Tkácová M, Varecková E
Institute of Virology, Slovak Academy of Sciences, Bratislava, Slovak Republic.
J Virol Methods. 1996 Jun;60(1):65-71. doi: 10.1016/0166-0934(96)02046-0.
A highly sensitive one-step immunocapture EIA for the detection of influenza A virus antigen directly in a clinical specimen was developed. The sensitivity was achieved by using two high-affinity cross-reactive influenza type A-specific monoclonal antibodies, recognizing independent nonoverlapping epitopes on the influenza A nucleoprotein. One of the two MAbs was used as a capture antibody, while the other was coupled with enzyme peroxidase and served as a detector. Sensitivity to detection of highly purified recombinant influenza A virus nucleoprotein by EIA reached approximately 10 pg. Fifteen purified human influenza A virus strains of H1, H2 and H3 subtypes, isolated during the period 1934-1992, were tested by this system. All the influenza A viruses tested positive, whereas two influenza B viruses used as a control were negative. The efficiency of the system for detection of influenza A viral antigen directly in clinical specimens was confirmed by testing nasal and nasopharyngeal washes and aspirates, tested previously by time-resolved fluoroimmunoassay and by virus culture confirmation assay.
开发了一种用于直接在临床标本中检测甲型流感病毒抗原的高灵敏度一步免疫捕获酶免疫测定法。通过使用两种高亲和力交叉反应的甲型流感特异性单克隆抗体实现了灵敏度,这两种抗体识别甲型流感核蛋白上独立且不重叠的表位。两种单克隆抗体中的一种用作捕获抗体,另一种与辣根过氧化物酶偶联并用作检测抗体。酶免疫测定法检测高度纯化的重组甲型流感病毒核蛋白的灵敏度达到约10皮克。用该系统检测了1934年至1992年期间分离的15株纯化的H1、H2和H3亚型人甲型流感病毒株。所有检测的甲型流感病毒均呈阳性,而用作对照的两种乙型流感病毒均为阴性。通过检测鼻腔和鼻咽冲洗液及吸出物,证实了该系统直接在临床标本中检测甲型流感病毒抗原的效率,这些标本先前已通过时间分辨荧光免疫测定法和病毒培养确认试验进行了检测。