The Adjuvant Effect of Ambient Particulate Matter Is Closely Reflected by the Particulate Oxidant Potential

被引:190
作者
Li, Ning [1 ]
Wang, Meiying [1 ,2 ]
Bramble, Lori A. [3 ]
Schmitz, Debra A. [2 ]
Schauer, James J. [4 ]
Sioutas, Constantinos [2 ,5 ]
Harkema, Jack R. [2 ,3 ]
Nel, Andre E. [1 ,2 ]
机构
[1] Univ Calif Los Angeles, Dept Med, Div NanoMed, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, So Calif Particle Ctr, Los Angeles, CA 90095 USA
[3] Michigan State Univ, Coll Vet Med, Dept Pathobiol & Diagnost Invest, E Lansing, MI 48824 USA
[4] Univ Wisconsin, Dept Civil & Environm Engn, Madison, WI 53706 USA
[5] Univ So Calif, Dept Civil & Environm Engn, Los Angeles, CA USA
关键词
adjuvant; allergic inflammation; allergic sensitization; ambient ultrafine particles; asthma; oxidant potential; oxidative stress; redox-active organic chemicals; T(H)2 immune response; DIESEL EXHAUST PARTICLES; POLYCYCLIC AROMATIC-HYDROCARBON; SYSTEMIC IMMUNE-RESPONSES; OXIDATIVE STRESS; AIRWAY INFLAMMATION; ULTRAFINE PARTICLES; EPITHELIAL-CELLS; MITE ALLERGEN; EX-VIVO; MICE;
D O I
10.1289/ehp.0800319
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
BACKGROUND: It has been demonstrated that ambient particulate matter (PM) can act as an adjuvant for allergic sensitization. Redox-active organic chemicals on the particle surface play an important role in PM adverse health effects and may determine the adjuvant effect of different particle types according to their potential to perturb redox equilibrium in the immune system. OBJECTIVES: We determined whether the adjuvant effect of ambient fine particles versus ultrafine particles (UFPs) is correlated to their prooxidant potential. METHODS: We have established an intranasal sensitization model that uses ambient PM as a potential adjuvant for sensitization to ovalbumin (OVA), which enhances the capacity for secondary OVA challenge to induce allergic airway inflammation. RESULTS: UFPs with a greater polycyclic aromatic hydrocarbon (PAH) content and higher oxidant potential enhanced OVA sensitization more readily than did fine particles. This manifests as enhanced allergic inflammation upon secondary OVA challenge, leading to eosinophilic inflammation and mucoid hyperplasia starting at the nasal turbinates all the way down to the small pulmonary airways. The thiol antioxidant N-acetyl cysteine was able to suppress some of these sensitization events. CONCLUSIONS: The adjuvant effects of ambient UFP is determined by their oxidant potential, which likely plays a role in changing the redox equilibrium in the mucosal immune system.
引用
收藏
页码:1116 / 1123
页数:8
相关论文
共 56 条
[1]   Ambient particulate pollutants in the ultrafine range promote early atherosclerosis and systemic oxidative stress [J].
Araujo, Jesus A. ;
Barajas, Berenice ;
Kleinman, Michael ;
Wang, Xuping ;
Bennett, Brian J. ;
Gong, Ke Wei ;
Navab, Mohamad ;
Harkema, Jack ;
Sioutas, Constantinos ;
Lusis, Aldons J. ;
Nel, Andre E. .
CIRCULATION RESEARCH, 2008, 102 (05) :589-596
[2]   Health effects of air pollution [J].
Bernstein, JA ;
Alexis, N ;
Barnes, C ;
Bernstein, IL ;
Bernstein, JA ;
Nel, A ;
Peden, D ;
Diaz-Sanchez, D ;
Tarlo, SM ;
Williams, PB .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2004, 114 (05) :1116-1123
[3]   Combustion-derived nanoparticles:: Mechanisms of pulmonary toxicity [J].
BeruBe, Kelly ;
Balharry, Dominique ;
Sexton, Keith ;
Koshy, Lata ;
Jones, Tim .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2007, 34 (10) :1044-1050
[4]   Organic compounds from diesel exhaust particles elicit a proinflammatory response in human airway epithelial cells and induce cytochrome p450 1A1 expression [J].
Bonvallot, V ;
Baeza-Squiban, A ;
Baulig, A ;
Brulant, S ;
Boland, S ;
Muzeau, F ;
Barouki, R ;
Marano, F .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2001, 25 (04) :515-521
[5]   Pro-oxidative diesel exhaust particle chemicals inhibit LPS-induced dendritic cell responses involved in T-helper differentiation [J].
Chan, Ray Chun-Fai ;
Wang, Meiying ;
Li, Ning ;
Yanagawa, Yoshiki ;
Onoe, Kazunori ;
Lee, James J. ;
Nel, Andre E. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2006, 118 (02) :455-465
[6]   Redox activity of airborne particulate matter at different sites in the Los Angeles Basin [J].
Cho, AK ;
Sioutas, C ;
Miguel, AH ;
Kumagai, Y ;
Schmitz, DA ;
Singh, M ;
Eiguren-Fernandez, A ;
Froines, JR .
ENVIRONMENTAL RESEARCH, 2005, 99 (01) :40-47
[7]   Environmental risk factors and allergic bronchial asthma [J].
D'Amato, G ;
Liccardi, G ;
D'Amato, M ;
Holgate, S .
CLINICAL AND EXPERIMENTAL ALLERGY, 2005, 35 (09) :1113-1124
[8]   Ultrafine but not fine particulate matter causes airway inflammation and allergic airway sensitization to co-administered antigen in mice [J].
de Haar, C. ;
Hassing, I. ;
Bol, M. ;
Bleumink, R. ;
Pieters, R. .
CLINICAL AND EXPERIMENTAL ALLERGY, 2006, 36 (11) :1469-1479
[9]   Potential role of ultrafine particles in associations between airborne particle mass and cardiovascular health [J].
Delfino, RJ ;
Sioutas, C ;
Malik, S .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2005, 113 (08) :934-946
[10]   Role of free radicals in the toxicity of airborne fine particulate matter [J].
Dellinger, B ;
Pryor, WA ;
Cueto, R ;
Squadrito, GL ;
Hegde, V ;
Deutsch, WA .
CHEMICAL RESEARCH IN TOXICOLOGY, 2001, 14 (10) :1371-1377