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三种诊断肺炎支原体感染血清学方法的比较

Comparison of three serological methods for diagnosing Mycoplasma pneumoniae infection.

作者信息

Karppelin M, Hakkarainen K, Kleemola M, Miettinen A

机构信息

Department of Biomedical Sciences, University of Tampere, Finland.

出版信息

J Clin Pathol. 1993 Dec;46(12):1120-3. doi: 10.1136/jcp.46.12.1120.

Abstract

AIMS

To compare the novel Serofast latex agglutination test (International Mycoplasma, Toulon-Cedex, France) with the complement fixation test and enzyme immunoassay (EIA) for diagnosing acute Mycoplasma pneumoniae infection.

METHODS

Paired sera from 60 patients with respiratory infection who had tested positive for M pneumoniae by complement fixation test were analysed with Serofast and indirect EIA for specific IgG and IgM antibodies.

RESULTS

Serofast was less sensitive than the two other tests. Only 30 (50%) out of 60 paired sera which showed a diagnostic seroconversion or had high positive, unchanged antibody titres by complement fixation test or EIA, or both, tested positive with Serofast. Positive test results with Serofast were associated with the presence of a complement fixation test titre of > or = 512 and high positive IgM antibody titres measurable by EIA; virtually all patients with a complement fixation test titre of < 256 or those responding primarily in the IgG class tested negative with Serofast. Based on analysis of sera taken at the acute phase of infection, 10 (17%) of the 60 patients tested positive by complement fixation test, 10 (17%) by EIA, and only four (7%) by Serofast.

CONCLUSIONS

Serofast was less sensitive than complement fixation test and EIA and it cannot be recommended as a replacement for either test in routine diagnostic use. It might prove useful in laboratories where non-specific tests, such as the determination of cold agglutinins, are still used for the diagnosis of M pneumoniae infection. Testing paired sera is, however, a prerequisite for obtaining acceptable sensitivity by Serofast as well as other serological methods currently available.

摘要

目的

比较新型血清快速乳胶凝集试验(法国土伦市国际支原体公司生产)与补体结合试验及酶免疫测定法(EIA)用于诊断急性肺炎支原体感染的效果。

方法

对60例呼吸道感染患者的配对血清进行分析,这些患者经补体结合试验检测肺炎支原体呈阳性,采用血清快速试验及间接EIA检测特异性IgG和IgM抗体。

结果

血清快速试验比其他两种试验的敏感性低。在60对配对血清中,只有30份(50%)通过补体结合试验或EIA或两者均显示诊断性血清转化或具有高阳性、不变的抗体滴度的血清,血清快速试验检测为阳性。血清快速试验阳性结果与补体结合试验滴度≥512以及EIA可检测到的高阳性IgM抗体滴度有关;几乎所有补体结合试验滴度<256的患者或主要产生IgG类反应的患者,血清快速试验检测为阴性。根据感染急性期采集的血清分析,60例患者中10例(17%)补体结合试验检测为阳性,10例(17%)EIA检测为阳性,只有4例(7%)血清快速试验检测为阳性。

结论

血清快速试验比补体结合试验和EIA敏感性低,不推荐在常规诊断中替代这两种试验使用。在仍使用非特异性试验(如冷凝集素测定)诊断肺炎支原体感染的实验室中,它可能有用。然而,检测配对血清是通过血清快速试验以及目前可用的其他血清学方法获得可接受敏感性的前提条件。

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