Abstract
The effects of ambient levels of NO2 on murine splenic T‐lymphocyte subpopulations and natural killer cells were investigated. AKR/cum and C57BL/6) mice were exposed, in inhalation chambers, to 0.25 ppm NO2 for 7 wk and 0.35 ppm NO3 for 12 wk, respectively. Monoclonal antibody technology was used in conjunction with fluorescence‐activated cell sorter (FACS) analysis to detect quantitative changes in total T‐lymphocytes (Thy‐1.2‐positive), mature T‐lymphocytes (Lyt‐1‐positive), T‐helperlin‐ducer lymphocytes (L3T4‐positive), T‐cytotoxic/suppressor lymphocytes (Lyt‐2‐positive), and natural killer cells (asialo GM1‐positive). Percentages of all T‐lymphocyte subpopulations tested and natural killer cells were lower in spleens of mice exposed to NO2 compared to filtered‐air controls. This is the first report providing evidence linking alterations in T‐lymphocyte subpopulations and natural killer cells to NO2 exposure at ambient levels. Changes in T‐lymphocyte subpopulations detected by FACS and correlated to impaired immune function may provide an extremely sensitive means of demonstrating NO2‐induced changes in the immune system.