Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK.
C.J. Calderwood and A. Sanchez Martinez contributed equally.
Eur Respir J. 2024 Nov 21;64(5). doi: 10.1183/13993003.00457-2024. Print 2024 Nov.
Concerted efforts aim to reduce the burden of 6 months of anti-tuberculous treatment for tuberculosis (TB). Treatment cessation at 8 weeks is effective for most but incurs increased risk of disease relapse. We tested the hypothesis that blood RNA signatures or C-reactive protein (CRP) measurements discriminate 8-week sputum culture status, as a prerequisite for a biomarker to stratify risk of relapse following treatment cessation at this time-point.
We identified blood RNA signatures of TB disease or cure by systematic review. We evaluated these signatures and CRP measurements in a pulmonary TB cohort, pre-treatment, at 2 and 8 weeks of treatment, and sustained cure after treatment completion. We tested biomarker discrimination of 8-week sputum culture status using area under the receiver operating characteristic curve (AUROC) analysis and, secondarily, assessed correlation of biomarker scores with time to culture positivity at 8 weeks of treatment.
12 blood RNA signatures were reproduced in the dataset from 44 individuals with sputum culture-positive pulmonary TB. These normalised over time from TB treatment initiation. 11 out of 44 cases with blood RNA, CRP and sputum culture results were sputum culture-positive at 8 weeks of treatment. None of the contemporary blood RNA signatures discriminated sputum culture status at this time-point or correlated with bacterial load. CRP achieved modest discrimination with AUROC 0.69 (95% CI 0.52-0.87).
Selected TB blood RNA signatures and CRP do not provide biomarkers of microbiological clearance to support TB treatment cessation at 8 weeks. Resolution of blood transcriptional host responses in sputum culture-positive individuals suggests may colonise the respiratory tract without triggering a detectable immune response.
为了减轻结核病(TB)6 个月抗结核治疗的负担,人们正在齐心协力。对于大多数患者来说,8 周时停止治疗是有效的,但会增加疾病复发的风险。我们检验了这样一个假设,即血液 RNA 特征或 C 反应蛋白(CRP)测量可区分 8 周痰培养状态,作为在此时点停止治疗后分层复发风险的生物标志物的先决条件。
我们通过系统评价确定了 TB 疾病或治愈的血液 RNA 特征。我们在一个肺结核队列中评估了这些特征和 CRP 测量值,包括治疗前、治疗 2 周和 8 周以及治疗完成后的持续治愈。我们使用接受者操作特征曲线(AUROC)分析测试了生物标志物对 8 周痰培养状态的区分能力,其次评估了生物标志物评分与治疗 8 周时培养阳性时间的相关性。
从 44 例痰培养阳性肺结核患者的数据集重现了 12 个血液 RNA 特征。这些特征从 TB 治疗开始时就随时间而变化。在血液 RNA、CRP 和痰培养结果为 44 例中有 11 例在治疗 8 周时痰培养阳性。没有任何当前的血液 RNA 特征可以在此时区分痰培养状态,也与细菌负荷无关。CRP 的 AUROC 为 0.69(95%CI 0.52-0.87),具有适度的区分能力。
选定的 TB 血液 RNA 特征和 CRP 不能提供微生物清除的生物标志物,以支持在 8 周时停止 TB 治疗。痰培养阳性者血液转录宿主反应的解决表明,细菌可能定植于呼吸道而不触发可检测的免疫反应。