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多发性硬化症患者中干扰素产生与临床疾病活动度之间的相关性。

Correlation between interferon production and clinical disease activity in patients with multiple sclerosis.

作者信息

Dettke M, Scheidt P, Prange H, Kirchner H

机构信息

German Cancer Research Center Heidelberg, Department of Tumorvirus-Immunology, Germany.

出版信息

J Clin Immunol. 1997 Jul;17(4):293-300. doi: 10.1023/a:1027374615106.

Abstract

We determined the interferon (IFN) serum levels and in vitro activated IFN production in eight patients with relapsing/ remitting multiple sclerosis (MS), using a whole-blood test system and the mitogen concanavalin A and the viral antigen Newcastle disease virus for induction of the IFN production. During the overall study period of 12 months we observed, in relation to clinical disease progression, a biphasic increase in the individual IFN alpha and IFN gamma production. While mitogen-induced IFN gamma synthesis showed a significant augmentation prior to the onset of a new relapse (P < 0.05), virus-induced IFN alpha production showed a temporal delayed increase which was related to clinical remission (P < 0.01). The observed fluctuations in the individual production of both IFN subtypes were not reflected in the sera of the patients. Although the reason for the temporal different imbalance in the production of both IFN subtypes remains unknown, the observed association between increased IFN alpha production and clinical remission emphasizes a possible role for type 1 IFNs in the resolution of the MS relapse.

摘要

我们采用全血检测系统,使用促有丝分裂原刀豆球蛋白A和病毒抗原新城疫病毒诱导干扰素产生,测定了8例复发缓解型多发性硬化症(MS)患者的血清干扰素(IFN)水平及体外激活的IFN产生情况。在为期12个月的整个研究期间,我们观察到,与临床疾病进展相关,个体的IFNα和IFNγ产生呈双相增加。虽然促有丝分裂原诱导的IFNγ合成在新的复发发作前显著增加(P < 0.05),但病毒诱导的IFNα产生出现时间延迟增加,这与临床缓解相关(P < 0.01)。患者血清中未体现出两种IFN亚型个体产生情况的观察到的波动。虽然两种IFN亚型产生时间不同失衡的原因尚不清楚,但观察到的IFNα产生增加与临床缓解之间的关联强调了1型IFN在MS复发缓解中可能发挥的作用。

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