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用于鉴定HLA分型试剂的可溶性HLA I类抗原酶联免疫测定法。

Solubilized HLA class I antigen enzyme-linked immunoassay to identify HLA-typing reagents.

作者信息

Baier K A, Meyer J A, O'Brien B J, Flora-Ginter G, Morris T L, Patterson T, Bryan C F

机构信息

Midwest Organ Bank, Westwood, Kansas.

出版信息

Hum Immunol. 1994 Jul;40(3):187-90. doi: 10.1016/0198-8859(94)90068-x.

Abstract

The objective of this study was to evaluate the use of sHLA in a solid-phase EIA as a rapid and sensitive way to identify potential IgG HLA class-I-typing reagents. To evaluate the efficacy of the sHLA EIA, we used the assay to screen 259 HLA-A, -B, and -C antisera that our laboratory had procured using the standard NIH LCA. A positive result obtained by the sHLA EIA, which was defined as an EIA ratio of 3 SD above the mean of 91 anti-HLA-negative sera, revealed that 91% (79 of 87) of the A-locus-typing reagents were positive, 96% (150 of 156) of the B-locus antisera were positive, and only 75% (12 of 16) of the C-locus reagents were positive. The typing reagents that were negative by EIA (n = 18) fell into two categories. First, 38% (7 of 18) were negative by sHLA EIA, as they were IgM-typing reagents (NIH LCA reactivity ameliorated by DTT). The second group of the 11 remaining typing reagents had a mean EIA ratio of 1.0 +/- 0.246 (mean +/- 1 SD), which was significantly (P < 0.001) higher than the mean of the 91 negative controls that were used to establish the negative cutoff. The overall sensitivity of the sHLA EIA to detect HLA class-I-directed IgG was 97.2%.

摘要

本研究的目的是评估在固相酶免疫测定(EIA)中使用可溶性人类白细胞抗原(sHLA)作为一种快速且灵敏的方法来鉴定潜在的IgG HLA I类分型试剂。为了评估sHLA EIA的有效性,我们使用该检测方法对我们实验室使用标准美国国立卫生研究院淋巴细胞毒试验(NIH LCA)采购的259种HLA - A、- B和 - C抗血清进行筛选。sHLA EIA获得的阳性结果定义为酶免疫测定比值比91份抗HLA阴性血清的平均值高3个标准差,结果显示87种A位点分型试剂中有91%(79种)呈阳性,156种B位点抗血清中有96%(150种)呈阳性,而16种C位点试剂中只有75%(12种)呈阳性。酶免疫测定呈阴性的分型试剂(n = 18)分为两类。第一类,38%(18种中的7种)sHLA EIA呈阴性,因为它们是IgM分型试剂(DTT改善了NIH LCA反应性)。其余11种分型试剂的第二组酶免疫测定比值平均为1.0 +/- 0.246(平均值 +/- 1个标准差),显著高于(P < 0.001)用于确定阴性临界值的91份阴性对照的平均值。sHLA EIA检测HLA I类定向IgG的总体敏感性为97.2%。

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