Yolken R H, Torsch V M
Infect Immun. 1981 Feb;31(2):742-50. doi: 10.1128/iai.31.2.742-750.1981.
Coxsackieviruses A are known to cause a wide range of human disease processes. However, because many coxsackieviruses A present in clinical specimens do not produce a recognizable cytopathic effect in readily available tissue culture systems, infections with coxsackieviruses A are often difficult to diagnose. We have thus developed enzyme-linked immunosorbent assay (ELISA) systems for the detection and serotyping of coxsackievirus A antigens. The assays consist of a double-antibody ELISA which utilizes type-specific monkey and mouse coxsackievirus antisera. Although some cross-reactivity was noted, the ELISA systems correctly identified the serotypes of 22 to 23 coxsackievirus A complement fixation antigens available for testing. Testing of tissue culture fluids revealed that antigen could often be detected by ELISA before the appearance of a cytopathic effect. In addition, the infecting coxsackievirus A antigen could be unequivocally identified in 8 of 11 stool specimens obtained from patients with coxsackievirus A infections. The ELISA system might thus represent an important tool in the diagnosis and study of coxsackievirus A infections.
已知A组柯萨奇病毒可引发多种人类疾病进程。然而,由于临床标本中存在的许多A组柯萨奇病毒在现有的组织培养系统中不会产生可识别的细胞病变效应,A组柯萨奇病毒感染往往难以诊断。因此,我们开发了用于检测A组柯萨奇病毒抗原并进行血清分型的酶联免疫吸附测定(ELISA)系统。这些测定包括一种双抗体ELISA,它利用了型特异性猴和小鼠A组柯萨奇病毒抗血清。尽管观察到了一些交叉反应,但ELISA系统正确鉴定了可用于检测的22至23种A组柯萨奇病毒补体结合抗原的血清型。对组织培养液的检测表明,在细胞病变效应出现之前,ELISA通常就能检测到抗原。此外,从A组柯萨奇病毒感染患者获得的11份粪便标本中,有8份能明确鉴定出感染性A组柯萨奇病毒抗原。因此,ELISA系统可能是诊断和研究A组柯萨奇病毒感染的重要工具。