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一种使用小鼠单克隆抗体检测狂犬病疑似标本中狂犬病病毒核衣壳的简单夹心酶联免疫吸附测定法(WELYSSA)。

A simple sandwich ELISA (WELYSSA) for the detection of lyssavirus nucleocapsid in rabies suspected specimens using mouse monoclonal antibodies.

作者信息

Xu Gelin, Weber Patrick, Hu Qiaoling, Xue Honggang, Audry Laurent, Li Chengping, Wu Jie, Bourhy Herve

机构信息

Wuhan Institute of Biological Products, Wuhan 430060, Hubei Province, China.

出版信息

Biologicals. 2007 Oct;35(4):297-302. doi: 10.1016/j.biologicals.2006.10.002. Epub 2007 Feb 2.

Abstract

Monoclonal antibody (MAb)-based capture enzyme-linked immunosorbent assays (ELISA) were developed for the diagnosis of rabies-suspect specimens. A combination of four mouse monoclonal antibodies directed against the rabies virus nucleocapsid was selected and used for the detection. The test was optimized and standardized so that maximum concordance could be maintained with the standard procedures of rabies diagnosis recommended by the WHO expert committee. Using prototype viruses from the different genotypes of lyssavirus and from various geographic origins and phylogenetic lineages, this paper presents a reliable, rapid and transferable diagnostic method, named WELYSSA that readily permits the detection of lyssaviruses belonging to the 7 genotypes of lyssavirus circulating in Europe, Africa, Asia and Oceania. The threshold of detection of lyssavirus nucleocapsids is low (0.8 ng/ml). With a panel of 1030 specimens received for rabies diagnostic testing, this test was found to be highly specific (0.999) and sensitive (0.970) when compared to other recommended rabies diagnostic methods.

摘要

开发了基于单克隆抗体(MAb)的捕获酶联免疫吸附测定(ELISA)用于诊断疑似狂犬病标本。选择了四种针对狂犬病病毒核衣壳的小鼠单克隆抗体组合并用于检测。对该检测方法进行了优化和标准化,以便与世界卫生组织专家委员会推荐的狂犬病诊断标准程序保持最大程度的一致性。利用来自不同基因型狂犬病病毒、不同地理来源和系统发育谱系的原型病毒,本文提出了一种可靠、快速且可转移的诊断方法,名为WELYSSA,该方法能够轻松检测出在欧洲、非洲、亚洲和大洋洲传播的属于7种基因型狂犬病病毒的病毒。狂犬病病毒核衣壳的检测阈值较低(0.8 ng/ml)。与其他推荐的狂犬病诊断方法相比,在一组1030份用于狂犬病诊断检测的标本中,该检测方法具有高度特异性(0.999)和敏感性(0.970)。

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