Suppr超能文献

通过电聚焦在多发性硬化症中发现的异常脑脊液蛋白组分。对26例临床确诊或疑似多发性硬化症患者及2例视神经炎患者的研究。

Aberrant CSF protein fractions found by electrofocusing in multiple sclerosis. A study of 26 cases with clinically verified or probable multiple sclerosis and 2 cases with optic neuritis.

作者信息

Kjellin K G, Siden A

出版信息

Eur Neurol. 1977;15(1):40-50. doi: 10.1159/000114787.

Abstract

The CSF gamma-globulin patterns found by electrofocusing in multiple sclerosis can be classified into five (a-e) mean patterns, where the individual bands lie very close together. However, in some patients with verified or probable multiple sclerosis conspicuous bands are found. The electrofocusing patterns from 28 such cases were compared with those reported by Kjellin and Vesterberg and with 20 cases of verified multiple sclerosis collected by chance. Differences were found with regard to the frequency of the different mean patterns, the occurrence of a double fraction in region '5', a single fraction in region '7' and a highly alkaline fraction. The electrofocusing findings have been compared with the clinical data of the 28 patients. There seems to be some correlation between the patterns of conspicuous bands and the duration and course of the disorder as well as probable sites of the CNS lesions. No indication was found, that either a high CSF gamma-globulin value and/or in a high degree of barrier damage was a prerequisite for the occurrence of conspicuous bands in the CSF gamma-globulin region. The aberrant electrofocusing patterns might be genetically determined or caused by some unusual agents (possible viral) or autoimmune reactions, modified by other than gentically divergent factors.

摘要

通过电聚焦法在多发性硬化症患者中发现的脑脊液γ-球蛋白模式可分为五种(a - e)平均模式,其中各个条带靠得很近。然而,在一些确诊或疑似多发性硬化症的患者中发现了明显的条带。将28例此类病例的电聚焦模式与Kjellin和Vesterberg报告的模式以及偶然收集的20例确诊多发性硬化症病例的模式进行了比较。在不同平均模式的频率、区域“5”中双组分的出现、区域“7”中单一组分的出现以及高碱性组分方面发现了差异。将电聚焦结果与这28例患者的临床数据进行了比较。明显条带的模式与疾病的持续时间和病程以及中枢神经系统病变的可能部位之间似乎存在某种相关性。未发现脑脊液γ-球蛋白值升高和/或高度屏障损伤是脑脊液γ-球蛋白区域出现明显条带的先决条件。异常的电聚焦模式可能是由基因决定的,或者是由某些不寻常的因素(可能是病毒)或自身免疫反应引起的,并受到非基因差异因素的影响。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验