Hm. Yang et al., Diesel exhaust particles suppress macrophage function and slow the pulmonary clearance of Listeria monocytogenes in rats, ENVIR H PER, 109(5), 2001, pp. 515-521
In this study, we tested the hypothesis that exposure to diesel exhaust par
ticles (DEP) may increase susceptibility of the host to pulmonary infection
. Male Sprague-Dawley rats received a single dose of DEP (5 mg/kg), carbon
black (CB, 5 mg/kg), or saline intratracheally. Three days later, the rats
were inoculated intratracheally with similar to5,000 Listeria monocytogenes
and sacrificed at 3, 5, and 7 days postinfection, and we determined the nu
mber of viable Listeria in the left lobe of lungs. The remaining lungs unde
rwent bronchoalveolar lavage (BAL) and the retrieved BAL cells were identif
ied and counted. Luminol-dependent chemiluminescence, a measure of reactive
oxygen species (ROS) formation, generated by BAL cells was monitored and t
he levels of nitric oxide and tumor necrosis factor (TNF)-alpha produced by
macrophages in culture were determined. At 7 days postinfection, we excise
d the lung-draining lymph nodes and phenotyped the lymphocyte subpopulation
s. Exposure of rats to DEP, but not to CB, decreased the clearance of Liste
ria from the lungs. Listeria-induced generation of luminol-dependent chemil
uminescence by pulmonary phagocytes decreased by exposure to DEP but not CB
. Similarly, Listeria-induced production of NO by alveolar macrophages was
negated at 3, 5, and 7 days after inoculation in DEP-exposed rats. In contr
ast, CB exposure had no effect on Listeria-induced NO production at 3 days
after infection and had a substantially smaller effect than DEP at later da
ys. Exposure to DEP or CB resulted in enlarged lung-draining lymph nodes an
d increased the number and percentage of CD4(+) and CD8(+) T cells. These r
esults showed that exposure to DEP decreased the ability of macrophages to
produce antimicrobial oxidants in response to Listeria, which may play a ro
le in the increased susceptibility of rats to pulmonary infection. This DEP
-induced suppression is caused partially by chemicals adsorbed onto the car
bon core of DEP, because impaired macrophage function and decreased Listeri
a clearance were not observed following exposure to CB.