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一种基于广泛反应性多克隆抗体的用于结核病诊断的多抗原检测方法。

A multiple-antigen detection assay for tuberculosis diagnosis based on broadly reactive polyclonal antibodies.

作者信息

Dai Zhenhua, Liu Zhiqiang, Xiu Bingshui, Yang Xiqin, Zhao Ping, Zhang Xuhui, Duan Cuimi, Que Haiping, Zhang Heqiu, Feng Xiaoyan

机构信息

Department of Bio-diagnosis, Beijing Institute of Basic Medical Sciences, 27 Taiping Road, Beijing 100850, China.

Chaoyang District Centre for Disease Control and Prevention, 25 Panjiayuan Huaweili, Beijing 100029, China.

出版信息

Iran J Basic Med Sci. 2017 Apr;20(4):360-367. doi: 10.22038/IJBMS.2017.8575.

Abstract

OBJECTIVES

Detection of circulating () antigens is promising in Tuberculosis (TB) diagnosis. However, not a single antigen marker has been found to be widely expressed in all TB patients. This study is aimed to prepare broadly reactive polyclonal antibodies targeting multiple antigen markers (multi-target antibodies) and evaluate their efficacies in TB diagnosis.

MATERIALS AND METHODS

A fusion gene consisting of 38kD, ESAT6, and CFP10 was constructed and overexpressed. The fusion polyprotein was used as an immunogen to elicit production of multi-target antibodies. Their reactivities were tested. Then, the multi-target antibodies and three corresponding antibodies elicited by each single antigen (mono-target antibodies) were evaluated with sandwich ELISA for detecting antigens. Their diagnostic efficacies for TB were also compared.

RESULTS

The polyprotein successfully elicited production of multi-target antibodies targeting 38kD, ESAT6, and CFP10 as analyzed by Western blotting. When used as coating antibodies, the multi-target antibodies were more efficient in capturing the three antigens than the corresponding mono-target antibodies. By testing clinical serum, the multi-target antibodies demonstrated significantly higher sensitivity for clinical TB diagnosis than all three mono-target antibodies.

CONCLUSION

The multi-target antibodies allowed detecting multiple antigens simultaneously and significantly enhanced TB detection compared to routine mono-target antibodies. Our study may provide a promising strategy for TB diagnosis.

摘要

目的

检测循环中的()抗原在结核病(TB)诊断中具有前景。然而,尚未发现单一抗原标志物能在所有TB患者中广泛表达。本研究旨在制备针对多种抗原标志物的广谱反应性多克隆抗体(多靶点抗体),并评估其在TB诊断中的效能。

材料与方法

构建并过表达由38kD、ESAT6和CFP10组成的融合基因。融合多蛋白用作免疫原以引发多靶点抗体的产生。测试它们的反应性。然后,用夹心ELISA评估多靶点抗体和由每种单一抗原引发的三种相应抗体(单靶点抗体)检测()抗原的能力。还比较了它们对TB的诊断效能。

结果

通过蛋白质印迹分析,多蛋白成功引发了针对38kD、ESAT6和CFP10的多靶点抗体的产生。当用作包被抗体时,多靶点抗体在捕获这三种抗原方面比相应的单靶点抗体更有效。通过检测临床血清,多靶点抗体对临床TB诊断的敏感性明显高于所有三种单靶点抗体。

结论

与常规单靶点抗体相比,多靶点抗体能够同时检测多种抗原,并显著提高TB检测能力。我们的研究可能为TB诊断提供一种有前景的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4baa/5425917/16df6f22e1ff/IJBMS-20-360-g001.jpg

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