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使用微酶联免疫吸附测定(ELISA)检测血小板抗体。

Detection of platelet antibodies using a micro-enzyme-linked immunosorbent assay (ELISA).

作者信息

Schiffer C A, Young V

出版信息

Blood. 1983 Feb;61(2):311-7.

PMID:6336958
Abstract

An enzyme-linked immunosorbent assay (ELISA) for the measurement of circulating platelet antibody and platelet-associated IgG (PAIgG) is described. The test is done in microtiter plates and rapidly provides quantitative and highly reproducible results. Alloantibodies from 28 of 30 multiple transfused patients and isoantibodies from 3 of 4 patients with immune thrombocytopenic purpura (ITP) were detected. PAIgG was elevated in all 4 patients with ITP, and HLA and platelet-specific antigens were reliably detected using HLA typing sera and anti-PIA1 antibody, respectively. Platelets preserved wither by dessication in the wells of the microtiter plates or in liquid suspension in saline at 4 degrees C gave results comparable to values using fresh platelets. Storage periods ranged from 30 days for dessicated platelets to more than 1 yr for platelets stored in suspension. The ability to utilize preserved platelets may allow relatively convenient screening of large numbers of potential platelet donors for alloimmunized patients.

摘要

本文描述了一种用于测量循环血小板抗体和血小板相关IgG(PAIgG)的酶联免疫吸附测定(ELISA)。该检测在微量滴定板中进行,可快速提供定量且高度可重复的结果。检测出了30例多次输血患者中28例的同种抗体以及4例免疫性血小板减少性紫癜(ITP)患者中3例的同种抗体。所有4例ITP患者的PAIgG均升高,分别使用HLA分型血清和抗PIA1抗体可靠地检测到了HLA和血小板特异性抗原。保存在微量滴定板孔中经干燥处理的血小板或保存在4℃盐溶液中的液体悬浮血小板,其检测结果与使用新鲜血小板时相当。保存期从干燥血小板的30天到悬浮保存血小板的1年以上不等。利用保存血小板的能力可能允许相对方便地对大量潜在血小板供体进行筛查,以用于同种免疫患者。

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