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Selective Harvesting of Marginating-pulmonary Leukocytes
Published on: March 11, 2016
Changes in immune status of circulating NK cells in patients with latent tuberculosis infection
Shuang Qin1, Ruiqi Chen2, Meihui Li3
1Department of Clinical Laboratory, Jinan People's Hospital Affiliated to Shandong First Medical University, China.
Insights
Latent tuberculosis infection (LTBI) impacts NK cell populations, with CD56bright NK cells playing a key role in immune balance. Specific NK cell markers can differentiate LTBI patients from healthy individuals.
Area of Science:
- Immunology
- Infectious Diseases
- Cell Biology
Background:
- Latent tuberculosis infection (LTBI) is a significant reservoir for tuberculosis (TB) transmission.
- Understanding the immune status of natural killer (NK) cells in LTBI is crucial for controlling the TB pandemic.
Purpose of the Study:
- To investigate the immune status and characteristics of NK cells in patients with latent tuberculosis infection (LTBI).
- To explore the potential of NK cell markers in differentiating LTBI from active pulmonary tuberculosis (APTB) and healthy controls (HCs).
Main Methods:
- Flow cytometry was used to detect NK cell markers in 21 LTBI patients, 25 APTB patients, and 25 HCs.
- Analysis included absolute counts of CD56bright and CD56dim NK cells, and frequencies of HLA-DR, granzyme B, granzyme A, perforin, and CXCR3 expressing NK cells.
Main Results:
- LTBI patients showed higher absolute numbers of CD56bright and CD56dim NK cells compared to APTB patients.
- A lower frequency of HLA-DR+ CD56bright NK cells was observed in LTBI patients versus HCs and APTB patients.
- LTBI patients exhibited elevated granzyme B but reduced granzyme A and perforin levels in CD56bright NK cells, along with lower frequencies of CXCR3+ NK cells.
Conclusions:
- Circulating CD56bright NK cells are vital for maintaining immune balance in LTBI patients.
- Elevated granzyme B+ CD56bright NK cells and reduced perforin+ CD56bright NK cells can effectively distinguish LTBI patients from healthy controls.
Introduction:
The presence of patients with latent tuberculosis infection (LTBI) has fueled the tuberculosis pandemic. We aimed to investigate the immune status of NK cells in LTBI patients.
Material And Methods:
Twenty-one LTBI patients, 25 active pulmonary tuberculosis (APTB) patients and 25 healthy controls (HCs) participated in our research. The markers of NK cells were detected by flow cytometry.
Results:
The absolute number of circulating CD56bright and CD56dim NK cells in LTBI patients was higher than that of APTB patients, but the frequency of HLA-DR+ CD56bright NK cells was significantly lower than that of HCs and APTB patients. Also, LTBI patients with CD56bright NK cells had intracellular levels of granzyme B that were as significantly elevated as those with APTB patients, but the levels of granzyme A and perforin were reduced. Meanwhile, the frequencies of CXCR3+ NK cells, CXCR3+ CD56bright and CXCR3+ CD56dim NK cells were significantly lower in LTBI patients.
Conclusions:
Circulating CD56bright NK cells exerted a significant role in maintaining immune balance in LTBI patients. An elevated frequency of granzyme B+ CD56bright NK cells and a reduced frequency of perforin+ CD56bright NK cells were effective in differentiating LTBI patients from HCs.
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