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Suppression of cell-mediated immune responses to Listeria infection by repeated exposure to diesel exhaust particles.

Authors
Yin-XJ; Dong-CC; Ma-JYC; Antonini-JM; Roberts-JR; Stanley-CF; Schafer-R; Ma-JKH
Source
Toxicol Sci 2004 Feb; 77(2):263-271
NIOSHTIC No.
20024356
Abstract
Diesel exhaust particles (DEP) have been shown to alter pulmonary immune responses to bacterial infection. Exposure of rats to 100 mg/m(3) DEP for 4 h was found to aggravate Listeria monocytogenes(Listeria) infection at 3 days postinfection, but the bacteria were largely cleared at 7 days postinfection due to the development of a strong T cell-mediated immunity. In the present study, we examined the effects of repeated DEP exposure at lower doses on pulmonary responses to bacterial infection. Brown Norway rats were exposed to DEP by inhalation at 20.62 +/- 1.31 mg/m 3 for 4 h/day for 5 days, followed by intratracheal inoculation with 100,000 Listeria at 2 h after the last DEP exposure. DEP-exposed rats showed a significant increase in lung bacterial load at both 3 and 7 days postinfection. The repeated DEP exposure was shown to suppress both the innate, orchestrated by alveolar macrophages (AM), and T cell-mediated responses to Listeria. DEP inhibited AM production of interleukin- (IL-) 1beta, tumor necrosis factor- (TNF-) alpha, and IL-12 but enhanced Listeria-induced AM production of IL-10, which has been shown to prolong the survival of intracellular pathogens such as Listeria. DEP exposure also suppressed the development of bacteria-specific lymphocytes from lung-draining lymph nodes, as indicated by the decreased numbers of T lymphocytes and their CD4(+) and CD8(+) subsets. Furthermore, the DEP exposure markedly inhibited the Listeria-induced lymphocyte secretion of IL-2 at day 7, IL-10 at days 3 and 7, and interferon- (IFN-) gamma at days 3 to 10 postinfection when compared to air-exposed controls. These results show a sustained pattern of downregulation of T cell-mediated immune responses by repeated low-dose DEP exposure, which is different from the results of a single high-dose exposure where the acute effect of DEP aggravated bacteria infection but triggered a strong T cell-mediated immunity.
Keywords
Diesel-exhausts; Particulates; Cardiopulmonary-system; Bacterial-infections; Animal-studies; Laboratory-animals; Lung-disorders; Pathogens; Lymphocytes; Immune-system-disorders; Immune-reaction; Immunology; Microorganisms
Contact
School of Pharmacy, West Virginia University, Morgantown, West Virginia 26506
CODEN
TOSCF2
Publication Date
20040201
Document Type
Journal Article
Email Address
jma@hsc.wvu.edu
Fiscal Year
2004
NTIS Accession No.
NTIS Price
Issue of Publication
2
ISSN
1096-6080
NIOSH Division
HELD
Source Name
Toxicological Sciences
State
WV
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