Go to The Journal of Clinical Investigation
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
  • Physician-Scientist Development
  • Current issue
  • Past issues
  • By specialty
    • COVID-19
    • Cardiology
    • Immunology
    • Metabolism
    • Nephrology
    • Oncology
    • Pulmonology
    • All ...
  • Videos
  • Collections
    • In-Press Preview
    • Resource and Technical Advances
    • Clinical Research and Public Health
    • Research Letters
    • Editorials
    • Perspectives
    • Physician-Scientist Development
    • Reviews
    • Top read articles

  • Current issue
  • Past issues
  • Specialties
  • In-Press Preview
  • Resource and Technical Advances
  • Clinical Research and Public Health
  • Research Letters
  • Editorials
  • Perspectives
  • Physician-Scientist Development
  • Reviews
  • Top read articles
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Transfers
  • Advertising
  • Job board
  • Contact
Blood transcriptomic diagnosis of pulmonary and extrapulmonary tuberculosis
Jennifer K Roe, … , Adrian Martineau, Mahdad Noursadeghi
Jennifer K Roe, … , Adrian Martineau, Mahdad Noursadeghi
Published October 6, 2016
Citation Information: JCI Insight. 2016;1(16):e87238. https://doi.org/10.1172/jci.insight.87238.
View: Text | PDF
Clinical Research and Public Health Infectious disease

Blood transcriptomic diagnosis of pulmonary and extrapulmonary tuberculosis

  • Text
  • PDF
Abstract

BACKGROUND. Novel rapid diagnostics for active tuberculosis (TB) are required to overcome the time delays and inadequate sensitivity of current microbiological tests that are critically dependent on sampling the site of disease. Multiparametric blood transcriptomic signatures of TB have been described as potential diagnostic tests. We sought to identify the best transcript candidates as host biomarkers for active TB, extend the evaluation of their specificity by comparison with other infectious diseases, and to test their performance in both pulmonary and extrapulmonary TB.

METHODS. Support vector machine learning, combined with feature selection, was applied to new and previously published blood transcriptional profiles in order to identify the minimal TB‑specific transcriptional signature shared by multiple patient cohorts including pulmonary and extrapulmonary TB, and individuals with and without HIV-1 coinfection.

RESULTS. We identified and validated elevated blood basic leucine zipper transcription factor 2 (BATF2) transcript levels as a single sensitive biomarker that discriminated active pulmonary and extrapulmonary TB from healthy individuals, with receiver operating characteristic (ROC) area under the curve (AUC) scores of 0.93 to 0.99 in multiple cohorts of HIV-1–negative individuals, and 0.85 in HIV-1–infected individuals. In addition, we identified and validated a potentially novel 4-gene signature comprising CD177, haptoglobin, immunoglobin J chain, and galectin 10 that discriminated active pulmonary and extrapulmonary TB from other febrile infections, giving ROC AUCs of 0.94 to 1.

CONCLUSIONS. Elevated blood BATF2 transcript levels provide a sensitive biomarker that discriminates active TB from healthy individuals, and a potentially novel 4-gene transcriptional signature differentiates between active TB and other infectious diseases in individuals presenting with fever.

FUNDING. MRC, Wellcome Trust, Rosetrees Trust, British Lung Foundation, NIHR.

Authors

Jennifer K Roe, Niclas Thomas, Eliza Gil, Katharine Best, Evdokia Tsaliki, Stephen Morris‑Jones, Sian Stafford, Nandi Simpson, Karolina D Witt, Benjamin Chain, Robert F Miller, Adrian Martineau, Mahdad Noursadeghi

×

Figure 11

Derivation of a single risk score from multiparametric classification of active tuberculosis (TB).

Options: View larger image (or click on image) Download as PowerPoint
Derivation of a single risk score from multiparametric classification of...
(A) Transformation of the distance of each of the test cases of active TB (AdjuVIT cohort, n = 23) and other infectious diseases (Fever cohort, n = 35) from the SVM separating hyperplane derived from the training half using CD177/HP/IGJ/CLC transcript data, to give a case-by-case probability of TB. (B) Receiver operating characteristic (ROC) analyses of support vector machine (SVM) discrimination of AdjuVIT active TB from pooled AdjuVIT after recovery and Fever cohort patients using expression levels of the 5 genes indicated by training half of the data and then testing on the second half of the data independently of the original derivation of the gene signature (Figure 7). ROC AUCs are shown in parentheses for each test. (C) Transformation of the distance of each test case in B from the SVM separating hyperplane derived from the training half, using all 5 genes indicated, to give a case-by-case probability of TB.

Copyright © 2025 American Society for Clinical Investigation
ISSN 2379-3708

Sign up for email alerts