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人类免疫缺陷病毒中和抗体的流行率、临床意义及毒株特异性

Prevalence, clinical significance, and strain specificity of neutralizing antibody to the human immunodeficiency virus.

作者信息

Prince A M, Pascual D, Kosolapov L B, Kurokawa D, Baker L, Rubinstein P

出版信息

J Infect Dis. 1987 Aug;156(2):268-72. doi: 10.1093/infdis/156.2.268.

Abstract

A semiautomated microtiter assay has been developed to quantitate neutralizing antibody to the human immunodeficiency virus. This assay has been found to be highly specific. Forty-four sera that were negative by enzyme-linked immunosorbent assay (ELISA) were tested under code: 42 were negative (less than 1:2), and 2 had titers of 1:2. By contrast, of 178 sera positive by western blot, 92.7% had detectable neutralizing antibody, and 12.5% had titers greater than or equal to 1:128. Neutralizing antibody titers correlated poorly with clinical diagnosis and T4/T8 ratios. Different isolates differed quantitatively in their sensitivity to neutralization by antibodies obtained from different patients; however, all strains tested so far have been neutralizable by all the sera tested. Neutralizing antibody titers correlated weakly, if at all, with direct or competition ELISA titers.

摘要

已开发出一种半自动微量滴定测定法来定量检测针对人类免疫缺陷病毒的中和抗体。该测定法具有高度特异性。对44份酶联免疫吸附测定(ELISA)呈阴性的血清进行了编码检测:42份为阴性(低于1:2),2份的效价为1:2。相比之下,在178份经蛋白质印迹法检测呈阳性的血清中,92.7%可检测到中和抗体,12.5%的效价大于或等于1:128。中和抗体效价与临床诊断及T4/T8比值的相关性较差。不同的病毒分离株对来自不同患者的抗体中和作用的敏感性在数量上存在差异;然而,迄今为止测试的所有菌株均可被所有测试血清中和。中和抗体效价与直接ELISA或竞争ELISA效价的相关性较弱(如果有相关性的话)。

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