Literature DB >> 1472443

Reductions in lymphocyte subpopulations after repeated exposure to 1.5 ppm nitrogen dioxide.

T Sandström1, M C Ledin, L Thomasson, R Helleday, N Stjernberg.   

Abstract

In this investigation the effects of repeated exposure to 1.5 ppm NO2 on immune competent cells in bronchoalveolar lavage (BAL) fluid was studied. Special attention was focused on effects on lymphocyte subpopulations. Eight healthy subjects were exposed to 1.5 ppm NO2 every second day on six occasions. Bronchoalveolar lavage fluid was collected at least three weeks before the exposure series as reference and 24 hours after the last exposure. The results obtained were analysed using a non-parametric test for paired observations, with each subject as his own control. Significant reductions were found in the total number and percentage of T cytotoxic-suppressor cells in BAL fluid; this caused an increase in the ratio of T helper-inducer: cytotoxic-suppressor cells. The total number of natural killer cells in the BAL fluid was also reduced. The numbers of all other cell types were unchanged after exposure. No reduction of phagocytosis of opsonised yeast particles by alveolar macrophages in vitro was detected. It is concluded that repeated short term exposures to 1.5 ppm NO2, a moderate occupational concentration, induces significant effects on immune competent bronchoalveolar lymphocytes. This indicates that previous findings of changes in the lymphoid immune system induced by NO2 in animals may well be applicable to humans.

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Year:  1992        PMID: 1472443      PMCID: PMC1061215          DOI: 10.1136/oem.49.12.850

Source DB:  PubMed          Journal:  Br J Ind Med        ISSN: 0007-1072


  20 in total

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Review 3.  Toxicological data on NOx: an overview.

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7.  Inflammatory cell response in bronchoalveolar lavage fluid after nitrogen dioxide exposure of healthy subjects: a dose-response study.

Authors:  T Sandström; N Stjernberg; A Eklund; M C Ledin; L Bjermer; B Kolmodin-Hedman; K Lindström; L Rosenhall; T Angström
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Authors:  M W Frampton; J N Finkelstein; N J Roberts; A M Smeglin; P E Morrow; M J Utell
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10.  Time--dose response for nitrogen dioxide exposure in an infectivity model system.

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