Blood transcriptomic signatures predict poor treatment outcomes in drug-susceptible pulmonary TB in Brazil
Mendelsohn, S. C.; Andrade, B. B.; Araujo-Pereira, M.; Amorim, G. C.; Erasmus, M.; Andrade, A. M.; Fisher, M.; Figueiredo, M. C.; Muwanga, V. M.; Kritski, A. L.; Cordeiro-Santos, M.; Rolla, V. C.; Hatherill, M.; Sterling, T. R.; Scriba, T. J.; RePORT-South Africa Consortium, ; RePORT-Brazil Consortium,
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BackgroundNon-sputum biomarkers to monitor tuberculosis (TB) treatment and predict poor outcomes are lacking. We evaluated host-blood transcriptomic signatures for treatment monitoring and prognosis (death, treatment failure, recurrence) in adults with pulmonary TB. MethodsAdults with culture-confirmed, drug-susceptible pulmonary TB were enrolled at five Brazilian sites. Whole-blood PAXgene samples were collected at baseline, month 2 (M2), and end of treatment (EoT). Treatment failure was defined as sputum culture positivity at month 5 or later. Participants were followed for 24 months from treatment initiation for clinical or microbiological TB recurrence. Unfavourable outcomes were matched [~]1:3 to recurrence-free cure. Twenty-two published blood transcriptomic signatures were measured by microfluidic RT-qPCR and benchmarked against the WHO Target Product Profile (TPP) criteria. ResultsWe matched 263 participants with recurrence-free cure to 33 with treatment failure, 24 who died (TB/unknown cause), and 9 with recurrence. Signature scores generally declined from baseline to EoT. Multiple signatures predicted recurrence at baseline and M2 (AUC range 0.71-0.91), with waning performance at EoT (AUC range 0.42-0.89). Against the WHO TPP, 2/22 signatures met minimum criteria at baseline, 13/22 at M2, and none at EoT. Prediction of treatment failure was poor across timepoints (AUC <0.70). In contrast, Thompson5 and others at baseline predicted death during treatment or follow-up (AUC [≥]0.80). ConclusionBlood transcriptomic signatures tracked treatment response and predicted recurrence and death, meeting WHO TPP benchmarks at baseline and M2. These findings support prospective, biomarker-guided trials to individualise TB therapy--shortening regimens for early responders and intensifying care for high-risk patients. FundingThis work was supported by the U.S. National Institutes of Health, CRDF Global, and Departamento de Ciencia e Tecnologia (DECIT) - Secretaria de Ciencia e Tecnologia (SCTIE), Ministerio da Saude (MS), Brazil.
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