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Updated: Jan 30, 2026

A Tuberculosis Molecular Bacterial Load Assay TB-MBLA
Published on: April 30, 2020
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.
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.
Background:
Clinical application of the CD8 response as measured by the newer interferon gamma release assay, QuantiFERON-TB Gold-Plus (QFT-Plus), remains to be investigated.
Method:
We performed this prospective study and recruited active TB patients, contacts with latent tuberculosis infection (LTBI) and contacts without LTBI in two centres in northern Taiwan in 2017. Subjects were tested with both QuantiFERON-TB Gold In-Tube (QFT-GIT) and QFT-Plus. LTBI was defined by positive result by QFT-GIT and exclusion of active TB.
Results:
A total of 336 participants (118 uninfected contacts, 105 LTBI, 113 active TB) were included. The concordance rate of QFT-GIT and QFT-Plus was high (n = 300, 89.3%). The kappa value was 0.811 among contacts and 0.708 among active TB. While TB1 and TB2 quantitative responses were not different between active TB and LTBI (TB1: 1.74 ± 2.73 IU/ml vs. 2.03 ± 2.28 IU/ml, p = 0.403; TB2: 2.21 ± 3.09 IU/ml vs. 2.15 ± 2.40 IU/ml, p = 0.867), CD8 response was higher in active TB than LTBI (0.47 ± 1.53 IU/ml vs. -0.06 ± 1.47 IU/ml, p = 0.011). Culture-confirmed TB had a higher CD8 response compared with LTBI (0.63 ± 1.74 IU/ml vs. -0.05 ± 1.47 IU/ml, p = 0.004).
Conclusions:
This study demonstrated specific CD8 responses among uninfected contacts, LTBI as well as active TB.
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