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首页> 外文期刊>Tuberculosis >Development of a time-resolved fluoroimmunoassay of CFP-10 for rapid diagnosis of tuberculous pleural effusion
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Development of a time-resolved fluoroimmunoassay of CFP-10 for rapid diagnosis of tuberculous pleural effusion

机译:建立可快速诊断结核性胸腔积液的CFP-10时间分辨荧光免疫测定法

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摘要

Tuberculous pleural effusion is the second most common form of extrapulmonary tuberculosis, which is very difficult to rapidly distinguish from malignant pleural effusion in the clinical setting. A timeresolved fluoroimmunoassay (TRF) of CFP-10, a low molecular weight protein secreted by pathogenic Mycobacterium tuberculosis, was developed to differentiate tuberculous pleural effusion from malignant one. The measuring range was 0.3-187.5 ng/ml with the doseeresponse coefficient of 0.9998 and detection limit of 0.036 ng/ml. The intra-assay and inter-assay coefficients of variation were 3.6-9.2% and 10.0-12.4%, respectively. The concentration of CFP-10 in malignant pleural effusion was less than 0.8 ng/ ml. The negative predictive value was 93.1% in malignant pleural effusion (n = 247) while the positive predictive value was 83.0% in tuberculous pleural effusion (n = 235). Moreover, there was a statistically significant difference in the CFP-10 concentration of pleural effusion between the groups before and after clinical therapy of tuberculosis (P < 0.001, n = 81). In addition, the stability of the diagnostic reagents lasted at least 1 year at 4 degrees C. Therefore, the TRF of CFP-10 may be used for the rapid diagnosis of tuberculous pleural effusion and further monitoring the clinical therapeutic efficacy of tuberculosis. (C) 2015 Elsevier Ltd. All rights reserved.
机译:结核性胸腔积液是肺外结核的第二种最常见形式,在临床上很难与恶性胸腔积液迅速地区分。 CFP-10的时间分辨荧光免疫测定(TRF)是一种由致病性结核分枝杆菌分泌的低分子量蛋白质,用于区分结核性胸腔积液和恶性胸腔积液。测量范围为0.3-187.5 ng / ml,剂量响应系数为0.9998,检出限为0.036 ng / ml。批内和批间变异系数分别为3.6-9.2%和10.0-12.4%。恶性胸腔积液中CFP-10的浓度小于0.8 ng / ml。恶性胸腔积液阴性预测值为93.1%(n = 247),结核性胸腔积液阳性预测值为83.0%(n = 235)。此外,在结核病临床治疗前后,两组之间胸腔积液的CFP-10浓度存在统计学差异(P <0.001,n = 81)。另外,诊断试剂的稳定性在4℃下持续至少1年。因此,CFP-10的TRF可用于快速诊断结核性胸腔积液并进一步监测结核的临床治疗效果。 (C)2015 Elsevier Ltd.保留所有权利。

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