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QuantiFERON-TB Gold Plus combined with HBHA-Induced IFN-? release assay improves the accuracy of identifying tuberculosis disease status - 30/09/20

Doi : 10.1016/j.tube.2020.101966 
Jinhua Tang a, 1, Yuan Huang a, 1, Shen Jiang b, Fang Huang c, Tingting Ma b, Yun Qi b, , Yueyun Ma a, d,
a Department of Clinical Laboratory, Xijing Hospital, Air Force Medical University (Fourth Military Medical University), Xi'an, China 
b Department of Gynecology and Pediatric Tuberculosis, Xi'an Chest Hospital, Xi'an, China 
c Department of Clinical Laboratory, Xi'an Chest Hospital, Xi'an, China 
d Department of Clinical Laboratory, Air Force Medical Center, Air Force Medical University, Beijing, China 

Corresponding author. Department of Clinical Laboratory, Air Force Medical Center, Air Force Medical University, 30 Fucheng Road, Beijing, 100142, China.Department of Clinical LaboratoryAir Force Medical CenterAir Force Medical University30 Fucheng RoadBeijing100142China∗∗Corresponding author. Department of Gynecology and Pediatric Tuberculosis, Xi'an Chest Hospital, East Hangtian Avenue, Xi'an, 710100, China.Department of Gynecology and Pediatric TuberculosisXi'an Chest HospitalEast Hangtian AvenueXi'an710100China

Abstract

Objective

QFT-Plus's newly added antigen elicited a specific CD8 T-cell response, which is closely related to active TB (ATB), and the IGRA based on Heparin-binding haemagglutinin (HBHA-IGRA) is a promising tool in latent tuberculosis infection (LTBI) diagnosis. The objective of our study is to evaluate whether the combination of QFT-Plus and HBHA-IGRA can improve the diagnosis accuracy of ATB and LTBI.

Methods

135 healthcare workers (HCWs) and 57 patients with active pulmonary TB in a Chinese TB Hospital were recruited, HCWs underwent screening for LTBI using the QFT-Plus assay. Flow cytometry was used to analyze the distribution of peripheral blood T lymphocyte subsets in active TB patients with positive culture result. Then, the patients with ATB, individuals with LTBI and healthy TB-uninfected controls (HC) were tested by QFT-Plus and HBHA-IGRA respectively, and the efficiency of distinguishing LTBI from ATB by QFT-Plus and HBHA-IGRA were evaluated by Receiver Operating Characteristic (ROC) curves.

Results

QFT-Plus TB2-TB1 which was positively correlated with CD8 T-cell response (r = 0.731, P < 0.001) in peripheral blood was significantly higher in ATB than LTBI and HC (median 0.47 IU/mL versus 0.02 IU/mL and 0.00 IU/mL, respectively; both P < 0.0001). While the HBHA-induced IFN-γ response did not differ between ATB and HC (median 12.12 pg/mL versus 10.95 pg/mL; P = 0.463), but was significantly higher in the LTBI (median 69.67 pg/mL; both P < 0.0001). The ROC area under the curve (AUC) for identifying ATB and LTBI was 0.769 (95% CI: 0.652–0.886; P = 0.0001) for QFT-Plus TB2-TB1, and 0.886 (95% CI:0.791–0.982; P<0.0001) for HBHA-IGRA. After combining the HBHA-IGRA with QFT-Plus results, the accuracy of identifying ATB and LTBI was improved to 85.7% from 74.3%.

Conclusions

HBHA-based IGRA better differentiates between LTBI and ATB compared to QFT-Plus CD8 T-cell response. In addition, combining HBHA-IGRA and QFT-Plus improves the accuracy of identifying tuberculosis disease status.

Le texte complet de cet article est disponible en PDF.

Highlights

QFT-Plus TB2-TB1 was positively correlated with CD8 response in peripheral blood.
QFT-Plus CD8 response was significantly higher in active TB than LTBI individuals.
HBHA-IGRA was significantly higher in LTBI individuals than active TB patients.
HBHA-IGRA better discriminates LTBI and active TB compared to QFT-Plus CD8 response.
Combining HBHA-IGRA and QFT-Plus improves the accuracy of identifying TB status.

Le texte complet de cet article est disponible en PDF.

Keywords : IGRA, QFT-Plus, HBHA, Active TB, LTBI


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Vol 124

Article 101966- septembre 2020 Retour au numéro
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