Abstract

Natural killer (NK) cell activity of freshly isolated peripheral blood mononuclear cells (MNC) or cells stimulated for 72h with 10μg/ml of a sonicate antigen of Mycobacterium tuberculosis H37Rv were studied in healthy responder and non-responder controls, as detected by lymphocyte proliferation with specific antigen, and in patients with pulmonary tuberculosis. K-652 cells were used as targets in a 4 h 51Cr release assay. MNC from patients exhibited a significant decrease in NK function as compared with responder controls (p<0.02). NK activity in responder individuals was highest 72 h after incubation with antigen. Non-stimulated cells were not cytotoxic. MNC from healthy responder and non-responder subjects incubated for 72 h with antigen yielded a significant increase in the percentage NK cytotoxicity at all effector/target ratios studied (p<0.01) as well as in the number of lytic units per culture (p<0.004). However, this increase was higher in responder individuals as compared to non-responder subjects (p=0.02). The response to antigen was not significant in the group of patients although a net increase was also observed in the whole group. Only 4 of 9 patients exhibited significant increased responses after antigenic stimulation, 3 showed moderate responses, 1 did not respond and in a further patient a decrease was observed. The decreased NK activity could be secondary to abnormalities in the production of lymphokines by tuberculous patients. Although the role of non-specific cytotoxic cells in tuberculosis is unknown, their alterations could contribute to the pathogenesis of the disease.

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