Grillner L, Landqvist M
Eur J Clin Microbiol. 1983 Feb;2(1):39-42. doi: 10.1007/BF02019921.
An enzyme-linked immunosorbent assay for herpes simplex virus was tested using commercially available peroxidase-conjugated and unconjugated rabbit antibodies to herpes simplex virus type 1 and type 2 (DAKO immunoglobulins A/S, Copenhagen, Denmark). One hundred and thirty-seven clinical specimens from vesicles and superficial cutaneous lesions were tested and the results compared with virus isolation. In addition 210 herpes simplex virus isolates were typed. Forty-four specimens yielded herpes simplex virus both in the enzyme-linked immunosorbent assay and in tissue culture and 79 were negative in both tests. Fourteen were positive in isolation but negative in the enzyme-linked immunosorbent assay. Seventy-three isolates were typed as herpes simplex virus type 1 and 137 as herpes simplex virus type 2. The enzyme-linked immunosorbent assay was found to be rapid and easy to perform but less sensitive than conventional isolation in routine diagnostic work. For typing of isolates it was found to be a useful method for distinguishing herpes simplex virus type 1 and type 2.
使用市售的与过氧化物酶结合和未结合的抗1型和2型单纯疱疹病毒兔抗体(丹麦哥本哈根达科免疫球蛋白A/S公司产品)对单纯疱疹病毒酶联免疫吸附试验进行了检测。对137份来自水疱和浅表皮肤损害的临床标本进行了检测,并将结果与病毒分离法进行了比较。此外,对210株单纯疱疹病毒分离株进行了分型。44份标本在酶联免疫吸附试验和组织培养中均产生了单纯疱疹病毒,79份在两项检测中均为阴性。14份标本病毒分离呈阳性,但酶联免疫吸附试验呈阴性。73株分离株被分型为1型单纯疱疹病毒,137株为2型单纯疱疹病毒。在常规诊断工作中,发现酶联免疫吸附试验快速且易于操作,但比传统的病毒分离法敏感性低。对于分离株的分型,发现它是区分1型和2型单纯疱疹病毒的一种有用方法。