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

被引:45
作者
Becking, Karlijn [1 ,2 ]
Haarman, Bartholomeus C. M. [2 ,3 ]
Grosse, Laura [4 ,5 ]
Nolen, Willem A. [2 ]
Claes, Stephan [6 ]
Arolt, Volker [4 ]
Schoevers, Robert A. [1 ,2 ,3 ]
Drexhage, Hemmo A. [5 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Interdisciplinary Ctr Psychopathol & Emot Regulat, Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Psychiat, Groningen, Netherlands
[3] Univ Groningen, Univ Med Ctr Groningen, Res Sch Behav & Cognit Neurosci BCN, Groningen, Netherlands
[4] Univ Munster, Dept Psychiat & Psychotherapy, Munster, Germany
[5] Erasmus MC, Dept Immunol, Rotterdam, Netherlands
[6] Univ Psychiat Ctr KU, Leuven, Belgium
基金
欧盟第七框架计划;
关键词
Leukocyte subset; T cell defect; Th17; Th2; Major depressive disorder; Bipolar disorder; T helper cell differentiation; NATURAL-KILLER-CELLS; T-CELLS; RATING-SCALE; RELIABILITY; ACTIVATION; EXPRESSION; INTERVIEW; VALIDITY; DISEASE; SYSTEM;
D O I
10.1016/j.jneuroim.2018.03.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 < .02). In BD patients, levels of Th17 and T regulatory cells were increased compared to HC (p = .03, p = .02, respectively), while MDD patients showed decreased levels of Th17 and Th2 compared to HC (p = .03, p = .01, respectively). Of the various medications only SSRI/SNRI usage could explain part of the Th2 decrease in MDD. 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.
引用
收藏
页码:28 / 36
页数:9
相关论文
共 65 条
[1]   Bipolar Disorder: Role of Immune-Inflammatory Cytokines, Oxidative and Nitrosative Stress and Tryptophan Catabolites [J].
Anderson, George ;
Maes, Michael .
CURRENT PSYCHIATRY REPORTS, 2015, 17 (02)
[2]  
[Anonymous], INT J NEUROPSYCHOPHA
[3]  
[Anonymous], 2001, DIAGN STAT MAN MENT, V4th
[4]  
[Anonymous], 1997, STRUCTURED CLIN INTE
[5]   Predominant recurrence polarity among 928 adult international bipolar I disorder patients [J].
Baldessarini, R. J. ;
Undurraga, J. ;
Vazquez, G. H. ;
Tondo, L. ;
Salvatore, P. ;
Ha, K. ;
Khalsa, H. -M. K. ;
Lepri, B. ;
Ha, T. H. ;
Chang, J. S. ;
Tohen, M. ;
Vieta, E. .
ACTA PSYCHIATRICA SCANDINAVICA, 2012, 125 (04) :293-302
[6]   The Immunology of Bipolar Disorder [J].
Barbosa, Izabela Guimaraes ;
Machado-Vieira, Rodrigo ;
Soares, Jair C. ;
Teixeira, Antonio L. .
NEUROIMMUNOMODULATION, 2014, 21 (2-3) :117-122
[7]   Inflammatory monocyte gene expression: trait or state marker in bipolar disorder? [J].
Becking K. ;
Haarman B.C.M. ;
van der Lek R.F.R. ;
Grosse L. ;
Nolen W.A. ;
Claes S. ;
Drexhage H.A. ;
Schoevers R.A. .
International Journal of Bipolar Disorders, 3 (1)
[8]  
Benazzi Franco, 2002, Ann Clin Psychiatry, V14, P97, DOI 10.3109/10401230209149096
[9]   High numbers of circulating activated T cells and raised levels of serum IL-2 receptor in bipolar disorder [J].
Breunis, MN ;
Kupka, RW ;
Nolen, WA ;
Suppes, T ;
Denicoff, KD ;
Leverich, GS ;
Post, RM ;
Drexhage, HA .
BIOLOGICAL PSYCHIATRY, 2003, 53 (02) :157-165
[10]   Sex, the aging immune system, and chronic disease [J].
Bupp, Melanie R. Gubbels .
CELLULAR IMMUNOLOGY, 2015, 294 (02) :102-110