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系统性硬化症(硬皮病)中的抗拓扑异构酶-I与临床发现

Anti-topoisomerase-I and clinical findings in systemic sclerosis (scleroderma).

作者信息

Shoenfeld Y, Grunebaum E, Laufer M, Zurgil N, Bakimer R, Lunderschmidt A, Valentini G, Tirri G, Blank M

机构信息

Department of Medicine B, Chaim Sheba Medical Center, Tel-Hashomer, Israel.

出版信息

Isr J Med Sci. 1996 Jul;32(7):537-42.

PMID:8756980
Abstract

The relationship between anti-topoisomerase-I antibodies and clinical findings was studied in 191 patients with definite systemic sclerosis. This was done by performing ELISA to detect antibodies to recombinant topoisomerase-I. Antibodies to topoisomerase-I were found in 72 patients (37%) with systemic sclerosis, which is a higher percentage than reported in most previous reports on a large unselected population. In 43 patients the presence of antibodies to recombinant topoisomerase-I was confirmed using both the immunodiffusion method and ELISA, with similar results. When classified into diffuse versus limited disease, a significant difference in antibody prevalence was demonstrated (P < 0.005), thus indicating that anti-topoisomerase-I antibody detection with ELISA may assist in early identification of systemic sclerosis subtypes.

摘要

在191例确诊的系统性硬化症患者中研究了抗拓扑异构酶-I抗体与临床症状之间的关系。通过进行酶联免疫吸附测定(ELISA)来检测针对重组拓扑异构酶-I的抗体。在72例(37%)系统性硬化症患者中发现了拓扑异构酶-I抗体,这一比例高于大多数以往针对未经过挑选的大样本人群的报告中所报道的比例。在43例患者中,使用免疫扩散法和ELISA均证实了重组拓扑异构酶-I抗体的存在,结果相似。当分为弥漫性疾病和局限性疾病时,抗体患病率存在显著差异(P<0.005),因此表明用ELISA检测抗拓扑异构酶-I抗体可能有助于早期识别系统性硬化症亚型。

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