McHugh T M, Miner R C, Logan L H, Stites D P
Department of Laboratory Medicine, University of California, San Francisco 94143.
J Clin Microbiol. 1988 Oct;26(10):1957-61. doi: 10.1128/jcm.26.10.1957-1961.1988.
A sensitive assay for the simultaneous detection of anti-cytomegalovirus and anti-herpes simplex virus antibodies was developed. Two different sizes of polystyrene microspheres were coated with purified viral antigens. Human antiviral antibodies were detected with a biotin-streptavidin amplification procedure with phycoerythrin as the fluorescent label. Microsphere-associated fluorescence was quantitated with a flow cytometer. Sixteen percent of samples initially scored as seronegative for cytomegalovirus and 35% of samples initially scored as seronegative for herpes simplex virus by conventional assays were clearly found positive by the microsphere technique. This flow cytometric assay can simultaneously detect several specific antibodies at levels which are below the sensitivity of standard assays. The dynamic range of this assay is at least sixfold greater than that of enzyme immunoassays. This technique is amenable to numerous serologic assays and could greatly expand the clinical laboratory applications of flow cytometry.
开发了一种用于同时检测抗巨细胞病毒和抗单纯疱疹病毒抗体的灵敏检测方法。两种不同大小的聚苯乙烯微球用纯化的病毒抗原包被。采用以藻红蛋白为荧光标记的生物素-链霉亲和素扩增程序检测人抗病毒抗体。用流式细胞仪对微球相关荧光进行定量。通过微球技术明确发现,最初通过传统检测方法判定为巨细胞病毒血清阴性的样本中有16%以及最初判定为单纯疱疹病毒血清阴性的样本中有35%呈阳性。这种流式细胞术检测方法能够以低于标准检测方法灵敏度的水平同时检测多种特异性抗体。该检测方法的动态范围比酶免疫测定法至少大六倍。这项技术适用于众多血清学检测,并且能够极大地扩展流式细胞术在临床实验室中的应用。