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Updated: Jan 2, 2026

Phenotypic and Functional Analysis of Activated Regulatory T Cells Isolated from Chronic Lymphocytic Choriomeningitis Virus-infected Mice
Published on: June 22, 2016
Insights in tuberculosis immunology: Role of NKT and T regulatory cells
Pooja Pandey1, Anuj Kumar Bhatnagar2, Anant Mohan3
1Department of Microbiology, All India Institute of Medical Sciences, New Delhi, India.
Background:
Tuberculosis (TB) control is challenging due to poor drug compliance and emerging resistance. The need of the hour is to determine the prediction of disease cure and relapse. Patients' immune response is crucial to the disease outcome. This study was designed to study the immune profile of TB patients during treatment and cure.
Methods:
The cross-sectional study included newly diagnosed pulmonary TB patients and healthy controls. Levels of serum cytokines/chemokines (Th1/Th2/Th17) were measured by BD cytometric bead array. The cell surface markers assessed in the study were CD3, CD4, CD8, CD16, CD56, and BD human regulatory T cell cocktail (CD4/CD25/CD127).
Results:
Data analysis observed statistically significant differences in CD3dim/CD56 + natural killer T (NKT) among TB patients with significantly low levels in healthy controls and after treatment completion (P < 0.0001). The analysis also revealed a high percentage of CD3dim/CD56 + NKT in fast responders. The percentage of T regulatory was found to be high in patients when compared with healthy controls; the values were statistically significant (0.0002). Interleukin-6 was significantly associated with the disease (P < 0.0485).
Discussion:
A comprehensive understanding of role of CD3dim/CD56+ NKT in antimycobacterial immunity may enable new possibilities for NK cell-based prophylactic and/or therapeutic strategies against TB.
Insights
This study highlights the role of natural killer T (NKT) cells in tuberculosis (TB) immunity. Higher NKT cell levels in TB patients may indicate faster treatment response and potential for new therapeutic strategies.
Area of Science:
- Immunology
- Infectious Diseases
- Cell Biology
Background:
- Tuberculosis (TB) control faces challenges from poor drug compliance and drug resistance.
- Predicting disease cure and relapse is critical for effective TB management.
- Patient immune response significantly influences TB disease outcomes.
Purpose of the Study:
- To investigate the immune profile of tuberculosis patients during treatment and cure.
- To identify immune markers associated with disease progression and treatment response.
- To explore the role of specific immune cells and cytokines in tuberculosis.
Main Methods:
- Cross-sectional study design involving newly diagnosed pulmonary TB patients and healthy controls.
- Measurement of serum cytokines/chemokines (Th1/Th2/Th17) using BD cytometric bead array.
- Assessment of cell surface markers including CD3, CD4, CD8, CD16, CD56, and regulatory T cells (CD4/CD25/CD127).
Main Results:
- Statistically significant differences observed in CD3dim/CD56+ natural killer T (NKT) cells between TB patients and healthy controls, with lower levels post-treatment (P < 0.0001).
- A higher percentage of CD3dim/CD56+ NKT cells was found in fast responders.
- Elevated levels of T regulatory cells and Interleukin-6 were significantly associated with the disease in TB patients (P = 0.0002 and P < 0.0485, respectively).
Conclusions:
- CD3dim/CD56+ NKT cells play a crucial role in antimycobacterial immunity.
- Understanding NKT cell function may lead to novel NK cell-based prophylactic and therapeutic strategies for TB.
- Immune profiling of TB patients offers insights into disease dynamics and potential treatment targets.
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