Abstract

There is a crucial need for non-sputum-based TB tests. Here, we evaluate the performance of RISK6, a human-blood transcriptomic signature, for TB screening, triage and treatment monitoring. RISK6 performance was also compared to that of two IGRAs: one based on RD1 antigens (QuantiFERON-TB Gold Plus, QFT-P, Qiagen) and one on recombinant M. tuberculosis HBHA expressed in Mycobacterium smegmatis (IGRA-rmsHBHA). In this multicenter prospective nested case–control study conducted in Bangladesh, Georgia, Lebanon and Madagascar, adult non-immunocompromised patients with bacteriologically confirmed active pulmonary TB (ATB), latent TB infection (LTBI) and healthy donors (HD) were enrolled. ATB patients were followed-up during and after treatment. Blood RISK6 scores were assessed using quantitative real-time PCR and evaluated by area under the receiver-operating characteristic curve (ROC AUC). RISK6 performance to discriminate ATB from HD reached an AUC of 0.94 (95% CI 0.89–0.99), with 90.9% sensitivity and 87.8% specificity, thus achieving the minimal WHO target product profile for a non-sputum-based TB screening test. Besides, RISK6 yielded an AUC of 0.93 (95% CI 0.85–1) with 90.9% sensitivity and 88.5% specificity for discriminating ATB from LTBI. Moreover, RISK6 showed higher performance (AUC 0.90, 95% CI 0.85–0.94) than IGRA-rmsHBHA (AUC 0.75, 95% CI 0.69–0.82) to differentiate TB infection stages. Finally, RISK6 signature scores significantly decreased after 2 months of TB treatment and continued to decrease gradually until the end of treatment reaching scores obtained in HD. We confirmed the performance of RISK6 signature as a triage TB test and its utility for treatment monitoring.

Highlights

  • There is a crucial need for non-sputum-based TB tests

  • The combined use of QuantiFERON-TB Plus (QFT-P) with the heparin-binding hemagglutinin antigen; HBHA-based IGRAs, that relies on the stimulation of whole blood with recombinant Mycobacterium tuberculosis (Mtb) HBHA protein expressed in Mycobacterium smegmatis (IGRAs-rmsHBHA)[10], recently revealed the potential for the stratification of TB stages (e.g. active pulmonary TB (ATB) vs latent TB infection (LTBI))[11,12,13,14]

  • This was conducted in four independent cohorts enrolling ethnically and geographically diverse participants, including ATB patients, LTBI individuals, and healthy donors (HD), in both high- and low-TB incidence settings

Read more

Summary

Introduction

There is a crucial need for non-sputum-based TB tests. Here, we evaluate the performance of RISK6, a human-blood transcriptomic signature, for TB screening, triage and treatment monitoring. RISK6 performance was compared to that of two IGRAs: one based on RD1 antigens (QuantiFERON-TB Gold Plus, QFT-P, Qiagen) and one on recombinant M. tuberculosis HBHA expressed in Mycobacterium smegmatis (IGRA-rmsHBHA) In this multicenter prospective nested case–control study conducted in Bangladesh, Georgia, Lebanon and Madagascar, adult non-immunocompromised patients with bacteriologically confirmed active pulmonary TB (ATB), latent TB infection (LTBI) and healthy donors (HD) were enrolled. Sputum samples may be difficult to obtain in some populations (e.g. children and HIV co-infected TB patients) as well as in ATB patients after symptom ­improvement[18] In this context, the World Health Organization (WHO) has declared an urgent need for alternative non-sputum-based TB tests with a series of target product profiles (TPPs) which detailed the minimal and optimal criteria that should be met to diagnose and monitor TB treatment ­response[19,20,21]. Those new TB tests need to be based on accessible biological samples such as whole blood or urine, and must be practical for field a­ pplications[22]

Objectives
Methods
Results
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.