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在麻疹和风疹免疫球蛋白M的“捕获”检测中使用抗人免疫球蛋白M单克隆抗体。

Use of monoclonal antibodies to human immunoglobulin M in "capture" assays for measles and rubella immunoglobulin M.

作者信息

Forghani B, Myoraku C K, Schmidt N J

出版信息

J Clin Microbiol. 1983 Sep;18(3):652-7. doi: 10.1128/jcm.18.3.652-657.1983.

Abstract

Monoclonal antibodies to human immunoglobulin M (IgM) were used in a four-phase enzyme immunofluorescence "capture" assay for determination of IgM antibodies to measles and rubella viruses. Little or no background reactivity was seen in the test system, and interfering effects of rheumatoid factor were avoided by preabsorption of test sera with aggregated human IgG. Virus-specific IgM antibody was demonstrable in 23 of 24 patients with serological evidence of measles virus infections and in 36 of 36 patients with serological evidence of postnatal rubella infection. A few of the rubella patients did not show IgM antibody until 5 days after onset of illness. The enzyme immunofluorescence assay was able to demonstrate rubella IgM antibody in congenitally infected newborns, whereas indirect immunofluorescence results for virus-specific IgM were negative. Viral IgM antibody was not detected in persons with past infections with the test viruses, in young children without evidence of past infection, or in patients infected with heterotypic viruses, rickettsiae, chlamydiae, or mycoplasmas.

摘要

用人免疫球蛋白M(IgM)单克隆抗体,采用四步法酶免疫荧光“捕获”试验,检测麻疹病毒和风疹病毒的IgM抗体。在该检测系统中几乎未见背景反应性,通过用聚合人IgG预先吸收检测血清,避免了类风湿因子的干扰作用。在24例有麻疹病毒感染血清学证据的患者中,有23例检测到病毒特异性IgM抗体;在36例有出生后风疹感染血清学证据的患者中,36例均检测到病毒特异性IgM抗体。少数风疹患者在发病5天后才出现IgM抗体。酶免疫荧光试验能够在先天性感染的新生儿中检测到风疹IgM抗体,而病毒特异性IgM的间接免疫荧光结果为阴性。在既往感染过检测病毒的人群、无既往感染证据的幼儿、感染异型病毒、立克次体、衣原体或支原体的患者中,均未检测到病毒IgM抗体。

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Antibody capture radioimmunoassay for anti-rubella IgM.抗风疹IgM抗体捕获放射免疫测定法
J Hyg (Lond). 1981 Apr;86(2):139-53. doi: 10.1017/s0022172400068856.
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Detection of measles IgM antibodies by enzyme-linked immunosorbent assay (ELISA).采用酶联免疫吸附测定(ELISA)检测麻疹IgM抗体。
Acta Pathol Microbiol Immunol Scand B. 1982 Apr;90(2):153-60. doi: 10.1111/j.1699-0463.1982.tb00098.x.

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