- Sabiiti, Wilber;
- Azam, Khalide;
- Farmer, Eoghan Charles William;
- Kuchaka, Davis;
- Mtafya, Bariki;
- Bowness, Ruth;
- Oravcova, Katarina;
- Honeyborne, Isobella;
- Evangelopoulos, Dimitrios;
- McHugh, Timothy Daniel;
- Khosa, Celso;
- Rachow, Andrea;
- Heinrich, Norbert;
- Kampira, Elizabeth;
- Davies, Geraint;
- Bhatt, Nilesh;
- Ntinginya, Elias N;
- Viegas, Sofia;
- Jani, Ilesh;
- Kamdolozi, Mercy;
- Mdolo, Aaron;
- Khonga, Margaret;
- Boeree, Martin J;
- Phillips, Patrick PJ;
- Sloan, Derek;
- Hoelscher, Michael;
- Kibiki, Gibson;
- Gillespie, Stephen H
In this comparative biomarker study, we analysed 1768 serial sputum samples from 178 patients at 4 sites in Southeast Africa. We show that tuberculosis Molecular Bacterial Load Assay (TB-MBLA) reduces time-to-TB-bacillary-load-result from days/weeks by culture to hours and detects early patient treatment response. By day 14 of treatment, 5% of patients had cleared bacillary load to zero, rising to 58% by 12th week of treatment. Fall in bacillary load correlated with mycobacterial growth indicator tube culture time-to-positivity (Spearmans r=-0.51, 95% CI (-0.56 to -0.46), p<0.0001). Patients with high pretreatment bacillary burdens (above the cohort bacillary load average of 5.5log10eCFU/ml) were less likely to convert-to-negative by 8th week of treatment than those with a low burden (below cohort bacillary load average), p=0.0005, HR 3.1, 95% CI (1.6 to 5.6) irrespective of treatment regimen. TB-MBLA distinguished the bactericidal effect of regimens revealing the moxifloxacin-20 mg rifampicin regimen produced a shorter time to bacillary clearance compared with standard-of-care regimen, p=0.008, HR 2.9, 95% CI (1.3 to 6.7). Our data show that the TB-MBLA could inform clinical decision making in real-time and expedite drug TB clinical trials.