首页> 美国卫生研究院文献>Chest >A Platelet Factor 4-Dependent Platelet Activation Assay Facilitates Early Detection of Pathogenic Heparin-Induced Thrombocytopenia Antibodies
【2h】

A Platelet Factor 4-Dependent Platelet Activation Assay Facilitates Early Detection of Pathogenic Heparin-Induced Thrombocytopenia Antibodies

机译:血小板因子4依赖性血小板活化测定有助于早期发现病原性肝素诱导的血小板减少症抗体

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

Heparin-induced thrombocytopenia (HIT) is a dangerous complication of heparin therapy. HIT diagnosis is established by recognizing thrombocytopenia and/or thrombosis in an affected patient and from the results of serological tests such as the platelet factor 4 (PF4)/heparin immunoassay (PF4 ELISA) and serotonin release assay (SRA). Recent studies suggest that HIT antibodies activate platelets by recognizing PF4 in a complex with platelet glycosaminoglycans (and/or polyphosphates) and that an assay based on this principle, the PF4-dependent P-selectin expression assay (PEA), may be even more accurate than the SRA for HIT diagnosis. Here, we demonstrate that the PEA detected pathogenic antibodies before the SRA became positive in two patients with HIT studied serially, in one case even before seropositivity in the PF4 ELISA. In one of the patients treated with plasma exchange, persistent dissociation between the PEA and SRA test results was observed. These results support a role for the PEA in early HIT diagnosis.
机译:肝素诱导的血小板减少症(HIT)是肝素治疗的危险并发症。通过识别患病患者的血小板减少和/或血栓形成以及血清学检测的结果(例如血小板因子4(PF4)/肝素免疫测定(PF4 ELISA)和血清素释放测定(SRA))来建立HIT诊断。最近的研究表明,HIT抗体可通过识别与血小板糖胺聚糖(和/或多磷酸盐)形成的复合物中的PF4来激活血小板,基于该原理的测定法,即PF4依赖性P-选择素表达测定法(PEA),可能更加准确比SRA用于HIT诊断。在这里,我们证明了在连续研究的两名HIT患者中,在SRA呈阳性之前,甚至在PF4 ELISA中血清阳性之前,PEA都检测到了致病性抗体。在其中一位接受血浆置换治疗的患者中,观察到PEA和SRA测试结果之间持续分离。这些结果支持了PEA在早期HIT诊断中的作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号