首页> 外文期刊>The international journal of tuberculosis and lung disease: the official journal of the International Union against Tuberculosis and Lung Disease >Humoral immune response against 38-kDa and 16-kDa mycobacterial antigens in bone and joint tuberculosis.
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Humoral immune response against 38-kDa and 16-kDa mycobacterial antigens in bone and joint tuberculosis.

机译:针对骨骼和关节结核中38 kDa和16 kDa分枝杆菌抗原的体液免疫反应。

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摘要

SETTING: The diagnosis of bone and joint tuberculosis (BTB) is difficult, and diagnostic delays often occur. A reliable serological test detecting anti-mycobacterial antibodies would thus be of some use in this form of the disease. OBJECTIVE: To evaluate the diagnostic accuracy of an assay detecting IgG against 38-kDa and 16-kDa recombinant mycobacterial antigens in BTB. MATERIALS AND METHODS: In a prospective study, serum samples from 124 subjects were examined: 30 BTB cases, 40 non-specific bone and joint infection patients (NSBI), 30 lung cancer patients (LC), and 24 healthy volunteers (HC). An ELISA-based test (Pathozyme TB complex plus) was used. RESULTS: The cut-off level was established at 150 U/ml according to receiver operating characteristic (ROC) curves. The quantified level of sensitivity of the test detecting BTB was 56%, at a specificity of 99%. The positive and negative predictive values were respectively 94% and 88%. Mean IgG level in the BTB group was 470 +/- 761 U/ml (mean +/- SD), and was significantly higher than the antibody level in the control groups (NSBI 58 +/- 42 U/ml, LC 43 +/- 38 U/ml, HC 40 +/- 29 U/ml). CONCLUSION: The test presents an acceptable level of sensitivity and very good specificity in the diagnosis of BTB, and can be used in combination with other methods to increase diagnostic accuracy in this disease.
机译:地点:骨和关节结核(BTB)的诊断很困难,并且常常会出现诊断延迟。因此,检测抗分枝杆菌抗体的可靠的血清学检测将在该疾病的这种形式中有用。目的:评估检测针对TBB中38 kDa和16 kDa重组分枝杆菌抗原的IgG的诊断准确性。材料与方法:在一项前瞻性研究中,检查了124位受试者的血清样本:30例BTB病例,40例非特异性骨和关节感染患者(NSBI),30例肺癌患者(LC)和24名健康志愿者(HC)。使用基于ELISA的测试(Pathozyme TB complex plus)。结果:根据接受者的工作特征(ROC)曲线将截断水平确定为150 U / ml。检测BTB的测试的定量灵敏度为56%,特异性为99%。阳性和阴性预测值分别为94%和88%。 BTB组的平均IgG水平为470 +/- 761 U / ml(平均值+/- SD),并且显着高于对照组的抗体水平(NSBI 58 +/- 42 U / ml,LC 43 + +/- 38 U / ml,HC 40 +/- 29 U / ml)。结论:该测试在BTB的诊断中表现出可接受的灵敏度和非常好的特异性,可以与其他方法结合使用以提高对该疾病的诊断准确性。

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