Division of Infectious Diseases, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Center for Clinical Global Health Education, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Eur Respir J. 2022 Apr 21;59(4). doi: 10.1183/13993003.00905-2021. Print 2022 Apr.
Biomarkers of unfavourable tuberculosis (TB) treatment outcomes are needed to accelerate new drug and regimen development. Whether plasma cytokine levels can predict unfavourable TB treatment outcomes is unclear.
We identified and internally validated the association between 20 selected plasma inflammatory markers and unfavourable treatment outcomes of failure, recurrence and all-cause mortality among adults with drug-sensitive pulmonary TB in India. We externally validated these findings in two independent cohorts of predominantly diabetic and HIV co-infected TB patients in India and South Africa, respectively.
Pre-treatment interferon-γ, interleukin (IL)-13 and IL-6 were associated with treatment failure in the discovery analysis. Internal validation confirmed higher pre-treatment IL-6 concentrations among failure cases compared with controls. External validation among predominantly diabetic TB patients found an association between pre-treatment IL-6 concentrations and subsequent recurrence and death. Similarly, external validation among predominantly HIV co-infected TB patients found an association between pre-treatment IL-6 concentrations and subsequent treatment failure and death. In a pooled analysis of 363 TB cases from the Indian and South African validation cohorts, high pre-treatment IL-6 concentrations were associated with higher risk of failure (adjusted OR (aOR) 2.16, 95% CI 1.08-4.33; p=0.02), recurrence (aOR 5.36, 95% CI 2.48-11.57; p<0.001) and death (aOR 4.62, 95% CI 1.95-10.95; p<0.001). Adding baseline IL-6 to a risk prediction model comprised of low body mass index, high smear grade and cavitation improved model performance by 15% (C-statistic 0.66 0.76; p=0.02).
Pre-treatment IL-6 is a biomarker for unfavourable TB treatment outcomes. Future studies should identify optimal IL-6 concentrations for point-of-care risk prediction.
需要生物标志物来加速新药物和治疗方案的开发,以改善不利的结核病(TB)治疗结果。目前尚不清楚血浆细胞因子水平是否可以预测不利的 TB 治疗结果。
我们在印度的药物敏感型肺结核成人患者中,确定并内部验证了 20 种选定的血浆炎症标志物与治疗失败、复发和全因死亡率等不利治疗结果之间的关联。我们在印度和南非的两个独立队列中对这些发现进行了外部验证,这些队列主要包括糖尿病和 HIV 合并感染的 TB 患者。
在发现分析中,治疗前干扰素-γ、白细胞介素(IL)-13 和 IL-6 与治疗失败相关。内部验证证实治疗失败病例的治疗前 IL-6 浓度高于对照组。在主要为糖尿病的 TB 患者中进行的外部验证发现,治疗前 IL-6 浓度与随后的复发和死亡之间存在关联。同样,在主要为 HIV 合并感染的 TB 患者中进行的外部验证发现,治疗前 IL-6 浓度与随后的治疗失败和死亡之间存在关联。在来自印度和南非验证队列的 363 例 TB 病例的汇总分析中,高治疗前 IL-6 浓度与较高的失败风险相关(调整后的比值比(aOR)2.16,95%CI 1.08-4.33;p=0.02)、复发(aOR 5.36,95%CI 2.48-11.57;p<0.001)和死亡(aOR 4.62,95%CI 1.95-10.95;p<0.001)。将基线 IL-6 添加到由低体重指数、高涂片等级和空洞组成的风险预测模型中,可使模型性能提高 15%(C 统计量 0.66 至 0.76;p=0.02)。
治疗前 IL-6 是不利 TB 治疗结果的生物标志物。未来的研究应该确定用于即时护理风险预测的最佳 IL-6 浓度。