Sorry, I don't understand your search. ×
Back to Search Start Over

The circulating levels of CD4+ t helper cells are higher in bipolar disorder as compared to major depressive disorder

Authors :
Volker Arolt
Bartholomeus C M Haarman
Willem A. Nolen
Laura Grosse
Robert A. Schoevers
Stephan Claes
Hemmo A. Drexhage
Karlijn Becking
Interdisciplinary Centre Psychopathology and Emotion regulation (ICPE)
Perceptual and Cognitive Neuroscience (PCN)
Clinical Cognitive Neuropsychiatry Research Program (CCNP)
Immunology
Source :
Journal of Neuroimmunology, Journal of Neuroimmunology, 319, 28-36. ELSEVIER SCIENCE BV, Journal of Neuroimmunology, 319, 28-36. Elsevier
Publication Year :
2018

Abstract

Introduction: Clinical differentiation between bipolar disorder (BD) and major depressive disorder (MDD) is difficult. Research has therefore focused on discriminatory biological markers. Previous studies in MDD reported T cell deficits, while the limited studies in BD reported T cell activation. Studies directly comparing circulating numbers of T cells and T cell subsets between BD and MDD are lacking. The studies in the MOODINFLAME consortium make such a comparison possible.Methods: The number of circulating leukocyte populations (lymphocytes, monocytes, NK cells, B cells, T cells, CD3+CD8+ T cytotoxic cells, CD3+CD4+ T helper cells, Th1, Th2, Th17 and T regulatory cells) was determined using FACS technology in a cohort of 83 euthymic BD patients, 8 BD patients with a current mood episode and 165 healthy controls (HC). Data were compared to those of 34 moderately and 56 severely depressed MDD patients.Results: Compared to MDD patients, BD patients showed significantly increased levels of Th17, Th2, Th1 and T regulatory cells (all p Conclusion: This study shows CD4+ T helper cell deficits in MDD patients, while normal or even raised levels of these cells were found in BD patients. The differences in CD4+ T helper cell differentiation was most outspoken for Th17 cells.

Details

ISSN :
01655728
Database :
OpenAIRE
Journal :
Journal of Neuroimmunology
Accession number :
edsair.doi.dedup.....680943731573e525734d45965ef6c76c
Full Text :
https://doi.org/10.1016/j.jneuroim.2018.03.004