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

被引:15
作者
Sumner, Tom [1 ]
Scriba, Thomas J. [2 ,3 ]
Penn-Nicholson, Adam [2 ,3 ]
Hatherill, Mark [2 ,3 ]
White, Richard G. [1 ]
机构
[1] London Sch Hyg & Trop Med, Ctr Math Modelling Infect Dis, Dept Infect Dis Epidemiol, TB Modelling Grp,TB Ctr, London, England
[2] Univ Cape Town, South African TB Vaccine Initiat, Div Immunol, Dept Pathol, Cape Town, South Africa
[3] Univ Cape Town, Inst Infect Dis & Mol Med, Cape Town, South Africa
关键词
GAMMA RELEASE ASSAYS;
D O I
10.1038/s41598-019-47645-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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-gamma 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.
引用
收藏
页数:10
相关论文
共 35 条
[1]  
[Anonymous], 2016, HIV ESTIMATES UNCERT
[2]  
[Anonymous], 2011, Intensified tuberculosis case-finding and isoniazid preventive therapy for people living with HIV in resource-constrained settings
[3]   Understanding the incremental value of novel diagnostic tests for tuberculosis [J].
Arinaminpathy, Nimalan ;
Dowdy, David .
NATURE, 2015, 528 (7580) :S60-S67
[4]  
Balcells ME, 2006, EMERG INFECT DIS, V12, P744
[5]  
Belgorodski N., 2017, RRISK DISTRIBUTIONS
[6]  
Churchyard G., 2014, S AFR MED J, V104
[7]   Diagnostic performance of an optimized transcriptomic signature of risk of tuberculosis in cryopreserved peripheral blood mononuclear cells [J].
Darboe, Fatoumatta ;
Mbandi, Stanley Kimbung ;
Thompson, Ethan G. ;
Fisher, Michelle ;
Rodo, Miguel ;
van Rooyen, Michele ;
Filander, Elizabeth ;
Bilek, Nicole ;
Mabwe, Simbarashe ;
Hatherill, Mark ;
Zak, Daniel E. ;
Penn-Nicholson, Adam ;
Scriba, Thomas J. .
TUBERCULOSIS, 2018, 108 :124-126
[8]  
Department of Health South Africa South African National AIDS Council, 2017, S AFR NAT STRAT PLAN
[9]   Prospects for Tuberculosis Elimination [J].
Dye, Christopher ;
Glaziou, Philippe ;
Floyd, Katherine ;
Raviglione, Mario .
ANNUAL REVIEW OF PUBLIC HEALTH, VOL 34, 2013, 34 :271-+
[10]   Considerations for biomarker-targeted intervention strategies for tuberculosis disease prevention [J].
Fiore-Gartland, Andrew ;
Carpp, Lindsay N. ;
Naidoo, Kogieleum ;
Thompson, Ethan ;
Zak, Daniel E. ;
Self, Steve ;
Churchyard, Gavin ;
Walzl, Gerhard ;
Penn-Nicholson, Adam ;
Scriba, Thomas J. ;
Hatherill, Mark .
TUBERCULOSIS, 2018, 109 :61-68