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用于检测人血清中抗单纯疱疹病毒1型和2型IgG及IgM抗体的酶联免疫吸附测定

ELISA for detection of IgG and IgM antibodies to HSV-1 and HSV-2 in human sera.

作者信息

Katz D, Hilliard J K, Mirkovic R R, Word R A

出版信息

J Virol Methods. 1986 Aug;14(1):43-55. doi: 10.1016/0166-0934(86)90006-6.

Abstract

A rapid, enzyme-linked immunoassay (ELISA) was applied to identify and measure specific IgG and IgM antibodies to herpes simplex viruses types 1 and 2 (HSV-1 and HSV-2). Detergent solubilized infected cells and mock-infected cells were used as antigens in the assay. Identification of type-specific antibodies was achieved by a competition assay in which clinical sera mixed with HSV-1 or HSV-2 antigens were assayed for reactivity to identical antigens coating wells of polystyrene microtiter plates. Reactivity and the specificity of the reactive immunoglobulin class was quantitated using biotinylated goat anti-IgG and biotinylated goat anti-IgM. Five paired sera from patients with diagnosed herpes simplex genital infections and one human anti-HSV-1 reference serum were tested with this assay and results were compared to results previously obtained using a complement fixation test and micro-SPRIA. The results indicate that the ELISA is a specific, sensitive and simple test which confirms the herpes simplex virus infection history of patients.

摘要

采用快速酶联免疫吸附测定法(ELISA)来鉴定和检测针对1型和2型单纯疱疹病毒(HSV-1和HSV-2)的特异性IgG和IgM抗体。在该测定中,将经去污剂溶解的感染细胞和模拟感染细胞用作抗原。通过竞争测定法实现对型特异性抗体的鉴定,在竞争测定中,将与HSV-1或HSV-2抗原混合的临床血清检测其对包被在聚苯乙烯微量滴定板孔中的相同抗原的反应性。使用生物素化山羊抗IgG和生物素化山羊抗IgM对反应性免疫球蛋白类别的反应性和特异性进行定量。用该测定法检测了5例诊断为单纯疱疹性生殖器感染患者的配对血清和1份人抗HSV-1参考血清,并将结果与先前使用补体结合试验和微量固相放射免疫测定法获得的结果进行比较。结果表明,ELISA是一种特异性强、灵敏度高且操作简便的检测方法,可确认患者的单纯疱疹病毒感染史。

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