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Blood test can predict risk of developing tuberculosis

Date:
March 23, 2016
Source:
NIH/National Institute of Allergy and Infectious Diseases
Summary:
Only a fraction of those infected with the bacterium that causes TB ever develops symptomatic illness. Now, an international team of researchers has identified biological markers in the blood of latently infected people that may lead doctors to a way to predict who is at high risk of developing active TB. If validated, a test based on these blood biomarkers would allow doctors to target therapies to at-risk people, thus preventing them from getting sick.
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One-third of the world's population is thought to be infected with Mycobacterium tuberculosis (Mtb), the bacterium that causes tuberculosis (TB), but just a small fraction ever develops symptomatic illness. Now, an international team of researchers has identified biological markers in the blood of latently infected people that may give doctors a tool they have long sought: a way to predict who is at high risk of developing active TB. If validated through additional clinical trials, a test based on these blood biomarkers would allow doctors to target therapies to at-risk people, thus preventing them from getting sick.

The decade-long research effort was led by investigators from the South African Tuberculosis Vaccine Initiative at the University of Cape Town, and the Center for Infectious Disease Research, Seattle. It was funded in part by the National Institutes of Health.

The biomarkers were identified in two stages. First, researchers collected blood samples for two years from more than 6,000 Mtb-infected but otherwise healthy adolescent volunteers in South Africa. Analysis of the samples revealed patterns of gene expression that differed between volunteers who eventually developed TB and those who remained healthy. This risk "signature," confined to a set of 16 genes, could be detected in a blood sample as early as 18 months before the infected person developed active TB.

Next, the team confirmed the genetic risk signature's predictive ability in a study of more than 4,500 volunteers in South Africa and The Gambia. Volunteers in this study were healthy but lived with people who had recently been diagnosed with active TB. The second study group was more varied in age, health status, ethnicity and exposure to locally common strains of Mtb than volunteers in the first study. Despite the differences, the same risk signature found in the first study was detected in the people who eventually developed active TB during the second trial.


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Materials provided by NIH/National Institute of Allergy and Infectious Diseases. Note: Content may be edited for style and length.


Journal Reference:

  1. Daniel E Zak, Adam Penn-Nicholson, Thomas J Scriba, Ethan Thompson, Sara Suliman, Lynn M Amon, Hassan Mahomed, Mzwandile Erasmus, Wendy Whatney, Gregory D Hussey, Deborah Abrahams, Fazlin Kafaar, Tony Hawkridge, Suzanne Verver, E Jane Hughes, Martin Ota, Jayne Sutherland, Rawleigh Howe, Hazel M Dockrell, W Henry Boom, Bonnie Thiel, Tom H M Ottenhoff, Harriet Mayanja-Kizza, Amelia C Crampin, Katrina Downing, Mark Hatherill, Joe Valvo, Smitha Shankar, Shreemanta K Parida, Stefan H E Kaufmann, Gerhard Walzl, Alan Aderem, Willem A Hanekom. A blood RNA signature for tuberculosis disease risk: a prospective cohort study. The Lancet, 2016; DOI: 10.1016/S0140-6736(15)01316-1

Cite This Page:

NIH/National Institute of Allergy and Infectious Diseases. "Blood test can predict risk of developing tuberculosis." ScienceDaily. ScienceDaily, 23 March 2016. <www.sciencedaily.com/releases/2016/03/160323185639.htm>.
NIH/National Institute of Allergy and Infectious Diseases. (2016, March 23). Blood test can predict risk of developing tuberculosis. ScienceDaily. Retrieved April 23, 2024 from www.sciencedaily.com/releases/2016/03/160323185639.htm
NIH/National Institute of Allergy and Infectious Diseases. "Blood test can predict risk of developing tuberculosis." ScienceDaily. www.sciencedaily.com/releases/2016/03/160323185639.htm (accessed April 23, 2024).

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