Airborne pollutants and the immune system

被引:27
作者
Albright, JF
Goldstein, RA
机构
关键词
D O I
10.1016/S0194-5998(96)70173-0
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
The effects of airborne pollutants on the immune system have been most widely studied in the respiratory tract, Entry may occur as a volatile gas (ozone, benzene), as liquid droplets (sulfuric acid, nitrogen dioxide), or as particulate matter (diesel exhaust, aromatic hydrocarbons), The subsequent interaction with the immune system may result in local and systemic responses, and studies have shown examples of disease occurring from both overactive immune responses and immunosuppression. For the most part, airborne pollutants (small molecular weight chemicals) have to be coupled with other substances (proteins or conjugates) before they can be recognized by the immune system and exert their effects. Fortunately, this encounter rarely causes immunologically mediated human disorders, The following briefly reviews some of the disorders that may occur, Immunologically nonspecific inflammation of the lung can occur after inhalation of ozone in anyone given sufficient dose and time of exposure, Immunologically specific cell-mediated (T lymphocyte) reactions appear to predominate in chronic beryllium disease, which results in a granulomatous form of lung disease, Beryllium alone does not appear to be antigenic but requires chemical linkage with a larger molecule, Mercury-induced autoimmune disease (immune system attacks self-antigens) affecting kidneys and lungs has been demonstrated in animal models (changes similar to those seen in people with Goodpasture's syndrome), Immunosuppression can be demonstrated after exposure to polycyclic aromatic hydrocarbons (2,3,7,8-tetrachlorodibenzo-p-dioxin). Hypersensitivity (or allergic) reactions can occur after exposure to toluene diisocyanate (occupational asthma). In summary, airborne pollutants may cause a wide spectrum of immunologically mediated disorders, There is clearly an underlying genetic basis for the susceptibility to immunologic disease resulting from exposure to pollutants, but knowledge in this area is rudimentary at present. Studies have been impeded by lack of appropriate in vitro models, as well as difficulties in identifying the biologically active substance.
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页码:232 / 238
页数:7
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共 35 条
  • [1] ALBRIGHT JF, 1992, TOXICOL IND HEALTH, V8, P215
  • [2] ATEN J, 1988, AM J PATHOL, V133, P127
  • [3] ANTIGENIC SPECIFICITIES OF GLOMERULAR-BOUND AUTOANTIBODIES IN MEMBRANOUS GLOMERULOPATHY INDUCED BY MERCURIC-CHLORIDE
    ATEN, J
    VENINGA, A
    BRUIJN, JA
    PRINS, FA
    DEHEER, E
    WEENING, JJ
    [J]. CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1992, 63 (01): : 89 - 102
  • [4] TRANSPORT-PROPERTIES OF OLIGOMERIC SUBUNIT STRUCTURES
    BERNAL, JMG
    DELATORRE, JG
    [J]. BIOPOLYMERS, 1981, 20 (01) : 129 - 139
  • [5] CYTOKINES IN METAL FUME FEVER
    BLANC, PD
    BOUSHEY, HA
    WONG, H
    WINTERMEYER, SF
    BERNSTEIN, MS
    [J]. AMERICAN REVIEW OF RESPIRATORY DISEASE, 1993, 147 (01): : 134 - 138
  • [6] BUCKLEY TL, 1994, J IMMUNOL, V153, P4169
  • [7] DEHART RL, 1992, MULTIPLE CHEM SENSIT, P35
  • [8] DIESEL EXHAUST PARTICLES INDUCE LOCAL IGE PRODUCTION IN-VIVO AND ALTER THE PATTERN OF IGE MESSENGER-RNA ISOFORMS
    DIAZSANCHEZ, D
    DOTSON, AR
    TAKENAKA, H
    SAXON, A
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (04) : 1417 - 1425
  • [9] MERCURIC CHLORIDE-INDUCED ANTI-GLOMERULAR BASEMENT-MEMBRANE ANTIBODIES IN RAT - GENETIC-CONTROL
    DRUET, E
    SAPIN, C
    GUNTHER, E
    FEINGOLD, N
    DRUET, P
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1977, 7 (06) : 348 - 351
  • [10] FINK JN, 1991, IMMUNOLOGICALLY MEDI, P399