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一种检测弓形虫免疫球蛋白M抗体的酶免疫测定法,该方法不受类风湿因子或免疫球蛋白G抗体的影响。

An enzyme immunoassay for immunoglobulin M antibodies to Toxoplasma gondii which is not affected by rheumatoid factor or immunoglobulin G antibodies.

作者信息

Lin T M, Chin-See M W, Halbert S P, Joseph J M

出版信息

J Clin Microbiol. 1986 Jan;23(1):77-82. doi: 10.1128/jcm.23.1.77-82.1986.

Abstract

An enzyme-linked immunosorbent assay (ELISA) for total antibodies to Toxoplasma gondii was modified to measure specific immunoglobulin M (IgM) antibodies. The assay requires three incubation periods totaling 2 h and enzyme-labeled-heavy-chain-specific antibodies to human IgM. The objective read-out in absorbance was normalized to percent of a standardized positive control for interpretations. No difference was observed between the assay results with or without previous absorption of the samples by Staphylococcus aureus protein A to remove most of the IgG antibodies. Addition of serum containing very high levels of IgG antibodies to another containing both IgG and IgM antibodies did not change the IgM assay values for the latter. None of the 22 sera containing high levels of IgM rheumatoid factor (RF) gave positive ELISA IgM results, even though 8 of them also had high levels of IgG toxoplasma antibodies. Mixtures of sera containing high concentrations of RF with sera having high levels of IgG toxoplasma antibodies also failed to show any false-positive reactions in the IgM toxoplasma assay. Thus, this ELISA for T. gondii IgM antibodies was not affected by IgG toxoplasma antibodies and RF.

摘要

一种用于检测弓形虫总抗体的酶联免疫吸附测定(ELISA)被改进以测量特异性免疫球蛋白M(IgM)抗体。该测定需要三个孵育期,总计2小时,并使用酶标记的针对人IgM的重链特异性抗体。吸光度的目标读数被标准化为标准化阳性对照的百分比以进行结果解读。在样品用金黄色葡萄球菌蛋白A预先吸收以去除大部分IgG抗体前后,测定结果没有差异。将含有非常高水平IgG抗体的血清添加到另一份同时含有IgG和IgM抗体的血清中,并未改变后者的IgM测定值。22份含有高水平IgM类风湿因子(RF)的血清中,没有一份ELISA IgM结果呈阳性,尽管其中8份血清也含有高水平的IgG弓形虫抗体。含有高浓度RF的血清与含有高水平IgG弓形虫抗体的血清混合,在IgM弓形虫测定中也未显示任何假阳性反应。因此,这种用于检测弓形虫IgM抗体的ELISA不受IgG弓形虫抗体和RF的影响。

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