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皮质醇对阿尔茨海默型老年痴呆症患者自然杀伤细胞细胞毒性活性的免疫抑制作用减弱。

Decreased immunosuppressive effect of cortisol on natural killer cytotoxic activity in senile dementia of the Alzheimer type.

作者信息

Solerte S B, Cerutti N, Severgnini S, Rondanelli M, Ferrari E, Fioravanti M

机构信息

Department of Internal Medicine, Geriatrics and Gerontology Clinic, University of Pavia, Italy.

出版信息

Dement Geriatr Cogn Disord. 1998 May-Jun;9(3):149-56. doi: 10.1159/000017040.

Abstract

Former studies have indicated alterations of the cytotoxic activity of natural killer (NK) cells in senile dementia of the Alzheimer type (SDAT). These changes may be related to the increased reactivity of NK cells with cytokines, even if an impairment of the immunosuppressive effect of glucocorticoids cannot be excluded. In the present study we have demonstrated a lower immunosuppressive effect of cortisol on NK cytolytic function in patients with SDAT than in healthy elders and in patients with dementia of multi-infarct origin (MID). This suppression is completely lacking when cortisol is employed at low concentrations (10(-7) M) and is significantly reduced after incubation at physiological (10(-6) M; p < 0.001) and supraphysiological concentrations (10(-5) M; p < 0.001). The addition of IL-2 (50 and 100 IU/ml/cells) significantly antagonizes the effects of cortisol in SDAT, whereas the cortisol-dependent immunosuppression is partially maintained in healthy elders and in patients with MID. Our data indicate that the defect of the immunosuppressive effect of cortisol may play a role in NK dysregulation in SDAT, contributing to the cytokine-mediated NK overactivity in this disease.

摘要

以往的研究表明,在阿尔茨海默型老年痴呆症(SDAT)中自然杀伤(NK)细胞的细胞毒性活性发生了改变。这些变化可能与NK细胞对细胞因子反应性的增加有关,尽管不能排除糖皮质激素免疫抑制作用受损的情况。在本研究中,我们已经证明,与健康老年人和多发梗死性痴呆(MID)患者相比,皮质醇对SDAT患者NK细胞溶解功能的免疫抑制作用较低。当使用低浓度(10^(-7) M)的皮质醇时,这种抑制作用完全不存在,而在生理浓度(10^(-6) M;p < 0.001)和超生理浓度(10^(-5) M;p < 0.001)孵育后,抑制作用显著降低。添加白细胞介素-2(50和100 IU/ml/细胞)可显著拮抗皮质醇对SDAT的作用,而在健康老年人和MID患者中,皮质醇依赖性免疫抑制作用部分得以维持。我们的数据表明,皮质醇免疫抑制作用的缺陷可能在SDAT的NK细胞失调中起作用,导致该病中细胞因子介导的NK细胞过度活性。

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