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用于检测循环免疫复合物的Cordia-IC酶联免疫吸附测定试剂盒的评估

Evaluation of a Cordia-IC enzyme-linked immunosorbent assay kit for the detection of circulating immune complexes.

作者信息

Landoy Z, West T E, Vladutiu A O, Fitzpatrick J E

出版信息

J Clin Microbiol. 1985 Aug;22(2):279-82. doi: 10.1128/jcm.22.2.279-282.1985.

Abstract

A commercial kit (Cordia-IC) from Cordis Laboratory, Miami, Fla., was compared with the Raji cell radioimmunoassay for its ability to detect circulating immune complexes (CIC) in sera from 30 control subjects and 118 patients with infectious diseases. The 118 patients were categorized into the following groups: (i) 23 patients with bacterial endocarditis, (ii) 41 patients with bacteremia from an infected intravascular catheter or access device, and (iii) 54 patients with Staphylococcus aureus bacteremia related to a deep tissue infection. The Cordia-IC was comparable to the Raji cell radioimmunoassay in intraassay variability (4.0 versus 8.0%) and interassay reproducibility (8.7 versus 20.0%). Neither assay found CIC amounts above 12.5 micrograms equivalents (eq) of aggregated human gamma globulin (AHG) per ml in any of the 30 control individuals. In group 1, Cordia-IC detected 19 of 23 positives (mean, 73.6 micrograms eq of AHG per ml), whereas the Raji cell detected 16 of 23 positives (mean, 54.8 micrograms eq of AHG per ml). In group 2, Cordia-IC detected 19 of 41 positives (mean, 20.6 micrograms eq of AHG per ml), whereas the Raji cell detected 16 of 41 positives (mean, 15.1 micrograms eq of AHG per ml). In group 3, Cordia-IC found 38 of 54 positives (mean, 28.0 micrograms eq of AHG per ml), whereas the Raji cell found 32 of 54 positives (mean, 23.9 micrograms eq of AHG per ml). Statistically, these findings were not significantly different in any of the three patient groups (P> 0.15), and there was an overall good correlation between the results obtained by the two assays (r+0.64, P<0.001). The Cordia-IC provided a suitable assay for the detection of CIC and might find application in routine clinical laboratories.

摘要

将佛罗里达州迈阿密市科迪斯实验室生产的一种商用试剂盒(Cordia - IC)与拉吉细胞放射免疫分析法进行比较,以检测30名对照受试者和118名传染病患者血清中的循环免疫复合物(CIC)。118名患者被分为以下几组:(i)23例细菌性心内膜炎患者;(ii)41例因感染性血管内导管或接入装置导致菌血症的患者;(iii)54例与深部组织感染相关的金黄色葡萄球菌菌血症患者。Cordia - IC在批内变异性(4.0%对8.0%)和批间重复性(8.7%对20.0%)方面与拉吉细胞放射免疫分析法相当。在30名对照个体中,两种检测方法均未发现每毫升血清中CIC含量超过12.5微克当量(eq)的聚合人γ球蛋白(AHG)。在第1组中,Cordia - IC检测出23例阳性中的19例(平均每毫升AHG为73.6微克当量),而拉吉细胞检测出23例阳性中的16例(平均每毫升AHG为54.8微克当量)。在第2组中,Cordia - IC检测出41例阳性中的19例(平均每毫升AHG为20.6微克当量),而拉吉细胞检测出41例阳性中的16例(平均每毫升AHG为15.1微克当量)。在第3组中,Cordia - IC检测出54例阳性中的38例(平均每毫升AHG为28.0微克当量),而拉吉细胞检测出54例阳性中的32例(平均每毫升AHG为23.9微克当量)。从统计学角度来看,在三个患者组中的任何一组中,这些结果均无显著差异(P>0.15),并且两种检测方法所获结果之间总体具有良好的相关性(r = 0.64,P<0.001)。Cordia - IC为检测CIC提供了一种合适的检测方法,可能在常规临床实验室中得到应用。

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Quantitation of soluble immune complexes by a microplate Raji cell-ELISA method.
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