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青霉胺诱发的重症肌无力。23例免疫临床相关性研究

[Myasthenia induced by D-penicillamine. Study of immuno-clinical correlations in 23 cases].

作者信息

d'Anglejan J, Morel E, Feuillet-Fieux M N, Raimond F, Vernet der Garabedian B, Jacob L, Bach J F

出版信息

Presse Med. 1985 Dec 28;14(46):2336-40.

PMID:2935832
Abstract

Sera from 23 patients with D-penicillamine-induced myasthenia gravis (MG) contained antibodies directed against the human muscle acetylcholine receptor (anti-AChR) in 83% of the cases at the onset of the disease. Twenty-one were patients with rheumatoid arthritis. The anti-AChR antibody titers were comparable to those of sera from ocular MG patients and were related to the presence of clinical signs but not to their severity. The anti-AChR antibodies persisted in autonomous MG (5 cases) and disappeared in the other cases. The same phenomenon occurred for antinuclear antibodies detected in sera from 13 patients at the onset of the disease: anti-ss DNA 9/13, antinuclear 4/13 and anti-histones 7/13. The latter antibodies seem to result from, and follow the D-penicillamine treatment.

摘要

23例D-青霉胺诱发的重症肌无力(MG)患者的血清在疾病发作时,83%的病例含有针对人肌肉乙酰胆碱受体的抗体(抗AChR)。其中21例为类风湿关节炎患者。抗AChR抗体滴度与眼肌型MG患者血清的滴度相当,且与临床体征的存在有关,但与体征的严重程度无关。抗AChR抗体在自发缓解型MG患者(5例)中持续存在,在其他病例中消失。在13例患者疾病发作时血清中检测到的抗核抗体也出现了同样的现象:抗单链DNA 9/13、抗核抗体4/13和抗组蛋白7/13。后一种抗体似乎是由D-青霉胺治疗引起的,并随着该治疗而出现。

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