Increased serum IL-6 and IL-1 receptor antagonist concentrations in major depression and treatment resistant depression

被引:548
作者
Maes, M
Bosmans, E
DeJongh, R
Kenis, G
Vandoolaeghe, E
Neels, H
机构
[1] CLIN RES CTR MENTAL HLTH,ANTWERP,BELGIUM
[2] ACAD HOSP ST JAN,SCHIEPSEBOS,GENK,BELGIUM
[3] OCMW HOSP,DEPT BIOL CLIN,ANTWERP,BELGIUM
[4] EUROGENET,TESSENDERLO,BELGIUM
关键词
cytokines; antidepressants; CC16; CD8; psychoneuroimmunology;
D O I
10.1006/cyto.1997.0238
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There is now some evidence that major depression is accompanied by an immune response with an increased production of pro-inflammatory cytokines, such as interleukin 1 (IL-1), IL-6 and interferon gamma (IFN-gamma). The aims of the present study were to examine serum IL-6, IL-1 receptor antagonist (IL-1Ra), IL-6R, Clara cell protein (CC16) and the soluble CD8 (sCD8) molecule in chronic, treatment resistant depression (TRD) both before and after subchronic treatment with antidepressants. Serum IL-6 and IL-1Ra were significantly higher in subjects with major depression and TRD than in normal controls, Subchronic treatment with antidepressants had no significant effects on serum IL-6, IL-1Ra, CC16 or sCD8, but reduced serum sIL-6R levels significantly, There were significant and positive correlations between serum IL-6, on the one hand, and sIL-6R, IL-1RA, sCD8, number of peripheral blood leukocytes, neutrophils, CD2(+)T and CD19(+)B cells (all positive) and serum zinc (negative), on the other, These results suggest that: (1) major depression and TRD are accompanied by an activation of the monocytic arm of cell-mediated immunity; (2) the latter may be related to the immune and acute phase response in major depression; and (3) the above disorders may persist despite successful antidepressive treatment. (C) 1997 Academic Press Limited.
引用
收藏
页码:853 / 858
页数:6
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