Suppr超能文献

在鉴别高滴度血小板反应性抗体时MAIPA检测法的局限性。

Limits of the MAIPA assay when differentiating high-titered platelet-reactive antibodies.

作者信息

Agildere A, Wernet D, Schnaidt M

机构信息

Abteilung für Transfusionsmedizin, Universitätsklinik Tübingen, Germany.

出版信息

Beitr Infusionsther Transfusionsmed. 1997;34:190-3.

PMID:9356673
Abstract

Experience with the MAIPA assay for the diagnosis of platelet-reactive antibodies has shown that high-titered antibodies falsify the test results. We here demonstrate 2 cases: i) A serum with high-titered HLA antibodies (100% panel reactivity in the LCT, titer between 4,000 and 12,000), and ii) Serum with a high-titered anti-HPA-1a (titer in the MAIPA assay 1,000). In both cases, it can be demonstrated that these antibodies led to unspecific reactions. In the 1st case, they interfered with the diagnosis of additional platelet-specific antibodies. Only the use of HLA-compatible platelets allowed a correct identification. On the other hand, in the high-titered anti-HPA-1a unspecific reactions were seen with the glycoproteins Ib/IX, Ia/IIa, and beta 2-microglobulin, leading to misinterpretations. These examples demonstrate that, in the test conditions as described, a correct diagnosis of high-titered sera might only be achieved by using compatible HLA or HPA cells.

摘要

血小板反应性抗体诊断的单克隆抗体固相血小板抗原分析(MAIPA)经验表明,高滴度抗体可使检测结果出现偏差。我们在此展示2个病例:i)一份含有高滴度HLA抗体的血清(淋巴细胞毒试验中100%的板反应性,滴度在4000至12000之间),以及ii)一份含有高滴度抗HPA-1a的血清(MAIPA试验中滴度为1000)。在这两个病例中,均可证明这些抗体导致了非特异性反应。在第一个病例中,它们干扰了其他血小板特异性抗体的诊断。只有使用HLA相容的血小板才能进行正确鉴定。另一方面,在高滴度抗HPA-1a的情况下,糖蛋白Ib/IX、Ia/IIa和β2-微球蛋白出现了非特异性反应,导致解读错误。这些例子表明,在所述检测条件下,只有使用相容的HLA或HPA细胞才能对高滴度血清进行正确诊断。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验