <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20106 receptor (<jats:styled-content style=\"fixed-case\">sIL<\/jats:styled-content>\u20106R), <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20105, <jats:styled-content style=\"fixed-case\">CCL<\/jats:styled-content>\u20103, <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u201017, and transforming growth factor\u2010beta 1 were not significantly altered in individuals with <jats:styled-content style=\"fixed-case\">MDD<\/jats:styled-content> compared to <jats:styled-content style=\"fixed-case\">HC<\/jats:styled-content>s. Heterogeneity was large (<jats:italic>I<\/jats:italic><jats:sup>2<\/jats:sup>: 51.6\u201397.7%), and sources of heterogeneity were explored (e.g., age, smoking status, and body mass index).<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>Our results further characterize a cytokine\/chemokine profile associated with <jats:styled-content style=\"fixed-case\">MDD<\/jats:styled-content>. Future studies are warranted to further elucidate sources of heterogeneity, as well as biosignature cytokines secreted by other immune cells.<\/jats:p><\/jats:sec>","DOI":"10.1111\/acps.12698","type":"journal-article","created":{"date-parts":[[2017,1,25]],"date-time":"2017-01-25T19:46:50Z","timestamp":1485373610000},"page":"373-387","source":"Crossref","is-referenced-by-count":1369,"title":["Peripheral cytokine and chemokine alterations in depression: a meta\u2010analysis of 82 studies"],"prefix":"10.1111","volume":"135","author":[{"given":"C. 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