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Open Access Highly Accessed Research article

Immune responses in the lungs of patients with tuberculous pleural effusion without pulmonary tuberculosis

Diana Qama12, Won-Il Choi1* and Kun Young Kwon3

Author Affiliations

1 Department of Internal Medicine, Dongsan Hospital, Keimyung University School of Medicine, Dalseong-ro 56, Jung-gu, Daegu, 700-712, Republic of Korea

2 Regional Hospital, Berat, Albania

3 Department of Pathology, Dongsan Hospital, Keimyung University School of Medicine, Dalseong-ro 56, Jung-gu, Daegu, 700-712, Republic of Korea

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BMC Immunology 2012, 13:45  doi:10.1186/1471-2172-13-45

Published: 13 August 2012

Abstract

Background

Tuberculous pleural effusion (TPE) is one of the most common forms of extrapulmonary tuberculosis. Because most studies of TPE focused on the pleural space, little information regarding lung parenchyma is available. We therefore aimed to investigate immune responses in the lung parenchyma of TPE patients without pulmonary tuberculosis.

Methods

Patients with any evidence of pulmonary tuberculosis, either from radiologic or bacteriologic evaluation, were excluded. Bronchoalveolar lavage fluid (BALF) was collected from 10 newly diagnosed, untreated, HIV-negative TPE patients and 10 healthy controls. We analyzed T-lymphocyte subpopulations and measured 10 cytokines in BALF. Cytokine levels in BALF were standardised using urea.

Results

The concentrations of interferon-γ (IFN-γ), tumor necrosis factor-α (TNF-α), vascular endothelial growth factor (VEGF), and the CD4+/CD8+ ratio of T-lymphocytes were significantly higher in TPE patients without pulmonary tuberculosis than in the controls. Of the cytokines measured in BALF, VEGF showed the highest concentration. No difference was observed in T-helper type 2 cytokines between the 2 groups.

Conclusion

There were significant immune responses and increases in IFN-γ, TNF-α, and VEGF in the lung parenchyma of TPE patients without pulmonary tuberculosis. This result suggests that TPE may induce a significant immune response in lung parenchyma.

Keywords:
Interferon-γ; Tuberculosis; Tumor necrosis factor-α; Vascular endothelial growth factor