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A decrease in PPD specific CD4 T cell CD38 and HLA-DR expression in pulmonary tuberculosis patients after 8 weeks of
Herry Priyanto1, Edmond Chua2, Paul Hutchinson3
1Department of Pulmonology and Respiratory Medicine, Faculty of Medicine, Syiah Kuala University, Banda Aceh, Indonesia.
Journal of Clinical Tuberculosis and Other Mycobacterial Diseases
|January 25, 2021
Summary
Standard tuberculosis (TB) treatment impacts the adaptive immune response. A decrease in CD38+HLA-DR+ Mycobacterium tuberculosis-specific CD4 T cells indicates successful TB treatment.
Area of Science:
- Immunology
- Infectious Diseases
- Public Health
Background:
- Tuberculosis (TB) poses a significant global health challenge, particularly in Indonesia.
- The adaptive immune response, mediated by CD4 T cells, is crucial for controlling Mycobacterium tuberculosis (MTB) infection.
Purpose of the Study:
- To investigate the early effects of standard TB therapy on CD4 T cells.
- To identify potential immune markers for assessing TB treatment efficacy.
Main Methods:
- Blood samples were collected from TB patients before and after 8 weeks of treatment.
- MTB-specific CD4 T cells were analyzed ex vivo using PPD stimulation.
- Flow cytometry was employed to measure intracellular cytokines and surface markers (CD38, HLA-DR).
Main Results:
- No significant difference was observed in the total number of PPD-specific CD4 T cells between pre-treatment and post-treatment groups.
- A significant decrease in the proportion of CD38+HLA-DR+ PPD-specific CD4 T cells was found in patients who became smear-negative after treatment.
- This reduction was not specific to Interferon gamma (IFNg), Interleukin-2 (IL-2), or Granulocyte Macrophage Colony Stimulating Factor (GM-CSF) producing cells.
Conclusions:
- Anti-TB treatment alters the adaptive immune response in a measurable way.
- The decrease in the CD38+HLA-DR+ PPD-specific CD4 T cell phenotype may serve as a valuable indicator of successful TB treatment.
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