» Articles » PMID: 28779999

Th17 Cells in Depression

Overview
Publisher Elsevier
Date 2017 Aug 7
PMID 28779999
Citations 75
Authors
Affiliations
Soon will be listed here.
Abstract

T helper 17 (Th17) cells have recently been implicated in depression, which adds to the list of several other diseases of the central nervous system (CNS) that are already known to involve Th17 cells. In CNS diseases, it is thought that the signature cytokine produced by Th17 cells, interleukin-17A (IL-17A), mediates the detrimental effects of Th17 cells. In depression, although Th17 cells increase, the lack of a consistent correlation between depression severity and blood IL-17A levels suggests that Th17 cells promote depressive symptoms, which may not be entirely dependent on IL-17. However, little is known about the mechanism of action of Th17 cells or the source of CNS Th17 cells in depression. It is likely that Th17 cells promote neuroinflammation and activation of microglia and astrocytes, actions that may contribute to neuronal damage. A source of Th17 cells is the small intestine where they are regulated by the composition of the microbiome. It remains to be determined through what mechanisms of action Th17 cells affect depression and if Th17 cells can be considered a novel therapeutic target in depression.

Citing Articles

The role of short-chain fatty acid in metabolic syndrome and its complications: focusing on immunity and inflammation.

Yu W, Sun S, Fu Q Front Immunol. 2025; 16:1519925.

PMID: 39991152 PMC: 11842938. DOI: 10.3389/fimmu.2025.1519925.


Interaction between Th17 and central nervous system in multiple sclerosis.

Lai S, Wu X, Liu Y, Liu B, Wu H, Ma K Brain Behav Immun Health. 2025; 43():100928.

PMID: 39845807 PMC: 11751430. DOI: 10.1016/j.bbih.2024.100928.


Developing a translational research framework for MDD: combining biomolecular mechanisms with a spiraling risk factor model.

van Baalen M, van der Velden L, van der Gronde T, Pieters T Front Psychiatry. 2025; 15():1463929.

PMID: 39839132 PMC: 11747824. DOI: 10.3389/fpsyt.2024.1463929.


Gut-brain axis as a bridge in obesity and depression: Mechanistic exploration and therapeutic prospects.

Fang R, Pan X, Zeng X, Li Z, Chen B, Zeng H World J Psychiatry. 2025; 15(1):101134.

PMID: 39831021 PMC: 11684226. DOI: 10.5498/wjp.v15.i1.101134.


Impact of the gut microbiota-Th17 cell axis on inflammatory depression.

Jia X, Wang J, Ren D, Zhang K, Zhang H, Jin T Front Psychiatry. 2024; 15:1509191.

PMID: 39655201 PMC: 11625820. DOI: 10.3389/fpsyt.2024.1509191.


References
1.
Miller A, Raison C . The role of inflammation in depression: from evolutionary imperative to modern treatment target. Nat Rev Immunol. 2015; 16(1):22-34. PMC: 5542678. DOI: 10.1038/nri.2015.5. View

2.
Colpitts S, Kasper L . Influence of the Gut Microbiome on Autoimmunity in the Central Nervous System. J Immunol. 2017; 198(2):596-604. DOI: 10.4049/jimmunol.1601438. View

3.
Bautista J, Foldvary-Schaefer N, Bingaman W, Luders H . Focal cortical dysplasia and intractable epilepsy in adults: clinical, EEG, imaging, and surgical features. Epilepsy Res. 2003; 55(1-2):131-6. DOI: 10.1016/s0920-1211(03)00118-9. View

4.
Jankovic D, Kugler D, Sher A . IL-10 production by CD4+ effector T cells: a mechanism for self-regulation. Mucosal Immunol. 2010; 3(3):239-46. PMC: 4105209. DOI: 10.1038/mi.2010.8. View

5.
Yang J, Sundrud M, Skepner J, Yamagata T . Targeting Th17 cells in autoimmune diseases. Trends Pharmacol Sci. 2014; 35(10):493-500. DOI: 10.1016/j.tips.2014.07.006. View