Soluble interleukin-1 receptor type II levels are elevated in cerebrospinal fluid in Alzheimer's disease patients

被引:73
作者
Garlind, A [1 ]
Brauner, A
Höjeberg, B
Basun, H
Schultzberg, M
机构
[1] Huddinge Univ Hosp, Dept Clin Neurosci Occupat Therapy & Elderly Care, Div Geriatr Med, S-14186 Huddinge, Sweden
[2] Karolinska Hosp, Dept Lab Med, Div Clin Microbiol, S-17176 Stockholm, Sweden
[3] Huddinge Univ Hosp, Dept Clin Neurosci Occupat Therapy & Elderly Care, Div Neurol, S-14186 Huddinge, Sweden
关键词
cytokine; diagnostic marker; ELISA; interleukin-6; microglia; tumour necrosis factor-alpha;
D O I
10.1016/S0006-8993(99)01092-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Evidence from epidemiological, clinical and experimental studies favour the hypothesis that inflammatory events are part of the neuropathology in Alzheimer's disease. Proinflammatory cytokines such as interleukin-1 (IL-1), interleukin-6 (IL-6) and tumour necrosis factor-alpha (TNF-alpha) have been found in activated microglia in the vicinity of amyloid plaques in Alzheimer's disease brain. In the present study, the levels of soluble IL-1 receptor type II (sIL-1R type II), IL-1 receptor antagonist (IL-1ra), IL-1 beta, IL-6 and TNF-alpha were analyzed in cerebrospinal fluid (CSF) samples from Alzheimer's disease patients and control subjects. The levels of sIL-1R type II were significantly higher in CSF from Alzheimer's disease patients than in CSF samples from control subjects (38.5 +/- 8 pg/ml (mean +/- S.E.M.) vs. 7.9 +/- 4 pg/ml, p < 0.05). Measurements of the proinflammatory cytokines IL-6 and TNF-alpha showed no significant difference between the two groups, and the levels of IL-1 beta and IL-1ra in the present material were too low to permit detection. The increased levels of sIL-1R type II may reflect a compensatory mechanism to balance an increased release of IL-1 receptor agonists in the Alzheimer's disease brain. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:112 / 116
页数:5
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