Four-Gene Pan-African Blood Signature Predicts Progression to Tuberculosis

Sara Suliman(University of Cape Town), Ethan Thompson(Center for Infectious Disease Research), Jayne S. Sutherland(MRC Unit the Gambia), January Weiner(Max Planck Institute for Infection Biology), Martin O. C. Ota(MRC Unit the Gambia), Smitha Shankar(Center for Infectious Disease Research), Adam Penn‐Nicholson(University of Cape Town), Bonnie Thiel(Case Western Reserve University), Mzwandile Erasmus(University of Cape Town), Jeroen Maertzdorf(Max Planck Institute for Infection Biology), Fergal J. Duffy(Center for Infectious Disease Research), Philip C. Hill(University of Otago), E. Jane Hughes(University of Cape Town), Kim Stanley(South African Medical Research Council), Katrina Downing(University of Cape Town), Michelle Fisher(University of Cape Town), Joe Valvo(Center for Infectious Disease Research), Shreemanta K. Parida(Max Planck Institute for Infection Biology), Gian van der Spuy(South African Medical Research Council), Gerard Tromp(South African Medical Research Council), Ifedayo Adetifa(MRC Unit the Gambia), Simon Donkor(MRC Unit the Gambia), Rawleigh Howe(Armauer Hansen Research Institute), Harriet Mayanja‐Kizza(Makerere University), W. Henry Boom(Case Western Reserve University), Hazel M. Dockrell(London School of Hygiene & Tropical Medicine), Tom H. M. Ottenhoff(Leiden University Medical Center), Mark Hatherill(University of Cape Town), Alan Aderem(Center for Infectious Disease Research), Willem A. Hanekom(University of Cape Town), Thomas J. Scriba(University of Cape Town), Stefan H. E. Kaufmann(Max Planck Institute for Infection Biology), Daniel E. Zak(Center for Infectious Disease Research), Gerhard Walzl(South African Medical Research Council)
American Journal of Respiratory and Critical Care Medicine
April 6, 2018
Cited by 266Open Access
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Abstract

Abstract Rationale Contacts of patients with tuberculosis (TB) constitute an important target population for preventive measures because they are at high risk of infection with Mycobacterium tuberculosis and progression to disease. Objectives We investigated biosignatures with predictive ability for incident TB. Methods In a case–control study nested within the Grand Challenges 6-74 longitudinal HIV-negative African cohort of exposed household contacts, we employed RNA sequencing, PCR, and the pair ratio algorithm in a training/test set approach. Overall, 79 progressors who developed TB between 3 and 24 months after diagnosis of index case and 328 matched nonprogressors who remained healthy during 24 months of follow-up were investigated. Measurements and Main Results A four-transcript signature derived from samples in a South African and Gambian training set predicted progression up to two years before onset of disease in blinded test set samples from South Africa, the Gambia, and Ethiopia with little population-associated variability, and it was also validated in an external cohort of South African adolescents with latent M. tuberculosis infection. By contrast, published diagnostic or prognostic TB signatures were predicted in samples from some but not all three countries, indicating site-specific variability. Post hoc meta-analysis identified a single gene pair, C1QC/TRAV27 (complement C1q C-chain / T-cell receptor-α variable gene 27) that would consistently predict TB progression in household contacts from multiple African sites but not in infected adolescents without known recent exposure events. Conclusions Collectively, we developed a simple whole blood–based PCR test to predict TB in recently exposed household contacts from diverse African populations. This test has potential for implementation in national TB contact investigation programs.


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