Abstract

BackgroundPulmonary tuberculosis (TB) in people living with HIV (PLH) frequently presents as sputum smear-negative. However, clinical trials of TB in adults often use smear-positive individuals to ensure measurable bacterial responses following initiation of treatment, thereby excluding HIV-infected patients from trials.MethodsIn this prospective case cohort study, 118 HIV-seropositive TB patients were assessed prior to initiation of standard four-drug TB therapy and at several time points through 35 days. Sputum bacillary load, as a marker of treatment response, was determined serially by: smear microscopy, Xpert MTB/RIF, liquid culture, and colony counts on agar medium.ResultsBy all four measures, patients who were baseline smear-positive had higher bacterial loads than those presenting as smear-negative, until day 35. However, most smear-negative PLH had significant bacillary load at enrolment and their mycobacteria were cleared more rapidly than smear-positive patients. Smear-negative patients’ decline in bacillary load, determined by colony counts, was linear to day 7 suggesting measurable bactericidal activity. Moreover, the decrease in bacterial counts was comparable to smear-positive individuals. Increasing cycle threshold values (Ct) on the Xpert assay in smear-positive patients to day 14 implied decreasing bacterial load.ConclusionOur data suggest that smear-negative PLH can be included in clinical trials of novel treatment regimens as they contain sufficient viable bacteria, but allowances for late exclusions would have to be made in sample size estimations. We also show that increases in Ct in smear-positive patients to day 14 reflect treatment responses and the Xpert MTB/RIF assay could be used as biomarker for early treatment response.

Highlights

  • In high tuberculosis (TB) burden settings HIV-infection confers markedly higher risk of TB infection and TB disease [1]

  • Our data suggest that smear-negative people living with HIV (PLH) can be included in clinical trials of novel treatment regimens as they contain sufficient viable bacteria, but allowances for late exclusions would have to be made in sample size estimations

  • We show that increases in cycle threshold values (Ct) in smear-positive patients to day 14 reflect treatment responses and the GeneXpert MTB/RIF (Xpert) MTB/RIF assay could be used as biomarker for early treatment response

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Summary

Introduction

In high tuberculosis (TB) burden settings HIV-infection confers markedly higher risk of TB infection and TB disease [1]. The Xpert MTB/RIF assay (Cepheid Innovation, Sunnyvale, CA) is based on nucleic acid amplification technology (NAAT) [15] It has a reported limit of detection (LOD) of as low as 112.6 CFU/ ml (colony forming units per millilitre) and is increasingly replacing smear microscopy as the primary diagnostic measure on sputum from individuals with presumptive pulmonary TB [16,17,18]. Cultures - providing evidence of mycobacterial viability, which smear microscopy and Xpert are unable to do - may not be of immediate value because positive results for bacterial cell counts take at least 3 weeks for bacteria to form colonies, and MGIT culture can take up to 42 days for a positive result [14] by which time decisions about initiating TB treatment likely have already been made. Clinical trials of TB in adults often use smear-positive individuals to ensure measurable bacterial responses following initiation of treatment, thereby excluding HIV-infected patients from trials

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