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使用 mRNA 表达特征相关风险检测来针对结核病预防性治疗,对结核病发病率产生潜在的人群水平影响。

Potential population level impact on tuberculosis incidence of using an mRNA expression signature correlate-of-risk test to target tuberculosis preventive therapy.

机构信息

TB Modelling Group, TB Centre, Centre for Mathematical Modelling of Infectious Diseases, Department of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, United Kingdom.

South African Tuberculosis Vaccine Initiative, Division of Immunology, Department of Pathology and Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Cape Town, South Africa.

出版信息

Sci Rep. 2019 Jul 31;9(1):11126. doi: 10.1038/s41598-019-47645-z.

Abstract

Achieving the WHO End-Tuberculosis (TB) targets requires approaches to prevent progression to TB among individuals with Mycobacterium tuberculosis (M.tb) infection. Effective preventive therapy (PT) exists, but current tests have low specificity for identifying who, among those infected, is at risk of developing TB. Using mathematical models, we assessed the potential population-level impact on TB incidence of using a new more specific mRNA expression signature (COR) to target PT among HIV-uninfected adults in South Africa. We compared the results to the use of the existing interferon-γ release assay (IGRA). With annual screening coverage of 30% COR-targeted PT could reduce TB incidence in 2035 by 20% (95% CI 15-27). With the same coverage, IGRA-targeted PT could reduce TB incidence by 39% (31-48) but would require greater use of PT resulting in a higher number needed to treat per TB case averted (COR: 49 (29-77); IGRA: 84 (59-123)). The relative differences between COR and IGRA were not sensitive to screening coverage. COR-targeted PT could contribute to reducing total TB burden in high incidence countries like South Africa by allowing more efficient targeting of treatment. To maximise impact, COR-like tests may be best utilised in the highest burden regions, or sub-populations, within these countries.

摘要

实现世界卫生组织(WHO)终结结核病(TB)目标需要采取措施,防止结核分枝杆菌(M.tb)感染者进展为结核病。目前已经有有效的预防性治疗(PT)方法,但现有的检测方法对识别哪些感染者有发展为结核病的风险特异性较低。我们使用数学模型,评估了在南非,针对 HIV 阴性成年人使用新的更具特异性的 mRNA 表达谱(COR)对 PT 进行靶向,对结核病发病率产生的潜在人群水平影响。我们将结果与使用现有干扰素-γ释放试验(IGRA)进行了比较。如果每年有 30%的成年人接受 COR 靶向的 PT 筛查,到 2035 年,TB 发病率将降低 20%(95%CI:15-27)。采用相同的覆盖率,IGRA 靶向的 PT 可以降低 39%(31-48)的发病率,但需要更多地使用 PT,从而导致每例结核病病例避免治疗的人数增加(COR:49(29-77);IGRA:84(59-123))。COR 与 IGRA 之间的相对差异不受筛查覆盖率的影响。在南非等发病率较高的国家,通过更有效地针对治疗,COR 靶向的 PT 可能有助于减少总结核病负担。为了最大程度地发挥影响,可能最好在这些国家发病率最高的地区或亚人群中使用类似 COR 的检测方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2ae/6668474/584bd8cf1a39/41598_2019_47645_Fig1_HTML.jpg

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