CD8 response measured by QuantiFERON-TB Gold Plus and tuberculosis disease status

Meng-Rui Lee1, Chia-Hao Chang2, Lih-Yu Chang2

  • 1Department of Internal Medicine, National Taiwan University Hospital Hsin-Chu Branch, Hsin-Chu, Taiwan; Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan; Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei, Taiwan.

The Journal of Infection
|February 2, 2019
PubMed

Insights

The QuantiFERON-TB Gold-Plus (QFT-Plus) assay shows specific CD8 responses in active tuberculosis (TB) and latent TB infection (LTBI). This new interferon gamma release assay offers potential for improved TB diagnostics.

Area of Science:

  • Immunology
  • Infectious Diseases
  • Diagnostics

Background:

  • The clinical utility of the QuantiFERON-TB Gold-Plus (QFT-Plus) interferon gamma release assay, which measures CD8 response, requires further investigation.
  • Existing interferon gamma release assays primarily focus on CD4 responses, leaving the role of CD8 responses in tuberculosis diagnosis underexplored.

Purpose of the Study:

  • To evaluate the performance of the QFT-Plus assay in distinguishing between active tuberculosis (TB), latent tuberculosis infection (LTBI), and uninfected individuals.
  • To assess the concordance between QFT-Plus and the established QuantiFERON-TB Gold In-Tube (QFT-GIT) assay.
  • To investigate the specific CD8 T-cell responses measured by QFT-Plus in different TB infection states.

Main Methods:

  • A prospective study was conducted in Taiwan involving active TB patients, LTBI contacts, and uninfected contacts.
  • Participants were tested using both QFT-GIT and QFT-Plus assays.
  • LTBI was defined by a positive QFT-GIT result with the exclusion of active TB.

Main Results:

  • High concordance (89.3%) was observed between QFT-GIT and QFT-Plus assays.
  • While TB1 and TB2 responses did not differ significantly between active TB and LTBI groups, CD8 responses were significantly higher in active TB patients compared to LTBI individuals (p=0.011).
  • Culture-confirmed TB cases exhibited higher CD8 responses than LTBI cases (p=0.004).

Conclusions:

  • The QFT-Plus assay demonstrates specific CD8 T-cell responses that can differentiate between active TB, LTBI, and uninfected individuals.
  • The findings suggest that QFT-Plus has potential clinical applications in TB diagnosis, particularly by leveraging CD8 responses.
  • Further research is warranted to fully elucidate the clinical utility of QFT-Plus in various TB epidemiological settings.
Abstract

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