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[抗着丝点抗体,作为与硬皮病不同的CREST综合征的生物标志物]

[Anti-centromere antibody, biological marker of the CREST syndrome as distinct from scleroderma].

作者信息

Rouquette-Gally A M, Stern M H, Prost A C, Abuaf N, Homberg J C, Combrisson A

出版信息

Presse Med. 1985;14(28):1497-500.

PMID:2931679
Abstract

Using HEp2 cells to study antinuclear antibodies has resulted in the discovery of the anti-centromere antibody which is thought to separate the CREST syndrome from progressive systemic sclerosis (scleroderma). This antibody seems to be exceptional in healthy subjects and are in patients with connective tissue diseases, except for scleroderma. It has also been found in CREST syndrome associated with other diseases, such as primary cirrhosis and neoplasias. In our study, the sensitivity of the anti-centromere antibody was 89.1% and its specificity 92.3% which shows that it is worth looking for.

摘要

利用人喉表皮样癌细胞(HEp2细胞)研究抗核抗体,发现了抗着丝点抗体,该抗体被认为可将CREST综合征与进行性系统性硬化症(硬皮病)区分开来。这种抗体在健康受试者中似乎罕见,在结缔组织病患者中也罕见,但硬皮病患者除外。在与其他疾病相关的CREST综合征中也发现了该抗体,如原发性胆汁性肝硬化和肿瘤。在我们的研究中,抗着丝点抗体的敏感性为89.1%,特异性为92.3%,这表明该抗体值得检测。

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