首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Comparison of immunofluorescence particle agglutination and enzyme immunoassays for detection of human T-cell leukemia virus type I antibody in African sera.
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Comparison of immunofluorescence particle agglutination and enzyme immunoassays for detection of human T-cell leukemia virus type I antibody in African sera.

机译:在非洲血清中检测人T细胞白血病病毒I型抗体的免疫荧光法颗粒凝集法和酶免疫法的比较。

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摘要

The effectiveness of four screening tests for detecting antibody to human T-cell leukemia virus type I (HTLV-I) was determined by using 2,700 African serum specimens. The tests studied were indirect immunofluorescence, particle agglutination from Fujirebio, and two enzyme immunoassays, one from Abbott Laboratories that used virus lysate from HUT 102 cells and the other from Cambridge BioScience Corp. that used an env recombinant protein. Positive and doubtful sera were confirmed by Western immunoblot and radioimmunoprecipitation assay with Food and Drug Administration seropositivity criteria. The best results were obtained with the two enzyme immunoassays, which were more sensitive (100 and 98.6% [Abbott and Cambridge, respectively]) and more specific (98.7 and 96.5%). Indirect immunofluorescence exhibited difficulties for reading and interpretation. With particle agglutination, prozone was observed for 9 of 78 HTLV-I-positive serum specimens. False-positives in any of the tests were not linked to cross-reactions with human immunodeficiency viruses. However, confirmation tests remain necessary for HTLV-I screening.
机译:通过使用2700份非洲血清标本,确定了四项筛选测试检测I型人T细胞白血病病毒(HTLV-1)抗体的有效性。所研究的测试包括间接免疫荧光法,Fujirebio的颗粒凝集法和两种酶免疫法,一种来自Abbott Laboratories,其使用了HUT 102细胞的病毒裂解液,另一种来自Cambridge BioScience Corp.,其使用了env重组蛋白。阳性和可疑血清通过Western免疫印迹和放射免疫沉淀测定法(符合美国食品药品管理局的血清阳性标准)进行确认。两种酶免疫测定法均获得最佳结果,其灵敏度更高(分别为100和98.6%[分别为Abbott和Cambridge])和特异性更高(分别为98.7和96.5%)。间接免疫荧光显示难以阅读和解释。通过颗粒凝集,在78例HTLV-I阳性血清样本中有9份观察到了前带。在任何测试中,假阳性都与人免疫缺陷病毒的交叉反应无关。但是,对于HTLV-1筛查仍然需要进行确认测试。

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