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通过酶联免疫吸附测定法检测针对爱泼斯坦-巴尔病毒抗原的抗体。

Detection of antibodies to Epstein-Barr virus antigens by enzyme-linked immunosorbent assay.

作者信息

Hopkins R F, Witmer T J, Neubauer R H, Rabin H

出版信息

J Infect Dis. 1982 Dec;146(6):734-40. doi: 10.1093/infdis/146.6.734.

Abstract

An enzyme-linked immunosorbent assay (ELISA) is described for the serologic analysis of antibodies to Epstein-Barr virus (EBV)-associated nuclear antigen (EBNA), viral capsid antigen (VCA), and early antigen (EA). The specificity of each of the ELISAs was demonstrated by the use of well-characterized human sera shown by immunofluorescence assay to be variously reactive for antibodies to one or more of the three viral antigens studied. The ELISA for EBNA was four to 256 times more sensitive than immunofluorescence assays with all 33 EBNA-positive sera tested. The ELISAs for VCA and EA were also more sensitive than immunofluorescence assays: approximately 50% of the sera tested showed higher antibody titers. Sera that were negative for all three antigens by immunofluorescence assay were also negative by ELISA for each antigen. These ELISAs for EBV are rapid, sensitive, and objective and thus provide new and valuable methods for the detection of antibodies to EBV-related antigens.

摘要

本文描述了一种酶联免疫吸附测定法(ELISA),用于对针对爱泼斯坦-巴尔病毒(EBV)相关核抗原(EBNA)、病毒衣壳抗原(VCA)和早期抗原(EA)的抗体进行血清学分析。通过使用经充分鉴定的人血清,经免疫荧光测定显示对所研究的三种病毒抗原中的一种或多种抗体具有不同反应性,从而证明了每种ELISA的特异性。对于所有测试的33份EBNA阳性血清,EBNA的ELISA比免疫荧光测定法敏感4至256倍。VCA和EA的ELISA也比免疫荧光测定法更敏感:约50%的测试血清显示出更高的抗体滴度。通过免疫荧光测定对所有三种抗原均呈阴性的血清在针对每种抗原的ELISA中也呈阴性。这些用于EBV的ELISA快速、灵敏且客观,因此为检测EBV相关抗原的抗体提供了新的有价值的方法。

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