Suppr超能文献

基于细胞因子和抗体的痰培养阳性肺结核诊断算法

Cytokine and Antibody Based Diagnostic Algorithms for Sputum Culture-Positive Pulmonary Tuberculosis.

作者信息

Chen Tao, Lin Jinfei, Wang Wei, Fleming Joy, Chen Liang, Wang Yunxia, Li Haicheng, Guo Huixin, Zhou Jie, Chen Xunxun, Chen Yuhui, Liao Qinghua, Shu Yang, Tan Yaoju, Yu Meiling, Li Guozhou, Zhou Lin, Zhong Qiu, Bi Lijun, Guo Lina, Zhao Meigui

机构信息

Center for Tuberculosis Control of Guangdong Province, Guangzhou, 510630, China.

Foshan Fourth People's Hospital, Foshan, 528000, China.

出版信息

PLoS One. 2015 Dec 16;10(12):e0144705. doi: 10.1371/journal.pone.0144705. eCollection 2015.

Abstract

BACKGROUND

Tuberculosis (TB) is one of the most serious infectious diseases globally and has high mortality rates. A variety of diagnostic tests are available, yet none are wholly reliable. Serum cytokines, although significantly and frequently induced by different diseases and thus good biomarkers for disease diagnosis and prognosis, are not sufficiently disease-specific. TB-specific antibody detection, on the other hand, has been reported to be highly specific but not sufficiently sensitive. In this study, our aim was to improve the sensitivity and specificity of TB diagnosis by combining detection of TB-related cytokines and TB-specific antibodies in peripheral blood samples.

METHODS

TB-related serum cytokines were screened using a human cytokine array. TB-related cytokines and TB-specific antibodies were detected in parallel with microarray technology. The diagnostic performance of the new protocol for active TB was systematically compared with other traditional methods.

RESULTS

Here, we show that cytokines I-309, IL-8 and MIG are capable of distinguishing patients with active TB from healthy controls, patients with latent TB infection, and those with a range of other pulmonary diseases, and that these cytokines, and their presence alongside antibodies for TB-specific antigens Ag14-16kDa, Ag32kDa, Ag38kDa and Ag85B, are specific markers for active TB. The diagnostic protocol for active TB developed here, which combines the detection of three TB-related cytokines and TB-specific antibodies, is highly sensitive (91.03%), specific (90.77%) and accurate (90.87%).

CONCLUSIONS

Our results show that combining detection of TB-related cytokines and TB-specific antibodies significantly enhances diagnostic accuracy for active TB, providing greater accuracy than conventional diagnostic methods such as interferon gamma release assays (IGRAs), TB antibody Colloidal Gold Assays and microbiological culture, and suggest that this diagnostic protocol has potential for clinical application.

摘要

背景

结核病是全球最严重的传染病之一,死亡率很高。有多种诊断测试方法,但没有一种是完全可靠的。血清细胞因子虽然在不同疾病中会显著且频繁地被诱导产生,因此是疾病诊断和预后的良好生物标志物,但疾病特异性不足。另一方面,据报道结核特异性抗体检测具有高度特异性,但灵敏度不够。在本研究中,我们的目的是通过联合检测外周血样本中的结核相关细胞因子和结核特异性抗体来提高结核病诊断的灵敏度和特异性。

方法

使用人细胞因子阵列筛选结核相关血清细胞因子。采用微阵列技术同时检测结核相关细胞因子和结核特异性抗体。系统地将新的活动性结核病诊断方案的诊断性能与其他传统方法进行比较。

结果

在此,我们表明细胞因子I-309、白细胞介素-8和巨噬细胞炎性蛋白诱导因子能够区分活动性结核病患者与健康对照、潜伏性结核感染患者以及一系列其他肺部疾病患者,并且这些细胞因子以及它们与结核特异性抗原Ag14-16kDa、Ag32kDa、Ag38kDa和Ag85B的抗体同时存在是活动性结核病的特异性标志物。这里开发的活动性结核病诊断方案,结合了三种结核相关细胞因子和结核特异性抗体的检测,具有高灵敏度(91.03%)、高特异性(90.77%)和高准确性(90.87%)。

结论

我们的结果表明,联合检测结核相关细胞因子和结核特异性抗体可显著提高活动性结核病的诊断准确性,比传统诊断方法如干扰素γ释放试验(IGRAs)、结核抗体胶体金试验和微生物培养具有更高的准确性,并表明该诊断方案具有临床应用潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1c0/4682626/9c30a31821d6/pone.0144705.g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验