Abstract

Background: It is known that natural killer (NK) cell activity in the lung of smokers (SM) is lower than in non-smokers (NS). However, little is known about the underlying mechanisms. Objective: The purpose of this work was to investigate the mechanisms of the inhibition of NK cell activity by alveolar macrophages (AM) in SM. Methods: Lung effector cells and AM were obtained using bronchoalveolar lavage. The NK cell activity was assayed by <sup>51</sup>Cr release method after incubation of 4 and 24 h, using K562 as target cell. AM were added at a concentration of 25% to effector cells. Results: Following 24-hour culture, NK cell activity significantly increased in the NS but not in the SM. Lung NK cell activity was significantly augmented by interleukin-2 in the NS but not in the SM. Addition of AM to the NK cell preparation from SM exerted a significantly greater suppressive effect on autologous blood NK cell activity than in the NS. Indomethacin, catalase or thiourea did not prevent AM-mediated suppression of NK cell activity, in contrast to superoxide dismutase. Conclusions: These results suggest that the suppression of NK cell activity by AM in SM may be caused by O<sup>–</sup><sub>2</sub> release rather than by prostaglandins, H<sub>2</sub>O<sub>2</sub> or OH release from AM.

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