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Plasma Levels of IL-23 and IL-17 before and after Antidepressant Treatment in Patients with Major Depressive Disorder

Authors
Kim, Jae-WonKim, Yong-KuHwang, Jung-AYoon, Ho-KyoungKo, Young-HoonHan, ChangsuLee, Heon-JeongHam, Byung-JooLee, Hong Seock
Issue Date
Sep-2013
Publisher
KOREAN NEUROPSYCHIATRIC ASSOC
Keywords
Cytokine; Th17 cell; IL-23; IL-17; Immune; Major depressive disorder
Citation
PSYCHIATRY INVESTIGATION, v.10, no.3, pp.294 - 299
Indexed
SCIE
SSCI
SCOPUS
KCI
Journal Title
PSYCHIATRY INVESTIGATION
Volume
10
Number
3
Start Page
294
End Page
299
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/102289
DOI
10.4306/pi.2013.10.3.294
ISSN
1738-3684
Abstract
Objective Cytokines are believed to have a role in the pathophysiology of major depression. The alteration in levels of pro-inflammatory cytokines [interleukin 1 beta (IL-1 beta), IL-2, IL-6, IL-12, interferon gamma, and tumor necrosis factor a] in major depression supports the cytokine hypothesis of this illness. IL-23 and IL-17 are also pro-inflammatory cytokines, but few studies have focused on their role in major depression. This study investigated the potential role of the IL-23 and IL-17 axis in major depression. Methods Plasma IL-23 and IL-17 levels were measured in 26 major depressive disorder (MDD) patients before and after 6-week treatment with antidepressants; these levels were measured in 28 age- and sex-matched normal controls. Depression severity was assessed using the Hamilton Depression Rating Scale (HDRS). IL-23 and IL-17 plasma levels were estimated using quantitative enzyme-linked immunosorbent assay. Results Pre-treatment plasma levels of IL-23 and IL-17 in MDD patients were not significantly different from those of normal controls. In MDD patients, IL-23 and IL-17 levels after 6 weeks of antidepressant treatment were not different from the baseline levels. There was no significant correlation between changes in the cytokine levels and changes in the HDRS scores representing the severity of depression. Conclusion The present study does not support a potential involvement of IL-23 and IL-17 axis in major depression. Replication and extension using a larger sample are required.
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