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用于检测人血清中布鲁氏菌抗原的酶联免疫吸附测定。

Enzyme-linked immunosorbent assay for brucella antigen detection in human sera.

作者信息

Al-Shamahy H A, Wright S G

机构信息

Department of Clinical Sciences, London School of Hygiene and Tropical Medicine.

出版信息

J Med Microbiol. 1998 Feb;47(2):169-72. doi: 10.1099/00222615-47-2-169.

Abstract

A sandwich enzyme-linked immunosorbent assay (ELISA) with monoclonal antibody coupled to the solid phase was evaluated for the detection of brucella antigen in serum samples. Under optimum conditions, 100 brucella cells/well or 10(5) fg/ml of lipopolysaccharide (LPS) were detected in spiked specimens. The standardised assay was performed on 1607 sera from random blood donors, 146 patients with brucellosis, 20 persons in high risk groups and 264 sera from patients with diseases other than brucellosis. Sensitivity was 100% compared with positive blood culture, and 44% compared with serological tests for brucella antibodies. Specificity was 99.5% among random blood donors and 99.2% in the patient population. These data showed a strong agreement between ELISA antigen detection and blood culture for the detection of brucella positive blood samples. Moreover, the results indicated that antigen detection by ELISA could be an acceptable alternative to blood culture for the diagnosis of brucellosis.

摘要

评估了一种将单克隆抗体偶联到固相上的夹心酶联免疫吸附测定(ELISA)法,用于检测血清样本中的布鲁氏菌抗原。在最佳条件下,在加标的样本中可检测到每孔100个布鲁氏菌细胞或10⁵ fg/ml的脂多糖(LPS)。对1607名随机献血者的血清、146名布鲁氏菌病患者的血清、20名高危人群的血清以及264名非布鲁氏菌病患者的血清进行了标准化检测。与阳性血培养相比,灵敏度为100%,与布鲁氏菌抗体血清学检测相比为44%。随机献血者中的特异性为99.5%,患者群体中的特异性为99.2%。这些数据表明,ELISA抗原检测与血培养在检测布鲁氏菌阳性血样方面具有高度一致性。此外,结果表明ELISA抗原检测可作为血培养的一种可接受的替代方法用于布鲁氏菌病的诊断。

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