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Effect of diesel exhaust particulate (DEP) on immune responses: contributions of particulate versus organic soluble components.

Authors
Siegel-PD; Saxena-RK; Saxena-QB; Ma-JKH; Ma-JYC; Yin-XJ; Castranova-V; Al-Humadi-N; Lewis-DM
Source
J Toxicol Environ Health, A 2004 Feb; 67(3):221-231
NIOSHTIC No.
20024289
Abstract
The effect of diesel exhaust particulate (DEP) exposure on innate, cellular and humoral pulmonary immunity was studied using high-dose, acute-exposure rat, mouse, and cell culture models. DEP consists of a complex mixture of petrochemical-derived organics adsorbed onto elemental carbon particles. DEP is a major component of particulate urban air pollution and a health concern in both urban and occupational environments. The alveolar macrophage is considered a key cellular component in pulmonary innate immunity. DEP and DEP organic extracts have been found to suppress alveolar macrophage function as demonstrated by reduced production of cytokines (interleukin-1 [IL-1], tumor necrosis factor- alpha [TNF- alpha]) and reactive oxygen species (ROS) in response to a variety of agents, including lipopolysaccharide (LPS), interferon- gamma (IFN- gamma), and bacteria. Fractionation of DEP organic extract suggests that this activity was predominately in polyaromatic-containing and more polar (resin) fractions. Organic-stripped DEP did not alter these innate pulmonary immune responses. DEP also depressed pulmonary clearance of Listeria monocytogenes and Bacillus Calmette-Guerin (BCG). The contribution of the organic component of DEP is less well defined with respect to acquired and humoral immunity. Indeed, both DEP and carbon black enhanced humoral immune responses (specific immunoglobulin [Ig] E and IgG) in an ovalbumin-sensitized rat model. It is concluded that both the particulate and adsorbed organics may contribute to DEP-mediated immune alterations.
Keywords
Diesel-emissions; Diesel-exhausts; Particulates; Pulmonary-system; Pulmonary-system-disorders; Aerosols; Animal-studies; Laboratory-animals; Petroleum-products; Occupational-exposure; Alveolar-cells
Contact
HELD, NIOSH, Morgantown, West Virginia 26505, USA
CODEN
JTEHD6
Publication Date
20040213
Document Type
Journal Article
Email Address
psiegel@cdc.gov
Fiscal Year
2004
NTIS Accession No.
NTIS Price
Issue of Publication
3
ISSN
0098-4108
NIOSH Division
HELD
Source Name
Journal of Toxicology and Environmental Health, Part A: Current Issues
State
WV
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