Alteration of pulmonary immunity to Listeria monocytogenes by diesel exhaust particles (DEPs). II. Effects of DEPs on T-cell-mediated immune responses in rats
Autor: | Rosana Schafer, Joseph K. H. Ma, Xue-Jun Yin, Jane Y. C. Ma, David N. Weissman, Paul D. Siegel, James M. Antonini, Jenny R. Roberts |
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Rok vydání: | 2003 |
Předmět: |
Male
T-Lymphocytes Health Toxicology and Mutagenesis medicine.medical_treatment Lymphocyte T cell Receptor expression Down-Regulation Biology Listeria infection Microbiology Immune system medicine Animals Listeriosis Lung Vehicle Emissions Air Pollutants Immunity Cellular Inhalation Exposure Public Health Environmental and Occupational Health medicine.disease biology.organism_classification Listeria monocytogenes Rats Cytokine medicine.anatomical_structure Listeria Cytokines Tumor necrosis factor alpha Research Article |
Zdroj: | Environmental Health Perspectives |
ISSN: | 1552-9924 0091-6765 |
DOI: | 10.1289/ehp.5709 |
Popis: | Previously, we showed that diesel exhaust particles (DEPs) suppressed pulmonary clearance of Listeria monocytogenes (Listeria) and inhibited the phagocytosis of alveolar macrophages and their response to Listeria in the secretion of interleukin (IL)-1 beta, tumor necrosis factor alpha, and IL-12. In this report we examined the effects of DEPs and/or Listeria on T-cell development and secretion of IL-2, IL-6, and interferon (IFN)-gamma. We exposed Brown Norway rats to clean air or DEPs at 50 or 100 mg/m3 for 4 hr by nose-only inhalation and inoculated with 100,000 Listeria. Lymphocytes in the lung-draining lymph nodes were isolated at 3 and 7 days postexposure, analyzed for CD4+ and CD8+ cells, and measured for cytokine production in response to concanavalin A or heat-killed L. monocytogenes. Listeria infection induced lymphocyte production of IL-6. At 7 days postinfection, lymphocytes from Listeria-infected rats showed significant increases in CD4+ and CD8+ cell counts and the CD8+/CD4+ ratio and exhibited increased production of IFN-gamma and IL-2 receptor expression compared with the noninfected control. These results suggest an immune response that involves the action of IL-6 on T-cell activation, yielding Listeria-specific CD8+ cells. DEP exposure alone enhanced lymphocyte production of both IL-2 and IL-6 but inhibited lymphocyte secretion of IFN-gamma. In rats exposed to 100 mg/m3 DEPs and Listeria, a 10-fold increase occurred in pulmonary bacterial count at 3 days postinfection when compared with the Listeria-only exposure group. The isolated lymphocytes showed a significant increase in the CD4+ and CD8+ cell counts and the CD8+/CD4+ ratio and exhibited increased IL-2 responsiveness and increased capacity in the secretion of IL-2, IL-6, and IFN-gamma. This T-cell immune response was sufficient to allow the Brown Norway rats to clear the bacteria at 7 days postinfection and overcome the down-regulation of the innate immunity by the acute DEP exposure. |
Databáze: | OpenAIRE |
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