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Updated: Aug 8, 2026

Impression Cytology of the Lid Wiper Area
Published on: August 9, 2016
Cytokine content in pleural effusion. Comparison between tuberculous and carcinomatous pleurisy
K Shimokata1, H Saka, T Murate
1First Department of Medicine, Nagoya University School of Medicine, Japan.
Insights
Tuberculous pleurisy fluid shows elevated levels of interleukin-2 (IL-2), interferon-gamma (IFN-gamma), and adenosine deaminase (ADA). These markers suggest active T lymphocyte involvement in local cellular immunity against tuberculosis.
Area of Science:
- Immunology
- Infectious Diseases
- Pulmonology
Background:
- Tuberculous pleurisy serves as a model for studying local cellular immunity.
- Pleural effusions in tuberculous pleurisy are expected to contain various cytokines due to immune cell accumulation.
Purpose of the Study:
- To investigate the levels of interleukin-1 (IL-1), interleukin-2 (IL-2), and interferon-gamma (IFN-gamma) in tuberculous pleural fluid.
- To compare these cytokine levels and adenosine deaminase (ADA) levels with those found in malignant pleural effusions.
Main Methods:
- Analysis of pleural fluid from 20 patients with tuberculous pleurisy and 20 with malignant pleurisy.
- Measurement of IL-1, IL-2, IFN-gamma, and ADA levels in both groups.
Main Results:
- Tuberculous pleural fluid exhibited significantly higher levels of IL-2, IFN-gamma, and ADA compared to malignant pleural fluid.
- IL-1 levels were also higher in tuberculous effusions, though the difference was less pronounced.
- Elevated levels of IL-2, IFN-gamma, and ADA were dominant markers distinguishing tuberculous from malignant pleurisy.
Conclusions:
- Activated T lymphocytes in tuberculous pleural fluid contribute to lymphokine production at the site of infection.
- These lymphokines play a crucial role in mediating local cellular immunity against tuberculosis.
- Elevated ADA levels can serve as a valuable indicator for diagnosing tuberculous pleurisy.
Abstract:
Tuberculous pleurisy is a good model for resolution of local cellular immunity. It would be expected that tuberculous pleural fluid contains a variety of immunologically important cytokines because of the accumulation of immunocompetent cells in the pleural cavity. We studied interleukin 1 (IL-1), interleukin 2 (IL-2), and interferon gamma (IFN-gamma) levels in pleural fluid of 20 patients with tuberculous pleurisy and compared them with those in pleural fluid of 20 patients with malignant pleurisy. We also evaluated adenosine deaminase (ADA) levels in both effusions. Tuberculous pleural fluid had higher levels of IL-1, IL-2, IFN-gamma, and ADA than malignant pleural fluid. Although the difference of IL-1 level between tuberculous and malignant pleural fluid was modest, that of IL-2, IFN-gamma, and ADA was dominant. These findings suggest that activated T lymphocytes in tuberculous pleural fluid concern the production of lymphokines at the morbid site and they effectively exert local cellular immunity through the action of such lymphokines.
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