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Publication : Inflammatory T helper 17 cells promote depression-like behavior in mice.

First Author  Beurel E Year  2013
Journal  Biol Psychiatry Volume  73
Issue  7 Pages  622-30
PubMed ID  23174342 Mgi Jnum  J:283170
Mgi Id  MGI:6382392 Doi  10.1016/j.biopsych.2012.09.021
Citation  Beurel E, et al. (2013) Inflammatory T helper 17 cells promote depression-like behavior in mice. Biol Psychiatry 73(7):622-30
abstractText  BACKGROUND: Recognition of substantial immune-neural interactions is revising dogmas about their insular actions and revealing that immune-neural interactions can substantially impact central nervous system functions. The inflammatory cytokine interleukin-6 promotes susceptibility to depression and drives production of inflammatory T helper 17 (Th17) T cells, raising the hypothesis that in mouse models, Th17 cells promote susceptibility to depression-like behaviors. METHODS: Behavioral characteristics were measured in male mice administered Th17 cells, CD4(+) cells, or vehicle and in retinoid-related orphan receptor-gammaT (RORgammaT)(+/GFP) mice or male mice treated with RORgammaT inhibitor or anti-interleukin-17A antibodies. RESULTS: Mouse brain Th17 cells were elevated by learned helplessness and chronic restraint stress, two common depression-like models. Th17 cell administration promoted learned helplessness in 89% of mice in a paradigm where no vehicle-treated mice developed learned helplessness, and impaired novelty suppressed feeding and social interaction behaviors. Mice deficient in the RORgammaT transcription factor necessary for Th17 cell production exhibited resistance to learned helplessness, identifying modulation of RORgammaT as a potential intervention. Treatment with the RORgammaT inhibitor SR1001, or anti-interleukin-17A antibodies to abrogate Th17 cell function, reduced Th17-dependent learned helplessness. CONCLUSIONS: These findings indicate that Th17 cells are increased in the brain during depression-like states, promote depression-like behaviors in mice, and specifically inhibiting the production or function of Th17 cells reduces vulnerability to depression-like behavior, suggesting antidepressant effects may be attained by targeting Th17 cells.
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