Suppr超能文献

多发性硬化相关因子。多发性硬化症患者的脑部和血清无法降低正常小鼠以及接种含有C型颗粒细胞的小鼠的多形核细胞计数。

Multiple sclerosis-associated agent. Failure of MS brain and serum to depress the polymorph count in normal mice and mice inoculated with cells containing C/type particles.

作者信息

Cobill J M, Hughes D, Keith A B, Cameron K R, Mason J, Caspary E A

出版信息

J Neurol Sci. 1979 Mar;41(1):11-6. doi: 10.1016/0022-510x(79)90135-7.

Abstract

The groups that originally reported and confirmed the demonstration of a multiple sclerosis associated agent (MSAA) are now, along with others, unable to reproduce this effect. In view of this confusion and the potential importance of this work for multiple sclerosis (MS) we have done a strict double-blind trial using larger groups of mice (10) and counting more cells (900) than in previous reports to offset the high variability of mouse polymorphonuclear neutrophil (PMN) counts. Sera from 5 active MS patients and 4 normal subjects were tested in mice, half of which had previously been injected with PAM line cells (containing C-type particles and subject to reduced cell yield when cultured with MS brain extract). No significant PMN depression was found in either MS or normals on any basis of comparison. However, a significant depression was seen following PAM cell injection irrespective of serum origin. Higher counting accuracy did not reduce PMN variability. A single MS brain specimen was also without effect. consequently we have been unable to confirm the existence of an MSAA as defined by PMN depression in mice.

摘要

最初报告并证实存在多发性硬化相关因子(MSAA)的研究团队,如今与其他团队一样,无法重现这一效应。鉴于这种混乱情况以及该研究对多发性硬化(MS)的潜在重要性,我们进行了一项严格的双盲试验,使用的小鼠数量比以往报告更多(10只),并且计数的细胞数量也更多(900个),以抵消小鼠多形核中性粒细胞(PMN)计数的高变异性。对5名活动性MS患者和4名正常受试者的血清在小鼠身上进行了测试,其中一半小鼠先前已注射PAM系细胞(含有C型颗粒,在用MS脑提取物培养时细胞产量会降低)。在任何比较基础上,无论是MS患者组还是正常受试者组,均未发现PMN有显著降低。然而,无论血清来源如何,注射PAM细胞后均出现了显著降低。更高的计数准确性并未降低PMN的变异性。单个MS脑标本也没有效果。因此,我们无法证实小鼠中PMN降低所定义的MSAA的存在。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验