Whole blood GBP5 protein levels in patients with and without active tuberculosis

被引:9
作者
Yao, Xiangyang [1 ]
Liu, Wei [2 ]
Li, Xiaofei [3 ]
Deng, Chenxi [2 ]
Li, Tingdong [2 ]
Zhong, Zhouyue [2 ]
Chen, Shuping [2 ]
Ge, Zhitan [2 ]
Zhang, Xuejie [2 ]
Zhang, Shiyin [2 ]
Wang, Yingbin [2 ]
Liu, Yongliang [2 ]
Zheng, Chao [1 ]
Ge, Shengxiang [2 ]
Xia, Ningshao [2 ]
机构
[1] Xiamen Univ, Xinglin Branch, Affiliated Hosp 1, Xiamen 361102, Fujian, Peoples R China
[2] Xiamen Univ, Collaborat Innovat Ctr Biol Prod, State Key Lab Mol Vaccinol & Mol Diagnost, Natl Inst Diagnost & Vaccine Dev Infect Dis,Sch P, South Xiangan Rd, Xiamen 361102, Peoples R China
[3] Third Peoples Hosp Kunming City, Kunming 650041, Yunnan, Peoples R China
关键词
Guanylate binding protein 5; Whole blood; Protein level; Active tuberculosis; Interferon-gamma release assay; PULMONARY TUBERCULOSIS; DIAGNOSTIC-ACCURACY; MTB/RIF ASSAY; SIGNATURE;
D O I
10.1186/s12879-022-07214-8
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background The host blood transcriptional levels of several genes, such as guanylate binding protein 5 (GBP5), have been reported as potential biomarkers for active tuberculosis (aTB) diagnosis. The aim of this study was to investigate whole blood GBP5 protein levels in aTB and non-tuberculosis patients. Methods An in-house immunoassay for testing GBP5 protein levels in whole blood was developed, and suspected aTB patients were recruited. Whole blood samples were collected and tested at enrolment using interferon-gamma release assay (IGRA) and the GBP5 assay. Results A total of 470 participants were enrolled, and 232 and 238 patients were finally diagnosed with aTB and non-TB, respectively. The GBP5 protein levels of aTB patients were significantly higher than those of non-tuberculosis patients (p < 0.001), and the area under the ROC curve of the GBP5 assay for aTB diagnosis was 0.76. The reactivity of the GBP5 assay between pulmonary and extrapulmonary tuberculosis patients was comparable (p = 0.661). With the optimal cut-off value, the sensitivity and specificity of the GBP5 assay for diagnosing aTB were 78.02 and 66.81%, respectively, while those of IGRA were 77.59 and 76.47%. The combination of the GBP5 assay and IGRA results in 88.52% accuracy for diagnosing aTB in 63.83% of suspected patients with a positive predictive value of 89.57% and a negative predictive value of 87.59%. Conclusions Whole blood GBP5 protein is a valuable biomarker for diagnosing of aTB. This study provides an important idea for realizing the clinical application of whole blood transcriptomics findings by immunological methods.
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页数:8
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