Description
Identification of blood biomarkers that prospectively predict progression of Mycobacterium tuberculosis  infection to tuberculosis disease might lead to interventions that combat the tuberculosis epidemic. We aimed to  assess whether global gene expression measured in whole blood of healthy people allowed identification of prospective  signatures of risk of active tuberculosis disease. RESULTS:Between July 6, 2005, and April 23, 2007, we enrolled 6363 from the ACS study and 4466 from independent  South African and Gambian cohorts. 46 progressors and 107 matched controls were identified in the ACS cohort. A  16 gene signature of risk was identified. The signature predicted tuberculosis progression with a sensitivity of 66·1%  (95% CI 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 sequencing 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 people at risk of developing active  tuberculosis, opening the possibility for targeted intervention to prevent the disease. Overall design: In this prospective cohort study, we followed up healthy, South African adolescents aged 12–18 years from  the adolescent cohort study (ACS) who were infected with M tuberculosis for 2 years. We collected blood samples from  study participants every 6 months and monitored the adolescents for progression to tuberculosis disease. A prospective  signature of risk was derived from whole blood RNA sequencing data by comparing participants who 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. Participants of the  independent cohorts were household contacts of adults with active pulmonary tuberculosis disease.