| Abstract: |
Antibodies can direct tumor cell lysis by activating complement-mediated and cell-mediated cytoxicities (antibody-dependent cell-mediated cytotoxicity, ADCC). Clinical translation of these effects into successful cancer therapy has been slow. Choosing an appropriate animal model to test new therapeutic strategies is difficult because of species differences in immunological effector functions. In previous work, we found that an unmodified anti-ganglioside mouse IgG3 monoclonal antibody (mAb), 3F8, could successfully treat clinical tumors in humans and experimental tumors in rats but not experimental tumors in mice. We explored the reasons for this species difference by performing in vitro antibody-dependent cytotoxicity assays comparing the potency of polymorphonuclear neutrophils (PMN), natural killer (NK) cells and complement from the three species: mouse, rat and human. 3F8- dependent complement-mediated cytotoxicity produced more than 70% specific release when human and rat sera were used and only 20% with mouse serum. PMN- mediated ADCC was 35%-70% with human effectors, 25%-60% with rat and undetectable with mouse. Human eosinophils did not contribute to this ADCC. Cytotoxicity utilizing interleukin-2-activated NK cells was antibody- independent in all three species but the specific release was 60%-70% with human and rat NK cells and 10% with mouse NK cells. These data suggest that, for mouse IgG3, the rat may provide a more relevant rodent model than the mouse for testing the in vivo antitumor effects of monoclonal antibodies. |
| Keywords: |
controlled study; unclassified drug; human cell; nonhuman; animal cell; mouse; animals; mice; tumor cells, cultured; mice, inbred balb c; monoclonal antibody; antibodies, monoclonal; species specificity; neutrophil; immunoglobulin g; rat; natural killer cell; killer cells, natural; neutrophils; rats; immunostimulation; cancer cell destruction; monoclonal antibody 3f8; interleukin-2; complement dependent cytotoxicity; complement; cell mediated cytotoxicity; cancer immunology; eosinophil; eosinophils; chromium; dose-response relationship, immunologic; complement system proteins; antibody-dependent cell cytotoxicity; humans; human; priority journal; article; antibody-dependent cytotoxicity
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