LYSIS OF TUMOR-CELLS BY HUMAN-BLOOD MONOCYTES BY A MECHANISM INDEPENDENT OF ACTIVATION OF THE OXIDATIVE BURST

  • 1 January 1985
    • journal article
    • research article
    • Vol. 45  (5) , 2058-2064
Abstract
Tumorilytic human blood monocytes recognize and destroy neoplastic cells by a mechanism that is nonphagocytic and requires cell-to-cell contact. The mechanism of cytolysis subsequent to binding is controversial. Release of reactive O2 intermediates by activated rodent macrophages was suggested as an important mechanism for tumor cell lysis in some short-term cytotoxicity assays. Whether O2 intermediates are also responsible for mediating the lysis of adherent human tumor cells was examined in a long-term (72-h) tumoricidal assay. Human blood monocytes were incubated with medium, concanavalin A-stimulated lymphokine [macrophage-activating factor (MAF)], lipopolysaccharide endotoxin, or human recombinant .gamma. interferon for 24 h prior to the addition of [125I]iododeoxyuridine-labeled A375 melanoma cells. The following evidence indicated that monocyte mediated tumor cell lysis was independent of superoxide anion (O2-) and H2O2 production: although human blood monocytes incubated for 24 h with .gamma. interferon produced twice as much O2- as control or MAF-treated monocytes, .gamma. interferon did not activate monocyte tumoricidal activity unless combined with lipopoylsaccharide endotoxin, 0.2 ng/ml or more; incubating the monocytes with 10 nM phorbol myristate acetate for 0.5 h stimulated O2- production but no cytotoxicity; the cytolytic activity of MAF-treated monocytes was not decreased in the presence of catalase or superoxide dismutase; and finally, peripheral blood monocytes were isolated from 6 patients with chronic granulomatous disease, activated by MAF or lipopolysaccharide endotoxin and then assayed for tumoricidal activity. While these activated chronic granulomatous disease monocytes did not produce O2- or H2O2, tumor cell lysis was normal in all 6 patients. Hence, lysis of tumor cells in a 72-h assay is not dependent upon the generation of O2- and/or H2O2 and is intact in chronic granulomatous disease monocytes.