Suppr超能文献

自身免疫性血小板减少症中自身抗体的特异性

Specificity of autoantibodies in autoimmune thrombocytopenia.

作者信息

van Leeuwen E F, van der Ven J T, Engelfriet C P, von dem Borne A E

出版信息

Blood. 1982 Jan;59(1):23-6.

PMID:7032627
Abstract

In 42 patients with autoimmune thrombocytopenia (AITP) and a positive direct platelet suspension immunofluorescence test (PSIFT), the antigenic specificity of the autoantibodies was studied. Because the autoantibodies were often not detectable in the serum and additional HLA antibodies may disturb the reaction pattern with the platelet panel, we used eluates prepared from the patients' platelets for this study. Thirty-five patients had antibodies equally reactive with normal platelets, irrespective of their antigenic make-up, but not with the platelets from two Glanzmann's disease patients. Absorption and elution experiments in two patients showed that his was probably not due to the presence of a combination of anti-Zwa and anti-Zwb antibodies. Thus, the majority of autoantibodies against platelets seems to be directed against antigenic determinants not present on Glanzmann's disease platelets, but perhaps located on the platelet-membrane glycoproteins IIb and/or IIIa. In ten patients, antibodies of no, or still unknown, specificity were detected. Three of these had additional antibodies not reactive with the platelets of the two Glanzmann patients.

摘要

在42例自身免疫性血小板减少症(AITP)且直接血小板悬液免疫荧光试验(PSIFT)呈阳性的患者中,研究了自身抗体的抗原特异性。由于自身抗体在血清中往往无法检测到,且额外的HLA抗体可能会干扰与血小板组的反应模式,因此本研究使用从患者血小板制备的洗脱液。35例患者的抗体与正常血小板具有同等反应性,无论其抗原组成如何,但与两名Glanzmann病患者的血小板无反应。对两名患者进行的吸收和洗脱实验表明,这可能不是由于抗Zwa和抗ZWb抗体组合的存在。因此,大多数针对血小板的自身抗体似乎是针对Glanzmann病血小板上不存在但可能位于血小板膜糖蛋白IIb和/或IIIa上的抗原决定簇。在10例患者中,检测到特异性不明确或仍未知的抗体。其中3例还存在与两名Glanzmann患者的血小板无反应的额外抗体。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验