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[自身免疫性疾病——免疫学基础]

[Autoimmune diseases - immunological bases].

作者信息

Jäger W

出版信息

Z Gesamte Inn Med. 1975 Nov 15;30(22):241-4 concl.

PMID:55002
Abstract

Autosensibilisations are essentially more frequent than hitherto was assumed. They, in the main, can be led back to 3 basic mechanisms: 1. Autosensibilisations by determination of the antibodies, where no immunotolerance was present, 2. fraction of the immunotolerance by antibodies (e. g. due to cross-reactions or adjuvant effects), 3. fraction of the immunotolerance by primary changes of immunocompetent cells (e. g. lymphoproliferation diseases). Even the natural immunotolerance is possibly maintained by enhancement effects of blocking autoantibodies. Pathogenic effects (auto-immune diseases) are above all to be expected, if the autoantibodies or by endogenic substances sensibilised T-lymphocytes may react with the antigen and these immune reactions lead to lesions of cells or other structures. Finally for the progression is also necessary the persistence and the autonomisation of the autosensibilisation. Finally is discussed in which range the criteria for the diagnostics of an auto-immune disease derived by Milgrom and Witebsky from the animal experiment may be transposed to the clinic.

摘要

自身致敏本质上比以往认为的更为常见。它们主要可归因于三种基本机制:1. 因抗体介导的自身致敏,此时不存在免疫耐受;2. 抗体导致免疫耐受部分丧失(例如由于交叉反应或佐剂效应);3. 免疫活性细胞的原发性改变导致免疫耐受部分丧失(例如淋巴细胞增殖性疾病)。甚至天然免疫耐受也可能通过阻断自身抗体的增强作用得以维持。如果自身抗体或由内源性物质致敏的T淋巴细胞与抗原发生反应,并且这些免疫反应导致细胞或其他结构的损伤,那么首先就可能预期会产生致病效应(自身免疫性疾病)。最后,自身致敏的持续存在和自主化对于病情进展也是必要的。最后讨论了米尔格罗姆和维特布斯基从动物实验得出的自身免疫性疾病诊断标准可应用于临床的范围。

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