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临床实验室中血小板抗体和抗原的检测与鉴定。

Detection and identification of platelet antibodies and antigens in the clinical laboratory.

作者信息

Curtis B R, McFarland J G

机构信息

BloodCenter of Wisconsin, Platelet and Neutrophil Immunology Laboratory, PO Box 2178, Milwaukee, Wisconsin 53201-2178, USA.

出版信息

Immunohematology. 2009;25(3):125-35.

Abstract

As a result of the unique functional properties of platelets, more-robust methods were required for detection of antibodies raised against them. Immunofluorescence detection by flow cytometry, solid-phase red cell adherence, and antigen capture ELISAs are some of the current tests that have been developed to meet the challenges of platelet antibody detection and identification and antigen phenotyping. Recently developed protein liquid bead arrays are becoming the next-generation platelet antibody tests. Fueled by development of PCR and determination of the molecular basis of the PlA1 human platelet antigen (HPA), serologic platelet typing has now been replaced by genotyping of DNA. Allele-specific PCR, melting curve analysis, and 5'-nuclease assays are now evolving into more high-throughput molecular tests. Laboratory testing for the diagnosis of immune platelet disorders has advanced considerably from its humble beginnings.

摘要

由于血小板具有独特的功能特性,因此需要更强大的方法来检测针对血小板产生的抗体。流式细胞术免疫荧光检测、固相红细胞黏附以及抗原捕获酶联免疫吸附测定是目前为应对血小板抗体检测、鉴定及抗原表型分析挑战而开发的一些检测方法。最近开发的蛋白质液体芯片正成为新一代的血小板抗体检测方法。在聚合酶链反应(PCR)发展以及人类血小板抗原1(HPA)分子基础确定的推动下,血清学血小板分型现已被DNA基因分型所取代。等位基因特异性PCR、熔解曲线分析和5'核酸酶测定正发展成为更高通量的分子检测方法。用于诊断免疫性血小板疾病的实验室检测已从其简陋的开端取得了长足的进步。

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