Immunologic variables in acute mania of bipolar disorder

被引:100
作者
Liu, HC
Yang, YY
Chou, YM
Chen, KP
Shen, WW
Leu, SJ
机构
[1] Taipei Med Univ, Grad Inst Cell Mol Biol, Taipei 110, Taiwan
[2] Taipei City Psychiat Ctr, Dept Psychiat, Taipei, Taiwan
[3] Taipei Med Univ, Sch Med Technol, Taipei, Taiwan
[4] Taipei Med Univ, Wan Fang Hosp, Dept Psychiat, Taipei, Taiwan
关键词
bipolar disorder; manic episode; IL-1 receptor antagonist; soluble CD4; soluble CD8; IFN-gamma;
D O I
10.1016/j.jneuroim.2004.01.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Macrophages, lymphocytes and their products, may be involved in the pathophysiology of psychiatric disorders. The cell-mediated immune activation response of manic patients during pre-medication and medication stages remains unclear. The purpose of this case-control study was to investigate the plasma levels of immunologic variables, including interleukin (IL)-1 receptor antagonist (IL-1RA), soluble CD 4 (sCD4) and sCD8, and TH1 (interferon [IFN]-gamma and IL-2) and TH2 (IL-4 and IL-10) cytokines in patients with pre-medicated, medicated bipolar mania. The study subjects, aged 16-44 years, were physically healthy patients with Young Mania Rating Scale (YMRS) scores greater than or equal to 26, and normal controls, aged 19-40 years, were matched for sex. The immune variables were measured in acute mania and in consequent remission (YMRS scores less than or equal to 12) among bipolar patients. The plasma levels of IL-1RA, sCD4, and sCD8 were found significantly increased in pre-medicated acute manic patients as compared to normal Controls. But only IL-1RA and sCD8 were found different in remitted bipolar patients as compared to normal controls, For TH1 cytokines, culture supernatant level of IFN-gamma was found significantly lower in manic patients of both acute and remission stages as compared to normal controls. No significant difference was found in IL-2 level in premedicated acute manic patients compared to controls. For TH2 cytokines, no significant differences in IL-4 and IL-10 levels were observed. We showed that cell-mediated immune response was activated in patients with bipolar disorder during the pre-medication, medication, and the remission stages. Our study findings suggest that the immune-modulation in patients with bipolar disorder may be abnormal. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:116 / 122
页数:7
相关论文
共 69 条
[41]  
MOORE KW, 1993, ANNU REV IMMUNOL, V11, P165, DOI 10.1146/annurev.iy.11.040193.001121
[42]   Interleukin-10 and the interleukin-10 receptor [J].
Moore, KW ;
Malefyt, RD ;
Coffman, RL ;
O'Garra, A .
ANNUAL REVIEW OF IMMUNOLOGY, 2001, 19 :683-765
[43]   CYTOKINE PATTERNS DURING THE PROGRESSION TO AIDS [J].
MOSMANN, TR .
SCIENCE, 1994, 265 (5169) :193-194
[44]   Psychoneuroimmunology and the cytokine action in the CNS: Implications for psychiatric disorders [J].
Muller, N ;
Ackenheil, M .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 1998, 22 (01) :1-33
[45]   Increased production of interleukin-2 (IL-2) but not soluble interleukin-2 receptors (sIL-2R) in unmedicated patients with schizophrenia and schizophreniform disorder [J].
ODonnell, MC ;
Catts, SV ;
Ward, PB ;
Liebert, B ;
Lloyd, A ;
Wakefield, D ;
McConaghy, N .
PSYCHIATRY RESEARCH, 1996, 65 (03) :171-178
[46]   CLONING OF A NEW CYTOKINE THAT INDUCES IFN-GAMMA PRODUCTION BY T-CELLS [J].
OKAMURA, H ;
TSUTSUI, H ;
KOMATSU, T ;
YUTSUDO, M ;
HAKURA, A ;
TANIMOTO, T ;
TORIGOE, K ;
OKURA, T ;
NUKADA, Y ;
HATTORI, K ;
AKITA, K ;
NAMBA, M ;
TANABE, F ;
KONISHI, K ;
FUKUDA, S ;
KURIMOTO, M .
NATURE, 1995, 378 (6552) :88-91
[47]  
Osaki T, 1998, J IMMUNOL, V160, P1742
[48]   NATURALLY-OCCURRING SOLUBLE CD4 IN PATIENTS WITH HUMAN-IMMUNODEFICIENCY-VIRUS INFECTION [J].
PEAKMAN, M ;
SENALDI, G ;
FOOTE, N ;
MCMANUS, TJ ;
VERGANI, D .
JOURNAL OF INFECTIOUS DISEASES, 1992, 165 (05) :799-804
[49]   RECOMBINANT INTERLEUKIN-4 SUPPRESSES THE PRODUCTION OF INTERFERON-GAMMA BY HUMAN MONONUCLEAR-CELLS [J].
PELEMAN, R ;
WU, J ;
FARGEAS, C ;
DELESPESSE, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 170 (05) :1751-1756
[50]  
PUI CH, 1991, LEUKEMIA, V5, P249