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A prospective blood RNA signature for tuberculosis disease risk

BACKGROUND: Identification of blood biomarkers that prospectively predict progression of Mycobacterium tuberculosis infection to tuberculosis disease may lead to interventions that impact the epidemic. METHODS: Healthy, M. tuberculosis infected South African adolescents were followed for 2 years; bl...

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Detalles Bibliográficos
Autores principales: Zak, Daniel E., Penn-Nicholson, Adam, Scriba, Thomas J., Thompson, Ethan, Suliman, Sara, Amon, Lynn M., Mahomed, Hassan, Erasmus, Mzwandile, Whatney, Wendy, Hussey, Gregory D., Abrahams, Deborah, Kafaar, Fazlin, Hawkridge, Tony, Verver, Suzanne, Hughes, E. Jane, Ota, Martin, Sutherland, Jayne, Howe, Rawleigh, Dockrell, Hazel M., Boom, W. Henry, Thiel, Bonnie, Ottenhoff, Tom H.M., Mayanja-Kizza, Harriet, Crampin, Amelia C, Downing, Katrina, Hatherill, Mark, Valvo, Joe, Shankar, Smitha, Parida, Shreemanta K, Kaufmann, Stefan H.E., Walzl, Gerhard, Aderem, Alan, Hanekom, Willem A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5392204/
https://www.ncbi.nlm.nih.gov/pubmed/27017310
http://dx.doi.org/10.1016/S0140-6736(15)01316-1
Descripción
Sumario:BACKGROUND: Identification of blood biomarkers that prospectively predict progression of Mycobacterium tuberculosis infection to tuberculosis disease may lead to interventions that impact the epidemic. METHODS: Healthy, M. tuberculosis infected South African adolescents were followed for 2 years; blood was collected every 6 months. A prospective signature of risk was derived from whole blood RNA-Sequencing data by comparing participants who ultimately developed active tuberculosis disease (progressors) with those who remained healthy (matched controls). After adaptation to multiplex qRT-PCR, the signature was used to predict tuberculosis disease in untouched adolescent samples and in samples from independent cohorts of South African and Gambian adult progressors and controls. The latter participants were household contacts of adults with active pulmonary tuberculosis disease. FINDINGS: Of 6,363 adolescents screened, 46 progressors and 107 matched controls were identified. A 16 gene signature of risk was identified. The signature predicted tuberculosis progression with a sensitivity of 66·1% (95% confidence interval, 63·2–68·9) and a specificity of 80·6% (79·2–82·0) in the 12 months preceding tuberculosis diagnosis. The risk signature was validated in an untouched group of adolescents (p=0·018 for RNA-Seq and p=0·0095 for qRT-PCR) and in the independent South African and Gambian cohorts (p values <0·0001 by qRT-PCR) with a sensitivity of 53·7% (42·6–64·3) and a specificity of 82·8% (76·7–86) in 12 months preceding tuberculosis. INTERPRETATION: The whole blood tuberculosis risk signature prospectively identified persons at risk of developing active tuberculosis, opening the possibility for targeted intervention to prevent the disease. FUNDING: Bill and Melinda Gates Foundation, the National Institutes of Health, Aeras, the European Union and the South African Medical Research Council (detail at end of text).