Abstract | OBJECTIVE: METHODS: Serum was obtained from 26 active pulmonary TB patients [14 early TB (E-TB), and 12 chronic refractory TB (CR-TB)] and 15 healthy tuberculin reactors (HTRs). The monocytes and peripheral blood mononuclear cells (PBMCs) were separated and stimulated with purified protein derivatives ( PPD) or the 30-kDa antigen of Mycobacterium tuberculosis. Pleural exudates were isolated from 25 patients with TBP and 24 non- TBP patients [ malignancy and congestive heart failure (CHF)]. The MCP-1 levels were measured by enzyme-linked immunosorbent assay (ELISA). RESULTS: In sera, the MCP-1 levels of TB patients were similar to those of HTRs. For monocytes, CR-TB patients spontaneously expressed more MCP-1, compared with HTRs and E-TB patients. In addition, MCP-1 production of PPD- or 30-kDa antigen-stimulated monocytes was significantly elevated in CR-TB patients than that from E-TB. Interestingly, the E-TB patients had significantly depressed MCP-1 production by PBMCs in response to PPD or 30-kDa, compared with HTRs and CR-TB patients. In pleural effusions, MCP-1 levels were significantly higher in patients with TBP than in patients with CHF, but lower than in malignant effusions. CONCLUSIONS: The data suggest that MCP-1 production is not uniquely elevated systemically in TB patients, although MCP-1 production might be elevated by monocytes in the chronic phase of TB or with a local pleural infection.
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Authors | J-S Lee, C-H Song, J-H Lim, K-S Lee, H-J Kim, J-K Park, T-H Paik, S-S Jung, E-K Jo |
Journal | Inflammation research : official journal of the European Histamine Research Society ... [et al.]
(Inflamm Res)
Vol. 52
Issue 7
Pg. 297-304
(Jun 2003)
ISSN: 1023-3830 [Print] Switzerland |
PMID | 12861395
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antigens, Bacterial
- Chemokine CCL2
- Tuberculin
- Tumor Necrosis Factor-alpha
- Interferon-gamma
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Topics |
- Adult
- Antigens, Bacterial
(immunology)
- Chemokine CCL2
(biosynthesis)
- Exudates and Transudates
(immunology)
- Female
- Humans
- Interferon-gamma
(biosynthesis)
- Male
- Monocytes
(metabolism)
- Mycobacterium tuberculosis
(immunology)
- Neutrophils
(metabolism)
- Pleura
(immunology)
- Tuberculin
(metabolism)
- Tuberculosis, Pleural
(metabolism)
- Tuberculosis, Pulmonary
(metabolism)
- Tumor Necrosis Factor-alpha
(biosynthesis)
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